In:
Clinical Chemistry, Oxford University Press (OUP), Vol. 53, No. 5 ( 2007-05-01), p. 845-851
Abstract:
Background: Hyperhomocysteinemia has been associated with a higher risk of cardiovascular disease (CVD) in epidemiological studies, but recent trials have failed to show a benefit of lowering homocysteine. To address this apparent paradox, we explored whether interaction between genetic and dietary factors related to homocysteine metabolism contributes to CVD risk. Methods: We evaluated the associations of homocysteine, methylenetetrahydrofolate reductase (MTHFR) 677C & gt;T genotype, and dietary intake of folate/B-vitamins with subsequent CVD events in 24 968 apparently healthy white American women followed for 10 years. Plasma homocysteine was measured using an enzymatic assay. MTHFR genotype was determined with a multiplex PCR using biotinylated primers. Results: In unadjusted analyses, homocysteine showed moderately strong linear associations with CVD, with hazard ratios (95% CI) comparing top with bottom quintiles for total CVD of 1.92 (1.55–2.37), myocardial infarction 2.32 (1.52–3.54), and ischemic stroke 2.25 (1.45–3.50), all Ptrend & lt;0.001. These ratios were markedly attenuated after adjusting for traditional risk factors and socioeconomic status to 1.08 (0.86–1.36), Ptrend = 0.12; 1.20 (0.76–1.87), Ptrend = 0.14; and 1.21 (0.75–1.94), Ptrend = 0.50, respectively. Homocysteine was associated with MTHFR genotype (1.4 μmol/L higher homocysteine for TT vs CC, P & lt;0.001) and inversely with intake of folate, vitamin B2, B6, and B12, all Ptrend & lt;0.001. However, there was no association of MTHFR genotype or dietary folate/B-vitamins with CVD. In addition, there were no gene–diet or gene–homocysteine interactions in relation to CVD. Conclusions: In this large-scale prospective study, the association of homocysteine with CVD was markedly attenuated after adjusting for risk factors and was not modified by MTHFR 677C & gt;T or intake of folate or B-vitamins.
Type of Medium:
Online Resource
ISSN:
0009-9147
,
1530-8561
DOI:
10.1373/clinchem.2006.083881
Language:
English
Publisher:
Oxford University Press (OUP)
Publication Date:
2007
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