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1Academic Journal
Authors: Molochkov A.V., Kupriyanova A.G., Karzanov O.V., Setdikova G.R., Bolshakova E.A., Kornyushenko V.O., Molochkov V.A.
Contributors: 1
Source: Almanac of Clinical Medicine; Vol 53, No 3 (2025); 160-167 ; Альманах клинической медицины; Vol 53, No 3 (2025); 160-167 ; 2587-9294 ; 2072-0505
Subject Terms: pemphigus vulgaris, rituximab, toxic epidermal necrolysis, biological targeted therapy, вульгарная пузырчатка, ритуксимаб, токсический эпидермальный некролиз, генно-инженерная биологическая терапия
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Relation: https://almclinmed.ru/jour/article/view/17546/1752; https://almclinmed.ru/jour/article/downloadSuppFile/17546/160674; https://almclinmed.ru/jour/article/downloadSuppFile/17546/160697; https://almclinmed.ru/jour/article/downloadSuppFile/17546/160698; https://almclinmed.ru/jour/article/downloadSuppFile/17546/160699; https://almclinmed.ru/jour/article/downloadSuppFile/17546/160700; https://almclinmed.ru/jour/article/downloadSuppFile/17546/160701; https://almclinmed.ru/jour/article/downloadSuppFile/17546/160702; https://almclinmed.ru/jour/article/downloadSuppFile/17546/160703; https://almclinmed.ru/jour/article/downloadSuppFile/17546/160704; https://almclinmed.ru/jour/article/downloadSuppFile/17546/160705; https://almclinmed.ru/jour/article/downloadSuppFile/17546/160706; https://almclinmed.ru/jour/article/downloadSuppFile/17546/160707; https://almclinmed.ru/jour/article/downloadSuppFile/17546/160708; https://almclinmed.ru/jour/article/downloadSuppFile/17546/160709; https://almclinmed.ru/jour/article/downloadSuppFile/17546/160710; https://almclinmed.ru/jour/article/downloadSuppFile/17546/160711; https://almclinmed.ru/jour/article/downloadSuppFile/17546/160712; https://almclinmed.ru/jour/article/downloadSuppFile/17546/160713; https://almclinmed.ru/jour/article/downloadSuppFile/17546/160714; https://almclinmed.ru/jour/article/view/17546
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2Academic Journal
Authors: Maria A. Leonova, Nikolay N. Murashkin, Alexander I. Materikin, Roman V. Epishev, Dmitriy V. Fedorov, Leonid A. Opryatin, Roman A. Ivanov, Ekaterina S. Pavlova, М. А. Леонова, Н. Н. Мурашкин, А. И. Материкин, Р. В. Епишев, Д. В. Федоров, Л. А. Опрятин, Р. А. Иванов, Е. С. Павлова
Contributors: Not declared., Отсутствует.
Source: Current Pediatrics; Том 23, № 5 (2024); 370-375 ; Вопросы современной педиатрии; Том 23, № 5 (2024); 370-375 ; 1682-5535 ; 1682-5527
Subject Terms: устекинумаб, palmoplantar psoriasis, methotrexate, genetically engineered biologic therapy, ustekinumab, ладонно-подошвенный псориаз, метотрексат, генно-инженерная биологическая терапия
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Relation: https://vsp.spr-journal.ru/jour/article/view/3611/1405; Gunter NV, Yap BJM, Chua CLL, Yap WH. Combining Understanding of Immunological Mechanisms and Genetic Variants Toward Development of Personalized Medicine for Psoriasis Patients. Front Genet. 2019;10:395. doi: https://doi.org/10.3389/fgene.2019.00395; Мурашкин Н.Н., Круглова Л.С., Коваленко Ю.А. и др. Коморбидности псориаза в детском возрасте // Вопросы современной педиатрии. — 2020. — Т. 19. — № 6. — С. 460–467. — doi: https://doi.org/10.15690/vsp.v19i6.2149; Paller AS, Schenfeld J, Accortt NA, Kricorian G. A retrospective cohort study to evaluate the development of comorbidities, including psychiatric comorbidities, among a pediatric psoriasis population. Pediatr Dermatol. 2019;36(3):290–297. doi: https://doi.org/10.1111/pde.13772; Damiani G, Bragazzi NL, Karimkhani Aksut C, et al. The Global, Regional, and National Burden of Psoriasis: Results and Insights From the Global Burden of Disease 2019 Study. Front Med (Lausanne). 2021;8:743180. doi: https://doi.org/10.3389/fmed.2021.743180; Kang BY, O’Haver J, Andrews ID. Pediatric Psoriasis Comorbidities: Screening Recommendations for the Primary Care Provider. J Pediatr Health Care. 2021;35(3):337–350. doi: https://doi.org/10.1016/j.pedhc.2020.12.006; Branisteanu DE, Georgescu S, Serban IL, et al. Management of psoriasis in children (Review). Exp Ther Med. 2021;22(6):1429. doi: https://doi.org/10.3892/etm.2021.10864; Elvina M. Pediatric Psoriasis: Clinical Features and Course. Open Acc J Bio Sci. 2020;1(5):207–209. doi: https://doi.org/10.38125/OAJBS.000147; Montes de Oca Pedrosa A, Oakley A, Rogers J, Rangaitaha Epiha M. PASI vs PO-PASI: Patient-Oriented PASI (PO-PASI) is comparable to clinician score PASI. Australas J Dermatol. 2022;63(1):e67–e70. doi: https://doi.org/10.1111/ajd.13738; Torrelo A. The use of biologics for childhood psoriasis. J Eur Acad Dermatol Venereol. 2019;33(10):1816. doi: https://doi.org/10.1111/jdv.15855. PMID: 31617632; Иванов Р.А., Мурашкин Н.Н. Выживаемость биологической терапии у детей, страдающих псориазом: когортное исследование // Вопросы современной педиатрии. — 2021. — Т. 20. — № 5. — С. 451–458. — doi: https://doi.org/10.15690/vsp.v20i5.2323; Мурашкин Н.Н., Амбарчян Э.Т. Сравнительная оценка эффективности и безопасности ингибиторов TNFα и IL12/23 в терапии псориаза у детей // Педиатрическая фармакология. — 2018. — Т. 15. — № 6. — С. 455–463. — doi: https://doi.org/10.15690/pf.v15i6.1983; Мурашкин Н.Н., Амбарчян Э.Т., Епишев Р.В. и др. Эффективность и безопасность устекинумаба у детей с бляшечной, эритродермической и ладонно-подошвенной формами псориаза: ретроспективное когортное исследование // Вопросы современной педиатрии. — 2020. — Т. 19. — № 6. — С. 531–537. — doi: https://doi.org/10.15690/vsp.v19i6.2153; Chovatiya R, Silverberg JI. Pathophysiology of Atopic Dermatitis and Psoriasis: Implications for Management in Children. Children (Basel). 2019;6(10):108. doi: https://doi.org/10.3390/children6100108; Aggarwal S, Ghilardi N, Xie MH, et al. Interleukin-23 promotes a distinct CD4 T cell activation state characterized by the production 215 of interleukin-17. J Biol Chem. 2003;278(3):1910–1914. doi: https://doi.org/10.1074/jbc.M207577200; Lee E, Trepicchio WL, Oestreicher JL, et al. Increased expression of interleukin 23 p19 and p40 in lesional skin of patients with psoriasis vulgaris. J Exp Med. 2004;199(1):125–130. doi: https://doi.org/10.1084/jem.20030451; Sun HY, Phan K, Paller AS, Sebaratnam DF. Biologics for pediatric psoriasis: A systematic review and meta-analysis. Pediatr Dermatol. 2022;39(1):42–48. doi: https://doi.org/10.1111/pde.14870; Paller AS, Siegfried EC, Langley RG, et al. Long-Term Safety and Efficacy of Etanercept in Children and Adolescents with Plaque Psoriasis. J Am Acad Dermatol. 2016;74(2):280–287.e1–e3. doi: https://doi.org/10.1016/j.jaad.2015.09.056; Papp K, Thaçi D, Marcoux D, et al. Efficacy and Safety of Adalimumab Every Other Week versus Methotrexate Once Weekly in Children and Adolescents with Severe Chronic Plaque Psoriasis: a Randomised, Double-Blind, Phase 3 Trial. Lancet. 2017;390(10089):40–49. doi: https://doi.org/10.1016/S0140-6736(17)31189-3; Philipp S, Menter A, Nikkels AF, et al. Ustekinumab for the treatment of moderate-to-severe plaque psoriasis in pediatric patients (6 to < 12 years of age): efficacy, safety, pharmacokinetic, and biomarker results from the open-label CADMUS Jr study. Br J Dermatol. 2020;183(4):664–672. doi: https://doi.org/10.1111/bjd.19018; Magnolo N, Kingo K, Laquer V, et al. A phase III open-label, randomized multicenter study to evaluate efficacy and safety of secukinumab in pediatric patients with moderate to severe plaque psoriasis: 24-week results. J Am Acad Dermatol. 2022;86(1): 122–130. doi: https://doi.org/10.1016/j.jaad.2021.08.066
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3Academic Journal
Authors: O. N. Titova, V. A. Volchkov, N. A. Kuzubova, D. B. Sklyarova, О. Н. Титова, В. А. Волчков, Н. А. Кузубова, Д. Б. Склярова
Source: Meditsinskiy sovet = Medical Council; № 23 (2023); 128-132 ; Медицинский Совет; № 23 (2023); 128-132 ; 2658-5790 ; 2079-701X
Subject Terms: иммуноглобулин Е, genetically engineered biological therapy, benralizumab, dupilumab, personalized medicine, eosinophilic inflammation, immunoglobulin E, генно-инженерная биологическая терапия, бенрализумаб, дупилумаб, персонализированная медицина, эозинофильное воспаление
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Relation: https://www.med-sovet.pro/jour/article/view/8011/7102; Asher MI, García-Marcos L, Pearce NE, Strachan DP. Trends in worldwide asthma prevalence. Eur Respir J. 2020;56(6):2002094. https://doi.org/10.1183/13993003.02094-2020.; Chung KF, Wenzel SE, Brozek JL, Bush A, Castro M, Sterk PJ et al. International ERS/ATS guidelines on definition, evaluation and treatment of severe asthma. Eur Respir J. 2014;43(2):343–373. https://doi.org/10.1183/09031936.00202013.; Trevor J, Lugogo N, Carr W, Moore C, Soong W, Panettieri Jr RA et al. Severe asthma exacerbations in the United States: Incidence, characteristics, predictors, and effects of biologic treatments. Ann Allergy Asthma Immunology. 2021;127(5):579–587. https://doi.org/10.1016/j.anai.2021.07.010.; Pavord ID. Eosinophilic phenotypes of airway disease. Ann Am Thorac Soc. 2013;(10):143–149. https://doi.org/10.1513/Annal-sATS.201306-168AW.; Kaur R, Chupp GJ. Phenotypes and endotypes of adult asthma: moving toward precision medicine. J Allergy Clin Immunol. 2019;144(1):1–12. https://doi.org/10.1016/j.jaci.2019.05.031.; Ramírez-Jiménez F, Pavón-Romero GF, Velásquez-Rodríguez JM, López-Garza MI, Lazarini-Ruiz JF, Gutiérrez-Quiroz KV, Teran LM. Biologic Therapies for Asthma and Allergic Disease: Past, Present, and Future. Pharmaceuticals (Basel). 2023;16(2):270. https://doi.org/10.3390/ph16020270.; Kavanagh JE, Hearn AP, Jackson DJ. A pragmatic guide to choosing biologic therapies in severe asthma. Breathe (Sheff). 2021;17(4):210144. https://doi.org/10.1183/20734735.0144-2021.; Kavanagh JE, Hearn AP, Dhariwal J, d’Ancona G, Douiri A, Roxas C et al. Real-world effectiveness of benralizumab in severe eosinophilic asthma. Chest. 2021;159(2):496–506. https://doi.org/10.1016/j.chest.2020.08.2083.; Bleecker ER, FitzGerald JM, Chanez P, Papi A, Weinstein SF, Barker P et al. Efficacy and safety of benralizumab for patients with severe asthma uncontrolled with high-dosage inhaled corticosteroids and long-acting β 2-agonists (SIROCCO): a randomised, multicentre, placebo-controlled phase 3 trial. Lancet. 2016;388(10056):2115–2127. https://doi.org/10.1016/S0140-6736(16)31324-1.; FitzGerald JM, Bleecker ER, Nair P, Korn S, Ohta K, Lommatzsch M et al. Benralizumab, an anti-interleukin-5 receptor alpha monoclonal antibody, as add-on treatment for patients with severe, uncontrolled, eosinophilic asthma (CALIMA): a randomised, double-blind, placebo-controlled phase 3 trial. Lancet. 2016;388(10056):2128–2141. https://doi.org/10.1016/S01406736(16)31322-8.; Pham DN. Spontaneous resolution of atopic dermatitis incidental to participation in benralizumab clinical trial for severe, uncontrolled asthma: a case report. J Med Case Rep. 2021;15(1):103. https://doi.org/10.1186/s13256-021-02663-2.; Guttman-Yassky E, Bahadori L, Brooks L, Ckark L, Grindebacke H, Ho CN et al. Lack of effect of benralizumab on signs and symptoms of moderate-to-severe atopic dermatitis: Results from the phase 2 randomized, double-blind, placebo-controlled HILLIER trial. J Eur Acad Dermatol Venereol. 2023;37(10):e1211–e1214. https://doi.org/10.1111/jdv.19195.; Alenazi SD. Atopic dermatitis: a brief review of recent advances in its management. Dermatol Reports. 2023;15(3):9678. https://doi.org/10.4081/dr.2023.9678.; Salter B, Lacy P, Mukherjee M. Biologics in Asthma: A Molecular Perspective to Precision Medicine. Front Pharmacol. 2022;(12):793409. https://doi.org/10.3389/fphar.2021.793409.; Sardon-Prado O, Diaz-Garcia C, Corcuera-Elosegui P, Korta-Murua J, Valverde-Molina J, Sanchez-Solis M. Severe Asthma and Biological Therapies: Now and the Future. J Clin Med. 2023;12(18):5846. https://doi.org/10.3390/jcm12185846.; Rogers L, Jesenak M, Bjermer L, Hanania NA, Seys SF, Diamant Z. Biologics in severe asthma: A pragmatic approach for choosing the right treatment for the right patient. Respir Med. 2023;218:107414. https://doi.org/10.1016/j.rmed.2023.107414.; López-Viña A, Díaz Campos RM, Trisan Alonso A, Melero Moreno C. Uncontrolled severe T2 asthma: Which biological to choose? A biomarker-based approach. Front Allergy. 2022;(3):1007593. https://doi.org/10.3389/falgy.2022.1007593.
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4Academic Journal
Authors: G. N. Tarasenko, I. V. Patronov, Г. Н. Тарасенко, И. В. Патронов
Source: Meditsinskiy sovet = Medical Council; № 14 (2024); 78-81 ; Медицинский Совет; № 14 (2024); 78-81 ; 2658-5790 ; 2079-701X
Subject Terms: псориатический артрит, genetically engineered biological therapy, pustular psoriasis, psoriatic arthritis, генно-инженерная биологическая терапия, пустулезный псориаз
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Relation: https://www.med-sovet.pro/jour/article/view/8536/7517; Кубанова АА, Кубанов АА, Самцов АВ, Аравийских ЕР. Федеральные клинические рекомендации. Дерматовенерология 2015: Болезни кожи. Инфекции, передаваемые половым путем. 5-е изд., перераб. и доп. М.: Деловой экспресс; 2016. 768 c. Режим доступа: https://studfile.net/preview/6439905.; Тарасенко ГН, Паценко МБ, Алехнович АВ. Генно-инженерная биологическая терапия псориаза: перспективное направление в военномедицинской организации. Госпитальная медицина: наука и практика. 2018;(1):75–78. Режим доступа: https://www.elibrary.ru/saunpw.; Grän F, Kerstan A, Serfling E, Goebeler M, Muhammad K, Grän F et al. Current Developments in the Immunology of Psoriasis. Yale J Biol Med. 2020;93(1):97–110. Available at: https://pubmed.ncbi.nlm.nih.gov/32226340.; Сарсур ШХР, Руднева НС. Результаты сравнения эффективности применения адалимумаба и иксекизумаба в лечении псориаза. Госпитальная медицина: наука и практика: 2024;7(1):17–22. Режим доступа: https://www.3hospital.ru/media/newspapers/1_2024_сайт.pdf; Молочков ВА, Бадокин ВВ, Альбанова ВИ, Волнухин ВА. Псориаз и псориатический артрит. М.: Товарищество научных изданий КМК; 2007. 300 с.; Кубанова АА (ред.). Псориаз: клинические рекомендации. М.: ДЭКС-Пресс; 2008. 56 с.; Parisi R, Iskandar IYK, Kontopantelis E, Augustin M, Griffiths CEM, Ashcroft DM; Global Psoriasis Atlas. National, regional, and worldwide epidemiology of psoriasis: systematic analysis and modelling study. BMJ. 2020;369:m1590. https://doi.org/10.1136/bmj.m1590.; Голдсмит ЛА, Кац СИ, Джилкрест БА, Паллер ЭС, Леффель ДД, Вольф К (ред.). Дерматология Фицпатрика в клинической практике. М.: Издательство Панфилова: БИНОМ, Лаборатория знаний; 2012. Т., 1168 с.; Скрипкин ЮК (ред.). Кожные и венерические болезни. М.: ГЭОТАР-Медиа; 2012. 544 с. Режим доступа: http://www.studmedlib.ru/book/ISBN9785970419939.html.; Gianfredi V, Casu G, Bricchi L, Kacerik E, Rongioletti F, Signorelli C et al. Epidemiology of psoriasis in Italy: burden, cost, comorbidities and patients’ satisfaction. Acta Biomed. 2022;93(6):e2022332. https://doi.org/10.23750/abm.v93i6.13177.; Reich K, Griffiths C, Barker J, Chimenti S, Daudén E, Giannetti A et al. Recommendations for the long-term treatment of psoriasis with infliximab: a dermatology expert group consensus. Dermatology. 2008;217(3):268–275. https://doi.org/10.1159/000149970.; Augey F, Renaudier P, Nicolas JF. General pustular psoriasis: a French epidemiological survey. Eur J Dermatol. 2006;16(6):669–673. Available at: https://pubmed.ncbi.nlm.nih.gov/17229609.; Тарасенко ГН, Патронов ИВ. Клинический случай эффективного лечения вульгарного псориаза генно-инженерным биологическим препаратом у пациента с сердечной недостаточностью. Эффективная фармакотерапия. 2022;18(25):28–30. Режим доступа: https://umedp.ru/upload/iblock/7dd/effektivnaya_farmakoterapiya_dermatovenerologiya_i_dermatokosmetologiya_2_3_2022.pdf; Тарасенко ГН, Патронов ИВ. Поражение ногтей при псориазе и возможности терапии. Госпитальная медицина: наука и практика. 2022;5(4):10–12. Режим доступа: https://www.elibrary.ru/yaohia.; Тарасенко ГН, Паценко МБ, Патронов ИВ, Кузьмина ЮВ. Биологическая терапия как перспектива лечения тяжелых форм псориаза. Военномедицинский журнал. 2018;339(6):81–82. Режим доступа: https://www.elibrary.ru/xypoeh.; Тарасенко ГН, Белякин СА, Рыжман НН, Кузьмина ЮВ. Антицитокиновая терапия тяжелых форм псориаза в многопрофильном госпитале. Российский журнал кожных и венерических болезней. 2013;16(1):30–33. Режим доступа: https://rjsvd.com/1560-9588/article/view/36773/24568.; Weisenseel P, Prinz JC. Sequential use of inliximab and etanercept in generalized pustular psoriasis. Cutis. 2006;78(3):197–199. Available at: https://pubmed.ncbi.nlm.nih.gov/17036664.
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5Academic Journal
Authors: N. V. Muravyova, B. S. Belov, Н. В. Муравьева, Б. С. Белов
Contributors: The article was prepared as part of the research work, government task №1021051503137-7., Статья подготовлена в рамках научно-исследовательской работы, № государственного задания 1021051503137-7.
Source: Modern Rheumatology Journal; Том 18, № 4 (2024); 115-120 ; Современная ревматология; Том 18, № 4 (2024); 115-120 ; 2310-158X ; 1996-7012
Subject Terms: рекомбинантная адъювантная вакцина, rheumatoid arthritis, systemic lupus erythematosus, glucocorticoids, Janus kinase inhibitors, biologic disease-modifying antirheumatic drugs, herpes zoster, vaccination, recombinant adjuvant vaccine, ревматоидный артрит, системная красная волчанка, глюкокортикоиды, ингибиторы Янус-киназ, генно-инженерная биологическая терапия, опоясывающий лишай, вакцинация
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Relation: https://mrj.ima-press.net/mrj/article/view/1629/1505; Ющук НД, Венгеров ЮЯ, редакторы. Инфекционные болезни: национальное руководство. Москва: ГЭОТАР-Медиа; 2021.; Johnson RW, Alvarez-Pasquin M-J, Bijl M, et al. Herpes zoster epidemiology, management, and disease and economic burden in Europe: a multidisciplinary perspective. Ther Adv Vaccines. 2015 Jul;3(4):109-20. doi:10.1177/2051013615599151.; Furer V, Rondaan C, Heijstek M, et al. Incidence and prevalence of vaccine preventable infections in adult patients with autoimmune inflammatory rheumatic diseases (AIIRD): a systemic literature review informing the 2019 update of the EULAR recommendations for vaccination in adult patients with AIIRD. RMD Open. 2019 Sep 19;5(2):e001041. doi:10.1136/rmdopen-2019-001041. eCollection 2019.; Chen SY, Suaya JA, Li Q, et al. Incidence of herpes zoster in patients with altered immune function. Infection. 2014 Apr;42(2): 325-34. doi:10.1007/s15010-013-0550-8. Epub 2013 Nov 10.; Dlamini ST, Htet KM, Theint ECC, et al. Herpes zoster risk in patients with rheumatoid arthritis and its association with medications used. Int J Environ Res Public Health. 2023 Jan 24;20(3):2123. doi:10.3390/ijerph20032123.; Liao TL, Lin CH, Chen HH, et al. Significant associations of neurological complications of herpes zoster with stroke in rheumatoid arthritis patients. J Am Heart Assoc. 2017 Jul 19;6(7):e006304. doi:10.1161/JAHA.117.006304.; Nakajima A, Urano W, Inoue E, et al. Incidence of herpes zoster in Japanese patients with rheumatoid arthritis from 2005 to 2010. Mod Rheumatol. 2015 Jul;25(4):558-61. doi:10.3109/14397595.2014.984829. Epub 2015 Feb 4.; Yamaguchi R, Tanaka E, Nakajima A, et al. Risk of herpes zoster in patients with rheumatoid arthritis in the biologics era from 2011 to 2015 and its association with methotrexate, biologics, and corticosteroids. Mod Rheumatol. 2022 Apr 18;32(3):522-527. doi:10.1093/mr/roab026.; Zhang N, Wilkinson S, Riaz M, et al. Does methotrexate increase the risk of varicella or herpes zoster infection in patients with rheumatoid arthritis? A systematic literature review. Clin Exp Rheumatol. 2012 Nov-Dec; 30(6):962-71. Epub 2012 Dec 17.; Wolfe F, Michaud K, Chakravarty EF. Rates and predictors of herpes zoster in patients with rheumatoid arthritis and non-inflammatory musculoskeletal disorders. Rheumatology (Oxford). 2006 Nov;45(11): 1370-5. doi:10.1093/rheumatology/kel328. Epub 2006 Sep 26.; Mok CC, Ho LY, Tse SM, et al. Prevalence and risk factors of herpes zoster infection in patients with rheumatic diseases not receiving biologic or targeted therapies. Clin Rheumatol. 2023 Apr;42(4):1019-1026. doi:10.1007/s10067-022-06450-2. Epub 2022 Nov 16.; Che H, Lukas C, Morel J, Combe B. Risk of herpes/herpes zoster during anti-tumor necrosis factor therapy in patients with rheumatoid arthritis. Systematic review and meta-analysis. Joint Bone Spine. 2014 May; 81(3):215-21. doi:10.1016/j.jbspin.2013.07.009. Epub 2013 Aug 7.; Redeker I, Albrecht K, Kekow J, et al. Risk of herpes zoster (shingles) in patients with rheumatoid arthritis under biologic, targeted synthetic and conventional synthetic DMARD treatment: data from the German RABBIT register. Ann Rheum Dis. 2022 Jan;81(1):41-47. doi:10.1136/annrheumdis2021-220651. Epub 2021 Jul 28.; Atzeni F, Gozza F, Riva A, et al. Conventional, biological disease-modifying antirheumatic drugs and Janus kinase inhibitors and varicella zoster virus. Expert Opin Pharmacother. 2023 Apr;24(6):679-689. doi:10.1080/14656566.2023.2195050. Epub 2023 Mar 28.; Sakai R, Kasai S, Hirano F, et al. No increased risk of herpes zoster in TNF inhibitor and non-TNF inhibitor users with rheumatoid arthritis: epidemiological study using the Japanese health insurance database. Int J Rheum Dis. 2018 Sep;21(9):1670-1677. doi:10.1111/1756-185X.13300. 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6Academic Journal
Authors: M. I. Kaleda, I. P. Nikishina, М. И. Каледа, И. П. Никишина
Contributors: Статья подготовлена в рамках фундаментальной темы №1021051302580-4.
Source: Modern Rheumatology Journal; Том 18, № 4 (2024); 99-105 ; Современная ревматология; Том 18, № 4 (2024); 99-105 ; 2310-158X ; 1996-7012
Subject Terms: детский возраст, glucocorticoids, biologic disease-modifying antirheumatic drugs, childhood, глюкокортикоиды, генно-инженерная биологическая терапия
File Description: application/pdf
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Targeted Therapy for SLE-What Works, What Doesn't, What's Next. J Clin Med. 2023 Apr 29;12(9): 3198. doi:10.3390/jcm12093198.; Isenberg D, Gordon C, Licu D, et al. Efficacy and safety of atacicept for prevention of flares in patients with moderate-to-severe systemic lupus erythematosus (SLE): 52-week data (APRIL-SLE randomised trial). Ann Rheum Dis. 2015 Nov;74(11):2006-15. doi:10.1136/annrheumdis-2013-205067. Epub 2014 Jun 20.; Zhang L, Cui JY, Zhang L. Clinical efficacy and safety of sirolimus in childhood-onset systemic lupus erythematosus in real world. Medicine (Baltimore). 2022 Nov 18; 101(46):e31551. doi:10.1097/MD.0000000000031551.; Sun L, Shen Q, Gong Y, et al. Safety and efficacy of telitacicept in refractory childhood-onset systemic lupus erythematosus: A self-controlled before-after trial. Lupus. 2022 Jul;31(8):998-1006. doi:10.1177/09612033221097812. Epub 2022 May 2.; Modica RF, Thatayatikom A, Bell-Brunson DH, Elder ME. Bortezomib is efficacious in the treatment of severe childhood-onset neuropsychiatric systemic lupus erythematosus with psychosis: a case series and mini-review of B-cell immunomodulation in antibody-mediated diseases. Clin Rheumatol. 2023 Jul;42(7):1965-1979. doi:10.1007/s10067-023-06559-y. Epub 2023 Mar 27.; Shaw KS, Rajeh A, Le T, et al. Anifrolumab for Adolescent Discoid Lupus Erythematosus. JAMA Netw Open. 2023 Oct 2;6(10): e2338200. doi:10.1001/jamanetworkopen.2023.38200.; Pin A, Tesser A, Pastore S, et al. Biological and Clinical Changes in a Pediatric Series Treated with Off-Label JAK Inhibitors. Int J Mol Sci. 2020 Oct 20;21(20):7767. doi:10.3390/ijms21207767.; Rossano M, Conti EA, Bocca P, et al. Novel heterozygous TREX1 mutation in a juvenile systemic lupus erythematosus patient with severe cutaneous involvement treated successfully with Jak-inhibitors: a case report. Front Immunol. 2023 Dec 6:14:1288675. doi:10.3389/fimmu.2023.1288675. eCollection 2023.; Brunner HI, Martini A, Lovell DJ, Ruperto N. Clinical trials in children and adolescents with systemic lupus erythematosus: methodological aspects, regulatory landscape and future opportunities. Ann Rheum Dis. 2019 Feb;78(2):162-170. doi:10.1136/annrheumdis-2018-213198. Epub 2018 Sep 19.
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7Academic Journal
Authors: I. A. Ruslyakova, E. Z. Shamsutdinova, L. B. Gaikovaya, И. А. Руслякова, Э. З. Шамсутдинова, Л. Б. Гайковая
Source: General Reanimatology; Том 20, № 2 (2024); 29-39 ; Общая реаниматология; Том 20, № 2 (2024); 29-39 ; 2411-7110 ; 1813-9779
Subject Terms: исход, severe community-acquired pneumonia, genetically engineered biological therapy, response, outcome, тяжелая внебольничная пневмония, генно-инженерная биологическая терапия, ответная реакция
File Description: application/pdf
Relation: https://www.reanimatology.com/rmt/article/view/2392/1812; https://www.reanimatology.com/rmt/article/view/2392/1820; https://www.reanimatology.com/rmt/article/downloadSuppFile/2392/919; Авдеев С. Н., Белобородов В. Б., Белоцерковский Б. З., Грицан А. И., Дехнич А. В., Зайцев А. А., Киров М. Ю., с соавт. Тяжелая внебольничная пневмония у взрослых. Клинические рекомендации Федерации анестезиологов и реаниматологов России. Анестезиология и реаниматология. 2022; (1): 6–35. DOI:10.17116/anaesthesiology20220116.; Cavallazzi R., Furmanek S., Arnold F. W., Beavin L. A., Wunderink R. G., Niederman M. S., Ramirez J. A. The burden of community-acquired pneumonia requiring admission to ICU in the United States. Chest. 2020; 158 (3): 1008–1016. DOI:10.1016/j.chest.2020.03.051. PMID: 32298730.; Rudd K. E., Johnson S. C., Agesa K. M., Shackelford K. A., Tsoi D., Kievlan D. R., Colombara D. V., et al. Global, regional, and national sepsis incidence and mortality, 1990-2017: analysis for the Global Burden of Disease study. Lancet. 2020; 395 (10219): 200–211. DOI:10.1016/S0140-6736 (19)32989-7. PMID: 31954465.; Martin-Loeches I., Torres A., Nagavci B., Aliberti S., Antonelli M., Bassetti M., Bos L. D., et al. ERS/ESICM/ESCMID/ALAT guidelines for the management of severe community-acquired pneumonia. Intensive Care Med. 2023; 49 (6): 615– 632. DOI:10.1007/s00134-023-07033-8. PMID: 37012484.; Wiersinga W. J., van der Poll T. Immunopathophysiology of human sepsis. EBioMedicine. 2022; 86: 104363. DOI:10.1016/j.ebiom.2022.104363. PMID: 36470832.; Vincent J. L., van der Poll T., Marshall J. C. The end of «One Size Fits All» sepsis therapies: toward an individualized approach. Biomedicines. 2022; 10 (9): 2260. DOI:10.3390/biomedicines10092260. PMID: 36140361.; Knox D. B., Lanspa M. J., Kuttler K. G., Brewer S. C., Brown S. M. Phenotypic clusters within sepsis-associated multiple organ dysfunction syndrome. Intensive Care Med. 2015; 41 (5): 814–822. DOI:10.1007/s00134-015-3764-7. PMID: 25851384.; Bhavani S. V., Semler M., Qian E. T., Verhoef P. A., Robichaux C., Churpek M. M., Coopersmith C. M. Development and validation of novel sepsis subphenotypes using trajectories of vital signs. Intensive Care Med. 2022; 48 (11): 1582–1592. DOI:10.1007/s00134-022-06890-z. PMID: 36152041.; Zhang Z., Zhang G., Goyal H., Mo L., Hong Y. Identification of subclasses of sepsis that showed different clinical outcomes and responses to amount of fluid resuscitation: a latent profile analysis. Crit Care. 2018; 22 (1): 347. DOI:10.1186/s13054-018-2279-3. PMID: 30563548.; Kudo D., Goto T., Uchimido R., Hayakawa M., Yamakawa K., Abe T., Shiraishi A., et al. Coagulation phenotypes in sepsis and effects of recombinant human thrombomodulin: an analysis of three multicentre observational studies. Crit Care. 2021; 25 (1): 114. DOI:10.1186/s13054-021-03541-5. PMID: 33741010.; Scicluna B. P., van Vught L. A., Zwinderman A. H., Wiewel M. A., Davenport E. E., Burnham K. L., Nürnberg P., et al.; MARS consortium. Classification of patients with sepsis according to blood genomic endotype: a prospective cohort study. Lancet Respir Med. 2017; 5 (10): 816–826. DOI:10.1016/S2213-2600 (17)30294-1. PMID: 28864056.; Komorowski M., Green A., Tatham K. C., Seymour C., Antcliffe D. Sepsis biomarkers and diagnostic tools with a focus on machine learning. EBioMedicine. 2022; 86: 104394. DOI:10.1016/j.ebiom.2022.104394. PMID: 36470834.; Barichello T., Generoso J. S., Singer M., Dal-Pizzol F. Biomarkers for sepsis: more than just fever and leukocytosis-a narrative review. Crit Care. 2022; 26 (1): 14. DOI:10.1186/s13054021-03862-5. PMID: 34991675.; da Silva J. F., Hernandez-Romieu A. C., Browning S. D., Bruce B. B., Natarajan P., Morris S. B., Gold J. A.W., et al. COVID-19 clinical phenotypes: presentation and temporal progression of disease in a cohort of hospitalized adults in Georgia, United States. Open Forum Infect Dis. 2020; 8 (1): ofaa596. DOI:10.1093/ofid/ofaa596. PMID: 33537363.; Cidade J. P., de Souza Dantas V. C., de Figueiredo Thompson A., de Miranda R. C.C.C., Mamfrim R., Caroli H., et al. Identification of distinct clinical phenotypes of critically ill COVID19 patients: results from a cohort observational study. J Clin Med. 2023; 12 (8): 3035. DOI:10.3390/jcm12083035. PMID: 37109370.; Ranard B. L., Megjhani M., Terilli K., Doyle K., Claassen J., Pinsky M. R., Clermont G., et al. Identification of endotypes of hospitalized COVID-19 patients. Front Med (Lausanne). 2021; 8: 770343. DOI:10.3389/fmed.2021.770343. PMID: 34859018.; Komorowski M. Clinical management of sepsis can be improved by artificial intelligence: yes. Intensive Care Med. 2020; 46 (2): 375–377. DOI:10.1007/s00134-019-05898-2. PMID: 31834423.; Davenport E. E., Burnham K. L., Radhakrishnan J., Humburg P., Hutton P., Mills T. C., Rautanen A., et al. Genomic landscape of the individual host response and outcomes in sepsis: a prospective cohort study. Lancet Respir Med. 2016; 4 (4): 259–271. DOI:10.1016/S2213-2600(16)00046-1. PMID: 26917434.; Sweeney T. E., Azad T. D., Donato M., Haynes W. A., Perumal T. M., Henao R., Bermejo-Martin J. F., et al. Unsupervised analysis of transcriptomics in bacterial sepsis across multiple datasets reveals three robust clusters. Crit Care Med. 2018; 46 (6): 915–925. DOI:10.1097/CCM.0000000000003084. PMID: 29537985.; Burnham K. L., Davenport E. E., Radhakrishnan J., Humburg P., Gordon A. C., Hutton P., Svoren-Jabalera E., et al. Shared and distinct aspects of the sepsis transcriptomic response to fecal peritonitis and pneumonia. Am J Respir Crit Care Med. 2017; 196 (3): 328–339. DOI:10.1164/rccm.201608-1685OC. PMID: 28036233.; Antcliffe D. B., Burnham K. L., Al-Beidh F., Santhakumaran S., Brett S. J., Hinds C. J., Ashby D., et al. Transcriptomic signatures in sepsis and a differential response to steroids. From the VANISH randomized trial. Am J Respir Crit Care Med. 2019; 199 (8): 980–986. DOI:10.1164/rccm.201807-1419OC. PMID: 30365341.; Wu X., Li R., He Z., Yu T., Cheng C. A value-based deep reinforcement learning model with human expertise in optimal treatment of sepsis. NPJ Digit Med. 2023; 6 (1): 15. DOI:10.1038/s41746-023-00755-5. PMID: 36732666.; DeMerle K.M., Angus D. C., Baillie J. K., Brant E., Calfee C. S., Carcillo J., Chang C. H., et al. Sepsis subclasses: a framework for development and interpretation. Crit Care Med. 2021; 49 (5): 748–759. DOI:10.1097/CCM.0000000000004842. PMID: 33591001.; Seymour C. W., Kennedy J. N., Wang S., Chang C. H., Elliott C. F., Xu Z., Berry S., et al. Derivation, validation, and potential treatment implications of novel clinical phenotypes for sepsis. JAMA. 2019; 321 (20): 2003–2017. DOI:10.1001/jama.2019.5791. PMID: 31104070.; Kalimouttou A., Lerner I., Cheurfa C., Jannot A. S., Pirracchio R. Machine-learning-derived sepsis bundle of care. Intensive Care Med. 2023; 49 (1): 26–36. DOI:10.1007/s00134-022-06928-2. PMID: 36446854.; Bruse N., Kooistra E. J., Jansen A., van Amstel R. B.E., de Keizer N. F., Kennedy J. N., Seymour C., et al. Clinical sepsis phenotypes in critically ill COVID-19 patients. Crit Care. 2022; 26 (1): 244. DOI:10.1186/s13054-022-04118-6. PMID: 35945618.; Reddy K., Sinha P., O’Kane C.M., Gordon A. C., Calfee C. S., McAuley D.F. Subphenotypes in critical care: translation into clinical practice. Lancet Respir Med. 2020; 8 (6): 631– 643. DOI:10.1016/S2213-2600(20)30124-7. PMID: 32526190.; Grasselli G., Calfee C. S., Camporota L., Poole D., Amato M. B.P., Antonelli M., Arabi Y. M., et al; European Society of Intensive Care Medicine Taskforce on ARDS. ESICM guidelines on acute respiratory distress syndrome: definition, phenotyping and respiratory support strategies. Intensive Care Med. 2023; 49 (7): 727–759. DOI:10.1007/s00134-023-07050-7. PMID: 37326646.; Профилактика, диагностика и лечение новой коронавирусной 2. инфекции (COVID-19). Временные методические рекомендации МЗ РФ. Версия 17 от 14.12.2022. Дата доступа: 05.09.2023. https: //static-0.minzdrav.gov.ru/system/attachments/attaches/000/061/252/original/%D0%92%D0%9C%D0%A0_COVID-19_V17.pdf; Заболотских И. Б., Киров М. Ю., Лебединский К. М., Проценко Д. Н., Авдеев С. Н., Андреенко А. А., Арсентьев Л. В., с соавт. Анестезиолого-реанимационное обеспечение пациентов с новой коронавирусной инфекцией COVID-19. Методические рекомендации Общероссийской общественной организации «Федерация анестезиологов и реаниматологов». Вестник интенсивной терапии имени А.И. Салтанова. 2022; (1): 5–140. DOI:10.21320/1818-474X-2022-1-5-140; Mandell L. A., Wunderink R. G., Anzueto A., Bartlett J. G., Campbell G. D., Dean N. C., Dowell S. F., et al. Infectious diseases society of America/American Thoracic Society consensus guidelines on the management of communityacquired pneumonia in adults. Clin Infect Dis. 2007; 44 Suppl 2 (Suppl 2): S27–72. DOI:10.1086/511159. PMID: 17278083.; Zimmerman J. E., Kramer A. A., McNair D.S., Malila F. M. Acute Physiology and Chronic Health Evaluation (APACHE) IV: hospital mortality assessment for today’s critically ill patients. Crit Care Med. 2006; 34 (5): 1297–310. DOI:10.1097/01.CCM.0000215112.84523.F0. PMID: 16540951.; Ata Ur-Rehman H. M., Ishtiaq W., Yousaf M., Bano S., Mujahid A. M., Akhtar A. Modified Nutrition Risk in Critically Ill (mNUTRIC) score to assess nutritional risk in mechanically ventilated patients: a prospective observational study from the Pakistani population. Cureus. 2018; 10 (12): e3786. DOI:10.7759/cureus.3786. PMID: 30854273.; «National Early Warning Score (NEWS) 2» https: //www.rcplondon.ac.uk/projects/outputs/national-early-warningscore-news-2.; Miyashita N., Matsushima T., Oka M., Japanese Respiratory Society. The JRS guidelines for the management of community-acquired pneumonia in adults: an update and new recommendations. Intern Med. 2006; 45 (7): 419–428. DOI:10.2169/internalmedicine.45.1691. PMID: 16679695.; Charles P. G., Wolfe R., Whitby M., Fine M. J., Fuller A. J., Stirling R., Wright A. A., et al.; Australian CommunityAcquired Pneumonia Study Collaboration; Grayson M. L. SMART-COP: a tool for predicting the need for intensive respiratory or vasopressor support in community-acquired pneumonia. Clin Infect Dis. 2008; 47 (3): 375–384. DOI:10.1086/589754. PMID: 18558884.; Le Gall J., Lemeshow S., Saulnier F. A New Simplified Acute Physiology Score (SAPS II) based on a European/North American multicenter study. JAMA. 1993; 270 (24): 2957–2963. DOI:10.1001/jama.1993.03510240069035. PMID: 8254858.; https://www.reanimatology.com/rmt/article/view/2392
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8Academic Journal
Authors: O. V. Kazmerchuk, E. A. Sobko, I. V. Demko, О. В. Казмерчук, Е. А. Собко, И. В. Демко
Contributors: The authors declare no funding for this study, Авторы заявляют об отсутствии финансирования при проведении исследования
Source: The Russian Archives of Internal Medicine; Том 14, № 6 (2024); 457-466 ; Архивъ внутренней медицины; Том 14, № 6 (2024); 457-466 ; 2411-6564 ; 2226-6704
Subject Terms: генно-инженерная биологическая терапия, dupilumab, achieving control, genetically engineered biological therapy, дупилумаб, достижение контроля
File Description: application/pdf
Relation: https://www.medarhive.ru/jour/article/view/1881/1371; https://www.medarhive.ru/jour/article/view/1881/1378; Soriano JB, Abajobir AA, Abate KH, et al. Global, regional, and national deaths, prevalence, disability-adjusted life years, and years lived with disability for chronic obstructive pulmonary disease and asthma, 1990–2015: a systematic analysis for the Global Burden of Disease Study 2015. Lancet Respir Med. 2017; 5(9): 691–706. DOI:10.1016/S2213-2600(17)30293-X.; Деев И.А., Кобякова О.С., Стародубов В.И. Общая заболеваемость детского населения России (0-14 лет) в 2023 г. ФГБУ «ЦНИИОИЗ» Минздрава России. 2024; 154-156. DOI:10.21045/978-5-94116-160-7-2024.; Чучалин А.Г. Достижения в лечении астмы в России в первой декаде нового тысячелетия. Consilium Medicum (Экстравыпуск). 2010; 11—12.; Uphoff E, Cabieses B, Pinart M, et al. A systematic review of socioeconomic position in relation to asthma and allergic diseases. Eur RespirJ. 2015. 46(2). 364–374. DOI:10.1183/09031936.00114514.; Masefield S, Edwards J, Hansen K, et al. The future of asthma research and development: a roadmap from the European Asthma Research and Innovation Partnership (EARIP). Eur Respir J. 2017; 49(5): 1602295. DOI:10.1183/13993003.02295-2016.; Bahadori K, Doyle-Waters MM, Marra C et al. Economic burden of asthma : a systematic review. BMC Pulm Med. 2009. 19(9). 24. DOI:10.1186/1471-2466-9-24.; Mathers CD. History of global burden of disease assessment at the World Health Organization. Arch Public Health. 2020. 24. 77-78. DOI:10.1186/s13690-020-00458-3.; Agache I. Severe asthma phenotypes and endotypes. Semin Immunol. 2019. 46:101. DOI:10.1016/j.smim.2019.101301.; Global Initiative for Asthma, GINA. 2023; 200-220. [Electronic resource]. URL: https://ginasthma.org/wp-content/uploads/2023/07/GINA-2023-Full-report-23_07_06-WMS (date of the application: 10. 08. 2024); McDowell P.J., Heaney L.G. Different endotypes and phenotypes drive the heterogeneity in severe asthma. Allergy. 2020; 75(2):302-310. DOI:10.1111/all.13966.; Rabe KF, Nair P, Brusselle G, Maspero JF et al. Efficacy and safety of dupilumab in glucocorticoid-dependent severe asthma. N Engl J Med. 2018. 378:2475–85. DOI:10.1056/NEJMoa1804093.; Wechsler ME, Ford LB, Maspero JF et al. Long-term safety and efficacy of dupilumab in patients with moderate-to-severe asthma (TRAVERSE): an open-label extension study. Lancet Respir Med. 2022. 10:11–25. DOI:10.1016/S2213-2600(21)00322-2.; Пирогов АБ, Приходько АГ, Перельман ЮМ. Участие макрофагов и эпителия в реакции бронхов на гиперосмолярный стимул при бронхиальной астме. Сибирское медицинское обозрение. 2024. 64-71. DOI:10.20333/25000136-2024-1-64-71.; Chung K.F. Asthma phenotyping: a necessity for improved therapeutic precision and new targeted therapies. J Intern Med. 2016. 192-204. DOI:10.1111/joim.12382.; Fajt ML, Wenzel SE. Asthma phenotypes and the use of biologic medications in asthma and allergic disease: the next steps toward personalized care. J Allergy Clin Immunol. 2015. 135(2). 299-310. DOI:10.1016/j.jaci.2014.12.1871.; Андрианова Г.Н., Каримова А.А. Фармакоэкономика : уч. пособие. ФГБОУ ВО УГМУ Минздрава России. Екатеринбург: Изд-во УГМУ. 2017. 196. ISBN 978-5-89895-828-2; Ягудина, Р. И. Методологические основы анализа «затраты - эффективность». Фармакоэкономика: теория и практика. 2014. Т. 2, № 2. С. 23-27.; Клинические рекомендации по бронхиальной астме Минздрава РФ. 2024; 60-80. [Электронный ресурс]. URL: http://disuria.ru/_ld/10/1037_kr21J45J46MZ.pdf?ysclid=l7un7hzve9180338084.(дата обращения: 01. 08. 2024).; Graham B.L., Steenbruggen I., Miller M.R. et al. Standardization of spirometry 2019. Update an official American Thoracic Society and European Respiratory Society technical statement. Am. J. Respir. Crit. Care Med. 2019. 70–88. DOI:10.1164/rccm.201908-1590ST.; Dupin C, Belhadi D, Guilleminault L, et al. Effectiveness and safety of dupilumab for the treatment of severe asthma in a real-life French multi-centre adult cohort. Clin Exp Allergy. 2020; 50(7): 789–98. DOI:10.1111/cea.13614.; Pelaia C, Lombardo N, Busceti MT, et al. Short-term evaluation of dupilumab effects in patients with severe asthma and nasal polyposis. J Asthma Allergy. 2021; 24(14): 1165–72. DOI:10.2147/JAA.S328988.; Крысанов И.С., Крысанова В.С., Ермакова В.Ю. Клинико-экономический анализ применения препарата дупилумаб при тяжёлой бронхиальной астме. Качественная клиническая практика. 2020; 5: 15-26. DOI:10.37489/2588-0519-2020-5-15-26.; https://www.medarhive.ru/jour/article/view/1881
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9Academic Journal
Source: Наука и здравоохранение. :66-80
Subject Terms: Ішектің сүлелі қабынбалы ауруы, воспалительная болезнь кишечника, Жаралы колит, гендік инженерлік биологиялық ем, кальпротектин, язвенный колит, тітіркенген ішек, раздраженный кишечник, calprotectin, irritable bowel, генно-инженерная биологическая терапия, Крон ауруы, inflammatory bowel disease, болезнь Крона, genetically engineered biological therapy, ulcerative colitis
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10Academic Journal
Authors: L. S. Kruglova, A. A. Hotko
Source: Качественная клиническая практика, Vol 0, Iss 1, Pp 46-55 (2021)
Subject Terms: число госпитализаций, количество обращений за амбулаторной помощью, псориаз, количество листов временной нетрудоспособности, дней временной нетрудоспособности, 3. Good health, генно-инженерная биологическая терапия, RS1-441, 03 medical and health sciences, Pharmacy and materia medica, 0302 clinical medicine, псориатический артрит, длительность госпитализаций, Medical technology, R855-855.5
Access URL: https://www.clinvest.ru/jour/article/download/562/574
https://doaj.org/article/9fa04cbb6b0142e0878259f5feb9a98f
https://www.clinvest.ru/jour/article/download/562/574
https://cyberleninka.ru/article/n/resursopotreblenie-i-trudosposobnost-patsientov-na-fone-primeneniya-sistemnoy-terapii-i-genno-inzhenernoy-biologicheskoy-terapii/pdf
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https://cyberleninka.ru/article/n/resursopotreblenie-i-trudosposobnost-patsientov-na-fone-primeneniya-sistemnoy-terapii-i-genno-inzhenernoy-biologicheskoy-terapii -
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12Academic Journal
Authors: B. S. Belov, E. S. Aronova, G. I. Gridneva, E. I. Nasonov, Б. С. Белов, Е. С. Аронова, Г. И. Гриднева, Е. Л. Насонов
Contributors: Исследование выполнено в рамках темы ФГБНУ «Научно-исследовательский институт ревматологии им. В.А. Насоновой», № государственного задания 1021051503137-7
Source: Rheumatology Science and Practice; Vol 61, No 4 (2023); 450-457 ; Научно-практическая ревматология; Vol 61, No 4 (2023); 450-457 ; 1995-4492 ; 1995-4484
Subject Terms: базисные противовоспалительные препараты, infection, post-COVID syndrome, rheumatoid arthritis, immunoinflammatory rheumatic diseases, bDMARDs, DMARDs, инфекция, постковидный синдром, ревматоидный артрит, иммуновоспалительные ревматические заболевания, генно-инженерная биологическая терапия
File Description: application/pdf
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13Academic Journal
Authors: E. V. Svechnikova, S. E. Zhufina, M. A. Morzhanaeva, Е. В. Свечникова, С. Е. Жуфина, М. А. Моржанаева
Source: Meditsinskiy sovet = Medical Council; № 2 (2023); 69-74 ; Медицинский Совет; № 2 (2023); 69-74 ; 2658-5790 ; 2079-701X
Subject Terms: нетакимаб, basic therapy, genetically engineered biological therapy, netakimab, базисная терапия, генно-инженерная биологическая терапия
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Relation: https://www.med-sovet.pro/jour/article/view/7390/6591; Kaushik S.B., Lebwohl M.G. Psoriasis: Which therapy for which patient: Psoriasis comorbidities and preferred systemic agents. J Am Acad Dermatol. 2019;80(1):27–40. https://doi.org/10.1016/j.jaad.2018.06.057.; Ito T., Takahashi H., Kawada A., Iizuka H., Nakagawa H., Japanese Society for Psoriasis Research. Epidemiological survey from 2009 to 2012 of psoriatic patients in Japanese Society for Psoriasis Research. J Dermatol. 2018;45(3):293–301. https://doi.org/10.1111/1346-8138.14105.; Kamiya K., Kishimoto M., Sugai J., Komine M., Ohtsuki M. Risk Factors for the Development of Psoriasis. Int J Mol Sci. 2019;20(18):4347. https://doi.org/10.3390/ijms20184347.; Swindell W.R., Johnston A., Xing X., Voorhees J.J., Elder J.T., Gudjonsson J.E. Modulation of epidermal transcription circuits in psoriasis: new links between inflammation and hyperproliferation. PLoS One. 2013;8(11):e79253. https://doi.org/10.1371/journal.pone.0079253.; Nestle F.O., Kaplan D.H., Barker J. Psoriasis. N Engl J Med. 2009;361(5):496–509. https://doi.org/10.1056/NEJMra0804595.; Kolbinger F., Loesche C., Valentin M.A., Jiang X., Cheng Y., Jarvis P. et al. β‐Defensin 2 is a responsive biomarker of IL‐17A‐driven skin pathology in patients with psoriasis. J Allergy Clin Immunol. 2017;139(3):923–32.e8. https://doi.org/10.1016/j.jaci.2016.06.038.; Korman N.J. Management of psoriasis as a systemic disease: what is the evidence? Br J Dermatol. 2020;182(4):840–848. https://doi.org/10.1111/bjd.18245.; Griffiths C.E.M., Fava M., Miller A.H., Russell J., Ball S.G., Xu W. et al. Impact of ixekizumab treatment on depressive symptoms and systemic inflammation in patients with moderate‐to‐severe psoriasis: an integrated analysis of three phase 3 clinical studies. Psychother Psychosom. 2017;86(5):260–267. https://doi.org/10.1159/000479163.; Wu J.J., Sundaram M., Cloutier M., Gauthier-Loiselle M., Guerin A., Sigh R., Ganduli A. The risk of cardiovascular events in psoriasis patients treated with tumor necrosis factor‐α inhibitors versus phototherapy: an observational cohort study. J Am Acad Dermatol. 2018;79(1):60–68. https://doi.org/10.1016/j.jaad.2018.02.050.; Wu J.J., Joshi A.A., Reddy S.P., Batech M., Egeberg A., Ahlehoff O., Mehta N.N. Anti‐inflammatory therapy with tumour necrosis factor inhibitors is associated with reduced risk of major adverse cardiovascular events in psoriasis. J Eur Acad Dermatol Venereol. 2018;32(8):1320–1326. https://doi.org/10.1111/jdv.14951.; Bellinato F., Gisondi P., Girolomoni G. Latest Advances for the Treatment of Chronic Plaque Psoriasis with Biologics and Oral Small Molecules. Biologics. 2021;(15):247–253. https://doi.org/10.2147/BTT.S290309.; Kostareva O., Svoeglazova A., Kolyadenko I., Nikulin A., Evdokimov S., Dzhus U. et al. Two Epitope Regions Revealed in the Complex of IL-17A and Anti-IL-17A V HH Domain. Int J Mol Sci. 2022;23(23):14904. https://doi.org/10.3390/ijms232314904.; Puig L., Bakulev A.L., Kokhan M.M., Samtsov A.V., Khairutdinov V.R., Morozova M.A. et al. Efficacy and Safety of Netakimab, A Novel AntiIL-17 Monoclonal Antibody, in Patients with Moderate to Severe Plaque Psoriasis. Results of A 54-Week Randomized Double-Blind PlaceboControlled PLANETA Clinical Trial. Dermatol Ther (Heidelb). 2021;11(4):1319–1332. https://doi.org/10.1007/s13555-021-00554-4.
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14Academic Journal
Authors: O. V. Zhukova, S. I. Artemyeva, О. В. Жукова, С. И. Артемьева
Source: Meditsinskiy sovet = Medical Council; № 14 (2023); 24-34 ; Медицинский Совет; № 14 (2023); 24-34 ; 2658-5790 ; 2079-701X
Subject Terms: Дерматологический индекс качества жизни, psoriatic arthritis, guselkumab, genetically engineered biologic therapy, interleukin 23 inhibitors, DLQI, псориатический артрит, гуселькумаб, генно-инженерная биологическая терапия, ингибиторы интерлейкина 23
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Br J Dermatol. 2017;176(3): 732–740. https://doi.org/10.1111/bjd.15149.; Mease PJ, Fleischmann R, Deodhar AA, Wollenhaupt M, Khraishi M, Kielar D et al. Effect of certolizumab pegol on signs and symptoms in patients with psoriatic arthritis: 24-week results of a phase 3 double-blind randomised placebo-controlled study (RAPID-PsA). Ann Rheumatic Dis. 2014;73(1):48–55. https://doi.org/10.1136/annrheumdis-2013-203696.; Syversen SW, Jorgensen KK, Goll GL, Brun MK, Sandanger Q, Bjorlykke KH et al. Effect of therapeutic drug monitoring vs standard therapy during maintenance infliximab therapy on disease control in patients with immune-mediated inflammatory diseases: a randomized clinical trial. JAMA. 2021;326(23):2375–2384. https://doi.org/10.1001/jama.2021.21316.; McInnes IB, Sawyer LM, Markus K, LeReun C, Sabry-Grant C, Helliwell PS. Targeted systemic therapies for psoriatic arthritis: a systematic review and comparative synthesis of short-term articular, dermatological, enthesitis and dactylitis outcomes. RMD Open. 2022;8(1):е002074. https://doi.org/10.1136/rmdopen-2021-002074.; Baraliakos X, Gossec L, Pournara E, Jeka S, Mera-Varela A, D´Angelo S et al. Secukinumab in patients with psoriatic arthritis and axial manifestations: results from the double-blind, randomised, phase 3 MAXIMISE trial. Ann Rheumc Dis. 2021;80(5):582–590. https://doi.org/10.1136/annrheumdis2020-218808.; Mease PJ, Landewe R, Rahman P, Tahir H, Singhal A, Boettcher E et al. Secukinumab provides sustained improvement in signs and symptoms and low radiographic progression in patients with psoriatic arthritis: 2-year (end-of-study) results from the FUTURE 5 study. RMD Open. 2021;7(2):е001600. https://doi.org/10.1136/rmdopen-2021-001600.; Gottlieb AB, Merola JF, Reich K, Behrens F, Nash P, Griffiths CEM et al. Efficacy of secukinumab and adalimumab in patients with psoriatic arthritis and concomitant moderate-to-severe plaque psoriasis: results from EXCEED, a randomized, double-blind head-to-head monotherapy study. Br J Dermatol. 2021;185(6):1124–1134. https://doi.org/10.1111/bjd.20413.; Gottlieb AB, Strand V, Kishimoto M, Mease P, Thaci D, Birt J et al. Ixekizumab improves patient-reported outcomes up to 52 weeks in bDMARD-naive patients with active psoriatic arthritis (SPIRIT-P1). Rheumatology. 2018;57(10):1777–1788. https://doi.org/10.1093/rheumatology/key161.; Deodhar A, Helliwell PS, Boehncke W-H, Kollmeier A, Hsia EC, Subramanian RA et al. Guselkumab in patients with active psoriatic arthritis who were biologic-naive or had previously received TNF alpha inhibitor treatment (DISCOVER-1): a double-blind, randomised, placebo-controlled phase 3 trial. Lancet. 2020;395(10230):1115–1125. https://doi.org/10.1016/s0140-6736(20)30265-8.; Mease PJ, Rahman P, Gottlieb AB, Kollmeier AP, Hsia EC, Xu XL et al. Guselkumab in biologic-naive patients with active psoriatic arthritis (DISCOVER-2): a doubleblind, randomised, placebo-controlled phase 3 trial. Lancet. 2020;395(10230): 1126–1136. https://doi.org/10.1016/s0140-6736(20)30263-4.; Sweet K, Song Q, Loza MJ, McInnes IB, Ma K, Leander K et al. Guselkumab induces robust reduction in acute phase proteins and type 17 effector cytokines in active psoriatic arthritis: results from phase 3 trials. RMD Open. 2021;7(2):е001679. https://doi.org/10.1136/rmdopen-2021-001679.; Stefan S, Loza MJ, Song Q, Mcinnes I, Sweet K. “THU0052 ustekinumab and guselkumab treatment results in differences in serum IL17A, IL17F and CRP levels in psoriatic arthritis patients: a comparison from ustekinumab ph3 and guselkumab ph2 programs.” BMJ. 2019;78(2):293. Available at: https://ard.bmj.com/content/annrheumdis/78/Suppl_2/293.1.full.pdf.; Bonifati C, Graceffa D. How effective is ustekinumab in controlling psoriatic arthritis? Dermatol Ther. 2016;(3):155–159. https://doi.org/10.1111/dth.12322.; Snekvik I, Smith CH, Nilsen TIL, Langan SM, Modalsli EH, Romundstad PR, Saunes M. Obesity, waist circumference, weight change, and risk of incident psoriasis: prospective data from the HUNT Study. J Invest Dermatol. 2017;137(12):2484–2490. https://doi.org/10.1016/j.jid.2017.07.822.; Petridis A, Panagakis P, Moustou E, Vergou T, Kallidis P, Mandekou-Lefaki I et al. A multicenter, prospective, observational study examining the impact of risk factors, such as BMI and waist circumference, on quality of life improvement and clinical response in moderate-to-severe plaque-type psoriasis patients treated with infliximab in routine care settings of Greece. J Eur Acad Dermatol Venereol. 2018;32(5):768–775. https://doi.org/10.1111/jdv.14802.; Araujo EP, De Souza CT, Ueno M, Cintra DE, Bertolo MB, Carvalheira JB et al. Infliximab restores glucose homeostasis in an animal model of diet-induced obesity and diabetes. Endocrinology. 2007;148(12):5991–5997. https://doi.org/10.1210/en.2007-0132.; Bykerk VP, Blauvelt A, Curtis JR, Gaujoux-Viala C, Kvien TK, Winthrop K et al. Associations between safety of certolizumab pegol, disease activity, and patient characteristics, including corticosteroid use and body mass index. ACR Open Rheumatol. 2021;3(8):501–511. https://doi.org/10.1002/acr2.11259.; Mahe E, Reguiai Z, Barthelemy H, Quiles-Tsimaratos, Chaby C, Esteve E et al. Evaluation of risk factors for body weight increment in psoriatic patients on infliximab: a multicentre, cross-sectional study. J Eur Acad Dermatol Venereol. 2014;28(2):151–159. https://doi.org/10.1111/jdv.12066.; Gisondi P, Conti A, Galdo G, Piaserico S, De Simone C, Girolomoni G. Ustekinumab does not increase body mass index in patients with chronic plaque psoriasis: a prospective cohort study. Br J Dermatol. 2013;168(5):1124–1127. https://doi.org/10.1111/bjd.12235.; Dalal RS, Allegretti JR. Ustekinumab dose optimization in Crohn disease: one size does not fit all. Inflamm Bowel Dis. 2021;27(6):e70. https://doi.org/10.1093/ibd/izab019.; Papp KA, Langley RG, Sigurgeirsson B, Abe M, Baker DR, Konno P et al. Efficacy and safety of secukinumab in the treatment of moderate-to-severe plaque psoriasis: a randomized, double-blind, placebo-controlled phase II dose-ranging study. Br J Dermatol. 2013;168(2):412–421. https://doi.org/10.1111/bjd.12110.; Gerdes S, Pinter A, Papavassilis C, Reinhardt M. Effects of secukinumab on metabolic and liver parameters in plaque psoriasis patients. J Eur Acad Dermatol Venereol. 2020;34(3):533–541. https://doi.org/10.1111/jdv.16004.; Papp K, Crowley J, Rubel D, Landells I, Song M, Wasfi Y et al. Consistency of response by weight across subgroups of patients with psoriasis treated with guselkumabl: results from the VOYAGE 1 and 2 Trials. Acta Dermato Venereol. 2018;79(3):20. https://doi.org/10.1016/j.jaad.2018.05.378.; Galluzzo M, Tofani L, Lombardo P, Petruzzellis A, Silvaggio D, Egan CG et al. Use of guselkumab for the treatment of moderate-to-severe plaque psoriasis: a 1 year real-life study. J Clin Med. 2020;9(7):2170. https://doi.org/10.3390/jcm9072170.; Regueiro M, Kip KE, Baidoo L, Swoger JM, Schraut W. Postoperative therapy with infliximab prevents long-term Crohn’s disease recurrence. Clin Gastroenterol Hepatol. 2014;12(9):1494-502.e1. https://doi.org/10.1016/j.cgh.2013.12.035.; Feagan BG, Sandborn WJ, Gasink C, Jacobstein D, Lang Y, Friedman JR et al. Ustekinumab as induction and maintenance therapy for Crohn’s disease. N Engl J Med. 2016;375(20):1946–1960. https://doi.org/10.1056/NEJMoa1602773.; Singh S, Murad MH, Fumery M, Dulai PS, Sandborn WJ. First- and second-line pharmacotherapies for patients with moderate to severely active ulcerative colitis: an updated network meta-analysis. Clin Gastroenterol Hepatol. 2020;18(10):2179–2191. https://doi.org/10.1016/j.cgh.2020.01.008.; Hueber W, Sands BE, Lewitzky S, Vandemeulebroecke M, Reinisch W, Higgins PDR et al. Secukinumab, a human anti-IL-17A monoclonal antibody, for moderate to severe Crohn’s disease: unexpected results of a randomised, double-blind placebo-controlled trial. Gut. 2012;61(12):1693–1700. https://doi.org/10.1136/gutjnl-2011-301668.; van de Kerkhof PCM, Griffiths CEM, Reich K, Leonardi CL, Blauvelt A, Tsai T-F et al. Secukinumab long-term safety experience: a pooled analysis of 10 phase II and III clinical studies in patients with moderate to severe plaque psoriasis. J Am Acad Dermatol. 2016;75(1):83–98. https://doi.org/10.1016/j.jaad.2016.03.024.; Gordon KB, Colombel J-F, Hardin DS. Phase 3 trials of ixekizumab in moderate-to-severe plaque psoriasis reply. N Engl J Med. 2016;375(21):2102. https://doi.org/10.1056/NEJMc1610828.; Sandborn WJ, D’Haens GR, Reinisch W, Panes J, Chan D, Gonzalez S et al. Guselkumab for the treatment of Crohn’s disease: induction results from the phase 2 GALAXI-1 study. Gastroenterology. 2022;162(6):1650–1664. https://doi.org/10.1053/j.gastro.2022.01.047.; Berman HS, Villa NM, Shi VY, Hsiao JL. Guselkumab in the treatment of concomitant hidradenitis suppurativa, psoriasis, and Crohn’s disease. J Dermatol Treat. 2021;32(2):261–263. https://doi.org/10.1080/09546634.2019.1654067.; Grossberg LB. A case report of successful treatment of Crohn’s disease and psoriasis with guselkumab. Inflamm Bowel Dis. 2019;25(7):E84-E. https://doi.org/10.1093/ibd/izz033.; Wu JJ, Guerin A, Sundaram M, Dea K, Cloutier M, Mulani P. Cardiovascular event risk assessment in psoriasis patients treated with tumor necrosis factor-alpha inhibitors versus methotrexate. J Am Acad Dermatol. 2017;76(1):81–90. https://doi.org/10.1016/j.jaad.2016.07.042.; Poizeau F, Nowak E, Kerbrat S, Le Nautout B, Droitcourt C, Drici M-D et al. Association between early severe cardiovascular events and the initiation of treatment with the anti-interleukin 12/23p40 antibody ustekinumab. JAMA Dermatol. 2020;156(11):1208–1215. https://doi.org/10.1001/jamadermatol.2020.2977.; Kimball AB, Papp KA, Wasfi Y, Chan D, Bissonnette R, Sofen H et al. Longterm efficacy of ustekinumab in patients with moderate-to-severe psoriasis treated for up to 5 years in the PHOENIX 1 study. J Eur Acad Dermatol Venereol. 2013;27(12):1535–1545. https://doi.org/10.1111/jdv.12046.; Papp K, Gottlieb AB, Naldi L, Pariser D, Ho V, Goyal K et al. Safety surveillance for ustekinumab and other psoriasis treatments from the Psoriasis Longitudinal Assessment and Registry (PSOLAR). J Drugs Dermatol. 2015;14(7):58–66. Available at: https://pubmed.ncbi.nlm.nih.gov/?term=39.%09Papp+K,+Gottlieb+AB,+Naldi+L+et+al.+Safety+surveillance+for+ustekinumab+and+other+psoriasis+treatments+from+the+Psoriasis+Longitudinal+Assessment+and+Registry+%28PSOLAR%29.+J+Drugs+Dermatology.+2015%3B14%3A5.; Lockshin B, Balagula Y, Merola JF. Interleukin 17, inflammation, and cardiovascular risk in patients with psoriasis. J Am Acad Dermatol. 2018;79(2): 345–352. https://doi.org/10.1016/j.jaad.2018.02.040.; de Brito M, Yiu ZZN. Cardiovascular Safety of biologics targeting interleukin (IL)-12 and/or IL-23: what does the evidence say? Am J Clin Dermatol. 2021;22(5):587–601. https://doi.org/10.1007/s40257-021-00612-9.; Crowley JJ, Warren RB, Cather JC. Safety of selective IL-23p19 inhibitors for the treatment of psoriasis. J Eur Acad Dermatol Venereol. 2019;33(9):1676–1684. https://doi.org/10.1111/jdv.15653.; Blauvelt A, Tsai T-F, Langley RG, Miller M, Shen Y-K, You Y et al. Consistent safety profile with up to 5 years of continuous treatment with guselkumab: pooled analyses from the phase 3 VOYAGE 1 and VOYAGE 2 trials of patients with moderate-to-severe psoriasis. J Am Acad Dermatol. 2022;86(4):827–834. https://doi.org/10.1016/j.jaad.2021.11.004.; Margolis D, Bilker W, Hennessy S, Vittorio C, Santanna J, Strom BL. The risk of malignancy associated with psoriasis. Arch Dermatol. 2001;137(6):778–783. Available at: https://pubmed.ncbi.nlm.nih.gov/?term=44.%09Margolis+D,+Bilker+W,+Hennessy+S,+Vittorio+C,+Santanna+J,+Strom+BL.+The+risk+of+malignancy+associated+with+psoriasis.+Arch+Dermatol.+2001%3B137%3A778%E2%80%93783.; Askling J, Fahrbach K, Nordstrom B, Ross S, Schmid CH, Symmons D. Cancer risk with tumor necrosis factor alpha (TNF) inhibitors: meta-analysis of randomized controlled trials of adalimumab, etanercept, and infliximab using patient level data. Pharmacoepidemiol Drug Saf. 2011;20(2):119–130. https://doi.org/10.1002/pds.2046.; Bongartz T, Sutton AJ, Sweeting MJ, Buchan I, Matteson EL, Montori V. AntiTNF antibody therapy in rheumatoid arthritis and the risk of serious infections and malignancies–systematic review and meta-analysis of rare harmful effects in randomized controlled trials. JAMA. 2006;295(19):2275–2285. https://doi.org/10.1001/jama.295.19.2275.; Gottlieb A, Lebwohl M, Liu C. Malignancy Rates in Brodalumab Clinical Studies for Psoriasis. Am J Clin Dermatol. 2020;21(3):421–430. https://doi.org/10.1007/s40257-020-00512-4.; Strober B, Leonardi C, Papp KA, Mrowietz U, Ohtsuki M, Bissonnette R et al. Short- and long-term safety outcomes with ixekizumab from 7 clinical trials in psoriasis: etanercept comparisons and integrated data. J Am Acad Dermatol. 2017;76(3):432–440. https://doi.org/10.1016/j.jaad.2016.09.026.; Papp KA, Griffiths CEM, Gordon K, Lebwohl M, Szapary Po, Wasfi Y et al. Long-term safety of ustekinumab in patients with moderate-to-severe psoriasis: final results from 5 years of follow-up. B J Dermatol. 2013;168(4):844–854. https://doi.org/10.1111/bjd.12214.; Gordon KB, Papp KA, Langley RG, Ho V, Kimball AB, Guzzo C et al. Long-term safety experience of ustekinumab in patients with moderate to severe psoriasis (part II of II): results from analyses of infections and malignancy from pooled phase II and III clinical trials. J Am Acad Dermatol. 2012;66(5):742–751. https://doi.org/10.1016/j.jaad.2011.06.041.; Strober B, Gooderham M, de Jong EMGJ, Kimball AB, Langley RG, Lakdawala N et al. Depressive symptoms, depression, and the effect of biologic therapy among patients in Psoriasis Longitudinal Assessment and Registry (PSOLAR). J Am Acad Dermatol. 2018;78(1):70–80. https://doi.org/10.1016/j.jaad.2017.08.051.; Langley RG, Feldman SR, Han C, Schenkel B, Szapary P, Hsu M-C et al. Ustekinumab significantly improves symptoms of anxiety, depression, and skin-related quality of life in patients with moderate-to-severe psoriasis: results from a randomized, double-blind, placebo-controlled phase III trial. J Am Acad Dermatol. 2010;63(3):457–465. https://doi.org/10.1016/j.jaad.2009.09.014.; Griffiths CEM, Fava M, Miller AH, Russell J, Ball SG, Xu W et al. Impact of ixekizumab treatment on depressive symptoms and systemic inflammation in patients with moderate-to-severe psoriasis: an integrated analysis of three phase 3 clinical studies. Psychother Psychosom. 2017;86(5):260–267. https://doi.org/10.1159/000479163.; Strober BE, Langley RGB, Menter A, Magid M, Porter B, Fox T et al. No elevated risk for depression, anxiety or suicidality with secukinumab in a pooled analysis of data from 10 clinical studies in moderate-to-severe plaque psoriasis. Br J Dermatol. 2018;178(2):E105-107. https://doi.org/10.1111/bjd.16051.; Komori T, Otsuka A, Honda Y, Kanameishi S, Honda T, Kabashima K. Exacerbation of depression in a psoriatic arthritis patient possibly induced by secukinumab. Eur J Dermatol. 2016;26(5):506–507. https://doi.org/10.1684/ejd.2016.2832.; Reich K, Gordon B, Strober BE, Armstrong AW, Miller M, Shen YK. Five‐year maintenance of clinical response and health‐related quality of life improvements in patients with moderate‐to‐severe psoriasis treated with guselkumab: results from VOYAGE 1 and VOYAGE 2. British Journal of Dermatol. 2021;185(6):1146–1159. https://doi.org/10.1111/bjd.20568.
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15Academic Journal
Authors: L. A. Smirnova, O. V. Simonova, E. N. Sukhikh, A. O. Shilyaeva, Л. А. Смирнова, О. В. Симонова, Е. Н. Сухих, А. О. Шиляева
Source: Rheumatology Science and Practice; Vol 60, No 5 (2022); 599-602 ; Научно-практическая ревматология; Vol 60, No 5 (2022); 599-602 ; 1995-4492 ; 1995-4484
Subject Terms: генно-инженерная биологическая терапия, secondary renal amyloidosis, nephrotic syndrome, chronic kidney disease, interleukin 6, genetic engineering biological therapy, вторичный амилоидоз почек, нефротический синдром, хроническая болезнь почек, ингибитор интерлейкина 6
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Relation: https://rsp.mediar-press.net/rsp/article/view/3229/2233; Hickson LJ, Crowson CS, Gabriel SE, McCarthy JT, Matteson EL. Development of reduced kidney function in rheumatoid arthritis. Am J Kidney Dis. 2014;63(2):206-213. doi:10.1053/j.ajkd.2013.08.010; Listing J, Kekow J, Manger B, Burmester GR, Pattloch D, Zink A, et al. Mortality in rheumatoid arthritis: the impact of disease activity, treatment with glucocorticoids, TNFα inhibitors and rituximab. Ann Rheum Dis. 2015;74(2):415-421. doi:10.1136/ annrheumdis-2013-204021; Оранский СП. Хроническая болезнь почек при ревматоидно артрите: ассоциация с сердечно-сосудистым риском. Фундаментальные исследования. 2013;12(2):285-288; Чеботарева НВ, Гуляев СВ, Андросова ТВ, Милованова ЛЮ. Хроническая болезнь почек у больных ревматоидным артритом: частота, факторы риска, варианты поражения почек. Терапевтический архив. 2019;91(5):129-133.; Makino H, Yoshinaga Y, Yamasaki Y, Morita Y, Hashimoto H, Yamamura M. Renal involvement in rheumatoid arthritis: analysis of renal biopsy specimens from 100 patients. Mod Rheumatol. 2002;12(2):148-154. doi:10.3109/s101650200025; Ребров АП, Тяпкина МА, Волошина ЕВ. Субклиническое поражение почек у пациентов с ревматоидным артритом. Лечащий врач. 2012;4:40-42.; Sipe JD, Benson MD, Buxbaum JN, Ikeda SI, Merlini G, Saraiva MJ, et al. Amyloid fibril proteins and amyloidosis: Chemical identification and clinical classification International Society of Amyloidosis 2016 Nomenclature Guidelines. Amyloid. 2016;23(4):209-213. doi:10.1080/13506129.2016.1257986; Li ZI, Chung AC, Zhou L, Huang XR, Liu F, Fu P, et al. C-reactive protein promotes acute renal inflammation and fibrosis in unilateral ureteral obstructive nephropathy in mice. Lab Invest. 2011;91(6):837-851. doi:10.1038/labinvest.2011.42; Kim HW, Lee CK, Cha HS, Choe JY, Park EJ, Kim J. Effect of antitumor necrosis factor alpha treatment of rheumatoid arthritis and chronic kidney disease. Rheumatol Int. 2015;35(4):727-734. doi:10.1007/s00296-014-3146-4; Sumida K, Molnar MZ, Potukuchi PK, Hassan F, Thomas F, Yamagata K, et al. Treatment of rheumatoid arthritis with biologic agents lowers the risk of incident chronic kidney disease. Kidney Int. 2018;93(5):1207-1216. doi:10.1016/j.kint.2017.11.025; Nakamura T, Kumon Y, Hirata S, Takaoka H. Abatacept may be effective and safe in patients with amyloid A amyloidosis secondary to rheumatoid arthritis. Clin Exp Rheumatol. 2014;32(4):501-508.; Nakamura T, Higashi S, Tomoda K, Tsukano M, Shono M. Etanercept can induce resolution of renal deterioration in patients with amyloid A amyloidosis secondary to rheumatoid arthritis. Clin Rheumatol. 2010;29(12):1395-1401. doi:10.1007/s10067-010-1469-4; Okuda Y. AA amyloidosis – Benefits and prospects of IL-6 inhibitors. Mod Rheumatol. 2019;29(2):268-274. doi:10.1080/14397595.2 018.1515145; Sato H, Sakai T, Sugaya T, Otaki Y, Aoki K, Ishii K, et al. Tocilizumab dramatically ameliorated life-threatening diarrhea due to secondary amyloidosis associated with rheumatoid arthritis. Clin Rheumatol. 2009;28(9):1113-1136. doi:10.1007/s10067-009-1185-0; Симонова ОВ, Сухих ЕН, Смирнова ЛА, Тимин МВ. Клинический случай успешной трансплантации почки у пациента с вторичным амилоидозом на фоне анкилозирующего спондилоартрита. Лечащий врач. 2020;1:36-38.; Smolen JS, Beaulieu A, Rubbert-Roth A, Ramos-Remus C, Rovensky J, Alecock E, et al.; OPTION Investigators. Effect of interleukin-6 receptor inhibition with tocilizumab in patients with rheumatoid arthritis (OPTION study): A double-blind, placebo-controlled, randomised trial. Lancet. 2008;371(9617):987-997. doi:10.1016/S0140-6736(08)60453-5; Насонов ЕЛ. Применение тоцилизумаба при ревматоидном артрите: новые данные. Научно-практическая ревматология. 2011;(6):46-56.
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16Academic Journal
Authors: A. Yu. Kraposhina, E. A. Sobko, I. V. Demko, A. B. Katser, O. V. Kazmerchuk, Yu. I. Abramov, S. V. Chubarova, А. Ю. Крапошина, Е. А. Собко, И. В. Демко, А. Б. Кацер, О. В. Казмерчук, Ю. И. Абрамов, С. В. Чубарова
Source: Meditsinskiy sovet = Medical Council; № 18 (2022); 20-28 ; Медицинский Совет; № 18 (2022); 20-28 ; 2658-5790 ; 2079-701X
Subject Terms: эозинофильное воспаление, asthma pathogenesis, targeted therapy, genetically engineered biological therapy, T2 endotype markers, eosinophilic inflammation, патогенез астмы, таргетная терапия, генно-инженерная биологическая терапия, маркеры Т2-эндотипа
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PLoS ONE. 2013;8(3):e59872. https://doi.org/10.1371/journal.pone.0059872.; Parker J.M., Oh C.K., LaForce C., Miller S.D., Pearlman D.S., Le C. et al. Safety profile and clinical activity of multiple subcutaneous doses of MEDI-528, a humanized anti-interleukin-9 monoclonal antibody, in two randomized phase 2a studies in subjects with asthma. BMC Pulm Med. 2011;11:14. https://doi.org/10.1186/1471-2466-11-14.; Cheng G., Arima M., Honda K., Hirata H., Eda F., Yoshida N. et al. Antiinterleukin-9 antibody treatment inhibits airway inflammation and hyperreactivity in mouse asthma model. Am J Respir Crit Care Med. 2002;166(3):409–416. https://doi.org/10.1164/rccm.2105079.; Yang G., Li L., Volk A., Emmell E., Petley T., Giles-Komar J. et al. Therapeutic dosing with anti-interleukin-13 monoclonal antibody inhibits asthma progression in mice. J Pharmacol Exp Ther. 2005;313(1):8–15. https://doi.org/10.1124/jpet.104.076133.; Singh D., Kane B., Molfino N.A., Faggioni R., Roskos L., Woodcock A. A phase 1 study evaluating the pharmacokinetics, safety and tolerability of repeat dosing with a human IL-13 antibody (CAT-354) in subjects with asthma. BMC Pulm Med. 2010;10:3. https://doi.org/10.1186/1471-2466-10-3.; Corren J., Lemanske R.F., Hanania N.A., Korenblat P.E., Parsey M.V., Arron J.R. et al. Lebrikizumab treatment in adults with asthma. N Engl J Med. 2011;365(12):1088–1098. https://doi.org/10.1056/NEJMoa1106469.; Laviolette M., Gossage D., Gauvreau G., Leigh R., Olivenstein R., Katial R. et al. Effects of benralizumab on airway eosinophils in asthmatic patients with sputum eosinophilia. J Allergy Clin Immunol. 2013;132(5):1086–1096. https://doi.org/10.1016/j.jaci.2013.05.020.; Pérez de Llano L.A., Cosío B.G., Domingo C., Urrutia I., Bobolea I., Valero A. et al. Efficacy and safety of reslizumab in patients with severe asthma with inadequate response to omalizumab: A multicenter, open-label pilot study. J Allergy Clin Immunol Pract. 2019;7(7):2277–2283.e2. https://doi.org/10.1016/j.jaip.2019.01.017.; Bleecker E.R., FitzGerald J.M., Chanez P., Papi A., Weinstein S.F., Barker P. et al. Efficacy and safety of benralizumab for patients with severe asthma uncontrolled with high-dosage inhaled corticosteroids and long-acting beta2-agonists (SIROCCO): a randomised, multicentre, placebo-controlled phase 3 trial. Lancet. 2016;388(10056):2115–2127. https://doi.org/10.1016/S0140-6736(16)31324-1.; FitzGerald J.M., Bleecker E., Nair P., Korn S., Ohta K., Lommatzsch M. et al. Benralizumab, an anti-interleukin-5 receptor alpha monoclonal antibody, as add-on treatment for patients with severe, uncontrolled, eosinophilic asthma (CALIMA): a randomised, double-blind, placebo-controlled phase 3 trial. Lancet. 2016;388(10056):2128–2141. https://doi.org/10.1016/S0140-6736(16)31322-8.; Parulekar A.D., Diamant Z., Hanania N.A. Role of biologics targeting type 2 airway inflammation in asthma: what have we learned so far? Curr Opin Pulm Med. 2017;23(1):3–11. https://doi.org/10.1097/MCP.0000000000000343.; Menzies-Gow A., Ponnarambil S., Downie J., Bowen K., Hellqvist Å., Colice G. DESTINATION: a phase 3, multicentre, randomized, doubleblind, placebo-controlled, parallel-group trial to evaluate the longterm safety and tolerability of tezepelumab in adults and adolescents with severe, uncontrolled asthma. Respir Res. 2020;21(1):279. https://doi.org/10.1186/s12931-020-01541-7.; Chung K.F., Wenzel S.E., Brozek J.L., Bush A., Castro M., Sterk P.J. et al. International ERS/ATS guidelines on definition, evaluation and treatment of severe asthma. Eur Respir J. 2014;43(2):343–373. https://doi.org/10.1183/09031936.00202013.
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17Academic Journal
Authors: Фентисов, В. В.
Subject Terms: медицина, внутренние болезни, ревматоидный артрит, генно-инженерная биологическая терапия, латентная туберкулезная инфекция
Availability: http://dspace.bsu.edu.ru/handle/123456789/52749
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18Academic Journal
Contributors: The article has been funded by Johnson & Johnson., Статья подготовлена при финансовой поддержке компании Johnson & Johnson.
Source: Current Pediatrics; Том 20, № 5 (2021); 451-458 ; Вопросы современной педиатрии; Том 20, № 5 (2021); 451-458 ; 1682-5535 ; 1682-5527
Subject Terms: бионаивность, children, survivability, genetically engineered biological therapy, ustekinumab, adalimumab, etanercept, bionaive, дети, выживаемость, генно-инженерная биологическая терапия, устекинумаб, адалимумаб, этанерцепт
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Relation: https://vsp.spr-journal.ru/jour/article/view/2746/1087; Michalek IM, Loring B, John SM. A systematic review of worldwide epidemiology of psoriasis. J Europ Acad Dermatol Venereol. 2016;31(2):205-212. doi:10.1111/jdv.13854; Murzina E. Pediatric Psoriasis: Clinical Features and Course. OAJBS. 2020;1(5):207-209. doi:10.38125/OAJBS.000147; Augustin M, Glaeske G, Radtke MA, et al. Epidemiology and comorbidity of psoriasis in children. Br J Dermatol. 2010;162(3):633-636. doi:10.1111/j.1365-2133.2009.09593.x; Gelfand JM, Weinstein R, Porter SB, et al. Prevalence and treatment of psoriasis in the United Kingdom: a population-based study. Arch Dermatol. 2005;141(12):1537-1541. doi:10.1001/archderm.141.12.1537; Кубанов А.А., Богданова Е.В. Организация и результаты оказания медицинской помощи по профилю «дерматовенерология» в Российской Федерации. Итоги 2018 года // Вестник дерматологии и венерологии. — 2019. — Т. 95. — № 4. — С. 8-23. doi:10.25208/0042-4609-2019-95-4-8-23; Torrelo A. The use of biologics for childhood psoriasis. J Eur Acad Dermatol Venereol. 2019;33(10):1816-1816. doi:10.1111/jdv.15855; Cramer JA, Roy A, Burrell A, et al. Medication Compliance and Persistence: Terminology and Definitions. Value Health. 2008;11(1):44-47. doi:10.1111/j.1524-4733.2007.00213.x; Phan C, Beauchet A, Burztejn A-C, et al. Biological treatments for paediatric psoriasis: A retrospective observational study on biological drug survival in daily practice in childhood psoriasis. J Eur Acad Dermatol Venereol. 2019;33(10):1984-1992. doi:10.1111/jdv.15579; Augustin M, Krger K, Radtke MA, et al. Disease severity, quality of life and health care in plaque-type psoriasis: a multicenter crosssectional study in Germany. Dermatology. 2008;216(4):366-372. doi:10.1159/000119415; Соколовский Е.В., Круглова Л.С., Понич Е.С. «Болевые» точки системной терапии биологическими препаратами при псориазе // Российский журнал кожных и венерических болезней. — 2015. — Т. 18. — № 6. — С. 32-38.; Лесная И.Н., Фриго Н.В., Каганова Н.Л. и др. Молекулярные маркеры в прогнозировании клинической эффективности инфликсимаба у больных псориазом // Вестник дерматологии и венерологии. — 2010. — Т. 86. — № 1. — C. 57-66. doi:10.25208/vdv827
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19Academic Journal
Authors: E. A. Pyadushkina, E. V. Derkach, M. Yu. Frolov, V. A. Rogov, A. S. Salasyuk, Е. А. Пядушкина, Е. В. Деркач, М. Ю. Фролов, В. А. Рогов, А. С. Саласюк
Contributors: Lilly Pharma sponsored the study «Cost-effectiveness analysis of active psoriatic arthritis treatment with ixekizumab in adult patients in Russian Federation health care system», «Лилли фарма» спонсировала исследование «Клинико-экономический анализ применения иксекизумаба у взрослых пациентов с активным псориатическим артритом в условиях здравоохранения РФ»
Source: Modern Rheumatology Journal; Том 15, № 1 (2021); 119-127 ; Современная ревматология; Том 15, № 1 (2021); 119-127 ; 2310-158X ; 1996-7012
Subject Terms: влияние на бюджет, biologic disease-modifying antirheumatic drugs, ixekizumab, secukinumab, ustekinumab, budget impact, генно-инженерная биологическая терапия, иксекизумаб, секукинумаб, устекинумаб
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Relation: https://mrj.ima-press.net/mrj/article/view/1110/1068; Коротаева ТВ, Корсакова ЮЛ, Логинова ЕЮ и др. Псориатический артрит. Клинические рекомендации по диагностике и лечению. Современная ревматология. 2018;12(2):22–35. doi:10.14412/1996-7012-2018-2-22-35; Статистический сборник «Общая заболеваемость взрослого населения России в 2017 году» https://www.rosminzdrav.ru/ministry/61/22/stranitsa-979/statisticheskie-i-informatsionnyematerialy/statisticheskiy-sbornik-2017-god; Статистический сборник «Заболеваемость всего населения России в 2017 году» https://www.rosminzdrav.ru/ministry/61/22/stranitsa-979/statisticheskie-i-informatsionnyematerialy/statisticheskiy-sbornik-2017-god; Статистический сборник «Заболеваемость взрослого населения России в 2017 году» https://www.rosminzdrav.ru/ministry/61/22/stranitsa-979/statisticheskie-i-informatsionnyematerialy/statisticheskiy-sbornik-2017-god; Лила АМ, Насонов ЕЛ, Коротаева ТВ. Псориатический артрит: патогенетические особенности и инновационные методы терапии. Научно-практическая ревматология. 2018;56(6):685-91.; Государственный реестр лекарственных средств. https://grls.rosminzdrav.ru/; Коротаева ТВ. Новые возможности ГИБП в терапии псориатического артрита: фокус на иксекизумаб. Opinion Leader. 2019;(9):60-6.; Распоряжение Правительства Российской Федерации от 23 ноября 2020 г. № 3073-р «Об утверждении перечня жизненно необходимых и важнейших лекарственных препаратов для медицинского применения на 2021 год, перечня лекарственных препаратов для медицинского применения, в том числе лекарственных препаратов для медицинского применения, назначаемых по решению врачебных комиссий медицинских организаций, перечня лекарственных препаратов, предназначенных для обеспечения лиц, больных гемофилией, муковисцидозом, гипофизарным нанизмом, болезнью Гоше, а также минимального ассортимента лекарственных препаратов, необходимых для оказания медицинской помощи». http://static.government.ru/media/files/XSa8p7I5b5HKbAYd2xmfvVzBsosxagSe.pdf; Постановление Правительства Российской Федерации от 7 декабря 2019 г. №1610 «О Программе государственных гарантий бесплатного оказания гражданам медицинской помощи на 2020 год и на плановый период 2021 и 2022 годов». https://tyumen.ldc.ru/userfiles/public/postanovlenie-1610.pdfhttps://tyumen.ldc.ru/userfiles/public/postanovlenie-1610.pdf; Коротаева ТВ, Корсакова ЮЛ, Логинова ЕЮ и др. Оптимизация диагностики, системы мониторинга и лечения псориатического артрита в реальной практике: общие принципы организации общероссийского регистра пациентов с псориатическим артритом. Научно-практическая ревматология. 2019;55(4):407-14. doi:10.14412/1995-4484-2019-407-414; Государственный реестр лекарственных средств. Инструкция по медицинскому применению препарата Талс. https://grls.rosminzdrav.ru/Grls_View_v2.aspx?routingGuid=c819bbb6-be51-4ff5-9344-050d1084f6a1&t=; National Institute for Health and Care Excellence. Ixekizumab for treating active psoriatic arthritis after inadequate response to DMARDs. [TA537]. https://www.nice.org.uk/guidance/ta537; Протокол Совещания профильной комиссии Экспертного совета Минздрава России по специальности «Ревматология» №23 от 28 сентября 2019 г. Научно-практическая ревматология. 2019;57(5):604-7.; Методические рекомендации по проведению сравнительной клинико-экономической оценки лекарственного препарата, утвержденные приказом ФГБУ «Центр экспертизы и контроля качества медицинской помощи» Минздрава России от 29 декабря 2018 г. №242-од. https://rosmedex.ru/hta/recom/; Методические рекомендации по оценке влияния на бюджет в рамках реализации программы государственных гарантий бесплатного оказания гражданам медицинской помощи, утвержденные приказом ФГБУ «Центр экспертизы и контроля качества медицинской помощи» Минздрава России от 29 декабря 2018 г. №242-од. https://rosmedex.ru/hta/recom/; Wu D, Yue J, Tam LS. Efficacy and safety of biologics targeting interleukin-6,-12/23 and-17 pathways for peripheral psoriatic arthritis: a network meta-analysis. Rheumatology (Oxford). 2018 Mar 1;57(3):563-71. doi:10.1093/rheumatology/kex452.; Реброва ОЮ, Федяева ВК. Вопросник для оценки достоверности сетевого метаанализа (в том числе непрямых и смешанных сравнений). Медицинские технологии. Оценка и выбор. 2016;(2):48-54.; Jansen JP, Trikalinos T, Cappelleri JC, et al. Indirect treatment comparison/network meta-analysis study questionnaire to assess relevance and credibility to inform health care decision-making: an ISPOR-AMCP-NPC Good Practice Task Force report. Value Health. 2014 Mar;17(2):157-73. doi:10.1016/j.jval.2014.01.004.; Данные о предельных размерах оптовых надбавок и предельных размерах розничных надбавок к ценам на жизненно необходимые и важнейшие лекарственные препараты, установленные в субъектах Российской Федерации (данные на 10 февраля 2020https://fas.gov.ru/documents/686367; Оценка численности постоянного населения на 1 января 2020 года и в среднем за 2019 г. Федеральная служба государственной статистики. http://www.gks.ru/free_doc/new_site/population/demo/Popul2020.xls; Инструкция по применению лекарственного препарата для медицинского применения Козэнтикс (секукинумаб). https://grls.rosminzdrav.ru/GRLS.aspx; Инструкция по применению лекарственного препарата для медицинского применения Стелара (устекинумаб). https://grls.rosminzdrav.ru/GRLS.aspx; Walpole SC, Prieto-Merino D, Edwards P, et al. The weight of nations: an estimation of adult human biomass. BMC Public Health. 2012 Jun 18;12:439. doi:10.1186/1471-2458-12-439.; Лила АМ, Древаль РО, Шипицын ВВ. Оценка организации медицинской помощи и лекарственного обеспечения при ревматических заболеваниях и социально-экономического бремени этих болезней в Российской Федерации. Современная ревматология. 2018;12(3):112–9. doi:10.14412/1996-7012-2018-3-112-119
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20Academic Journal
Authors: P. A. Shesternya, O. D. Gritsenko, P. A. Astanin, A. Yu. Stepanenko, N. V. Popov, П. А. Шестерня, О. Д. Гриценко, П. А. Астанин, А. Ю. Степаненко, Н. В. Попов
Contributors: The investigation has been conducted within scientific topic № AAA-A20-120022890005-5 «Personified Clinicoimmunological Strategy of spondyloarthritis treatment with biological disease modifying anti-rheumatic drugs», Работа выполнена в рамках Государственного задания Минзрава России «Персонифицированная клинико-иммунологическая стратегия генно-инженерной биологической терапии спондилоартрита» (№АААА-А20-120022890005-5)
Source: Modern Rheumatology Journal; Том 15, № 2 (2021); 29-34 ; Современная ревматология; Том 15, № 2 (2021); 29-34 ; 2310-158X ; 1996-7012
Subject Terms: ремиссия, axial spondyloarthritis, Magnetic resonance imaging (MRI), biological disease modifying anti-rheumatic drugs therapy (bDMARDs), sacroiliitis, remission, аксиальный спондилоартрит, магнитно-резонансная томография, генно-инженерная биологическая терапия, сакроилиит
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Relation: https://mrj.ima-press.net/mrj/article/view/1119/1078; Румянцева ДГ, Эрдес ШФ. Аксиальный спондилоартрит: современный взгляд на концепцию и эволюцию болезни. Современная ревматология. 2019;13(4):4-10. doi:10/14412/1996-7012-2019-4-4-10; Bennett AN, Marzo-Ortega H, KaurPapadakis D, et al. The use of magnetic resonance imaging in axial spondyloarthritis: time to bridge the gap between radiologists and rheumatologists. J Rheumatol. 2017 Jun; 44(6):780-5. doi:10.3899/jrheum.161337. Epub 2017 Apr 1.; Baraliakos X, Richter A, Feldmann D, et al. Which factors are associated with bone marrow oedema suspicious of axial spondyloarthritis as detected by MRI in the sacroiliac joints and the spine in the general population? Ann Rheum Dis. 2020 Nov 25; annrheumdis-2020-218669. doi:10.1136/annrheumdis-2020-218669. Online ahead of print.; Chan SC, Li PH, Lee KH, et al. Diagnostic utility of whole spine and thoracic spine MRI corner inflammatory lesions in axial spondyloarthritis. Ther Adv Musculoskelet Dis. 2020 Nov 24;12: 1759720X20973922. doi:10.1177/1759720X20973922. eCollection 2020.; Bakker PAC, Ramiro S, Ez-Zaitouni Z, et al. Is it Useful to Repeat Magnetic Resonance Imaging of the Sacroiliac Joints After Three Months or One Year in the Diagnosis of Patients With Chronic Back Pain and Suspected Axial Spondyloarthritis? Arthritis Rheumatol. 2019 Mar;71(3):382-91. doi:10.1002/art.40718. Epub 2019 Feb 6.; Гайдукова ИЗ, Ребров АП, Коротаева ТВ, и др. Ремиссия при аксиальных спондилоартритах – определение и инструменты оценки (рекомендации Экспертной группы по изучению спондилоартритов при Общероссийской общественной организации Ассоциация ревматологов России.). Научно-практическая ревматология. 2018;56(1):10-4.; Andreasen RA, Kristensen LE, Baraliakos X, et al. Assessing the effect of interventions for axial spondyloarthritis according to the endorsed ASAS/OMERACT core outcome set: a meta-research study of trials included in Cochrane reviews. Arthritis Res Ther. 2020 Jul 25;22(1):177. doi:10.1186/s13075-020-02262-4.; Schwartzman M, Maksymowych WP. Is there a role for MRI to establish treatment indications and effectively monitor response in patients with axial spondyloarthritis? Rheum Dis Clin North Am. 2019 Aug;45(3): 341-58. doi:10.1016/j.rdc.2019.04.009. Epub 2019 Jun 5.; Ward MM, Deodhar A, Gensler LS, et al. 2019 Update of the American College of Rheumatology/Spondylitis Association of America/Spondyloarthritis Research and Treatment Network Recommendations for the Treatment of Ankylosing Spondylitis and Nonradiographic Axial Spondyloarthritis. Arthritis Care Res (Hoboken). 2019 Oct; 71(10):1285-99. doi:10.1002/acr.24025. Epub 2019 Aug 21.; Machado PM, Landewe R, van der Heijde D, et al. Ankylosing Spondylitis Disease Activity Score (ASDAS): 2018 update of the nomenclature for disease activity states. Ann Rheum Dis. 2018 Oct; 77(10):1539-40. doi:10.1136/annrheumdis2018-213184. Epub 2018 Feb 16.; Эрдес Ш, Смирнов АВ. Технология диагностики воспалительных изменений скелета при анкилозирующем спондилите по данным магнитно-резонансной томографии. Научно-практическая ревматология. 2019;57(6):678-84.; Madari Q, Sepriano A, Ramiro S, et al. 5-year follow- up of spinal and sacroiliac MRI abnormalities in early axial spondyloarthritis: data from the Desir cohort. RMD Open. 2020 Feb;6(1):e001093. doi:10.1136/rmdopen-2019-001093.; Huang Y, Chen Y, Liu T, et al. Impact of tumor necrosis factor α inhibitors on MRI inflammation in axial spondyloarthritis assessed by Spondyloarthritis Research Consortium Canada score: A metaanalysis. PLoS One. 2020 Dec 31;15(12):e0244788. doi:10.1371/journal.pone.0244788. eCollection 2020.; Эрдес Ш, Румянцева ДГ, Смирнов АВ и др. Активность заболевания и двухлетняя динамика изменений крестцово-подвздошных суставов по данным инструментальных методов исследованияу больных ранним аксиальным спондилоартритом когорты КоРСАр. Научно-практическая ревматология. 2019;57(2):186-90.; Krabbe S, Eshed I, S∅rensen IJ, et al. Novel whole-body magnetic resonance imaging response and remission criteria document diminished inflammation during golimumab treatment in axial spondyloarthritis. Rheumatology (Oxford). 2020 Nov 1;59(11): 3358-68. doi:10.1093/rheumatology/keaa153.; Smolen JS, Schö ls M, Braun J, et al. Treating axial spondyloarthritis and peripher al spondyloarthritis, especially psoriatic arthritis, to target: 2017 update of recommendations by an international task force. Ann Rheum Dis. 2018 Jan;77(1):3-17. doi:10.1136/annrheumdis-2017-211734; Акулова АИ, Дорогойкина КД, Гайдукова ИЗ и др. Качество жизни пациентов со спондилоартритами, получающих генно-инженерную биологическую терапию. Современная ревматология. 2019; 13(4):36-40. doi:10.14412/1996-7012-2019-4-36-40