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.
引用
收藏
页数:15
相关论文
共 43 条
  • [1] ACE gene polymorphism in cardiovascular disease -: Meta-analyses of small and large studies in whites
    Agerholm-Larsen, B
    Nordestgaard, BG
    Tybjaerg-Hansen, A
    [J]. ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 2000, 20 (02) : 484 - 492
  • [2] [Anonymous], 2001, SYSTEMATIC REV HLTH
  • [3] Smoking and a complement gene polymorphism interact in promoting cardiovascular disease morbidity and mortality
    Arason, G. J.
    Kramer, J.
    Blasko, B.
    Kolka, R.
    Thorbjornsdottir, P.
    Einarsdottir, K.
    Sigfusdottir, A.
    Sigurdarson, S. T.
    Sigurdsson, G.
    Ronai, Z.
    Prohaszka, Z.
    Sasvari-Szekely, M.
    Boddvarsson, S.
    Thorgeirsson, G.
    Fust, G.
    [J]. CLINICAL AND EXPERIMENTAL IMMUNOLOGY, 2007, 149 (01) : 132 - 138
  • [4] Genetics of ischaemic stroke among persons of non-European descent: A meta-analysis of eight genes involving; 32,500 individuals
    Ariyaratnam, Roshan
    Casas, Juan P.
    Whittaker, John
    Smeeth, Liam
    Hingorani, Aroon D.
    Sharma, Pankaj
    [J]. PLOS MEDICINE, 2007, 4 (04) : 728 - 736
  • [5] Relevance of genetics and genomics for prevention and treatment of cardiovascular disease - A scientific statement from the American Heart Association Council on epidemiology and prevention, the stroke council, and the functional genomics and translational biology interdisciplinary working group
    Arnett, Donna K.
    Baird, Alison E.
    Barkley, Ruth A.
    Basson, Craig T.
    Boerwinkle, Eric
    Ganesh, Santhi K.
    Herrington, David M.
    Hong, Yuling
    Jaquish, Cashell
    McDermott, Deborah A.
    O'Donnell, Christopher J.
    [J]. CIRCULATION, 2007, 115 (22) : 2878 - 2901
  • [6] Attia John, 2007, J Stroke Cerebrovasc Dis, V16, P173, DOI 10.1016/j.jstrokecerebrovasdis.2007.03.002
  • [7] Renin-angiotensin-aldosterone system in brain infarction and vascular death
    Brenner, D
    Labreuche, J
    Poirier, O
    Cambien, F
    Amarenco, P
    [J]. ANNALS OF NEUROLOGY, 2005, 58 (01) : 131 - 138
  • [8] Endothelial nitric oxide synthase genotype and ischemic heart disease - Meta-analysis of 26 studies involving 23028 subjects
    Casas, JP
    Bautista, LE
    Humphries, SE
    Hingorani, AD
    [J]. CIRCULATION, 2004, 109 (11) : 1359 - 1365
  • [9] Meta-analysis of genetic studies in ischemic stroke - Thirty-two genes involving approximately 18 000 cases and 58 000 controls
    Casas, JP
    Hingorani, AD
    Bautista, LE
    Sharma, P
    [J]. ARCHIVES OF NEUROLOGY, 2004, 61 (11) : 1652 - 1661
  • [10] Casas JP, 2005, LANCET, V365, P224, DOI 10.1016/S0140-6736(05)70152-5