Differences in Common Genetic Predisposition to Ischemic Stroke by Age and Sex

被引:26
作者
Traylor, Matthew [1 ]
Rutten-Jacobs, Loes C. A. [1 ]
Holliday, Elizabeth G. [2 ,4 ]
Malik, Rainer [5 ]
Sudlow, Cathie [6 ,7 ]
Rothwell, Peter M. [8 ]
Maguire, Jane M. [3 ,9 ]
Koblar, Simon A. [10 ,11 ]
Bevan, Steve [1 ]
Boncoraglio, Giorgio [12 ]
Dichgans, Martin [5 ,13 ]
Levi, Chris [4 ,14 ]
Lewis, Cathryn M. [15 ,16 ]
Markus, Hugh S. [1 ]
机构
[1] Univ Cambridge, Stroke Res Grp, Clin Neurosci, Cambridge CB2 0QQ, England
[2] Univ Newcastle, Sch Med & Publ Hlth, Callaghan, NSW 2308, Australia
[3] Univ Newcastle, Sch Nursing & Midwifery, Callaghan, NSW 2308, Australia
[4] Hunter Med Res Inst, Clin Res Design IT & Stat Support Unit, Newcastle, NSW, Australia
[5] Univ Munich, Klinikum Univ Munchen, Inst Stroke & Dementia Res, Munich, Germany
[6] Univ Edinburgh, Ctr Clin Brain Sci, Edinburgh, Midlothian, Scotland
[7] Univ Edinburgh, Inst Genet & Mol Med, Edinburgh, Midlothian, Scotland
[8] Univ Oxford, Nuffield Dept Clin Neurosci, Stroke Prevent Res Unit, Oxford, England
[9] Hunter Med Res Inst, Newcastle, NSW, Australia
[10] Univ Adelaide, Sch Med, Stroke Res Program, Adelaide, SA, Australia
[11] Univ Adelaide, Adelaide Ctr Neurosci Res, Adelaide, SA, Australia
[12] IRCCS, Ist Neurol Carlo Besta, Dept Cerebrovasc Dis, Milan, Italy
[13] Munich Cluster Syst Neurol SyNergy, Munich, Germany
[14] John Hunter Hosp, Dept Neurol, Newcastle, NSW, Australia
[15] Kings Coll London, Dept Med & Mol Genet, London, England
[16] Kings Coll London, Inst Psychiat, Social Genet & Dev Psychiat Ctr, London, England
基金
英国惠康基金;
关键词
GENOME-WIDE ASSOCIATION; RISK-FACTORS; CLINICAL PRESENTATION; IDENTIFIES COMMON; METAANALYSIS; VARIANTS; DISEASE; HERITABILITY; MENOPAUSE; SUBTYPES;
D O I
10.1161/STROKEAHA.115.009816
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background and Purpose-Evidence from epidemiological studies points to differences in factors predisposing to stroke by age and sex. Whether these arise because of different genetic influences remained untested. Here, we use data from 4 genome-wide association data sets to study the relationship between genetic influence on stroke with both age and sex. Methods-Using genomic-relatedness-matrix restricted maximum likelihood methods, we performed 4 analyses: (1) we calculated the genetic correlation between groups divided by age and (2) by sex, (3) we calculated the heritability of age-at-stroke-onset, and (4) we evaluated the evidence that heritability of stroke is greater in women than in men. Results-We found that genetic factors influence age at stroke onset (h2 [SE]=18.0 [6.8]; P=0.0038), with a trend toward a stronger influence in women (women: h2 [SE]=21.6 [3.5]; Men: h2 [SE]=13.9 [2.8]). Although a moderate proportion of genetic factors was shared between sexes (rG [SE]=0.68 [0.16]) and between younger and older cases (rG [SE]=0.70 [0.17]), there was evidence to suggest that there are genetic susceptibility factors that are specific to sex (P=0.037) and to younger or older groups (P=0.056), particularly for women (P=0.0068). Finally, we found a trend toward higher heritability of stroke in women although this was not significantly greater than in men (P=0.084). Conclusions-Our results indicate that there are genetic factors that are either unique to or have a different effect between younger and older age groups and between women and men. Performing large, well-powered genome-wide association study analyses in these groups is likely to uncover further associations. © 2015 American Heart Association, Inc.
引用
收藏
页码:3042 / 3047
页数:6
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