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    Academic Journal

    Source: Rheumatology Science and Practice; Vol 60, No 5 (2022); 538-545 ; Научно-практическая ревматология; Vol 60, No 5 (2022); 538-545 ; 1995-4492 ; 1995-4484

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    Relation: https://rsp.mediar-press.net/rsp/article/view/3220/2224; Gabrielli A, Avvedimento EV, Krieg T. Scleroderma. N Engl J Med. 2009;360(19):1989-2003. doi:10.1056/NEJMra0806188; Marie I, Gehanno JF. Environmental risk factors of systemic sclerosis. Semin Immunopathol. 2015;37(5):463-473. doi:10.1007/ s00281-015-0507-3; Elhai M, Avouac J, Walker UA, Matucci-Cerinic M, Riemekasten G, Airò P, et al.; EUSTAR co-authors. A gender gap in primary and secondary heart dysfunctions in systemic sclerosis: A EUSTAR prospective study. Ann Rheum Dis. 2016;75(1):163-169. doi:10.1136/annrheumdis-2014-206386; Ruzehaji N, Avouac J, Elhai M, Frechet M, Frantz C, Ruiz B, et al. Combined effect of genetic background and gender in a mouse model of bleomycin-induced skin fibrosis. Arthritis Res Ther. 2015;17(1):145. doi:10.1186/s13075-015-0659-5; D’Amico F, Skarmoutsou E, Mazzarino MC. The sex bias in systemic sclerosis: On the possible mechanisms underlying the female disease preponderance. 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JAMA. 2002;288(3):321-333. doi:10.1001/jama.288.3.321; Балан ВЕ, Андреева ЕН, Юренева СВ, Ткачева ОН, Илюхин ЕА. Риск и польза менопаузальной гормональной терапии. Акушерство и гинекология. 2020;3:33-41.; Крюков ЕВ, Паневин ТС. Антитромбогенная активность сосудистой стенки в период пери- и постменопаузы у женщин с климактерической миокардиодистрофией. Вестник национального медико-хирургического центра им. Н.И. Пиро - гова. 2020;15(2):67-70.; Крюков ЕВ, Паневин ТС, Попова ЛВ. Возрастные изменения системы гемостаза. Клиническая медицина. 2020;98(1):9-12.; Крюков ЕВ, Попова ЛВ, Васильев СВ, Паневин ТС, Паневина АС, Стромская УА, и др. Ультранизкодозированная менопаузальная гормонотерапия с дидрогестероном: роль в профилактике развития и прогрессирования атеросклероза. Вестник Российской военно-медицинской академии. 2021;1(73):9-14.; Kowal-Bielecka O, Fransen J, Avouac J, Becker M, Kulak A, Allanore Y, et al.; EUSTAR Coauthors. Update of EULAR recommendations for the treatment of systemic sclerosis. Ann Rheum Dis. 2017;76(8):1327-1339. doi:10.1136/annrheumdis-2016-209909; Aida-Yasuoka K, Peoples C, Yasuoka H, Hershberger P, Thiel K, Cauley JA, et al. Estradiol promotes the development of a fibrotic phenotype and is increased in the serum of patients with systemic sclerosis. Arthritis Res Ther. 2013;15(1):R10. doi:10.1186/ar4140; Кашникова ЛН, Гроздова МД, Панасюк АФ. Значение эстрадиола в развитии фиброза при системной склеродермии (основы половой прерасположенности к заболеванию). Бюллетень экспериментальной биологии и медицины. 1991;111(4):365-367.; Soldano S, Montagna P, Brizzolara R, Sulli A, Parodi A, Seriolo B, et al. Effects of estrogens on extracellular matrix synthesis in cultures of human normal and scleroderma skin fibroblasts. Ann N Y Acad Sci. 2010;1193:25-29. doi:10.1111/j.1749-6632.2009.05296.x; Avouac J, Pezet S, Gonzalez V, Baudoin L, Cauvet A, Ruiz B, et al. Estrogens counteract the profibrotic effects of TGF-β and their inhibition exacerbates experimental dermal fibrosis. J Invest Dermatol. 2020;140(3):593-601.e7. doi:10.1016/ j.jid.2019.07.719; Hall G, Phillips TJ. Estrogen and skin: the effects of estrogen, menopause, and hormone replacement therapy on the skin. J Am Acad Dermatol. 2005;53(4):555-568. doi:10.1016/ j.jaad.2004.08.039; Brincat M, Kabalan S, Studd JW, Moniz CF, de Trafford J, Montgomery J. A study of the decrease of skin collagen content, skin thickness, and bone mass in the postmenopausal woman. Obstet Gynecol. 1987;70(6):840-845.; Maheux R, Naud F, Rioux M, Grenier R, Lemay A, Guy J, et al. A randomized, double-blind, placebo-controlled study on the effect of conjugated estrogens on skin thickness. Am J Obstet Gynecol. 1994;170(2):642-649. doi:10.1016/s0002-9378(94)70242-x; Vinet É, Bernatsky S, Hudson M, Pineau CA, Baron M; Canadian Scleroderma Research Group. Effect of menopause on the modified Rodnan skin score in systemic sclerosis. Arthritis Res Ther. 2014;16(3):R130. doi:10.1186/ar4587; Medsger TA Jr. Natural history of systemic sclerosis and the assessment of disease activity, severity, functional status, and psychologic well-being. Rheum Dis Clin North Am. 2003;29(2):255-273. doi:10.1016/s0889-857x(03)00023-1; Omair MA, Pagnoux C, McDonald-Blumer H, Johnson SR. Low bone density in systemic sclerosis. A systematic review. J Rheumatol. 2013;40(11):1881-1890. doi:10.3899/jrheum.130032; Dovio A, Data V, Carignola R, Calzolari G, Vitetta R, Ventura M, et al. Circulating osteoprotegerin and soluble RANK ligand in systemic sclerosis. J Rheumatol. 2008;35(11):2206-2213. doi:10.3899/ jrheum.080192; Kilic G, Kilic E, Akgul O, Ozgocmen S. Increased risk for bone loss in women with systemic sclerosis: A comparative study with rheumatoid arthritis. Int J Rheum Dis. 2016;19(4):405-411. doi:10.1111/1756-185X.12242; Добровольская ОВ, Демин НВ, Смирнов АВ, Гарзанова ЛА, Торопцова НВ, Алекперов РТ. Состояние минеральной плотности кости у пациентов с системной склеродермией. Современная ревматология. 2019;13(1):58-63.; Добровольская ОВ, Демин НВ, Смирнов АВ, Торопцова НВ. Состояние минеральной плотности костной ткани и потребность в противоостеопоротической терапии у женщин в постменопаузе с системной склеродермией. Медицинский совет. 2019;(9):72-79.; John G. Systemic sclerosis and urinary symptoms: A complex pathophysiology. Clin Rheumatol. 2020;39(1):5-8. doi:10.1007/ s10067-019-04714-y; John G, Avouac J, Piantoni S, Polito P, Fredi M, Cozzi F, et al. Prevalence and disease-specific risk factors for lower urinary tract symptoms in systemic sclerosis: An international multicenter study. Arthritis Care Res (Hoboken). 2018;70(8):1218-1227. doi:10.1002/ acr.23454; Irwin DE, Milsom I, Hunskaar S, Reilly K, Kopp Z, Herschorn S, et al. Population-based survey of urinary incontinence, overactive bladder, and other lower urinary tract symptoms in five countries: Results of the EPIC study. Eur Urol. 2006;50(6):1306-1314. doi:10.1016/j.eururo.2006.09.019; Zigman JS, Yazdany J, Trinidad J, Yazdany T. Scleroderma and pelvic organ prolapse: A multidisciplinary approach to patient care and surgical planning. J Gynecol Surg. 2017;33(5):198-201. doi:10.1089/gyn.2017.0014; John G, Allanore Y, Polito P, Piantoni S, Fredi M, Avouac J, et al. The limited cutaneous form of systemic sclerosis is associated with urinary incontinence: An international multicentre study. Rheumatology (Oxford). 2017;56(11):1874-1883. doi:10.1093/ rheumatology/kex230; Motegi SI, Sekiguchi A, Sekine Y, Nakayama H, Suzuki K, Ishikawa O. Prevalence and clinical characteristics of overactive bladder in systemic sclerosis. Mod Rheumatol. 2020;30(2):327-331. doi:10.1080/14397595.2019.1589913; Kucharz EJ, Jonderko G, Rubisz-Brzezinska J, Końca A, Jarczyk R. Premictional volume and contractility of the urinary bladder in patients with systemic sclerosis. Clin Rheumatol. 1996;15(2):118-120. doi:10.1007/BF02230326; Kondo A, Susset JG. Viscoelastic properties of bladder. II. Comparative studies in normal and pathologic dogs. Invest Urol. 1974;11(6):459-465.; Minervini R, Morelli G, Minervini A, Pampaloni S, Tognetti A, Fiorentini L, et al. Bladder involvement in systemic sclerosis: Urodynamic and histological evaluation in 23 patients. Eur Urol. 1998;34(1):47-52. doi:10.1159/000019678; Leinwand I, Duryee AW, Richter MN. Scleroderma; based on a study of over 150 cases. Ann Intern Med. 1954;41(5):1003- 1041. doi:10.7326/0003-4819-41-5-1003; Bertinotti L, Bracci S, Nacci F, Colangelo N, Del Rosso A, Casale R, et al. The autonomic nervous system in systemic sclerosis. A review. Clin Rheumatol. 2004;23(1):1-5. doi:10.1007/ s10067-003-0812-4; Compérat E, Reitz A, Delcourt A, Capron F, Denys P, ChartierKastler E. Histologic features in the urinary bladder wall affected from neurogenic overactivity – A comparison of inflammation, oedema and fibrosis with and without injection of botulinum toxin type A. Eur Urol. 2006;50(5):1058-1064. doi:10.1016/ j.eururo.2006.01.025; Thoua NM, Abdel-Halim M, Forbes A, Denton CP, Emmanuel AV. Fecal incontinence in systemic sclerosis is secondary to neuropathy. Am J Gastroenterol. 2012;107(4):597-603. doi:10.1038/ ajg.2011.399; Singh J, Mehendiratta V, Del Galdo F, Jimenez SA, Cohen S, DiMarino AJ, et al. Immunoglobulins from scleroderma patients inhibit the muscarinic receptor activation in internal anal sphincter smooth muscle cells. Am J Physiol Gastrointest Liver Physiol. 2009;297(6):G1206-G1213. doi:10.1152/ajpgi.00286.2009; Fetscher C, Fleichman M, Schmidt M, Krege S, Michel MC. M(3) muscarinic receptors mediate contraction of human urinary bladder. 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The use of antihypertensive medication and the risk of breast cancer in a case-control study in a Spanish population: The MCC-spain study. PLoS One. 2016;11(8):e0159672. doi:10.1371/journal.pone.0159672; Lu TY, Hill CL, Pontifex EK, Roberts-Thomson PJ. Breast cancer and systemic sclerosis: A clinical description of 21 patients in a population-based cohort study. Rheumatol Int. 2008;28(9): 895-899. doi:10.1007/s00296-008-0540-9; De Angelis R, Di Battista J, Smerilli G, Cipolletta E, Di Carlo M, Salaffi F. Association of silicone breast implants, breast cancer and anti-RNA polymerase III autoantibodies in systemic sclerosis: Case-based review. Open Access Rheumatol. 2020;12:207-213. doi:10.2147/OARRR.S262428

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