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Volumn 7, Issue 3, 2000, Pages 197-200

A common polymorphism in methionine synthase reductase increases risk of premature coronary artery disease

Author keywords

Coronary artery disease; Folate; Homocysteine; Methionine synthase reductase; Vitamin B12

Indexed keywords

COBALAMIN; CYANOCOBALAMIN; FOLIC ACID; HOMOCYSTEINE; METHIONINE SYNTHASE; OXIDOREDUCTASE;

EID: 0033912873     PISSN: 13506277     EISSN: None     Source Type: Journal    
DOI: 10.1177/204748730000700306     Document Type: Article
Times cited : (67)

References (18)
  • 1
    • 0000167774 scopus 로고
    • Disorder of transsulfuration
    • Scriver CR, Beaudet AL, Sly WS, Valle D (editors). New York: McGraw-Hill
    • 1 Mudd SH, Levy HL, Skovby F. Disorder of transsulfuration. In: Scriver CR, Beaudet AL, Sly WS, Valle D (editors): The metabolic basis of inherited disease. New York: McGraw-Hill; 1995. p. 1279.
    • (1995) The Metabolic Basis of Inherited Disease , pp. 1279
    • Mudd, S.H.1    Levy, H.L.2    Skovby, F.3
  • 3
    • 0030971062 scopus 로고    scopus 로고
    • Homocysteine and thrombotic disease
    • 3 D'Angelo A, Selhub J. Homocysteine and thrombotic disease. Blood 1997; 90:1-11.
    • (1997) Blood , vol.90 , pp. 1-11
    • D'Angelo, A.1    Selhub, J.2
  • 4
    • 0030797307 scopus 로고    scopus 로고
    • Hyperhomocysteinemia as a risk factor for arterial and venous disease. A review of evidence and relevance
    • 4 Boers GHJ. Hyperhomocysteinemia as a risk factor for arterial and venous disease. A review of evidence and relevance. Thromb Haemost 1997; 77:520-522.
    • (1997) Thromb Haemost , vol.77 , pp. 520-522
    • Boers, G.H.J.1
  • 5
    • 0029066299 scopus 로고
    • A quantitative assessment of plasma homocysteine as a risk factor for vascular disease: Probable benefits of raising folic acid intakes
    • 5 Boushey CJ, Beresford SAA, Omenn G, Motulsky AG. A quantitative assessment of plasma homocysteine as a risk factor for vascular disease: probable benefits of raising folic acid intakes. JAMA 1995; 274:1049-1057.
    • (1995) JAMA , vol.274 , pp. 1049-1057
    • Boushey, C.J.1    Beresford, S.A.A.2    Omenn, G.3    Motulsky, A.G.4
  • 6
    • 0026533906 scopus 로고
    • The pathogenesis of homocysteinemia: Interruption of the coordinate regulation by S-adenosylmethionine of the remethylation and transsulfuration of homocysteine
    • 6 Selhub J, Miller JW. The pathogenesis of homocysteinemia: interruption of the coordinate regulation by S-adenosylmethionine of the remethylation and transsulfuration of homocysteine. Am J Clin Nutr 1991; 55:131-138.
    • (1991) Am J Clin Nutr , vol.55 , pp. 131-138
    • Selhub, J.1    Miller, J.W.2
  • 7
    • 0029924647 scopus 로고    scopus 로고
    • Homocysteine metabolism and risk of myocardial infarction: Relation with vitamins B6, B12 and folate
    • 7 Verhoef P, Stampfer MJ, Buring JE, Gaziano JM, Allen RH, Stabler SP, et al. Homocysteine metabolism and risk of myocardial infarction: relation with vitamins B6, B12 and folate. Am J Epidemiol 1996; 143:845-859.
    • (1996) Am J Epidemiol , vol.143 , pp. 845-859
    • Verhoef, P.1    Stampfer, M.J.2    Buring, J.E.3    Gaziano, J.M.4    Allen, R.H.5    Stabler, S.P.6
  • 8
    • 0032555167 scopus 로고    scopus 로고
    • Prospective study of coronary heart disease incidence in relation to fasting total homocysteine, related genetic polymorphisms and B vitamins
    • 8 Folsom AR, Nieto FJ, McGovern PG, Tsai MY, Malinow MR, Eckfeldt JH, et al. Prospective study of coronary heart disease incidence in relation to fasting total homocysteine, related genetic polymorphisms and B vitamins. Circulation 1998; 98:204-210.
    • (1998) Circulation , vol.98 , pp. 204-210
    • Folsom, A.R.1    Nieto, F.J.2    McGovern, P.G.3    Tsai, M.Y.4    Malinow, M.R.5    Eckfeldt, J.H.6
  • 9
    • 0030027668 scopus 로고    scopus 로고
    • Relation between folate status, a common mutation in methylenetetrahydrofolate reductase, and plasma homocysteine concentrations
    • 9 Jacques PF, Bostom AG, Williams RR, Ellison RC, Eckfeldt JH, Rosenberg IH, et al. Relation between folate status, a common mutation in methylenetetrahydrofolate reductase, and plasma homocysteine concentrations. Circulation 1996; 93:7-9.
    • (1996) Circulation , vol.93 , pp. 7-9
    • Jacques, P.F.1    Bostom, A.G.2    Williams, R.R.3    Ellison, R.C.4    Eckfeldt, J.H.5    Rosenberg, I.H.6
  • 10
    • 0032081312 scopus 로고    scopus 로고
    • Methylenetetrahydrofolate reductase C677T mutation, plasma homocysteine, and folate in subjects from northern Italy with or without angiographically documented severe coronary atherosclerotic disease: Evidence for an important genetic-environmental interaction
    • 10 Girelli D, Friso S, Trabetti E, Olivierei O, Russo C, Pessotto R, et al. Methylenetetrahydrofolate reductase C677T mutation, plasma homocysteine, and folate in subjects from northern Italy with or without angiographically documented severe coronary atherosclerotic disease: evidence for an important genetic-environmental interaction. Blood 1998; 91:4158-4163.
    • (1998) Blood , vol.91 , pp. 4158-4163
    • Girelli, D.1    Friso, S.2    Trabetti, E.3    Olivierei, O.4    Russo, C.5    Pessotto, R.6
  • 11
    • 0000443712 scopus 로고
    • Inherited disorders of folate transport and metabolism
    • Scriver CR, Beaudet AL, Sly WS, Valle D (editors). New York: McGraw-Hill
    • 11 Rosenblatt D. Inherited disorders of folate transport and metabolism. In: Scriver CR, Beaudet AL, Sly WS, Valle D (editors): The metabolic basis of inherited disease. New York: McGraw-Hill; 1995. pp. 3111-3128.
    • (1995) The Metabolic Basis of Inherited Disease , pp. 3111-3128
    • Rosenblatt, D.1
  • 12
    • 0000526332 scopus 로고
    • Inherited disorders of cobalamin transport and metabolism
    • Scriver CR, Beaudet AL, Sly WS, Valle D (editors). New York: McGraw-Hill
    • 12 Fenton WA, Rosenberg LE. Inherited disorders of cobalamin transport and metabolism. In: Scriver CR, Beaudet AL, Sly WS, Valle D (editors): The metabolic basis of inherited disease. New York: McGraw-Hill; 1995. pp. 3129-3149.
    • (1995) The Metabolic Basis of Inherited Disease , pp. 3129-3149
    • Fenton, W.A.1    Rosenberg, L.E.2
  • 14
    • 13144282730 scopus 로고    scopus 로고
    • Cloning and mapping of a cDNA for methionine synthase reductase, a flavoprotein defective in patients with homocystinuria
    • 14 Leclerc D, Wilson A, Dumas R, Gafuik C, Song D, Watkins D, et al. Cloning and mapping of a cDNA for methionine synthase reductase, a flavoprotein defective in patients with homocystinuria. Proc Natl Acad Sci USA 1998; 95:3059-3064.
    • (1998) Proc Natl Acad Sci USA , vol.95 , pp. 3059-3064
    • Leclerc, D.1    Wilson, A.2    Dumas, R.3    Gafuik, C.4    Song, D.5    Watkins, D.6
  • 15
    • 0032862179 scopus 로고    scopus 로고
    • Molecular basis for methionine synthase reductase deficiency in patients belonging to the cblE complementation group of disorders in folate/cobalamin metabolism
    • 15 Wilson A, Leclerc D, Rosenblatt DS, Gravel RA. Molecular basis for methionine synthase reductase deficiency in patients belonging to the cblE complementation group of disorders in folate/cobalamin metabolism. Human Molec Genet 1999; 8:2009-2016.
    • (1999) Human Molec Genet , vol.8 , pp. 2009-2016
    • Wilson, A.1    Leclerc, D.2    Rosenblatt, D.S.3    Gravel, R.A.4
  • 17
    • 0021993033 scopus 로고
    • Wllcoxon-type test for trend
    • 17 Cuzick JA. Wllcoxon-type test for trend. Statist Med 1985; 4:87-90.
    • (1985) Statist Med , vol.4 , pp. 87-90
    • Cuzick, J.A.1
  • 18
    • 0022629577 scopus 로고
    • Binomial regression in GLIM: Estimating risk ratios and risk differences
    • 18 Wacholder S. Binomial regression in GLIM: estimating risk ratios and risk differences. Am J Epidemiol 1986; 123:174-184.
    • (1986) Am J Epidemiol , vol.123 , pp. 174-184
    • Wacholder, S.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.