메뉴 건너뛰기




Volumn 49, Issue 2, 2008, Pages 237-243

Factor VLeiden and prothrombin G20210A gene polymorphisms in patients with coronary artery disease

Author keywords

Coronary artery disease; Factor VLeiden; Prothrombin G20210A gene

Indexed keywords

ADENINE; APOLIPOPROTEIN A; APOLIPOPROTEIN B; BLOOD CLOTTING FACTOR 5 LEIDEN; CHOLESTEROL; GUANINE; HIGH DENSITY LIPOPROTEIN CHOLESTEROL; LIPOPROTEIN A; LOW DENSITY LIPOPROTEIN CHOLESTEROL; PROTHROMBIN; TRIACYLGLYCEROL; VERY LOW DENSITY LIPOPROTEIN CHOLESTEROL;

EID: 44649202315     PISSN: 05135796     EISSN: None     Source Type: Journal    
DOI: 10.3349/ymj.2008.49.2.237     Document Type: Article
Times cited : (15)

References (39)
  • 1
    • 0034015006 scopus 로고    scopus 로고
    • The role of plaque rupture and thrombosis in coronary artery disease
    • Zaman AG, Helft G, Worthley SG, Badimon JJ. The role of plaque rupture and thrombosis in coronary artery disease. Atherosclerosis 2000;149:251-66.
    • (2000) Atherosclerosis , vol.149 , pp. 251-266
    • Zaman, A.G.1    Helft, G.2    Worthley, S.G.3    Badimon, J.J.4
  • 3
    • 0030809456 scopus 로고    scopus 로고
    • Fibrinolytic and inflammatory markers for arterial occlusion: The evolving epidemiology of thrombosis and hemostasis
    • Ridker PM. Fibrinolytic and inflammatory markers for arterial occlusion: the evolving epidemiology of thrombosis and hemostasis. Thromb Haemost 1997;78: 53-9.
    • (1997) Thromb Haemost , vol.78 , pp. 53-59
    • Ridker, P.M.1
  • 4
    • 0000087729 scopus 로고    scopus 로고
    • Hemostatic risk factors for cardiovascular disease
    • Schechter GP, Hoffman R, Schrier SL, eds, Washington. DC: American Society of Haematology;
    • Cushman M. Hemostatic risk factors for cardiovascular disease. In: Schechter GP, Hoffman R, Schrier SL, eds. Hematology. Washington. DC: American Society of Haematology; 1999.
    • (1999) Hematology
    • Cushman, M.1
  • 5
    • 0030809467 scopus 로고    scopus 로고
    • Clinical relevance of polymorphic markers of arterial thrombosis
    • Di Minno G, Grandone E, Margaglione M. Clinical relevance of polymorphic markers of arterial thrombosis. Thromb Haemost 1997;78:462-6.
    • (1997) Thromb Haemost , vol.78 , pp. 462-466
    • Di Minno, G.1    Grandone, E.2    Margaglione, M.3
  • 6
    • 0030780237 scopus 로고    scopus 로고
    • Polymorphisms of coagulation/fibrinolysis genes: Gene environment interactions and vascular risk
    • Grant PJ. Polymorphisms of coagulation/fibrinolysis genes: gene environment interactions and vascular risk Prostaglandins Leukot Essent Fatty Acids 1997;57:473-7.
    • (1997) Prostaglandins Leukot Essent Fatty Acids , vol.57 , pp. 473-477
    • Grant, P.J.1
  • 7
    • 0030811925 scopus 로고    scopus 로고
    • Genetic predisposition to hyperhomocysteinemia: Deficiency of methylenetetrahydrofolate reductase (MTHFR)
    • Rozen R. Genetic predisposition to hyperhomocysteinemia: deficiency of methylenetetrahydrofolate reductase (MTHFR). Thromb Haemost 1997;78:523-6.
    • (1997) Thromb Haemost , vol.78 , pp. 523-526
    • Rozen, R.1
  • 9
    • 0029850530 scopus 로고    scopus 로고
    • A common genetic variation in the 3′-untranslated region of the prothrombin gene is associated with elevated plasma prothrombin levels and an increase in venous thrombosis
    • Poort SR, Rosendaal FR, Reitsma PH, Bertina RM. A common genetic variation in the 3′-untranslated region of the prothrombin gene is associated with elevated plasma prothrombin levels and an increase in venous thrombosis. Blood 1996;88:3698-703.
    • (1996) Blood , vol.88 , pp. 3698-3703
    • Poort, S.R.1    Rosendaal, F.R.2    Reitsma, P.H.3    Bertina, R.M.4
  • 11
    • 44649160212 scopus 로고    scopus 로고
    • Kapur RK, Mills LA, Spitzer SG, Hultin MB. A prothrombin gene mutation is significantly associated with venous thrombosis. Arterioscler Thromb Vasc Biol
    • Kapur RK, Mills LA, Spitzer SG, Hultin MB. A prothrombin gene mutation is significantly associated with venous thrombosis. Arterioscler Thromb Vasc Biol
  • 12
    • 0030608645 scopus 로고    scopus 로고
    • Co-inheritance of the 20210A allele of the prothrombin gene increases the risk of thrombosis in subjects with familial thrombophilia
    • Makris M, Preston FE, Beauchamp NJ, Cooper PC, Daly ME, Hampton KK, et al. Co-inheritance of the 20210A allele of the prothrombin gene increases the risk of thrombosis in subjects with familial thrombophilia. Thromb Haemost 1997;78:1426-9.
    • (1997) Thromb Haemost , vol.78 , pp. 1426-1429
    • Makris, M.1    Preston, F.E.2    Beauchamp, N.J.3    Cooper, P.C.4    Daly, M.E.5    Hampton, K.K.6
  • 13
    • 0030714108 scopus 로고    scopus 로고
    • Prevalence of the prothrombin gene variant (nt20210A) in venous thrombosis and arterial disease
    • Arruda VR, Annichino-Bizzacchi JM, Gonçalves MS, Costa FF. Prevalence of the prothrombin gene variant (nt20210A) in venous thrombosis and arterial disease. Thromb Haemost 1997;78:1430-3.
    • (1997) Thromb Haemost , vol.78 , pp. 1430-1433
    • Arruda, V.R.1    Annichino-Bizzacchi, J.M.2    Gonçalves, M.S.3    Costa, F.F.4
  • 14
    • 0343035591 scopus 로고    scopus 로고
    • Increased prevalence of a polymorphism in the gene coding for human prothrombin in patients with coronary heart disease
    • Watzke HH, Schüttrumpf J, Graf S, Huber K, Panzer S. Increased prevalence of a polymorphism in the gene coding for human prothrombin in patients with coronary heart disease. Thromb Res 1997;87:521-6.
    • (1997) Thromb Res , vol.87 , pp. 521-526
    • Watzke, H.H.1    Schüttrumpf, J.2    Graf, S.3    Huber, K.4    Panzer, S.5
  • 15
    • 0032525101 scopus 로고    scopus 로고
    • Prothrombin G20210A mutant genotype is a risk factor for cerebrovascular ischemic disease in young patients
    • De Stefano V, Chiusolo P, Paciaroni K, Casorelli I, Rossi E, Molinari M, et al. Prothrombin G20210A mutant genotype is a risk factor for cerebrovascular ischemic disease in young patients. Blood 1998;91:3562-5.
    • (1998) Blood , vol.91 , pp. 3562-3565
    • De Stefano, V.1    Chiusolo, P.2    Paciaroni, K.3    Casorelli, I.4    Rossi, E.5    Molinari, M.6
  • 16
    • 0030921663 scopus 로고    scopus 로고
    • A common prothrombin variant (20210 G to A) increases the risk of myocardial infarction in young women
    • Rosendaal FR, Siscovick DS, Schwartz SM, Psaty BM, Raghunathan TE, Vos HL. A common prothrombin variant (20210 G to A) increases the risk of myocardial infarction in young women. Blood 1997;90:1747-50.
    • (1997) Blood , vol.90 , pp. 1747-1750
    • Rosendaal, F.R.1    Siscovick, D.S.2    Schwartz, S.M.3    Psaty, B.M.4    Raghunathan, T.E.5    Vos, H.L.6
  • 17
    • 0031442537 scopus 로고    scopus 로고
    • The heterozygous 20210 G/A prothrombin genotype is associated with early venous thrombosis in inherited thrombophilias and is not increased in frequency in artery disease
    • Ferraresi P, Marchetti G, Legnani C, Cavallari E, Castoldi E, Mascoli F, et al. The heterozygous 20210 G/A prothrombin genotype is associated with early venous thrombosis in inherited thrombophilias and is not increased in frequency in artery disease. Arterioscler Thromb Vasc Biol 1997;17:2418-22.
    • (1997) Arterioscler Thromb Vasc Biol , vol.17 , pp. 2418-2422
    • Ferraresi, P.1    Marchetti, G.2    Legnani, C.3    Cavallari, E.4    Castoldi, E.5    Mascoli, F.6
  • 18
    • 0030664938 scopus 로고    scopus 로고
    • The venous thrombosis risk factor 20210A allele of the prothrombin gene is not a major risk factor for arterial thrombotic disease
    • Corral J, Gonzalez-Conjero R, Lozano ML, Rivera J, Heras I, Vicente V. The venous thrombosis risk factor 20210A allele of the prothrombin gene is not a major risk factor for arterial thrombotic disease. Br J Haematol 1997;99:304-7.
    • (1997) Br J Haematol , vol.99 , pp. 304-307
    • Corral, J.1    Gonzalez-Conjero, R.2    Lozano, M.L.3    Rivera, J.4    Heras, I.5    Vicente, V.6
  • 19
    • 0344765521 scopus 로고    scopus 로고
    • Risk of stroke in young women and two prothrombotic mutations: Factor VLeiden and Prothrombin gene variant (G20210A)
    • Longstreth WT Jr, Rosendaal FR, Siscovic DS, Vos HL, Schwartz SM, Psaty BM, et al. Risk of stroke in young women and two prothrombotic mutations: factor VLeiden and Prothrombin gene variant (G20210A). Stroke 1998;29:577-80.
    • (1998) Stroke , vol.29 , pp. 577-580
    • Longstreth Jr, W.T.1    Rosendaal, F.R.2    Siscovic, D.S.3    Vos, H.L.4    Schwartz, S.M.5    Psaty, B.M.6
  • 20
    • 0028902044 scopus 로고
    • Mutation in a coagulation factor V associated with resistance to activated protein C in patients with coronary artery disease
    • März W, Seydewitz H, Winkelmann B, Chen M, Nauck M, Witt I. Mutation in a coagulation factor V associated with resistance to activated protein C in patients with coronary artery disease. Lancet 1995;345:526.
    • (1995) Lancet , vol.345 , pp. 526
    • März, W.1    Seydewitz, H.2    Winkelmann, B.3    Chen, M.4    Nauck, M.5    Witt, I.6
  • 21
    • 0030032237 scopus 로고    scopus 로고
    • Prevalence of factor V gene mutation amongst myocardial infarction patients and healthy controls is higher in Sweden than in other countries
    • Holm J, Zöller B, Berntorp E, Erhardt L, Dahlbäck B. Prevalence of factor V gene mutation amongst myocardial infarction patients and healthy controls is higher in Sweden than in other countries. J Intern Med 1996;239:221-6.
    • (1996) J Intern Med , vol.239 , pp. 221-226
    • Holm, J.1    Zöller, B.2    Berntorp, E.3    Erhardt, L.4    Dahlbäck, B.5
  • 22
    • 0030984288 scopus 로고    scopus 로고
    • Factor VLeiden (resistance to activated protein C) increases the risk of myocardial infarction in young women
    • Rosendaal FK, Siscovick DS, Schwartz SM, Beverly RK, Psaty BM, Longstreth WT Jr, et al. Factor VLeiden (resistance to activated protein C) increases the risk of myocardial infarction in young women. Blood 1997; 89:2817-21.
    • (1997) Blood , vol.89 , pp. 2817-2821
    • Rosendaal, F.K.1    Siscovick, D.S.2    Schwartz, S.M.3    Beverly, R.K.4    Psaty, B.M.5    Longstreth Jr, W.T.6
  • 23
  • 24
    • 0028910906 scopus 로고
    • Mutation in the gene coding for coagulation factor V and the risk of myocardial infarction, stroke and venous thrombosis in apparently healthy men
    • Ridker PM, Hennekens CH, Lindpaintner Stampfer MJ, Eisenberg PR, Miletich JP: Mutation in the gene coding for coagulation factor V and the risk of myocardial infarction, stroke and venous thrombosis in apparently healthy men. N Engl J Med 1995;332:912-7.
    • (1995) N Engl J Med , vol.332 , pp. 912-917
    • Ridker, P.M.1    Hennekens, C.H.2    Lindpaintner Stampfer, M.J.3    Eisenberg, P.R.4    Miletich, J.P.5
  • 27
    • 0027241856 scopus 로고    scopus 로고
    • Ross R The pathogenesis of atherosclerosis: a perspective for the 1990s. Nature 1993;362:801-9.
    • Ross R The pathogenesis of atherosclerosis: a perspective for the 1990s. Nature 1993;362:801-9.
  • 28
    • 0028519887 scopus 로고
    • Conner Memorial Lecture. Mechanisms leading to myocardial infarction: Insights from studies of vascular biology
    • Fuster V, Lewis A. Conner Memorial Lecture. Mechanisms leading to myocardial infarction: insights from studies of vascular biology. Circulation 1994;90: 2126.
    • (1994) Circulation , vol.90 , pp. 2126
    • Fuster, V.1    Lewis, A.2
  • 29
    • 44649121659 scopus 로고    scopus 로고
    • Farmer JA, Gotto AM Jr. Dyslipidemia and other risk factors for coronary artery disease. In: Braunwa E, editor. Heart disease. A textbook of cardiovascular medicine. 5th ed. Philadelphia, PA: W.B. Saunders; 1997.
    • Farmer JA, Gotto AM Jr. Dyslipidemia and other risk factors for coronary artery disease. In: Braunwa E, editor. Heart disease. A textbook of cardiovascular medicine. 5th ed. Philadelphia, PA: W.B. Saunders; 1997.
  • 30
    • 0033121115 scopus 로고    scopus 로고
    • Synergistic effects of prothrombic polymorphisms and atherogenic factors on the risk of myocardial infarction in young males
    • Inbal A, Freimark D, Modan B, Chetrit A, Matetzky S, Rosenberg N, et al. Synergistic effects of prothrombic polymorphisms and atherogenic factors on the risk of myocardial infarction in young males. Blood 1999; 93:2186-90.
    • (1999) Blood , vol.93 , pp. 2186-2190
    • Inbal, A.1    Freimark, D.2    Modan, B.3    Chetrit, A.4    Matetzky, S.5    Rosenberg, N.6
  • 31
    • 0035933001 scopus 로고    scopus 로고
    • G20210A prothrombin gene polymorphism and prothrombin activity in subjects with or without angiographically documented coronary artery disease
    • Russo C, Girelli D, Olivieri O, Guarini P, Manzato F, Pizzolo F, et al. G20210A prothrombin gene polymorphism and prothrombin activity in subjects with or without angiographically documented coronary artery disease. Circulation 2001;103:243640.
    • (2001) Circulation , vol.103 , pp. 243640
    • Russo, C.1    Girelli, D.2    Olivieri, O.3    Guarini, P.4    Manzato, F.5    Pizzolo, F.6
  • 32
    • 0032562254 scopus 로고    scopus 로고
    • Interaction of coagulation defects and cardiovascular risk factors: Increased risk of myocardial infarction associated with factor VLeiden or prothrombin 20210A
    • Doggen CJ, Cats VM, Bertina RM, Rosendaal FR. Interaction of coagulation defects and cardiovascular risk factors: increased risk of myocardial infarction associated with factor VLeiden or prothrombin 20210A. Circulation 1998;97:1037-41.
    • (1998) Circulation , vol.97 , pp. 1037-1041
    • Doggen, C.J.1    Cats, V.M.2    Bertina, R.M.3    Rosendaal, F.R.4
  • 33
    • 0036403373 scopus 로고    scopus 로고
    • Increased prevalence of the G20210A prothrombin gene variant in acute coronary syndromes without metabolic or acquired risk factors or with limited extent of disease
    • Burzotta F, Paciaroni K, De Stefano V, Chiusolo P, Manzoli A, Casorelli I, et al. Increased prevalence of the G20210A prothrombin gene variant in acute coronary syndromes without metabolic or acquired risk factors or with limited extent of disease. Eur Heart J 2002;23:26-30.
    • (2002) Eur Heart J , vol.23 , pp. 26-30
    • Burzotta, F.1    Paciaroni, K.2    De Stefano, V.3    Chiusolo, P.4    Manzoli, A.5    Casorelli, I.6
  • 34
    • 0033953537 scopus 로고    scopus 로고
    • Resistance to activated protein C and FV Leiden mutation in patients with a history of acute myocardial infarction or primary hypertension
    • Makris TK, Krespi PC, Hatzizacharias AN, Gialeraki AE, Anastasiadis G, Triposkiadis FK, et al. Resistance to activated protein C and FV Leiden mutation in patients with a history of acute myocardial infarction or primary hypertension. Am J Hypertens 2000,13:61-5.
    • (2000) Am J Hypertens , vol.13 , pp. 61-65
    • Makris, T.K.1    Krespi, P.C.2    Hatzizacharias, A.N.3    Gialeraki, A.E.4    Anastasiadis, G.5    Triposkiadis, F.K.6
  • 35
    • 0033515068 scopus 로고    scopus 로고
    • G20210A mutation in prothrombin gene and risk of myocardial infarction, stroke, and venous thrombosis in a large cohort of US men
    • Ridker PM, Hennekens CH, Miletich JP. G20210A mutation in prothrombin gene and risk of myocardial infarction, stroke, and venous thrombosis in a large cohort of US men. Circulation 1999;99:999-1004.
    • (1999) Circulation , vol.99 , pp. 999-1004
    • Ridker, P.M.1    Hennekens, C.H.2    Miletich, J.P.3
  • 36
    • 0035069631 scopus 로고    scopus 로고
    • Factor VLeiden and its relation to left ventricular thrombus in acute myocardial infarction
    • Çelik S, Ovali E, Baykan M, Uçar F, Erdöl C, Durmuş I, et al. Factor VLeiden and its relation to left ventricular thrombus in acute myocardial infarction. Acta Cardiol 2001; 56:1-6.
    • (2001) Acta Cardiol , vol.56 , pp. 1-6
    • Çelik, S.1    Ovali, E.2    Baykan, M.3    Uçar, F.4    Erdöl, C.5    Durmuş, I.6
  • 38
    • 0028888446 scopus 로고
    • Myocardial infarction, Arg506 to G1n factor V mutation, and activated protein C resistance
    • Emmerich J, Poirier O, Evans A, Margues-Vidal P, Arveiler D, Luc G, et al. Myocardial infarction, Arg506 to G1n factor V mutation, and activated protein C resistance. Lancet 1995;345:321.
    • (1995) Lancet , vol.345 , pp. 321
    • Emmerich, J.1    Poirier, O.2    Evans, A.3    Margues-Vidal, P.4    Arveiler, D.5    Luc, G.6
  • 39
    • 0028951045 scopus 로고
    • Premature ischaemic heart disease and the gene for coagulation factor V
    • van Bockxmeer FM, Baker RI, Taylor RR. Premature ischaemic heart disease and the gene for coagulation factor V. Nat Med 1995;1:185.
    • (1995) Nat Med , vol.1 , pp. 185
    • van Bockxmeer, F.M.1    Baker, R.I.2    Taylor, R.R.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.