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Volumn 20, Issue 4, 2009, Pages 252-256

Factor v G1691A, prothrombin G20210A and methylenetetrahydrofolate reductase polymorphism C677T are not associated with coronary artery disease and type 2 diabetes mellitus in western Iran

Author keywords

Coronary artery disease; Diabetes; Factor v leiden; Iran; Methylentetrahydrofolate reductase; Prothrombin g2021 OA; Western

Indexed keywords

5,10 METHYLENETETRAHYDROFOLATE REDUCTASE (FADH2); BLOOD CLOTTING FACTOR 5 LEIDEN; PROTHROMBIN;

EID: 67649531257     PISSN: 09575235     EISSN: None     Source Type: Journal    
DOI: 10.1097/MBC.0b013e3283255487     Document Type: Article
Times cited : (23)

References (34)
  • 2
    • 0035909969 scopus 로고    scopus 로고
    • Genetic variation in coagulation and fibrinolytic proteins and their relation with acute myocardial infarction
    • Boekholdt SM, Bijslerveld NR, Moons AHM, Levi M, BullerHR, Peters RJG. Genetic variation in coagulation and fibrinolytic proteins and their relation with acute myocardial infarction. Circulatio. 2001; 104:3063-3068.
    • (2001) Circulatio , vol.104 , pp. 3063-3068
    • Boekholdt, S.M.1    Bijslerveld, N.R.2    Moons, A.H.M.3    Levi, M.4    Buller, H.R.5    Peters, R.J.G.6
  • 3
    • 0030921663 scopus 로고    scopus 로고
    • A common prothrombin variant (20210G 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 (20210G to A) increases the risk of myocardial infarction in young women. Stoo. 1997; 90:1747-1750.
    • (1997) Stoo , 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
  • 4
    • 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 K, Stampeer 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 Me. 1995; 332:912-917.
    • (1995) N Engl J Me , vol.332 , pp. 912-917
    • Ridker, P.M.1    Hennekens, C.H.2    Lindpaintner, K.3    Stampeer, M.J.4    Eisenberg, P.R.5    Miletich, J.P.6
  • 5
    • 0033515068 scopus 로고    scopus 로고
    • G2021 OA 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. G2021 OA mutation in prothrombin gene and risk of myocardial infarction, stroke, and venous thrombosis in a large cohort of US men. Circulatio. 1999; 99:999-1004.
    • (1999) Circulatio , vol.99 , pp. 999-1004
    • Ridker, P.M.1    Hennekens, C.H.2    Miletich, J.P.3
  • 6
    • 0030984288 scopus 로고    scopus 로고
    • Factor V Leiden (resistance to activated protein C) increases the risk of myocardial infarction in young women
    • Rosendaal FR, Siscovick DS, Schwartz SM, Beverly RK, Psaty BM, Longstreth WT Jr, ef al. Factor V Leiden (resistance to activated protein C) increases the risk of myocardial infarction in young women. Bloo. 1997; 89:2817-2821.
    • (1997) Bloo , vol.89 , pp. 2817-2821
    • Rosendaal, F.R.1    Siscovick, D.S.2    Schwartz, S.M.3    Beverly, R.K.4    Psaty, B.M.5    Longstreth Jr, W.T.6    ef al7
  • 7
    • 0033121115 scopus 로고    scopus 로고
    • Synergistic effects of prothrombotic 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 prothrombotic polymorphisms and atherogenic factors on the risk of myocardial infarction in young males. Bloo. 1999; 93:2186-2190.
    • (1999) Bloo , vol.93 , pp. 2186-2190
    • Inbal, A.1    Freimark, D.2    Modan, B.3    Chetrit, A.4    Matetzky, S.5    Rosenberg, N.6
  • 8
    • 4444233897 scopus 로고    scopus 로고
    • Factor V G1691A, prothrombin G20210A, and methylenetetrahydrofolate reductase [MTHFR] C677T gene polymorphism in angiographically documented coronary artery disease
    • Almawi WY, Ameen G, Tamin H, Finan RR, Irani-Hakime N. Factor V G1691A, prothrombin G20210A, and methylenetetrahydrofolate reductase [MTHFR] C677T gene polymorphism in angiographically documented coronary artery disease. J Thromb Thrombolysi. 2004; 17:199-205.
    • (2004) J Thromb Thrombolysi , vol.17 , pp. 199-205
    • Almawi, W.Y.1    Ameen, G.2    Tamin, H.3    Finan, R.R.4    Irani-Hakime, N.5
  • 9
    • 14444281536 scopus 로고    scopus 로고
    • Prevalence of factor V Leiden (APCR) and other inherited thrombophilias in young patients with myocardial infarction and normal coronary arteries
    • Dacosta A, Tardy-Poncet B, Isaaz K, Cerisier A, Mismetti P, Simitsidis S, et al. Prevalence of factor V Leiden (APCR) and other inherited thrombophilias in young patients with myocardial infarction and normal coronary arteries. Hear. 1998; 80:338-340.
    • (1998) Hear , vol.80 , pp. 338-340
    • Dacosta, A.1    Tardy-Poncet, B.2    Isaaz, K.3    Cerisier, A.4    Mismetti, P.5    Simitsidis, S.6
  • 10
    • 0035877010 scopus 로고    scopus 로고
    • Correlation of polymorphisms to coagulation and biochemical risk factors for cardiovascular diseases
    • Wu AH, Tsongalis GJ. Correlation of polymorphisms to coagulation and biochemical risk factors for cardiovascular diseases. Am J Cardio. 2001; 87:1361-1366.
    • (2001) Am J Cardio , vol.87 , pp. 1361-1366
    • Wu, A.H.1    Tsongalis, G.J.2
  • 11
    • 0030470762 scopus 로고    scopus 로고
    • lacoviello L Association of coagulation factor V-Arg506Gln mutation with noninsulin-dependent diabetes mellitus
    • Krekora K, Delucia D, Capani F, Donati MD, lacoviello L Association of coagulation factor V-Arg506Gln mutation with noninsulin-dependent diabetes mellitus. Lance. 1996; 348:1666-1667.
    • (1996) Lance , vol.348 , pp. 1666-1667
    • Krekora, K.1    Delucia, D.2    Capani, F.3    Donati, M.D.4
  • 12
    • 0032988612 scopus 로고    scopus 로고
    • Prevalence of variants in candidate genes for type 2 diabetes mellitus in the Netherlands: The Rotterdam study and the Hoorn study
    • *
    • Hart LM, Stolk RP, Dekker JM, Nijpels G, Grobbee DE, Heine PJ, Maassen JA. Prevalence of variants in candidate genes for type 2 diabetes mellitus in the Netherlands: the Rotterdam study and the Hoorn study. J Clin Endocrinol Meta. 1999; 84:1002-1006. *
    • (1999) J Clin Endocrinol Meta , vol.84 , pp. 1002-1006
    • Hart, L.M.1    Stolk, R.P.2    Dekker, J.M.3    Nijpels, G.4    Grobbee, D.E.5    Heine, P.J.6    Maassen, J.A.7
  • 14
    • 41649111625 scopus 로고    scopus 로고
    • Part 1: Diagnosis and classification of diabetes mellitus
    • World Health Organization: Geneva;
    • WHO Study Group Report of a WHO consultation. Part 1: Diagnosis and classification of diabetes mellitus. World Health Organization: Geneva; 1999.
    • (1999) WHO Study Group Report of a WHO consultation
  • 15
    • 0002804385 scopus 로고
    • Gene analysis
    • Weatherall DJ, editor., London: Churchill Livingstone;
    • Old JM, Higgs DR. Gene analysis. In: Weatherall DJ, editor. Methods in hematology. The thalassemias. (Vol. 6). London: Churchill Livingstone; 1983. pp. 74-101.
    • (1983) Methods in hematology. The thalassemias , vol.6 , pp. 74-101
    • Old, J.M.1    Higgs, D.R.2
  • 16
    • 0028314865 scopus 로고    scopus 로고
    • Bertina RM, Koeleman BPC, Koster T, Rosendaal FR, Dirven RJ.de Ronde H, et al. Mutation in blood coagulation factor V associated with resistance to activated protein C. Natur. 1994; 369:64-67.
    • Bertina RM, Koeleman BPC, Koster T, Rosendaal FR, Dirven RJ.de Ronde H, et al. Mutation in blood coagulation factor V associated with resistance to activated protein C. Natur. 1994; 369:64-67.
  • 17
    • 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. Bloo. 1996; 88:3698-3703.
    • (1996) Bloo , vol.88 , pp. 3698-3703
    • Poort, S.R.1    Rosendaal, F.R.2    Reitsma, P.H.3    Bertina, R.M.4
  • 18
    • 0029049553 scopus 로고    scopus 로고
    • Frosst P, Blom HI, Milos R, Goyette P, Sheppard CA, Matthews RG, et al. A candidate genetic risk factor for vascular disease: a common mutation in methylenetetrahydrofolate reductase. Na. Genef 1995; 10:111 -113.
    • Frosst P, Blom HI, Milos R, Goyette P, Sheppard CA, Matthews RG, et al. A candidate genetic risk factor for vascular disease: a common mutation in methylenetetrahydrofolate reductase. Na. Genef 1995; 10:111 -113.
  • 19
    • 13844254899 scopus 로고    scopus 로고
    • High prevalence of thrombophilia among young patients with myocardial infarction and few conventional risk factors
    • Segev A, Ellis MH, Segev F, Friedman Z, Reshef T, Sparkes JD, et al. High prevalence of thrombophilia among young patients with myocardial infarction and few conventional risk factors. Int J Cardio. 2005; 98: 421 -424.
    • (2005) Int J Cardio , vol.98 , pp. 421-424
    • Segev, A.1    Ellis, M.H.2    Segev, F.3    Friedman, Z.4    Reshef, T.5    Sparkes, J.D.6
  • 20
    • 44649129978 scopus 로고    scopus 로고
    • Prevalence of factor V Leiden (G1691A) and prothrombin (G20210A) among Kurdish population from Western Iran
    • Rahimi Z, Vaisi-Raygani A, Mozafari H, Kharrazi H, Rezaei M, Nagel RL. Prevalence of factor V Leiden (G1691A) and prothrombin (G20210A) among Kurdish population from Western Iran. J Thromb Thrombolysi. 2008; 25:280-283.
    • (2008) J Thromb Thrombolysi , vol.25 , pp. 280-283
    • Rahimi, Z.1    Vaisi-Raygani, A.2    Mozafari, H.3    Kharrazi, H.4    Rezaei, M.5    Nagel, R.L.6
  • 23
    • 35848934784 scopus 로고    scopus 로고
    • Association between factor V Leiden mutation and coronary artery disease in the northeast region of Turkey. Stood
    • Gurlertop HY, Gundogdu F, Pirim I, Islamoglu Y, Egercia N, Sevimli S, et al. Association between factor V Leiden mutation and coronary artery disease in the northeast region of Turkey. Stood Coagul Fibrinolysi. 2007; 18:719-722.
    • (2007) Coagul Fibrinolysi , vol.18 , pp. 719-722
    • Gurlertop, H.Y.1    Gundogdu, F.2    Pirim, I.3    Islamoglu, Y.4    Egercia, N.5    Sevimli, S.6
  • 24
    • 0036770450 scopus 로고    scopus 로고
    • Prevalence of the 2021OG→A prothrombin variant and its association with coronary artery disease in a Middle Eastern Arab population
    • Abu-Amero KK, Wyngaard CA, Kambouris M, Dzimiri N. Prevalence of the 2021OG→A prothrombin variant and its association with coronary artery disease in a Middle Eastern Arab population. Arch Pathol Lab Me. 2002; 126:1087-1090.
    • (2002) Arch Pathol Lab Me , vol.126 , pp. 1087-1090
    • Abu-Amero, K.K.1    Wyngaard, C.A.2    Kambouris, M.3    Dzimiri, N.4
  • 25
    • 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. Circulatio. 2001; 103:2436-2440.
    • (2001) Circulatio , vol.103 , pp. 2436-2440
    • Russo, C.1    Girelli, D.2    Olivieri, O.3    Guarini, P.4    Manzato, F.5    Pizzolo, F.6
  • 28
    • 0034662779 scopus 로고    scopus 로고
    • Effect of common methylenetetrahydrofolate reductase gene mutation on coronary artery disease in familial hypercholesterolemia
    • Kawashiri M, Kajinami K, Nohara A, Yagi K, Inazu A, Koizumi J, Mabuchi H. Effect of common methylenetetrahydrofolate reductase gene mutation on coronary artery disease in familial hypercholesterolemia. Am J Cardio. 2000; 86:840-845.
    • (2000) Am J Cardio , vol.86 , pp. 840-845
    • Kawashiri, M.1    Kajinami, K.2    Nohara, A.3    Yagi, K.4    Inazu, A.5    Koizumi, J.6    Mabuchi, H.7
  • 29
    • 0029827313 scopus 로고    scopus 로고
    • Homocysteine and risk of premature coronary heart disease: Evidence for a common gene mutation
    • Gallagher PM, Meleady R, Shields DC, Tan KS, McMaster D, Rozen R, et al. Homocysteine and risk of premature coronary heart disease: evidence for a common gene mutation. Circulatio. 1996; 94:2154-2158.
    • (1996) Circulatio , vol.94 , pp. 2154-2158
    • Gallagher, P.M.1    Meleady, R.2    Shields, D.C.3    Tan, K.S.4    McMaster, D.5    Rozen, R.6
  • 30
    • 0037163849 scopus 로고    scopus 로고
    • MTHFR 677C→T polymorphism and risk of coronary heart disease: A metaanalysis
    • Klerk M, Verhoef P, Clarke R, Blom HJ, Kok FJ, Schouten EG. MTHFR 677C→T polymorphism and risk of coronary heart disease: a metaanalysis. JAM. 2002; 288:2023-2031.
    • (2002) JAM , vol.288 , pp. 2023-2031
    • Klerk, M.1    Verhoef, P.2    Clarke, R.3    Blom, H.J.4    Kok, F.J.5    Schouten, E.G.6
  • 31
    • 4644301651 scopus 로고    scopus 로고
    • The methylenetetrahydrofolate reductase gene polymorphism (C677T) is associated with increased cardiovascular mortality in Hungary
    • Kalina A, Czeizel AE. The methylenetetrahydrofolate reductase gene polymorphism (C677T) is associated with increased cardiovascular mortality in Hungary. Int J Cardio. 2004; 97:333-334.
    • (2004) Int J Cardio , vol.97 , pp. 333-334
    • Kalina, A.1    Czeizel, A.E.2
  • 32
    • 0036488108 scopus 로고    scopus 로고
    • A low prevalence of the C677T mutation in the methylenetetrahydrofolate reductase gene in Asian Indians
    • Mukherjee M, Joshi S, Bagadi S, Dalvi M, Rao A, Shetty KR. A low prevalence of the C677T mutation in the methylenetetrahydrofolate reductase gene in Asian Indians. Clin Gene. 2002; 61:155-159.
    • (2002) Clin Gene , vol.61 , pp. 155-159
    • Mukherjee, M.1    Joshi, S.2    Bagadi, S.3    Dalvi, M.4    Rao, A.5    Shetty, K.R.6
  • 33
    • 0033782287 scopus 로고    scopus 로고
    • The methylenetetrahydrofolate reductase gene is associated with increased cardiovascular risk in Japan, but not in other populations
    • Jee SH, Beaty TH, Suh I, Yoon Y, Appel U. The methylenetetrahydrofolate reductase gene is associated with increased cardiovascular risk in Japan, but not in other populations. Atherosclerosi. 2000; 153:161 -168.
    • (2000) Atherosclerosi , vol.153 , pp. 161-168
    • Jee, S.H.1    Beaty, T.H.2    Suh, I.3    Yoon, Y.4    Appel, U.5
  • 34
    • 37849022695 scopus 로고    scopus 로고
    • Demirer AN, Alikasifoglu M, Tuncbilek E, Karakus S, Erbas T. Factor V Leiden mutation and type 1 diabetes mellitus. Stood Coagul Fibrinolysi. 2008; 19:70-74.
    • Demirer AN, Alikasifoglu M, Tuncbilek E, Karakus S, Erbas T. Factor V Leiden mutation and type 1 diabetes mellitus. Stood Coagul Fibrinolysi. 2008; 19:70-74.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.