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1Academic Journal
Authors: Alekseeva K.B., Kruchina T.К., Maljarova M.S., Novik G.A.
Contributors: 1
Source: Annals of the Russian academy of medical sciences; Vol 78, No 5 (2023); 498-504 ; Вестник Российской академии медицинских наук; Vol 78, No 5 (2023); 498-504 ; 2414-3545 ; 0869-6047 ; 10.15690/vramn.785
Subject Terms: antiarrhythmic therapy, propafenone, children, idiopathic premature ventricular contractions, антиаритмическая терапия, пропафенон, дети, идиопатическая желудочковая экстрасистолия
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Relation: https://vestnikramn.spr-journal.ru/jour/article/view/13677/1892; https://vestnikramn.spr-journal.ru/jour/article/view/13677/1855; https://vestnikramn.spr-journal.ru/jour/article/view/13677/1868; https://vestnikramn.spr-journal.ru/jour/article/downloadSuppFile/13677/109166; https://vestnikramn.spr-journal.ru/jour/article/downloadSuppFile/13677/145519; https://vestnikramn.spr-journal.ru/jour/article/downloadSuppFile/13677/145520
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2Academic Journal
Authors: M. M. Rogova, N. A. Mironova, E. S. Rodionova, T. A. Malkina, K. A. Zykov, Zh. D. Bespalova, R. Sh. Bibilashvili, E. E. Efremov, S. P. Golitsyn
Source: Рациональная фармакотерапия в кардиологии, Vol 8, Iss 5, Pp 647-654 (2015)
Subject Terms: идиопатическая желудочковая экстрасистолия, антитела, β –адренорецептор, М -холинорецептор, Therapeutics. Pharmacology, RM1-950, Diseases of the circulatory (Cardiovascular) system, RC666-701
File Description: electronic resource
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3Academic Journal
Authors: M. Rogova M., N. Mironova A., E. Rodionova S., T. Malkina A., K. Zykov A., Zh. Bespalova D., R. Bibilashvili Sh., E. Efremov E., S. Golitsyn P., М. Рогова М., Н. Миронова А., Е. Родионова С., Т. Малкина А., К. Зыков А., Ж. Беспалова Д., Р. Бибилашвили Ш., Е. Ефремов Е., С. Голицын П.
Source: Rational Pharmacotherapy in Cardiology; Vol 8, No 5 (2012); 647-654 ; Рациональная Фармакотерапия в Кардиологии; Vol 8, No 5 (2012); 647-654 ; 2225-3653 ; 1819-6446 ; 10.20996/1819-6446-2012-8-5
Subject Terms: idiopathic ventricular premature beats, antibodies, β1-adrenergic receptor, the M2 acetylcholine receptor, идиопатическая желудочковая экстрасистолия, антитела, β –адренорецептор, М -холинорецептор
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Autoimmun Rev 2008; 7: 209–213.; Gleicher N., Elkayam U. Peripartum cardiomyopathy, an autoimmune manifestation of allograft rejection? Autoimmun Rev 2009; 8: 384–387.; Zifman E., Amital H., Gilburd B., Shoenfeld Y. Antioxidants and smoking in autoimmune disease-opposing sides of the seesaw? Autoimmun Rev 2008; 8: 165–169.; Sitia S., Atzeni F., Sarzi-Puttini P. et al. Cardiovascular involvement in systemic autoimmune diseases. Autoimmun Rev 2009; 8: 281–286.; Gleicher N., Barad D., Weghofer A. Functional autoantibodies, a new paradigm in autoimmunity? Autoimmun Rev 2007; 7: 42–45.; Fritzler M.J. Challenges to the use of autoantibodies as predictors of disease onset, diagnosis and outcomes. Autoimmun Rev 2008; 7: 616–620.; Briani C., Samaroo D., Alaedini A. Celiac disease: from gluten to autoimmunity. Autoimmun Rev 2008; 7: 644–650.; Li Y., Heuser J.S., Cunningham L.C. et al. Mimicry and antibody-mediated cell signaling in autoimmune myocarditis. J Immunol 2006; 177: 8234–8240.; Deubner N., Berliner D., Schlipp A. et al. Cardiac beta1— adrenoceptor autoantibodies in human heart disease: rationale and design of the Etiology, Titre-Course, and Survival (ETiCS) Study. Eur J Heart Fail 2010; 12: 753–762.; Kaya Z., Katus H.A., Rose N.R. Cardiac troponins and autoimmunity: their role in the pathogenesis of myocarditis and of heart failure. Clin Immunol 2010; 134(1):80–8.; Chiale P.A., Ferrari .I, Mahler E. et al. Differential profile and biochemical effects of antiautonomic membrane receptor antibodies in ventricular arrhythmias and sinus nodedysfunction. Circulation 2001; 103(13): 1765–71.; Baba A., Yoshikawa T., Fukuda Y. et al. Autoantibodies against M2-muscarinic acetylcholine receptors: new upstream targets in atrial fibrillation in patients with dilated cardiomyopathy. Eur Heart J 2004; 25(13): 1108–15.; Villecco A.S., de Liberali E., Bianchi F.B., Pisi E. Antibodies to cardiac conducting tissue and abnormalities of cardiac conduction in rheumatoid arthritis. Clin Exp Immunol 1983; 53(3): 536–40.; Chiale P.A., Rosenbaum M.B., Elizari M.V. et al. High prevalence of antibodies against beta 1- and beta 2-adrenoceptors in patients with primary electrical cardiac abnormalities. J Am Coll Cardiol 1995; 26(4): 864–9.; Nussinovitch U., Shoenfeld Y. Anti-troponin autoantibodies and the cardiovascular system. Heart 2010; 96: 1518–1524.; Chiale P.A., Garro H.A., Schmidberg J. et al. Inappropriate sinus tachycardia may be related to an immunologic disorder involving cardiac beta adrenergic receptors. Heart Rhythm 2006; 3: 1182–1186.; Magnusson Y., Marullo S., Hoyer S. et al. Mapping of a functional autoimmune epitope on the beta 1-adrenergic receptor in patients with idiopathic dilated cardiomyopathy. J Clin Invest 1990; 86: 1658– 1663.; Liu H.R., Zhao R.R., Zhi J.M. et al. Screening of serum autoantibodies to cardiac beta1-adrenocep-tors and M2- muscarinic acetylcholine receptors in 408 healthy subjects of varying ages. Autoimmunity 1999; 29: 43–51.; Jahns R., Boivin V., Siegmund C. et al. Activating beta-1-adrenoceptor antibodies are not associated with cardiomyopathies secondary to valvular or hypertensive heart disease. J Am Coll Cardiol 1999; 34: 1545–1551.; Nikolaev V.O., Boivin V., Stork S. et al. A novel fluorescence method for the rapid detection of functional beta1-adrenergic receptor autoantibodies in heart failure. J Am Coll Cardiol 2007; 50: 423–431.; Chiale P.A., Ferrari I., Mahler E. et al. Differential profile and biochemical effects of antiautonomic membrane receptor antibodies in ventricular arrhythmias and sinus node dysfunction. Circulation 2001; 103: 1765–1771.; Hoebeke J. Structural basis of autoimmunity against G protein-coupled membrane receptors. Int J Car-diol 1996; 54: 103–111.; Caforio A.L., Mahon N.J., Tona F., McKenna W.J. Circulating cardiac autoantibodies in dilated car-diomyopathy and myocarditis: pathogenetic and clinical significance. Eur J Heart Fail 2002; 4: 411– 417.; Rose N.R. Infection, mimics, and autoimmune disease. J Clin Invest 2001; 107: 943–944.; Eriksson U., Ricci R., Hunziker L. et al. Dendritic cell-induced autoimmune heart failure requires cooperation between adaptive and innate immunity. Nat Med 2003; 9: 1484–1490.; Yoshikawa T., Baba A., Nagatomo Y. Autoimmune mechanisms underlying dilated cardiomyopathy. Circ J 2009; 73: 602–607.; Nagatomo Y., Yoshikawa T., Kohno T. et al. A pilot study on the role of autoantibody targeting the beta1-adrenergic receptor in the response to beta-blocker therapy for congestive heart failure. J Card Fail 2009; 15: 224–232.; Stork S., Boivin V., Horf R. et al. Stimulating autoantibodies directed against the cardiac beta1-adrenergic receptor predict increased mortality in idiopathic cardiomyopathy. Am Heart J 2006; 152: 697– 704.; Christ T., Wettwer E., Dobrev D. et al. Autoantibodies against the beta1 adrenoceptor from patients with dilated cardiomyopathy prolong action potential duration and enhance contractility in isolated cardiomyocytes. J Mol Cell Cardiol 2001; 33: 1515–1525.; Sterin-Borda L., Cossio P.M., Gimeno M.F. et al. Effect of chagasic sera on the rat isolated atrial preparation: immunological, morphological and function aspects. Cardiovasc Res 1976; 10: 613–622.; Caforio A.L., Tona F., Bottaro S. et al. Clinical implications of anti-heart autoantibodies in myocardi-tis and dilated cardiomyopathy. Autoimmunity 2008; 41: 35–45.; Mobini R., Staudt A., Felix S.B. et al. Hemodynamic improvement and removal of autoantibodies against beta1-adrenergic receptor by immunoadsorption therapy in dilated cardiomyopathy. J Autoimmun 2003; 20: 345–350.; Muller J., Wallukat G., Dandel M. et al. Immunoglobulin adsorption in patients with idiopathic dilated cardiomyopathy. 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Clin Rheumatol 2010; 29: 1353–1356.; Nussinovitch U., Katz U., Nussinovitch M., Nussinovitch N. Late ventricular potentials and QT dispersion in familial dysautonomia. Pediatr Cardiol 2009; 30: 747–751.; Wallukat G., Nissen E., Morwinski R., Muller J. Autoantibodies against the beta- and muscarinic receptors in cardiomyopathy. Herz 2000; 25: 261–266.; Wallukat G., Fu H.M., Matsui S. et al. Autoantibodies against M2 muscarinic receptors in patients with cardiomyopathy display non-desensitized agonist-like effects. Life Sci 1999; 64: 465–469.; Wang W.Z., Zhao R.R., Wu B.W. et al. Effects of anti-peptide antibodies against human M2 muscarinic receptors on cardiac function in rats in vivo. Blood Press Suppl 1996; 3: 25–27.; Goin J.C., Leiros C.P., Borda E., Sterin-Borda L. Interaction of human chagasic IgG with the second extracellular loop of the human heart muscarinic acetylcholine receptor: functional and pathological implications. FASEB J 1997; 11: 77–83.; https://www.rpcardio.com/jour/article/view/576
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4Academic Journal
Authors: Рогова, Мария, Миронова, Наталия, Родионова, Екатерина, Малкина, Татьяна, Зыков, Кирилл, Беспалова, Жанна, Бибилашвили, Роберт, Ефремов, Евгений, Голицын, Сергей
Subject Terms: ИДИОПАТИЧЕСКАЯ ЖЕЛУДОЧКОВАЯ ЭКСТРАСИСТОЛИЯ, АНТИТЕЛА, В -АДРЕНОРЕЦЕПТОР, М2-ХОЛИНОРЕЦЕПТОР, В -ADRENERGIC RECEPTOR
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5Academic Journal
Source: Рациональная фармакотерапия в кардиологии.
Subject Terms: 0301 basic medicine, ИДИОПАТИЧЕСКАЯ ЖЕЛУДОЧКОВАЯ ЭКСТРАСИСТОЛИЯ, АНТИТЕЛА, В -АДРЕНОРЕЦЕПТОР, М2-ХОЛИНОРЕЦЕПТОР, В -ADRENERGIC RECEPTOR, 0303 health sciences, 03 medical and health sciences, 3. Good health
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