Serum homocysteine, thermolabile variant of methylene tetrahydrofolate reductase (MTHFR), and venous thromboembolism: Longitudinal investigation of thromboembolism etiology,(LITE)

被引:61
作者
Tsai, AW
Cushman, M
Tsai, MY
Heckbert, SR
Rosamond, WD
Aleksic, N
Yanez, ND
Psaty, BM
Folsom, AR
机构
[1] Univ Minnesota, Sch Publ Hlth, Div Epidemiol, Minneapolis, MN 55454 USA
[2] Univ Vermont, Dept Med, Div Hematol Oncol, Burlington, VT USA
[3] Univ Minnesota, Dept Pathol & Lab Med, Minneapolis, MN 55454 USA
[4] Univ Washington, Dept Epidemiol, Seattle, WA 98195 USA
[5] Univ N Carolina, Collaborat Studies Coordinating Ctr, Chapel Hill, NC 27515 USA
[6] Univ Texas, Sch Med, Div Hematol, Houston, TX USA
[7] Univ Washington, Dept Biostat, Seattle, WA 98195 USA
[8] Univ Washington, Dept Med, Epidemiol Serv, Seattle, WA 98195 USA
[9] Univ Washington, Dept Med, Hlth Serv, Cardiovasc Hlth Res Unit, Seattle, WA 98195 USA
关键词
deep vein thrombosis; epidemiology; homocysteine; MTHFR; pulmonary embolism;
D O I
10.1002/ajh.10287
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
We sought to examine prospectively the association of serum homocysteine and the methylene tetrahydrofolate reductase (MTHFR) C677T gene polymorphism with risk of venous thromboembolism (VTE). We studied these relationships in a nested case-control study of 303 VTE cases and 635 matched controls from a population-based cohort of 21,680 adults from six U.S. communities. The highest quintile of serum homocysteine carried a non-statistically significant adjusted odds ratio of 1.55 (95% Cl, 0.93-2.58) compared to the lowest quintile in the overall cohort but a significant association among adults aged 45-64 years (OR = 2.05, 95% Cl, 1.10-3.83) and an inverse association in those greater than or equal to65 years of age. Carriers of the MTHFR C677T polymorphism were not at higher risk for VTE than those with normal genotype (OR = 0.74, 95% Cl = 0.56-0.98). Our prospective data showed, at most, a weak relationship between homocysteine and VTE risk, with associations larger among younger participants. MTHFR C677T was not a risk factor for VTE. (C) 2003 Wiley-Liss, Inc.
引用
收藏
页码:192 / 200
页数:9
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