Causal Relationship of Susceptibility Genes to Ischemic Stroke: Comparison to Ischemic Heart Disease and Biochemical Determinants

被引:69
作者
Bentley, Paul [1 ]
Peck, George [1 ]
Smeeth, Liam [2 ]
Whittaker, John [2 ]
Sharma, Pankaj [1 ]
机构
[1] Univ London Imperial Coll Sci Technol & Med, Charing Cross Hosp, Imperial Coll Cerebrovasc Res Unit, London, England
[2] London Sch Hyg & Trop Med, Dept Epidemiol & Populat Hlth, London WC1, England
来源
PLOS ONE | 2010年 / 5卷 / 02期
基金
英国惠康基金;
关键词
PLASMINOGEN-ACTIVATOR INHIBITOR; CORONARY-ARTERY-DISEASE; CARDIOVASCULAR-DISEASE; MYOCARDIAL-INFARCTION; PRIMARY PREVENTION; RISK; METAANALYSIS; POLYMORPHISM; ASSOCIATION; PLASMA;
D O I
10.1371/journal.pone.0009136
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Interrelationships between genetic and biochemical factors underlying ischemic stroke and ischemic heart disease are poorly understood. We: 1) undertook the most comprehensive meta-analysis of genetic polymorphisms in ischemic stroke to date; 2) compared genetic determinants of ischemic stroke with those of ischemic heart disease, and 3) compared effect sizes of gene-stroke associations with those predicted from independent biochemical data using a mendelian randomization strategy. Electronic databases were searched up to January 2009. We identified: 1) 187 ischemic stroke studies (37,481 cases; 95,322 controls) interrogating 43 polymorphisms in 29 genes; 2) 13 meta-analyses testing equivalent polymorphisms in ischemic heart disease; and 3) for the top five gene-stroke associations, 146 studies (65,703 subjects) describing equivalent gene-biochemical relationships, and 28 studies (46,928 subjects) describing biochemical-stroke relationships. Meta-analyses demonstrated positive associations with ischemic stroke for factor V Leiden Gln506, ACE I/D, MTHFR C677T, prothrombin G20210A, PAI-1 5G allele and glycoprotein IIIa Leu33Pro polymorphisms (ORs: 1.11-1.60). Most genetic associations show congruent levels of risk comparing ischemic stroke with ischemic heart disease, but three genes-glycoprotein IIIa, PAI-1 and angiotensinogen-show significant dissociations. The magnitudes of stroke risk observed for factor V Leiden, ACE, MTHFR and prothrombin, but not PAI-1, polymorphisms, are consistent with risks associated with equivalent changes in activated protein C resistance, ACE activity, homocysteine, prothrombin, and PAI-1 levels, respectively. Our results demonstrate causal relationships for four of the most robust genes associated with stroke while also showing that PAI-1 4G/5G polymorphism influences cardiovascular risk via a mechanism not simply related to plasma levels of PAI-1 (or tPA) alone.
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页数:15
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