Prospective study of circulating factor XI and incident venous thromboembolism: The Longitudinal Investigation of Thromboembolism Etiology (LITE)

被引:25
|
作者
Folsom, Aaron R. [1 ]
Tang, Weihong [1 ]
Roetker, Nicholas S. [1 ]
Heckbert, Susan R. [2 ]
Cushman, Mary [3 ,4 ]
Pankow, James S. [1 ]
机构
[1] Univ Minnesota, Sch Publ Hlth, Div Epidemiol & Community Hlth, Minneapolis, MN 55454 USA
[2] Univ Washington, Dept Epidemiol, Seattle, WA 98195 USA
[3] Univ Vermont, Dept Med, Burlington, VT USA
[4] Univ Vermont, Dept Pathol, Burlington, VT 05405 USA
关键词
GENOME-WIDE ASSOCIATION; DEEP-VEIN THROMBOSIS; RISK-FACTORS; VARIANTS; COHORTS;
D O I
10.1002/ajh.24168
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Elevated plasma concentrations of coagulation factor XI may increase risk of venous thromboembolism (VTE), but prospective data are limited. We studied prospectively the associations of plasma factor XI and a key F11 genetic variant with incident VTE in whites and African-Americans. We measured factor XI in 16,299 participants, initially free of VTE, in two prospective population cohorts. We also measured the F11 single nucleotide polymorphism rs4241824, which a genome-wide association study had linked to factor XI concentration. During follow-up, we identified 606 VTEs. The age, race, sex, and study-adjusted hazard ratio of VTE increased across factor XI quintiles (P<0.001 for trend), and the hazard ratio was 1.51 (95% CI 1.16, 1.97) for the highest versus lowest quintile overall, and was 1.42 (95% CI 1.03, 1.95) in whites and 1.72 (95% CI 1.08, 2.73) in African-Americans. In whites, the F11 variant was associated with both factor XI concentration and VTE incidence (1.15-fold greater incidence of VTE per risk allele). In African-Americans, these associations were absent. In conclusion, this cohort study documented that an elevated plasma factor XI concentration is a risk factor for VTE over extended follow-up, not only in whites but also in African-Americans. In whites, the association of the F11 genetic variant with VTE suggests a causal relation, but we did not observe this genetic relation in African-Americans. Am. J. Hematol. 90:1047-1051, 2015. (c) 2015 Wiley Periodicals, Inc.
引用
收藏
页码:1047 / 1051
页数:5
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