Hereditary hemochromatosis genotypes and risk of ischemic stroke

被引:33
作者
Ellervik, C.
Tybjaerg-Hansen, A.
Appleyard, M.
Sillesen, H.
Boysen, G.
Nordestgaard, B. G.
机构
[1] Herlev Univ Hosp, Dept Clin Biochem, DK-2730 Herlev, Denmark
[2] Univ Copenhagen Hosp, Rigshosp, Dept Clin Biochem, DK-2100 Copenhagen, Denmark
[3] Univ Copenhagen Hosp, Rigshosp, Dept Vasc Surg, DK-2100 Copenhagen, Denmark
[4] Univ Copenhagen, Bispebjerg Univ Hosp, Copehagen City Heart Study, Copenhagen, Denmark
[5] Univ Copenhagen, Bispebjerg Univ Hosp, Dept Neurol, Copenhagen, Denmark
关键词
D O I
10.1212/01.wnl.0000257814.77115.d6
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Objective: We tested the hypothesis that the HFE genotypes H63D/H63D, H63D/wild type, C282Y/H63D, C282Y/C282Y, and C282Y/wild type are risk factors for symptomatic carotid atherosclerosis, ischemic cerebrovascular disease (ICVD), and ischemic stroke. Methods: We performed an age- and gender- matched case- control study of 701 cases with symptomatic carotid atherosclerosis vs 2,777 controls, and a prospective study of 9,178 individuals from the Danish general population followed for 24 years, during which 504 developed ICVD, of whom 393 had ischemic stroke. Results: Genotype was not consistently associated with symptomatic carotid atherosclerosis. The cumulative incidences of ICVD and ischemic stroke by age were increased for H63D/H63D vs wild type/wild type (log- rank: p = 0.003 and p = 0.001). H63D/H63D vs wild type/wild type had an age- and multifactorially adjusted hazard ratio of 2.0 (95% CI: 1.2 to 3.2; p = 0.007) and 2.1 (1.3 to 3.5; p = 0.004) for ICVD and of 2.4 (1.4 to 4.0; p = 0.001) and 2.8 (1.7 to 4.6; p = 0.001) for ischemic stroke; these remained significant after correction for multiple comparisons. Other hereditary hemochromatosis genotypes were not associated with ICVD or ischemic stroke. Conclusions: Hereditary hemochromatosis H63D homozygosity predicts a two- to threefold risk of ICVD and ischemic stroke.
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页码:1025 / 1031
页数:7
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