Methylenetetrahydrofolate Reductase 677 C → T Mutation and Coronary Heart Disease Risk in UK Indian Asians

Author:

Chambers John C.1,Ireland Helen1,Thompson Elizabeth1,Reilly Peter1,Obeid Omar A.1,Refsum Helga1,Ueland Per1,Lane David A.1,Kooner Jaspal S.1

Affiliation:

1. From the National Heart and Lung Institute (J.C.C., P.R., J.S.K.), Imperial College School of Medicine, Hammersmith Hospital; the Department of Haematology (H.I., E.T., D.L.), Imperial College School of Medicine, Charing Cross Hospital; and the Department of Human Nutrition (O.A.O.), St Bartholomew’s and Royal London School of Medicine & Dentistry, Queen Mary and Westfield College, London, UK; and the Department of Pharmacology (H.R., P.U.), University of Bergen, Armauer Hansen Hus, Bergen, Norway.

Abstract

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 CT 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 CT genotype, and conventional CHD risk factors were measured. The prevalence of homozygous MTHFR 677 T 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 μmol/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 677 T 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 677 T 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.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Cardiology and Cardiovascular Medicine

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