Literature DB >> 11073851

Methylenetetrahydrofolate reductase 677 C-->T mutation and coronary heart disease risk in UK Indian Asians.

J C Chambers1, H Ireland, E Thompson, P Reilly, O A Obeid, H Refsum, P Ueland, D A Lane, J S Kooner.   

Abstract

Plasma homocysteine concentrations are elevated in UK Indian Asians and may contribute to twice as many coronary heart disease (CHD) deaths in this group compared with European whites. The mechanisms underlying elevated homocysteine concentrations among Indian Asians are not well understood. In this study, we have investigated the extent to which the methylenetetrahydrofolate reductase (MTHFR) 677 C-->T mutation accounts for elevated plasma homocysteine and increased CHD risk in Indian Asians compared with European whites. We investigated 454 male cases (with myocardial infarction or angiographically proven CHD: 224 Indian Asians, 230 European whites) and 805 healthy male controls (381 Indian Asians, 424 European whites). Fasting homocysteine concentrations, MTHFR 677 C-->T genotype, and conventional CHD risk factors were measured. The prevalence of homozygous MTHFR 677T in Indian Asian controls was less than one third that in European white controls (3.1% versus 9. 7%, P<0.001). In Indian Asians, the TT MTHFR genotype was not associated with homocysteine concentrations and was not present in any of the Asian controls with hyperhomocysteinemia (>15 micromol/L). In contrast, among European whites, the TT MTHFR genotype was strongly related to elevated plasma homocysteine concentrations and was found in 27% of the European controls with hyperhomocysteinemia. Elevated homocysteine in Indian Asian compared with European white controls was accounted for by their reduced levels of B vitamins but not by the MTHFR 677T genotype. However, neither the TT MTHFR genotype nor B vitamin levels explained the elevated homocysteine concentrations in CHD cases compared with controls. TT MTHFR was not a risk factor for early-onset CHD in Indian Asians (odds ratio, 0.5; 95% confidence interval, 0.1 to 2.4; P=0.39), unlike in European whites (odds ratio, 2.1; 95% confidence interval, 1.1 to 4. 1; P=0.02). We conclude that the MTHFR 677T: mutation does not contribute to elevated plasma homocysteine concentrations or increased CHD risk in Indian Asians compared with European whites. Our results suggest that novel genetic defects and/or environmental factors influence homocysteine metabolism in Indian Asians residing in the United Kingdom.

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Year:  2000        PMID: 11073851     DOI: 10.1161/01.atv.20.11.2448

Source DB:  PubMed          Journal:  Arterioscler Thromb Vasc Biol        ISSN: 1079-5642            Impact factor:   8.311


  14 in total

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Journal:  Proc Natl Acad Sci U S A       Date:  2001-03-13       Impact factor: 11.205

2.  Folate and cobalamin deficiencies and hyperhomocysteinemia in Bangladesh.

Authors:  Mary V Gamble; Habibul Ahsan; Xinhua Liu; Pam Factor-Litvak; Vesna Ilievski; Vesna Slavkovich; Faruque Parvez; Joseph H Graziano
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3.  Association of MTHFR C677T (rs1801133) and A1298C (rs1801131) Polymorphisms with Serum Homocysteine, Folate and Vitamin B12 in Patients with Young Coronary Artery Disease.

Authors:  Rajni R Shivkar; Gayatri C Gawade; Meghana K Padwal; Arundhati G Diwan; Sumiran A Mahajan; Charushila Y Kadam
Journal:  Indian J Clin Biochem       Date:  2021-05-18

4.  The association of the MTHFR c.1625A>C genetic variant with the risk of congenital heart diseases in the Chinese.

Authors:  Yuting Wang; Lei Sun; Weina Du; Shuang Song; Shuo Wang; Weiju Jiang; Tianchu Huang; Hui Li
Journal:  Genet Test Mol Biomarkers       Date:  2015-01

5.  Lack of association of methylenetetrahydrofolate reductase 677C>T mutation with coronary artery disease in a Pakistani population.

Authors:  M Perwaiz Iqbal; Tasneem Fatima; Siddiqa Parveen; Farzana A Yousuf; Majid Shafiq; Naseema Mehboobali; Abrar H Khan; Iqbal Azam; Philippe M Frossard
Journal:  J Mol Genet Med       Date:  2005-07-28

6.  MTHFR Gene variants C677T, A1298C and association with Down syndrome: A Case-control study from South India.

Authors:  Cyrus Cyril; Padmalatha Rai; N Chandra; P M Gopinath; K Satyamoorthy
Journal:  Indian J Hum Genet       Date:  2009-05

7.  Polymorphisms of methylenetetrahydrofolate reductase gene as the genetic predispositions of coronary artery diseases in eastern India.

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8.  Association of polymorphism in the thermolabile 5, 10-methylene tetrahydrofolate reductase gene and hyperhomocysteinemia with coronary artery disease.

Authors:  Mohammad A Alam; Syed A Husain; Rajiv Narang; Shayam S Chauhan; Madhulika Kabra; Suman Vasisht
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9.  Detailed analysis of gene polymorphisms associated with ischemic stroke in South Asians.

Authors:  Sunaina Yadav; Nazeeha Hasan; Thomas Marjot; Muhammad S Khan; Kameshwar Prasad; Paul Bentley; Pankaj Sharma
Journal:  PLoS One       Date:  2013-03-07       Impact factor: 3.240

10.  Genetic interactions between MTHFR (C677T), methionine synthase (A2756G, C2758G) variants with vitamin B12 and folic acid determine susceptibility to premature coronary artery disease in Indian population.

Authors:  V V Ravi Kanth; Jaya Prakash Golla; B K S Sastry; Sudhir Naik; Nitin Kabra; Madireddi Sujatha
Journal:  J Cardiovasc Dis Res       Date:  2011-07
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