Literature DB >> 15528878

Potential confounding by intermediate phenotypes in studies of the genetics of ischaemic stroke.

Enrico Flossmann1, Ursula G R Schulz, Peter M Rothwell.   

Abstract

BACKGROUND: Family history (FHx) of stroke is perceived to be an important risk factor for ischaemic stroke. However, there are several intermediate phenotypes that are often involved in the aetiology of ischaemic stroke and that have a substantial genetic component themselves. We studied FHx of ischaemic heart disease (IHD), hypertension (HTN) and diabetes mellitus (DM) as risk factors for ischaemic stroke.
METHODS: We performed a systematic review of case-control and cohort studies reporting on FHx(IHD), FHx(HTN) or FHx(DM) as risk factors for stroke using bibliographic databases, and by hand searching reference lists and journals. Odds ratios of FHx as a risk factor for stroke were calculated within individual studies. We included unpublished data from two Oxfordshire population-based studies to assess effects on subtypes of ischaemic stroke.
RESULTS: We identified 54 studies that investigated the odds of stroke conferred by a positive FHx, 24 of which reported data on FHx of one or more intermediate phenotypes in addition to FHx of stroke. Most studies reported an increased frequency of FHx(IHD) and FHx(HTN) in stroke patients versus controls. The association was significant in 6 out of 14 studies for FHx(IHD) and 4 out of 11 studies for FHx(HTN). In contrast, FHx(DM) was not associated with stroke. FHx(IHD) was particularly associated with large vessel strokes (OR 1.72, CI 1.3-2.2, p = 0.00004).
CONCLUSIONS: FHx(IHD) and FHx(HTN) are both risk factors for stroke. It is likely that the apparent heritability of stroke is partly accounted for by heritability of HTN and large vessel atherosclerosis. Analyses of heritability of stroke and candidate gene studies should be adjusted accordingly.

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Year:  2004        PMID: 15528878     DOI: 10.1159/000081905

Source DB:  PubMed          Journal:  Cerebrovasc Dis        ISSN: 1015-9770            Impact factor:   2.762


  15 in total

1.  An rs13293512 polymorphism in the promoter of let-7 is associated with a reduced risk of ischemic stroke.

Authors:  Li Zhang; Junsu Yang; Qiang Xue; Dong Yang; Yibing Lu; Xuefeng Guang; Weihua Zhang; Ruiqiong Ba; Hongwen Zhu; Xiang Ma
Journal:  J Thromb Thrombolysis       Date:  2016-11       Impact factor: 2.300

2.  Family history of stroke and severity of neurologic deficit after stroke.

Authors:  J F Meschia; L D Case; B B Worrall; R D Brown; T G Brott; M Frankel; S Silliman; S S Rich
Journal:  Neurology       Date:  2006-10-24       Impact factor: 9.910

3.  Correlations between MMP-2/MMP-9 promoter polymorphisms and ischemic stroke.

Authors:  Shu-Wei Nie; Xiao-Feng Wang; Zong-Chun Tang
Journal:  Int J Clin Exp Med       Date:  2014-02-15

4.  Parental occurrence of stroke and risk of stroke in their children: the Framingham study.

Authors:  Sudha Seshadri; Alexa Beiser; Aleksandra Pikula; Jayandra J Himali; Margaret Kelly-Hayes; Stephanie Debette; Anita L DeStefano; Jose R Romero; Carlos S Kase; Philip A Wolf
Journal:  Circulation       Date:  2010-03-08       Impact factor: 29.690

5.  Sex-specific responses to stroke.

Authors:  L Christine Turtzo; Louise D McCullough
Journal:  Future Neurol       Date:  2010-01-01

6.  Association between family risk of stroke and myocardial infarction with prevalent risk factors and coexisting diseases.

Authors:  Richard E Kennedy; George Howard; Rodney C Go; Peter M Rothwell; Hemant K Tiwari; Rui Feng; Leslie A McClure; Ronald J Prineas; Amitava Banerjee; Donna K Arnett
Journal:  Stroke       Date:  2012-02-09       Impact factor: 7.914

7.  Association of ALOX5AP with ischemic stroke in eastern Chinese.

Authors:  Yao Wang; Gan-Nan Wang; Hao Sun; Chen Chen; Hang Xiao; Jin-Song Zhang
Journal:  World J Emerg Med       Date:  2012

8.  Genetic susceptibility for ischemic infarction and arteriolosclerosis based on neuropathologic evaluations.

Authors:  Sh-Y Chou; J M Shulman; B T Keenan; E A Secor; A S Buchman; J Schneider; D A Bennett; P L De Jager
Journal:  Cerebrovasc Dis       Date:  2013-10-12       Impact factor: 2.762

9.  Estimating the magnitude of genetic factors by calculating the genetic relative risk of stroke in first-ever lacunar stroke patients.

Authors:  Iris L H Knottnerus; Marij Gielen; Jan Lodder; Rob P W Rouhl; Julie Staals; Robert Vlietinck; Robert J van Oostenbrugge
Journal:  PLoS One       Date:  2011-06-29       Impact factor: 3.240

10.  Common variants at 6p21.1 are associated with large artery atherosclerotic stroke.

Authors:  Elizabeth G Holliday; Jane M Maguire; Tiffany-Jane Evans; Simon A Koblar; Jim Jannes; Jonathan W Sturm; Graeme J Hankey; Ross Baker; Jonathan Golledge; Mark W Parsons; Rainer Malik; Mark McEvoy; Erik Biros; Martin D Lewis; Lisa F Lincz; Roseanne Peel; Christopher Oldmeadow; Wayne Smith; Pablo Moscato; Simona Barlera; Steve Bevan; Joshua C Bis; Eric Boerwinkle; Giorgio B Boncoraglio; Thomas G Brott; Robert D Brown; Yu-Ching Cheng; John W Cole; Ioana Cotlarciuc; William J Devan; Myriam Fornage; Karen L Furie; Sólveig Grétarsdóttir; Andreas Gschwendtner; M Arfan Ikram; W T Longstreth; James F Meschia; Braxton D Mitchell; Thomas H Mosley; Michael A Nalls; Eugenio A Parati; Bruce M Psaty; Pankaj Sharma; Kari Stefansson; Gudmar Thorleifsson; Unnur Thorsteinsdottir; Matthew Traylor; Benjamin F J Verhaaren; Kerri L Wiggins; Bradford B Worrall; Cathie Sudlow; Peter M Rothwell; Martin Farrall; Martin Dichgans; Jonathan Rosand; Hugh S Markus; Rodney J Scott; Christopher Levi; John Attia
Journal:  Nat Genet       Date:  2012-09-02       Impact factor: 38.330

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