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Volumn 164, Issue 17, 2004, Pages 1932-1937

Prothrombin 20210A mutation: A mild risk factor for venous thromboembolism but not for arterial thrombotic disease and pregnancy-related complications in a family study

Author keywords

[No Author keywords available]

Indexed keywords

PROTHROMBIN;

EID: 4644268361     PISSN: 00039926     EISSN: None     Source Type: Journal    
DOI: 10.1001/archinte.164.17.1932     Document Type: Article
Times cited : (95)

References (37)
  • 1
    • 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;88:3698-3703.
    • (1996) Blood , vol.88 , pp. 3698-3703
    • Poort, S.R.1    Rosendaal, F.R.2    Reitsma, P.H.3    Bertina, R.M.4
  • 2
    • 0030714108 scopus 로고    scopus 로고
    • Prevalence of the prothrombin gene variant (nt20210A) in venous thrombosis and arterial disease
    • Arruda VR, Annichino-Bizzacchi JM, Goncalves MS, Costa FF. Prevalence of the prothrombin gene variant (nt20210A) in venous thrombosis and arterial disease. Thromb Haemost. 1997;78:1430-1433.
    • (1997) Thromb Haemost , vol.78 , pp. 1430-1433
    • Arruda, V.R.1    Annichino-Bizzacchi, J.M.2    Goncalves, M.S.3    Costa, F.F.4
  • 3
    • 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;90:1747-1750.
    • (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
  • 4
    • 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, Schuttrumpf 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;87:521-526.
    • (1997) Thromb Res , vol.87 , pp. 521-526
    • Watzke, H.H.1    Schuttrumpf, J.2    Graf, S.3    Huber, K.4    Panzer, S.5
  • 5
    • 0032976317 scopus 로고    scopus 로고
    • Interaction between the G20210A mutation of the prothrombin gene and oral contraceptive use in deep vein thrombosis
    • Martinelli I, Taioli E, Bucciarelli P, Akhavan S, Mannucci PM. Interaction between the G20210A mutation of the prothrombin gene and oral contraceptive use in deep vein thrombosis. Arterioscler Thromb Vasc Biol. 1999;19:700-703 .
    • (1999) Arterioscler Thromb Vasc Biol , vol.19 , pp. 700-703
    • Martinelli, I.1    Taioli, E.2    Bucciarelli, P.3    Akhavan, S.4    Mannucci, P.M.5
  • 6
    • 0032612369 scopus 로고    scopus 로고
    • The 20210 G→A mutation in the 3′-untranslated region of the prothrombin gene and the risk for arterial thrombotic disease
    • Franco RF, Trip MD, ten Gate H, et al. The 20210 G→A mutation in the 3′-untranslated region of the prothrombin gene and the risk for arterial thrombotic disease. Br J Haematol. 1999;104:50-54.
    • (1999) Br J Haematol , vol.104 , pp. 50-54
    • Franco, R.F.1    Trip, M.D.2    Ten Gate, H.3
  • 7
    • 0032892886 scopus 로고    scopus 로고
    • The risk of early recurrent venous thromboembolism after oral anticoagulant therapy in patients with the G20210A transition in the prothrombin gene
    • Eichinger S, Minar E, Hirschl M, et al. The risk of early recurrent venous thromboembolism after oral anticoagulant therapy in patients with the G20210A transition in the prothrombin gene. Thromb Haemost. 1999;81:14-17.
    • (1999) Thromb Haemost , vol.81 , pp. 14-17
    • Eichinger, S.1    Minar, E.2    Hirschl, M.3
  • 8
    • 0032743845 scopus 로고    scopus 로고
    • The prothrombin gene G20210A mutation and the platelet glycoprotein Ilia polymorphism PI(A2) in patients with central retinal vein occlusion
    • Larsson J, Hillarp A. The prothrombin gene G20210A mutation and the platelet glycoprotein Ilia polymorphism PI(A2) in patients with central retinal vein occlusion. Thromb Res. 1999;96:323-327.
    • (1999) Thromb Res , vol.96 , pp. 323-327
    • Larsson, J.1    Hillarp, A.2
  • 9
    • 0033539096 scopus 로고    scopus 로고
    • The risk of recurrent deep venous thrombosis among heterozygous carriers of both factor V Leiden and the G20210A prothrombin mutation
    • De Stefano V, Martinelli I, Mannucci PM, et al. The risk of recurrent deep venous thrombosis among heterozygous carriers of both factor V Leiden and the G20210A prothrombin mutation. N Engl J Med. 1999;341:801-806.
    • (1999) N Engl J Med , vol.341 , pp. 801-806
    • De Stefano, V.1    Martinelli, I.2    Mannucci, P.M.3
  • 10
    • 0034511765 scopus 로고    scopus 로고
    • Risk of venous thrombosis in carriers of the prothrombin G20210A variant and factor V Leiden and their interaction with oral contraceptives
    • Aznar J, Vaya A, Estelles A, et al. Risk of venous thrombosis in carriers of the prothrombin G20210A variant and factor V Leiden and their interaction with oral contraceptives. Haematologica. 2000;85:1271-1276.
    • (2000) Haematologica , vol.85 , pp. 1271-1276
    • Aznar, J.1    Vaya, A.2    Estelles, A.3
  • 11
    • 0034994092 scopus 로고    scopus 로고
    • The risk of recurrent venous thromboembolism among heterozygous carriers of the G20210A prothrombin gene mutation
    • De Stefano V, Martinelli I, Mannucci PM, et al. The risk of recurrent venous thromboembolism among heterozygous carriers of the G20210A prothrombin gene mutation. Br J Haematol. 2001;113:630-635.
    • (2001) Br J Haematol , vol.113 , pp. 630-635
    • De Stefano, V.1    Martinelli, I.2    Mannucci, P.M.3
  • 12
    • 0036998067 scopus 로고    scopus 로고
    • Can screening for genetic markers improve peripheral artery bypass patency?
    • Kibbe MR, Cortese HA, McSherry F, et al. Can screening for genetic markers improve peripheral artery bypass patency? J Vasc Surg. 2002;36:1198-1206.
    • (2002) J Vasc Surg , vol.36 , pp. 1198-1206
    • Kibbe, M.R.1    Cortese, H.A.2    McSherry, F.3
  • 13
    • 0037340390 scopus 로고    scopus 로고
    • Prothrombin G20210A mutation and oral contraceptives increase upper-extremity deep vein thrombotic risk
    • Vaya A, Mira Y, Mateo J, et al. Prothrombin G20210A mutation and oral contraceptives increase upper-extremity deep vein thrombotic risk. Thromb Haemost. 2003;89:452-457.
    • (2003) Thromb Haemost , vol.89 , pp. 452-457
    • Vaya, A.1    Mira, Y.2    Mateo, J.3
  • 14
    • 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
  • 15
    • 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, et al. G20210A prothrombin gene polymorphism and prothrombin activity in subjects with or without angiographically documented coronary artery disease. Circulation. 2001;103:2436-2440.
    • (2001) Circulation , vol.103 , pp. 2436-2440
    • Russo, C.1    Girelli, D.2    Olivieri, O.3
  • 16
    • 0037418247 scopus 로고    scopus 로고
    • No evidence of association between prothrombic gene polymorphisms and the development of acute myocardial infarction at a young age
    • Atherosclerosis, Thrombosis, and Vascular Biology Italian Study Group. No evidence of association between prothrombic gene polymorphisms and the development of acute myocardial infarction at a young age. Circulation. 2003;107:1117-1128.
    • (2003) Circulation , vol.107 , pp. 1117-1128
  • 17
    • 0035909969 scopus 로고    scopus 로고
    • Genetic variation in coagulation and fibrinolytic proteins and their relation with acute myocardial infarction: A systematic review
    • Boekholdt SM, Bijsterveld NR, Moons AM, Buller HR, Peters RG. Genetic variation in coagulation and fibrinolytic proteins and their relation with acute myocardial infarction: a systematic review. Circulation. 2001;104:3063-3068.
    • (2001) Circulation , vol.104 , pp. 3063-3068
    • Boekholdt, S.M.1    Bijsterveld, N.R.2    Moons, A.M.3    Buller, H.R.4    Peters, R.G.5
  • 18
    • 0031767657 scopus 로고    scopus 로고
    • Thrombophilia: A mechanism of disease in women with adverse pregnancy outcome and thrombotic lesions in the placenta
    • Arias F, Romero R, Joist H, Kraus FT. Thrombophilia: a mechanism of disease in women with adverse pregnancy outcome and thrombotic lesions in the placenta. J Matern Fetal Med. 1998;7:277-286.
    • (1998) J Matern Fetal Med , vol.7 , pp. 277-286
    • Arias, F.1    Romero, R.2    Joist, H.3    Kraus, F.T.4
  • 19
    • 0036178694 scopus 로고    scopus 로고
    • Lower birth-weight in neonates of mothers carrying factor V G1691A and factor II A(20210) mutations
    • Grandone E, Margaglione M, Colaizzo D, et al. Lower birth-weight in neonates of mothers carrying factor V G1691A and factor II A(20210) mutations. Haematologica. 2002;87:177-181.
    • (2002) Haematologica , vol.87 , pp. 177-181
    • Grandone, E.1    Margaglione, M.2    Colaizzo, D.3
  • 20
    • 0033531184 scopus 로고    scopus 로고
    • Increased frequency of genetic thrombophilia in women with complications of pregnancy
    • Kupferminc MJ, Eldor A, Steinman N, et al. Increased frequency of genetic thrombophilia in women with complications of pregnancy. N Engl J Med. 1999;340:9-13.
    • (1999) N Engl J Med , vol.340 , pp. 9-13
    • Kupferminc, M.J.1    Eldor, A.2    Steinman, N.3
  • 21
    • 0034919759 scopus 로고    scopus 로고
    • Thrombophilic gene mutations and recurrent spontaneous abortion: Prothrombin mutation increases the risk in the first trimester
    • Pihusch R, Buchholz T, Lohse P, et al. Thrombophilic gene mutations and recurrent spontaneous abortion: prothrombin mutation increases the risk in the first trimester. Am J Reprod Immunol. 2001;46:124-131.
    • (2001) Am J Reprod Immunol , vol.46 , pp. 124-131
    • Pihusch, R.1    Buchholz, T.2    Lohse, P.3
  • 22
    • 0037443934 scopus 로고    scopus 로고
    • Thrombophilic disorders and fetal loss: A meta-analysis
    • Rey E, Kahn S, David M, Schrier I. Thrombophilic disorders and fetal loss: a meta-analysis. Lancet. 2003;361:901-908.
    • (2003) Lancet , vol.361 , pp. 901-908
    • Rey, E.1    Kahn, S.2    David, M.3    Schrier, I.4
  • 23
    • 0025708282 scopus 로고
    • Recurrent miscarriage, I: Definition and epidemiology
    • Stirrat GM. Recurrent miscarriage, I: definition and epidemiology. Lancet. 1990;336:673-675.
    • (1990) Lancet , vol.336 , pp. 673-675
    • Stirrat, G.M.1
  • 24
    • 0020082393 scopus 로고
    • Syndrome of hemolysis, elevated liver enzymes, and low platelet count: A severe consequence of hypertension in pregnancy
    • Weinstein L. Syndrome of hemolysis, elevated liver enzymes, and low platelet count: a severe consequence of hypertension in pregnancy. Am J Obstet Gynecol. 1982;142:159-167.
    • (1982) Am J Obstet Gynecol , vol.142 , pp. 159-167
    • Weinstein, L.1
  • 25
    • 0023893418 scopus 로고
    • The classification and definition of the hypertensive disorders of pregnancy
    • Davey DA, MacGillivray I. The classification and definition of the hypertensive disorders of pregnancy. Am J Obstet Gynecol. 1988;158:892-898.
    • (1988) Am J Obstet Gynecol , vol.158 , pp. 892-898
    • Davey, D.A.1    MacGillivray, I.2
  • 28
    • 0034023197 scopus 로고    scopus 로고
    • Prothrombin 20210 G→A, MTHFR C677T mutations in women with venous thromboembolism associated with pregnancy
    • McColl MD, Ellison J, Reid F, Tait RC, Walker ID, Greer IA. Prothrombin 20210 G→A, MTHFR C677T mutations in women with venous thromboembolism associated with pregnancy. BJOG. 2000;107:565-569.
    • (2000) BJOG , vol.107 , pp. 565-569
    • McColl, M.D.1    Ellison, J.2    Reid, F.3    Tait, R.C.4    Walker, I.D.5    Greer, I.A.6
  • 29
    • 0031985328 scopus 로고    scopus 로고
    • The incidence of venous thromboembolism in family members of patients with factor V Leiden mutation and venous thrombosis
    • Middeldorp S, Henkens CM, Koopman MM, et al. The incidence of venous thromboembolism in family members of patients with factor V Leiden mutation and venous thrombosis. Ann Intern Med. 1998;128:15-20.
    • (1998) Ann Intern Med , vol.128 , pp. 15-20
    • Middeldorp, S.1    Henkens, C.M.2    Koopman, M.M.3
  • 30
    • 0000662461 scopus 로고    scopus 로고
    • Incidence of venous thromboembolism in families with inherited thrombophilia
    • Simioni P, Sanson BJ, Prandoni P, et al. Incidence of venous thromboembolism in families with inherited thrombophilia. Thromb Haemost. 1999;81:198-202.
    • (1999) Thromb Haemost , vol.81 , pp. 198-202
    • Simioni, P.1    Sanson, B.J.2    Prandoni, P.3
  • 31
    • 0344765521 scopus 로고    scopus 로고
    • Risk of stroke in young women and two prothrombotic mutations: Factor V Leiden and prothrombin gene variant (G20210A)
    • Longstreth WTJ, Rosendaal FR, Siscovick DS, et al. Risk of stroke in young women and two prothrombotic mutations: factor V Leiden and prothrombin gene variant (G20210A). Stroke. 1998;29:577-580.
    • (1998) Stroke , vol.29 , pp. 577-580
    • Longstreth, W.T.J.1    Rosendaal, F.R.2    Siscovick, D.S.3
  • 32
    • 0033169099 scopus 로고    scopus 로고
    • Prothrombotic genetic risk factors in young survivors of myocardial infarction
    • Ardissino D, Mannucci PM, Merlini PA, et al. Prothrombotic genetic risk factors in young survivors of myocardial infarction. Blood. 1999;94:46-51.
    • (1999) Blood , vol.94 , pp. 46-51
    • Ardissino, D.1    Mannucci, P.M.2    Merlini, P.A.3
  • 33
    • 4644352758 scopus 로고
    • Evaluation of early pregnancy loss
    • Reed GB, Claireaux AE, Cockburn F, eds. London, England: Chapman & Hall
    • Bieber FR, Driscoll SG. Evaluation of early pregnancy loss. In: Reed GB, Claireaux AE, Cockburn F, eds. Diseases of the Fetus and Newborn. 2nd ed. London, England: Chapman & Hall; 1995:175-186.
    • (1995) Diseases of the Fetus and Newborn. 2nd Ed. , pp. 175-186
    • Bieber, F.R.1    Driscoll, S.G.2
  • 34
    • 0025970806 scopus 로고
    • Mortality in hereditary antithrombin-III deficiency-1830 to 1989
    • Rosendaal FR, Heijboer H, Briet E, et al. Mortality in hereditary antithrombin-III deficiency-1830 to 1989. Lancet. 1991;337:260-262.
    • (1991) Lancet , vol.337 , pp. 260-262
    • Rosendaal, F.R.1    Heijboer, H.2    Briet, E.3
  • 35
    • 0028356345 scopus 로고
    • Heart disease, cancer, and stroke mortality trends and their interrelations: An international perspective
    • Thorn TJ, Epstein FH. Heart disease, cancer, and stroke mortality trends and their interrelations: an international perspective. Circulation. 1994;90:574-582.
    • (1994) Circulation , vol.90 , pp. 574-582
    • Thorn, T.J.1    Epstein, F.H.2
  • 36
    • 0037085791 scopus 로고    scopus 로고
    • Incidence of venous thromboembolism in asymptomatic family members who are carriers of factor V Leiden: A prospective cohort study
    • Simioni P, Tormene D, Prandoni P, et al. Incidence of venous thromboembolism in asymptomatic family members who are carriers of factor V Leiden: a prospective cohort study. Blood. 2002;99:1938-1942.
    • (2002) Blood , vol.99 , pp. 1938-1942
    • Simioni, P.1    Tormene, D.2    Prandoni, P.3
  • 37
    • 0026764834 scopus 로고
    • A prospective study of the incidence of deep-vein thrombosis within a defined urban population
    • Nordstrom M, Lindblad B, Bergqvist D, Kjellstrom T. A prospective study of the incidence of deep-vein thrombosis within a defined urban population. J Intern Med. 1992;232:155-160.
    • (1992) J Intern Med , vol.232 , pp. 155-160
    • Nordstrom, M.1    Lindblad, B.2    Bergqvist, D.3    Kjellstrom, T.4


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