ГЕНЕТИЧЕСКИЕ АСПЕКТЫ ФИБРИЛЛЯЦИИ ПРЕДСЕРДИЙ
Аннотация
Об авторах
В. А. ШульманРоссия
С. Ю. Никулина
Россия
О. О. Исаченко
Россия
Н. В. Аксютина
Россия
С. Н. Романенко
Россия
В. Н. Максимов
Россия
И. В. Куликов
Россия
С. Н. Устинов
Россия
Ю. Л. Казаринова
Россия
А. Г. Ромащенко
Россия
М. И. Воевода
Россия
Список литературы
1. Allessie М. A. Is atrial fibrillation sometimes a genetic disease? //N. Engl. J. Med. - 1997. - V.336. - P..950 - 952.
2. Allessie M.A., Lammers W.J.E.P., Bonke F.I.M., Hollen J. Experimental evacuation of Moe’s multiple wavelet hypothesis of atrial fibrillation. Cardiac Electrophysiology and Arrhythmias. - N.Y.: Grune & Stratton, 1985. - P.265-276.
3. Amat-y-Leon F., Racki A.J., Denes P. et al. Familial atrial dysrhythmia with A-V block. Intracellular microelectrode, clinical electrophysiologic and morphologic observations // Circulation. - 1974. - V.50. - P.1097-1104.
4. Bellocq C., van Ginneken A.C.G., Bezzina C.R. et al. Mutation in the KCNQl gene leading to the short QT-interval syndrome // Circulation. - 2004. - V. 109. - P.2394 - 2397.
5. Bertram H., Paul T., Beyer F., Kallfelz H.C. Familial idiopathic atrial fibrillation with the electrocardiographic patterns of right bundle branch block and ST- segment elevation in precordial leads V l-V3 // Circulation.- 2002.- V l05.- P.73-8.
6. Brugada R., Brugada J., Roberts R. Genetics of cardiovascular disease with emphasis on atrial fibrillation // J. Interv Card. Electrophysiol. - 1999. - V.3. - P.7-13.
7. Bmgada R., Tapscott T., Czemusczewicz G.S. et al. Identification of a genetic locus for familial atrial fibrillation // N. Engl. J. Med. - 1997. - V.336. - P.905-911.
8. Calum A. MacRae, M.B. Familial atrial fibrillation // N. Engl. J. Med. - 1997 - V.337. - P.350.
9. Campbell R. W. Atrial fibrillation // Eur. Heart J. - 1998. - V.19. (Suppl. E). - P 41-45, 60-63.
10. Campbell R. W., Smith R. A., Gallagher J. J. et all. Atrial fibrillation in the preexcitation syndrome // Amer. J. Cardiol. - 1977. - V.40. - P..514-520.
11. Chen Y-H., Xu S-J., Bendahhou S. et al. KCNQl Gainof-function mutation infFamilial atrial fibrillation // Science. - 2003. - V.299 - P .251-254.
12. Ellinor PT., Moore R.K., Patton K.K. et al. Mutations in the long QT gene, KCNQI, are an uncommon cause of atrial fibrillation // Heart. - 2004. - V.90. - P.1487-1488.
13. Ellinor P T., Shin J. T., Moore R. K. et al. Locus for atrial fibrillation maps to chromosome 6ql4-16 // Circulation. - 2003. - V.107. - P.2880-2883.
14. Firouzi M., Ramanna H., Kok B. et al. Association of human connexin40 gene polymorphisms with atrial vulnerability as a risk factor for Idiopathic atrial fibrillation // Circ. Research. - 2004. - V.5. - P.29.
15. Fox C. S., Parise H., D’Agostino R. B. et al. Parental atrial fibrillation as a risk factor for atrial fibrillation in offspring // JAMA. - 2004. - V.291. - P.2851-2855.
16. Gensini F., Padeletti L., Fatini C. et al. Angiotensinconverting enzyme and ehdothelial nitric oxide synthase polymorphisms in patients with atrial fibrillation. // Am. J. Cardiol. - 2003. - V. 91. - P 678-683.
17. Gillor A., Korsch E. Familial manifestation of idiopathic atrial flutter // Monatsschr. Kinderheilkd. -1992. - V. 140, - P.47-50.
18. Girona J., Domingo A., Albert D. et al. Familial auricular fibrillation // Rev. Esp. Cardiol. - 1997. - V.50. - P.548-51.
19. Gollob M.H., Green M.S., Tang A.S. et al. Identification of a gene responsible for familial Wolff-Parkinson-White syndrome // N. Engl. J. Med.- 2001.- V.344.- P.1823-31.
20. Gollob M.H., Roberts R. AMP - activated protein kinase and familial Wolff-Parkinson-White syndrome: new perspectives on heart development and arrhythmogenesis // Eur. Heart J. - 2002. - V.23. - P.679-681.
21. Gollob M.H., Seger J. J., Gollob T.N. et al. Novel PRKAG2 mutation responsible for the genetic syndrome of ventricular preexcitation and conduction system disease with childhood onset and absence of cardiac hypertrophy // Circulation. - 2001. - V.104, - P.3030-3033.
22. Gould L., Reddy V., Becher H. The sick sinus syndrome // J. Electrocardiol. - 1978. - V.ll. - P.11-14.
23. Gruver E., Fatkin D., Dodds G. Et al. Familial hypertrophic caerdiomyopathy and atrial fibrillation caused by Arg66His beta-cardiac myosin heavy chain mutation// J. Cardiol.. -1999. - V. 83. - P 13-18.
24. Kevy S., Breithardt G., Campbell R.W. et al. Atrial fibrillation: current knowedge end recommendations for management. Working Group on Arrhythmias of the European Society of Cardiology//Eur. Heart J.- 1998.-V.19.-P.1294-1320.
25. Kyndt F., Schott J.-J., Probst V, Le Marec H. A new locus for isolated cardiac conduction defect maps to 16q23-24. // Circulation. - 2000. - V.102. (Suppl. II). - P.358.
26. Lai L.P, Lin J.L., Lin C.S. et al. Functional genomic study on atrial fibrillation using cDNA microarray and two-dimensional protein electrophoresis techniques and identification of the myosin regulatory light chain isoform reprogramming in atrial fibrillation. // J. Cardiovasc. Electrophysiol. - 2004. - V.15. - P.214-223.
27. Lai L.P, Su M.J., Yeh H.M. et al. Association of the human minK gene 38G allele with atrial fibrillation: evidence of possible genetic control on the pathogenesis of atrial fibrillation // Am. Heart J. - 2002. - V.144. - P.485-490.
28. Lai L.P, Tsai C.C., Su M.J. et al. Atrial fibrillation is associated with accumulation of aging-related common type mitochondrial DNA deletion mutation in human atrial tissue // Chest. - 2003. - V.123. - P.539-544.
29. Levy S. Epidemiologi and classification of atrial fibrillation// J. Cardiovasc. Electrophyol. - 1998. - V.9. - P.78-82.
30. Nattel S. Ionic Determinants of Atrial Fibrillation and Ca2+Channel Abnormalities // Circ. Research.-1999.- V.85. _ P 473-476.
31. Olson T.M., Michels V.V., Ballew J.D. et al. Sodium channel mutations and susceptibility to heart failure and atrial fibrillation // JAMA. - 2005. - V. 293, - P.491-493.
32. OMIM - Online Mendelian Inheritance in Men, Web site: http://www.ncbi.nlm.nih.gov
33. Poret P, Mabo P, Deplace C. et al. Is isolated atrial fibrillation genetically determined? Apropos of a familial history // Arch. Mai. Coeur. Vaiss. - 1996. - V.89. - P.1197-1203.
34. Dostal S., von Beckerath N. et al. C825T polymorphism of the G-protein beta3 subunit gene and atrial fibrillation: association of the TT genotype with a reduced risk for atrial fibrillation // Am. Heart J. - 2004. - V.148. - P.545-550.
35. Schreieck J., Dostal S., von Beckerath N. et al. C825T polymorphism of the protein beta-3 subunit gene and atrial fibrilation: association of the gehotype with a reduced risk for atrial fibrillation.// Heart.- 2004 - V. .90 - P 1310-1314.
36. Sparks E., Fraizier L. Heritable cardiovascular disease in women.// J. Obstet. Gynecol. Neonatal Nurs. - 2002. -V. 31. -P 217-228.
37. Takachimoto J. Pathological study of human sinoatrial node. On the changes associated with aging, atrial fibrillation and cardiac suddem death // Shikoku Acta. Med. - 1977. -V.33. - P.185-194.
38. Tikanoja T., Kirkinen P, Nikolajev K. et al. Familial atrial fibrillation witl fetal onset.// Heart. - 1998.- V.79. P 637-641.
39. Tsai C., Lai L., Chang F. Et al. Renin-angiotensin gene polymorphism and atrial fibrillation. // Clin. Sci. - 2004. - V. 106. - P 653-659.
40. Wolf P, Damber T., Thomas H., Kannel W. Epidemiologic assesmentof chronic atrial fibrillation and the risk of stroke: the Framingham study.// Neurology- 1978- V.28, P 973-978.
41. Yamashita T., Hayami N., Ajiki K. Is ACE gene polymorphism associated with lone atrial fibrillation? // Jpn. Heart J. - 1997. - V.38, - P.637-641.
42. Yan H., Chen J.Z., Zhu J.H. et al. Expression of connexin in atrium of patients with atrial fibrillation and its signal transduction pathway // Zhonghua Yi Xue Za Zhi. 2004. - V.84, - P.209-213.
43. Yang H., Xia M., Jin Q. et al. Identification of a KCNE2 - gain of function mutation in patients with familial atrial fibrillation. Am. J. Pathol. - 2004. - V.165. - P.1010-1032.
Рецензия
Для цитирования:
Шульман В.А., Никулина С.Ю., Исаченко О.О., Аксютина Н.В., Романенко С.Н., Максимов В.Н., Куликов И.В., Устинов С.Н., Казаринова Ю.Л., Ромащенко А.Г., Воевода М.И. ГЕНЕТИЧЕСКИЕ АСПЕКТЫ ФИБРИЛЛЯЦИИ ПРЕДСЕРДИЙ. Вестник аритмологии. 2006;(46):57-60.
For citation:
Shul’man V.A., Nikulina S.Yu., Isachenko O.O., Aksyutina N.V., Romanenko S.N., Maksimov V.N., Kulikov I.V., Ustinov S.N., Kazarinova Yu.L., Romashchenko A.G., Voevoda M.I. GENETIC ASPECTS OF ATRIAL FIBRILLATION. Journal of Arrhythmology. 2006;(46):57-60. (In Russ.)