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GWAS Study

Cerebral small vessel disease genomics and its implications across the lifespan.

Sargurupremraj M, Suzuki H, Jian X et al.

33293549 PubMed ID
GWAS Study Type
46055 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

SM
Sargurupremraj M
SH
Suzuki H
JX
Jian X
SC
Sarnowski C
ET
Evans TE
BJ
Bis JC
EG
Eiriksdottir G
SS
Sakaue S
TN
Terzikhan N
HM
Habes M
ZW
Zhao W
AN
Armstrong NJ
HE
Hofer E
YL
Yanek LR
HS
Hagenaars SP
KR
Kumar RB
VD
van den Akker EB
MR
McWhirter RE
TS
Trompet S
MA
Mishra A
SY
Saba Y
SC
Satizabal CL
BG
Beaudet G
PL
Petit L
TA
Tsuchida A
ZL
Zago L
SS
Schilling S
SS
Sigurdsson S
GR
Gottesman RF
LC
Lewis CE
AN
Aggarwal NT
LO
Lopez OL
SJ
Smith JA
VH
Valdés Hernández MC
VD
van der Grond J
WM
Wright MJ
KM
Knol MJ
DM
Dörr M
TR
Thomson RJ
BC
Bordes C
LG
Le Grand Q
DM
Duperron MG
SA
Smith AV
KD
Knopman DS
SP
Schreiner PJ
ED
Evans DA
RJ
Rotter JI
BA
Beiser AS
MS
Maniega SM
BM
Beekman M
TJ
Trollor J
SD
Stott DJ
VM
Vernooij MW
WK
Wittfeld K
NW
Niessen WJ
SA
Soumaré A
BE
Boerwinkle E
SS
Sidney S
TS
Turner ST
DG
Davies G
TA
Thalamuthu A
VU
Völker U
VB
van Buchem MA
BR
Bryan RN
DJ
Dupuis J
BM
Bastin ME
AD
Ames D
TA
Teumer A
AP
Amouyel P
KJ
Kwok JB
BR
Bülow R
DI
Deary IJ
SP
Schofield PR
BH
Brodaty H
JJ
Jiang J
TY
Tabara Y
SK
Setoh K
MS
Miyamoto S
YK
Yoshida K
NM
Nagata M
KY
Kamatani Y
MF
Matsuda F
PB
Psaty BM
BD
Bennett DA
DJ
De Jager PL
MT
Mosley TH
SP
Sachdev PS
SR
Schmidt R
WH
Warren HR
EE
Evangelou E
TD
Trégouët DA
IM
Ikram MA
WW
Wen W
DC
DeCarli C
SV
Srikanth VK
JJ
Jukema JW
SE
Slagboom EP
KS
Kardia SLR
OY
Okada Y
MB
Mazoyer B
WJ
Wardlaw JM
NP
Nyquist PA
MK
Mather KA
GH
Grabe HJ
SH
Schmidt H
VD
Van Duijn CM
GV
Gudnason V
LW
Longstreth WT
LL
Launer LJ
LM
Lathrop M
SS
Seshadri S
TC
Tzourio C
AH
Adams HH
MP
Matthews PM
FM
Fornage M
DS
Debette S
Chapter II

Abstract

Summary of the research findings

White matter hyperintensities (WMH) are the most common brain-imaging feature of cerebral small vessel disease (SVD), hypertension being the main known risk factor. Here, we identify 27 genome-wide loci for WMH-volume in a cohort of 50,970 older individuals, accounting for modification/confounding by hypertension. Aggregated WMH risk variants were associated with altered white matter integrity (p = 2.5×10-7) in brain images from 1,738 young healthy adults, providing insight into the lifetime impact of SVD genetic risk. Mendelian randomization suggested causal association of increasing WMH-volume with stroke, Alzheimer-type dementia, and of increasing blood pressure (BP) with larger WMH-volume, notably also in persons without clinical hypertension. Transcriptome-wide colocalization analyses showed association of WMH-volume with expression of 39 genes, of which four encode known drug targets. Finally, we provide insight into BP-independent biological pathways underlying SVD and suggest potential for genetic stratification of high-risk individuals and for genetically-informed prioritization of drug targets for prevention trials.

46,055 European ancestry individuals

Chapter III

Study Statistics

Key metrics and study information

46055
Total Participants
GWAS
Study Type
No
Replicated
European, African American or Afro-Caribbean
Ancestry
Austria, France, Germany, Iceland, Netherlands, Republic of Ireland, U.K., U.S., Australia
Recruitment Country
Chapter IV

AI-Generated Summary

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