Citation: Stroke. 44(6):1578-83, 2013 Jun..Journal: Stroke; a journal of cerebral circulation.ISSN: 0039-2499.Full author list: Devan WJ; Falcone GJ; Anderson CD; Jagiella JM; Schmidt H; Hansen BM; Jimenez-Conde J; Giralt-Steinhauer E; Cuadrado-Godia E; Soriano C; Ayres AM; Schwab K; Kassis SB; Valant V; Pera J; Urbanik A; Viswanathan A; Rost NS; Goldstein JN; Freudenberger P; Stogerer EM; Norrving B; Tirschwell DL; Selim M; Brown DL; Silliman SL; Worrall BB; Meschia JF; Kidwell CS; Montaner J; Fernandez-Cadenas I; Delgado P; Greenberg SM; Roquer J; Lindgren A; Slowik A; Schmidt R; Woo D; Rosand J; Biffi A; International Stroke Genetics Consortium.UI/PMID: 23559261.Subject(s): Adult | Aged | Aged, 80 and over | Apolipoproteins E/ge [Genetics] | Case-Control Studies | *Cerebral Hemorrhage/di [Diagnosis] | *Cerebral Hemorrhage/ge [Genetics] | Cerebral Hemorrhage/mo [Mortality] | Female | *Genetic Predisposition to Disease/ge [Genetics] | *Genetic Variation/ge [Genetics] | *Genome-Wide Association Study | Genotype | Hematoma/ge [Genetics] | Hematoma/pa [Pathology] | Humans | Male | Middle Aged | Phenotype | Prognosis | Risk Factors | *Severity of Illness Index | Survival RateInstitution(s): MedStar Heart & Vascular InstituteActivity type: Journal Article.Medline article type(s): Journal Article | Research Support, N.I.H., Extramural | Research Support, Non-U.S. Gov'tOnline resources: Click here to access onlineDigital Object Identifier: http://dx.doi.org/10.1161/STROKEAHA.111.000089 (Click here)Abbreviated citation: Stroke. 44(6):1578-83, 2013 Jun.Local Holdings: Available online from MWHC library: 1970 - present, Available in print through MWHC library: 1999 - 2006.Abstract: BACKGROUND AND PURPOSE: Previous studies suggest that genetic variation plays a substantial role in occurrence and evolution of intracerebral hemorrhage (ICH). Genetic contribution to disease can be determined by calculating heritability using family-based data, but such an approach is impractical for ICH because of lack of large pedigree-based studies. However, a novel analytic tool based on genome-wide data allows heritability estimation from unrelated subjects. We sought to apply this method to provide heritability estimates for ICH risk, severity, and outcome.Abstract: METHODS: We analyzed genome-wide genotype data for 791 ICH cases and 876 controls, and determined heritability as the proportion of variation in phenotype attributable to captured genetic variants. Contribution to heritability was separately estimated for the APOE (encoding apolipoprotein E) gene, an established genetic risk factor, and for the rest of the genome. Analyzed phenotypes included ICH risk, admission hematoma volume, and 90-day mortality.Abstract: RESULTS: ICH risk heritability was estimated at 29% (SE, 11%) for non-APOE loci and at 15% (SE, 10%) for APOE. Heritability for 90-day ICH mortality was 41% for non-APOE loci and 10% (SE, 9%) for APOE. Genetic influence on hematoma volume was also substantial: admission volume heritability was estimated at 60% (SE, 70%) for non-APOEloci and at 12% (SE, 4%) for APOE.Abstract: CONCLUSIONS: Genetic variation plays a substantial role in ICH risk, outcome, and hematoma volume. Previously reported risk variants account for only a portion of inherited genetic influence on ICH pathophysiology, pointing to additional loci yet to be identified.