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Chauhan, G.* ; Adams, H.H.H.* ; Satizabal, C.L.* ; Bis, J.C.* ; Teumer, A.* ; Sargurupremraj, M.* ; Hofer, E.* ; Trompet, S.* ; Hilal, S.* ; Smith, A.V.* ; Jian, X.* ; Malik, R.* ; Traylor, M.* ; Pulit, S.L.* ; Amouyel, P.* ; Mazoyer, B.* ; Zhu, Y.C.* ; Kaffashian, S.* ; Schilling, S.* ; Beecham, G.W.* ; Montine, T.J.* ; Schellenberg, G.D.* ; Kjartansson, O.* ; Guðnason, V.* ; Knopman, D.S.* ; Griswold, M.E.* ; Windham, B.G.* ; Gottesman, R.F.* ; Mosley, T.H.* ; Schmidt, R.* ; Saba, Y.* ; Schmidt, H.* ; Takeuchi, F.* ; Yamaguchi, S.* ; Nabika, T.* ; Kato, N.* ; Rajan, K.B.* ; Aggarwal, N.T.* ; de Jager, P.L.* ; Evans, D.A.* ; Psaty, B.M.* ; Rotter, J.I.* ; Rice, K.* ; Lopez, O.L.* ; Liao, J.M.* ; Chen, C.* ; Cheng, C.Y.* ; Wong, T.Y.* ; Ikram, M.K.* ; van der Lee, S.J.* ; Amin, N.* ; Chouraki, V.* ; DeStefano, A.L.* ; Aparicio, H.J.* ; Romero, J.R.* ; Maillard, P.* ; Decarli, C.* ; Wardlaw, J.M.* ; Hernández, M.D.C.V.* ; de Bakker, P.I.W.* ; Asselbergs, F.W.* ; Srikanth, V.* ; Thomson, R.J.* ; McWhirter, R.E.* ; Moran, C.* ; Callisaya, M.* ; Phan, T.* ; Rutten-Jacobs, L.C.A.* ; Bevan, S.* ; Tzourio, C.* ; Mather, K.A.* ; Sachdev, P.S.* ; van Duijn, C.M.* ; Worrall, B.B.* ; Dichgans, M.* ; Kittner, S.J.* ; Markus, H.S.* ; Ikram, M.A.* ; Fornage, M.* ; Launer, L.J.* ; Seshadri, S.* ; Longstreth, W.T. Jr.* ; Debette, S.* ; Müller-Nurasyid, M. ; Strauch, K. ; Baumert, J.J. ; Meisinger, C. ; Wichmann, H.-E. ; Illig, T. ; Klopp, N. ; Lichtner, P.

Genetic and lifestyle risk factors for MRI-defined brain infarcts in a population-based setting.

Neurology 92, e486-e503 (2019)
Verlagsversion DOI PMC
Open Access Gold (Paid Option)
Creative Commons Lizenzvertrag
OBJECTIVE: To explore genetic and lifestyle risk factors of MRI-defined brain infarcts (BI) in large population-based cohorts. METHODS: We performed meta-analyses of genome-wide association studies (GWAS) and examined associations of vascular risk factors and their genetic risk scores (GRS) with MRI-defined BI and a subset of BI, namely, small subcortical BI (SSBI), in 18 population-based cohorts (n = 20,949) from 5 ethnicities (3,726 with BI, 2,021 with SSBI). Top loci were followed up in 7 population-based cohorts (n = 6,862; 1,483 with BI, 630 with SBBI), and we tested associations with related phenotypes including ischemic stroke and pathologically defined BI. RESULTS: The mean prevalence was 17.7% for BI and 10.5% for SSBI, steeply rising after age 65. Two loci showed genome-wide significant association with BI: FBN2, p = 1.77 × 10-8; and LINC00539/ZDHHC20, p = 5.82 × 10-9. Both have been associated with blood pressure (BP)-related phenotypes, but did not replicate in the smaller follow-up sample or show associations with related phenotypes. Age- and sex-adjusted associations with BI and SSBI were observed for BP traits (p value for BI, p [BI] = 9.38 × 10-25; p [SSBI] = 5.23 × 10-14 for hypertension), smoking (p [BI] = 4.4 × 10-10; p [SSBI] = 1.2 × 10-4), diabetes (p [BI] = 1.7 × 10-8; p [SSBI] = 2.8 × 10-3), previous cardiovascular disease (p [BI] = 1.0 × 10-18; p [SSBI] = 2.3 × 10-7), stroke (p [BI] = 3.9 × 10-69; p [SSBI] = 3.2 × 10-24), and MRI-defined white matter hyperintensity burden (p [BI] = 1.43 × 10-157; p [SSBI] = 3.16 × 10-106), but not with body mass index or cholesterol. GRS of BP traits were associated with BI and SSBI (p ≤ 0.0022), without indication of directional pleiotropy. CONCLUSION: In this multiethnic GWAS meta-analysis, including over 20,000 population-based participants, we identified genetic risk loci for BI requiring validation once additional large datasets become available. High BP, including genetically determined, was the most significant modifiable, causal risk factor for BI.
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Publikationstyp Artikel: Journalartikel
Dokumenttyp Wissenschaftlicher Artikel
Korrespondenzautor
ISSN (print) / ISBN 0028-3878
e-ISSN 1526-632X
Zeitschrift Neurology
Quellenangaben Band: 92, Heft: 5, Seiten: e486-e503 Artikelnummer: , Supplement: ,
Verlag Lippincott Williams & Wilkins
Nichtpatentliteratur Publikationen
Begutachtungsstatus Peer reviewed
Institut(e) Institute of Genetic Epidemiology (IGE)
Institute of Epidemiology (EPI)
Institute of Epidemiology II (EPI2)
Institute of Human Genetics (IHG)
Förderungen NCATS NIH HHS
NHLBI NIH HHS
Biotechnology and Biological Sciences Research Council
British Heart Foundation
NINDS NIH HHS
Medical Research Council
NIA NIH HHS