Literature DB >> 32517579

Common Genetic Variation Indicates Separate Causes for Periventricular and Deep White Matter Hyperintensities.

Nicola J Armstrong1, Karen A Mather2,3, Muralidharan Sargurupremraj4, Maria J Knol5, Rainer Malik6, Claudia L Satizabal7,8,9, Lisa R Yanek10, Wei Wen2, Vilmundur G Gudnason11,12, Nicole D Dueker13, Lloyd T Elliott14,15, Edith Hofer16,17, Joshua Bis18, Neda Jahanshad19, Shuo Li20, Mark A Logue21,20,22, Michelle Luciano23, Markus Scholz24, Albert V Smith12, Stella Trompet25,26, Dina Vojinovic5, Rui Xia27, Fidel Alfaro-Almagro15, David Ames28,29, Najaf Amin5, Philippe Amouyel30,31, Alexa S Beiser8,9,20, Henry Brodaty2,32, Ian J Deary23, Christine Fennema-Notestine33,34, Piyush G Gampawar35, Rebecca Gottesman36, Ludovica Griffanti15, Clifford R Jack37, Mark Jenkinson15, Jiyang Jiang2, Brian G Kral10, John B Kwok38,39, Leonie Lampe40, David C M Liewald23, Pauline Maillard41, Jonathan Marchini42, Mark E Bastin23,43, Bernard Mazoyer44, Lukas Pirpamer45, José Rafael Romero8,9, Gennady V Roshchupkin5,46, Peter R Schofield38,3, Matthias L Schroeter47,48,49, David J Stott50, Anbupalam Thalamuthu2,3, Julian Trollor2,51, Christophe Tzourio4,52, Jeroen van der Grond53, Meike W Vernooij5,46, Veronica A Witte54,40, Margaret J Wright55,56, Qiong Yang20, Zoe Morris57, Siggi Siggurdsson7,8,9, Bruce Psaty18, Arno Villringer48,49, Helena Schmidt35, Asta K Haberg58,59, Cornelia M van Duijn5,60, J Wouter Jukema61,62, Martin Dichgans6,63,64, Ralph L Sacco65,66,67, Clinton B Wright68, William S Kremen69,70, Lewis C Becker10, Paul M Thompson19, Thomas H Mosley71, Joanna M Wardlaw23,43, M Arfan Ikram5, Hieab H H Adams5,46,72, Sudha Seshadri11, Perminder S Sachdev2,73, Stephen M Smith15, Lenore Launer74, William Longstreth18, Charles DeCarli75, Reinhold Schmidt16, Myriam Fornage27,76, Stephanie Debette4,77, Paul A Nyquist10,78,79.   

Abstract

BACKGROUND AND
PURPOSE: Periventricular white matter hyperintensities (WMH; PVWMH) and deep WMH (DWMH) are regional classifications of WMH and reflect proposed differences in cause. In the first study, to date, we undertook genome-wide association analyses of DWMH and PVWMH to show that these phenotypes have different genetic underpinnings.
METHODS: Participants were aged 45 years and older, free of stroke and dementia. We conducted genome-wide association analyses of PVWMH and DWMH in 26,654 participants from CHARGE (Cohorts for Heart and Aging Research in Genomic Epidemiology), ENIGMA (Enhancing Neuro-Imaging Genetics Through Meta-Analysis), and the UKB (UK Biobank). Regional correlations were investigated using the genome-wide association analyses -pairwise method. Cross-trait genetic correlations between PVWMH, DWMH, stroke, and dementia were estimated using LDSC.
RESULTS: In the discovery and replication analysis, for PVWMH only, we found associations on chromosomes 2 (NBEAL), 10q23.1 (TSPAN14/FAM231A), and 10q24.33 (SH3PXD2A). In the much larger combined meta-analysis of all cohorts, we identified ten significant regions for PVWMH: chromosomes 2 (3 regions), 6, 7, 10 (2 regions), 13, 16, and 17q23.1. New loci of interest include 7q36.1 (NOS3) and 16q24.2. In both the discovery/replication and combined analysis, we found genome-wide significant associations for the 17q25.1 locus for both DWMH and PVWMH. Using gene-based association analysis, 19 genes across all regions were identified for PVWMH only, including the new genes: CALCRL (2q32.1), KLHL24 (3q27.1), VCAN (5q27.1), and POLR2F (22q13.1). Thirteen genes in the 17q25.1 locus were significant for both phenotypes. More extensive genetic correlations were observed for PVWMH with small vessel ischemic stroke. There were no associations with dementia for either phenotype.
CONCLUSIONS: Our study confirms these phenotypes have distinct and also shared genetic architectures. Genetic analyses indicated PVWMH was more associated with ischemic stroke whilst DWMH loci were implicated in vascular, astrocyte, and neuronal function. Our study confirms these phenotypes are distinct neuroimaging classifications and identifies new candidate genes associated with PVWMH only.

Entities:  

Keywords:  brain; genome-wide association study; neuroimaging; risk factors; white matter

Mesh:

Year:  2020        PMID: 32517579      PMCID: PMC7365038          DOI: 10.1161/STROKEAHA.119.027544

Source DB:  PubMed          Journal:  Stroke        ISSN: 0039-2499            Impact factor:   7.914


  50 in total

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2.  White Matter Hyperintensities Are Under Strong Genetic Influence.

Authors:  Perminder S Sachdev; Anbupalam Thalamuthu; Karen A Mather; David Ames; Margaret J Wright; Wei Wen
Journal:  Stroke       Date:  2016-05-10       Impact factor: 7.914

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Review 10.  Genome-wide meta-analysis identifies 3 novel loci associated with stroke.

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