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GWAS Study

Transferability of European-derived Alzheimer's disease polygenic risk scores across multiancestry populations.

Nicolas A, Sherva R, Grenier-Boley B et al.

40533518 PubMed ID
GWAS Study Type
99796 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

NA
Nicolas A
SR
Sherva R
GB
Grenier-Boley B
KY
Kim Y
KM
Kikuchi M
TJ
Timsina J
DR
de Rojas I
DM
Dalmasso MC
ZX
Zhou X
LG
Le Guen Y
AC
Arboleda-Bustos CE
CB
Camargos Bicalho MA
GM
Guerchet M
VD
van der Lee S
GM
Goss M
CA
Castillo A
BC
Bellenguez C
KF
Küçükali F
SC
Satizabal CL
FB
Fongang B
YQ
Yang Q
PO
Peters O
SA
Schneider A
DM
Dichgans M
RD
Rujescu D
SN
Scherbaum N
DJ
Deckert J
RS
Riedel-Heller S
HL
Hausner L
ML
Molina-Porcel L
DE
Düzel E
GT
Grimmer T
WJ
Wiltfang J
HS
Heilmann-Heimbach S
MS
Moebus S
TT
Tegos T
SN
Scarmeas N
DO
Dols-Icardo O
MF
Moreno F
PJ
Pérez-Tur J
BM
Bullido MJ
PP
Pastor P
SR
Sánchez-Valle R
ÁV
Álvarez V
CH
Cao H
IN
Ip NY
FA
Fu AKY
IF
Ip FCF
ON
Olivar N
MC
Muchnik C
CC
Cuesta C
CL
Campanelli L
SP
Solis P
PD
Politis DG
KS
Kochen S
BL
Brusco LI
BM
Boada M
GP
García-González P
PR
Puerta R
MP
Mir P
RL
Real LM
PG
Piñol-Ripoll G
GJ
García-Alberca JM
RJ
Royo JL
RE
Rodriguez-Rodriguez E
SH
Soininen H
HS
Heikkinen S
DM
de Mendonça A
MS
Mehrabian S
TL
Traykov L
HJ
Hort J
VM
Vyhnalek M
RK
Rasmussen KL
TJ
Thomassen JQ
PY
Pijnenburg YAL
HH
Holstege H
VS
van Swieten JC
SH
Seelaar H
CJ
Claassen JAHR
JW
Jansen WJ
RI
Ramakers I
VF
Verhey F
VD
van der Lugt A
SP
Scheltens P
OJ
Ortega-Rojas J
CM
Concha Mera AG
MM
Mahecha MF
PR
Pardo R
AG
Arboleda G
BS
Bahrami S
FV
Fominykh V
SG
Selbæk G
GC
Graff C
PG
Papenberg G
GV
Giedraitis V
BA
Boland A
DJ
Deleuze JF
DM
de Marco LA
DM
de Moraes EN
DM
de Mattos Viana B
TG
Túlio Gualberto Cintra M
JT
Juarez-Cedillo T
GA
Griswold AJ
FT
Forund T
HJ
Haines J
FL
Farrer L
DA
DeStefano A
WE
Wijsman E
MR
Mayeux R
PM
Pericak-Vance M
KB
Kunkle B
GA
Goate A
SG
Schellenberg GD
VB
Vardarajan B
WL
Wang LS
LY
Leung YY
DC
Dalgard CL
NG
Nicolas G
WD
Wallon D
DC
Dufouil C
PF
Pasquier F
HO
Hanon O
DS
Debette S
GE
Grünblatt E
PJ
Popp J
AB
Angel B
GS
Gloger S
CM
Chacon MV
AR
Aranguiz R
OP
Orellana P
SA
Slachevsky A
GC
Gonzalez-Billault C
AC
Albala C
FP
Fuentes P
SP
Sachdev P
MK
Mather KA
HR
Hauger RL
MV
Merritt V
PM
Panizzon M
ZR
Zhang R
GJ
Gaziano JM
GR
Ghidoni R
GD
Galimberti D
AB
Arosio B
MP
Mecocci P
SV
Solfrizzi V
PL
Parnetti L
SA
Squassina A
TL
Tremolizzo L
BB
Borroni B
NB
Nacmias B
CP
Caffarra P
SD
Seripa D
RI
Rainero I
DA
Daniele A
PF
Piras F
LH
Leonard HL
YJ
Yokoyama JS
NM
Nalls MA
MA
Miyashita A
HN
Hara N
OK
Ozaki K
NS
Niida S
WJ
Williams J
MC
Masullo C
AP
Amouyel P
PP
Preux PM
MP
Mbelesso P
BB
Bandzouzi B
SA
Saykin A
JF
Jessen F
KP
Kehoe PG
VD
Van Duijn C
BS
Ben Salem N
FR
Frikke-Schmidt R
CL
Cherni L
GM
Greicius MD
TM
Tsolaki M
SP
Sánchez-Juan P
RS
Romano Silva MA
PT
Porter T
LS
Laws SM
SK
Sleegers K
IM
Ingelsson M
DJ
Dartigues JF
SS
Seshadri S
RG
Rossi G
ML
Morelli L
HM
Hiltunen M
SR
Sims R
VD
van der Flier W
AO
Andreassen OA
AH
Arboleda H
CC
Cruchaga C
EV
Escott-Price V
RA
Ruiz A
LK
Lee KH
IT
Ikeuchi T
RA
Ramirez A
GJ
Gim J
LM
Logue M
LJ
Lambert JC
Chapter II

Abstract

Summary of the research findings

A polygenic score (PGS) for Alzheimer's disease (AD) was derived recently from data on genome-wide significant loci in European ancestry populations. We applied this PGS to populations in 17 European countries and observed a consistent association with the AD risk, age at onset and cerebrospinal fluid levels of AD biomarkers, independently of apolipoprotein E locus (APOE). This PGS was also associated with the AD risk in many other populations of diverse ancestries. A cross-ancestry polygenic risk score improved the association with the AD risk in most of the multiancestry populations tested when the APOE region was included. Finally, we found that the PGS/polygenic risk score captured AD-specific information because the association weakened as the diagnosis was broadened. In conclusion, a simple PGS captures the AD-specific genetic information that is common to populations of different ancestries, although studies of more diverse populations are still needed to better characterize the genetics of AD.

36,659 European ancestry cases, 63,137 European ancestry controls

Chapter III

Study Statistics

Key metrics and study information

99796
Total Participants
GWAS
Study Type
No
Replicated
European
Ancestry
Portugal, Switzerland, Spain, Greece, Austria, Czech Republic, Netherlands, Sweden, Belgium, Norway, Finland, Denmark, Italy, U.K., Bulgaria, France, Germany
Recruitment Country
Chapter IV

Analysis

Comprehensive review of health and genetic findings

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Analysis In Progress

Our analysis of this publication is currently being prepared. Please check back soon for comprehensive insights into the health and genetic findings discussed in this research.