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
相关论文
共 24 条
  • [1] New gene variants associated with venous thrombosis: a replication study in White and Black Americans
    Austin, H.
    de Staercke, C.
    Lally, C.
    Bezemer, I. D.
    Rosendaal, F. R.
    Hooper, W. C.
    [J]. JOURNAL OF THROMBOSIS AND HAEMOSTASIS, 2011, 9 (03) : 489 - 495
  • [2] Gene variants associated with deep vein thrombosis
    Bezemer, Irene D.
    Bare, Lance A.
    Doggen, Carine J. M.
    Arellano, Andre R.
    Tong, Carmen
    Rowland, Charles M.
    Catanese, Joseph
    Young, Bradford A.
    Reitsma, Pieter H.
    Devlin, James J.
    Rosendaal, Frits R.
    [J]. JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2008, 299 (11): : 1306 - 1314
  • [3] Factor XI Antisense Oligonucleotide for Prevention of Venous Thrombosis
    Bueller, Harry R.
    Bethune, Claudette
    Bhanot, Sanjay
    Gailani, David
    Monia, Brett P.
    Raskob, Gary E.
    Segers, Annelise
    Verhamme, Peter
    Weitz, Jeffrey I.
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 2015, 372 (03) : 232 - 240
  • [4] Deep vein thrombosis and pulmonary embolism in two cohorts: The longitudinal investigation of thromboembolism etiology
    Cushman, M
    Tsai, AW
    White, RH
    Heckbert, SR
    Rosamond, WD
    Enright, P
    Folsom, AR
    [J]. AMERICAN JOURNAL OF MEDICINE, 2004, 117 (01) : 19 - 25
  • [5] Coagulation factors IX through XIII and the risk of future venous thrombosis: the Longitudinal Investigation of Thromboembolism Etiology
    Cushman, Mary
    O'Meara, Ellen S.
    Folsom, Aaron R.
    Heckbert, Susan R.
    [J]. BLOOD, 2009, 114 (14) : 2878 - 2883
  • [6] Fried Linda P., 1991, Annals of Epidemiology, V1, P263
  • [7] FACTOR-XI ACTIVATION IN A REVISED MODEL OF BLOOD-COAGULATION
    GAILANI, D
    BROZE, GJ
    [J]. SCIENCE, 1991, 253 (5022) : 909 - 912
  • [8] Genetics of Venous Thrombosis: Insights from a New Genome Wide Association Study
    Germain, Marine
    Saut, Noemie
    Greliche, Nicolas
    Dina, Christian
    Lambert, Jean-Charles
    Perret, Claire
    Cohen, William
    Oudot-Mellakh, Tiphaine
    Antoni, Guillemette
    Alessi, Marie-Christine
    Zelenika, Diana
    Cambien, Francois
    Tiret, Laurence
    Bertrand, Marion
    Dupuy, Anne-Marie
    Letenneur, Luc
    Lathrop, Mark
    Emmerich, Joseph
    Amouyel, Philippe
    Tregouet, David-Alexandre
    Morange, Pierre-Emmanuel
    [J]. PLOS ONE, 2011, 6 (09):
  • [9] A genome-wide association study of venous thromboembolism identifies risk variants in chromosomes 1q24.2 and 9q
    Heit, J. A.
    Armasu, S. M.
    Asmann, Y. W.
    Cunningham, J. M.
    Matsumoto, M. E.
    Petterson, T. M.
    De Andrade, M.
    [J]. JOURNAL OF THROMBOSIS AND HAEMOSTASIS, 2012, 10 (08) : 1521 - 1531
  • [10] Concept, Design and Implementation of a Cardiovascular Gene-Centric 50 K SNP Array for Large-Scale Genomic Association Studies
    Keating, Brendan J.
    Tischfield, Sam
    Murray, Sarah S.
    Bhangale, Tushar
    Price, Thomas S.
    Glessner, Joseph T.
    Galver, Luana
    Barrett, Jeffrey C.
    Grant, Struan F. A.
    Farlow, Deborah N.
    Chandrupatla, Hareesh R.
    Hansen, Mark
    Ajmal, Saad
    Papanicolaou, George J.
    Guo, Yiran
    Li, Mingyao
    DerOhannessian, Stephanie
    de Bakker, Paul I. W.
    Bailey, Swneke D.
    Montpetit, Alexandre
    Edmondson, Andrew C.
    Taylor, Kent
    Gai, Xiaowu
    Wang, Susanna S.
    Fornage, Myriam
    Shaikh, Tamim
    Groop, Leif
    Boehnke, Michael
    Hall, Alistair S.
    Hattersley, Andrew T.
    Frackelton, Edward
    Patterson, Nick
    Chiang, Charleston W. K.
    Kim, Cecelia E.
    Fabsitz, Richard R.
    Ouwehand, Willem
    Price, Alkes L.
    Munroe, Patricia
    Caulfield, Mark
    Drake, Thomas
    Boerwinkle, Eric
    Reich, David
    Whitehead, A. Stephen
    Cappola, Thomas P.
    Samani, Nilesh J.
    Lusis, A. Jake
    Schadt, Eric
    Wilson, James G.
    Koenig, Wolfgang
    McCarthy, Mark I.
    [J]. PLOS ONE, 2008, 3 (10):