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GWAS Study

Genome-wide association study of 40,000 individuals identifies two novel loci associated with bipolar disorder.

Hou L, Bergen SE, Akula N et al.

27329760 PubMed ID
GWAS Study Type
40255 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

HL
Hou L
BS
Bergen SE
AN
Akula N
SJ
Song J
HC
Hultman CM
LM
Landén M
AM
Adli M
AM
Alda M
AR
Ardau R
AB
Arias B
AJ
Aubry JM
BL
Backlund L
BJ
Badner JA
BT
Barrett TB
BM
Bauer M
BB
Baune BT
BF
Bellivier F
BA
Benabarre A
BS
Bengesser S
BW
Berrettini WH
BA
Bhattacharjee AK
BJ
Biernacka JM
BA
Birner A
BC
Bloss CS
BC
Brichant-Petitjean C
BE
Bui ET
BW
Byerley W
CP
Cervantes P
CC
Chillotti C
CS
Cichon S
CF
Colom F
CW
Coryell W
CD
Craig DW
CC
Cruceanu C
CP
Czerski PM
DT
Davis T
DA
Dayer A
DF
Degenhardt F
DZ
Del Zompo M
DJ
DePaulo JR
EH
Edenberg HJ
ÉB
Étain B
FP
Falkai P
FT
Foroud T
FA
Forstner AJ
FL
Frisén L
FM
Frye MA
FJ
Fullerton JM
GS
Gard S
GJ
Garnham JS
GE
Gershon ES
GF
Goes FS
GT
Greenwood TA
GM
Grigoroiu-Serbanescu M
HJ
Hauser J
HU
Heilbronner U
HS
Heilmann-Heimbach S
HS
Herms S
HM
Hipolito M
HS
Hitturlingappa S
HP
Hoffmann P
HA
Hofmann A
JS
Jamain S
JE
Jiménez E
KJ
Kahn JP
KL
Kassem L
KJ
Kelsoe JR
KS
Kittel-Schneider S
KS
Kliwicki S
KD
Koller DL
KB
König B
LN
Lackner N
LG
Laje G
LM
Lang M
LC
Lavebratt C
LW
Lawson WB
LM
Leboyer M
LS
Leckband SG
LC
Liu C
MA
Maaser A
MP
Mahon PB
MW
Maier W
MM
Maj M
MM
Manchia M
ML
Martinsson L
MM
McCarthy MJ
MS
McElroy SL
MM
McInnis MG
MR
McKinney R
MP
Mitchell PB
MM
Mitjans M
MF
Mondimore FM
MP
Monteleone P
MT
Mühleisen TW
NC
Nievergelt CM
NM
Nöthen MM
NT
Novák T
NJ
Nurnberger JI
NE
Nwulia EA
ÖU
Ösby U
PA
Pfennig A
PJ
Potash JB
PP
Propping P
RA
Reif A
RE
Reininghaus E
RJ
Rice J
RM
Rietschel M
RG
Rouleau GA
RJ
Rybakowski JK
SM
Schalling M
SW
Scheftner WA
SP
Schofield PR
SN
Schork NJ
ST
Schulze TG
SJ
Schumacher J
SB
Schweizer BW
SG
Severino G
ST
Shekhtman T
SP
Shilling PD
SC
Simhandl C
SC
Slaney CM
SE
Smith EN
SA
Squassina A
ST
Stamm T
SP
Stopkova P
SF
Streit F
SJ
Strohmaier J
SS
Szelinger S
TS
Tighe SK
TA
Tortorella A
TG
Turecki G
VE
Vieta E
VJ
Volkert J
WS
Witt SH
WA
Wright A
ZP
Zandi PP
ZP
Zhang P
ZS
Zollner S
MF
McMahon FJ
Chapter II

Abstract

Summary of the research findings

Bipolar disorder (BD) is a genetically complex mental illness characterized by severe oscillations of mood and behaviour. Genome-wide association studies (GWAS) have identified several risk loci that together account for a small portion of the heritability. To identify additional risk loci, we performed a two-stage meta-analysis of >9 million genetic variants in 9,784 bipolar disorder patients and 30,471 controls, the largest GWAS of BD to date. In this study, to increase power we used ∼2,000 lithium-treated cases with a long-term diagnosis of BD from the Consortium on Lithium Genetics, excess controls, and analytic methods optimized for markers on the X-chromosome. In addition to four known loci, results revealed genome-wide significant associations at two novel loci: an intergenic region on 9p21.3 (rs12553324, P = 5.87 × 10 - 9; odds ratio (OR) = 1.12) and markers within ERBB2 (rs2517959, P = 4.53 × 10 - 9; OR = 1.13). No significant X-chromosome associations were detected and X-linked markers explained very little BD heritability. The results add to a growing list of common autosomal variants involved in BD and illustrate the power of comparing well-characterized cases to an excess of controls in GWAS.

7,647 European ancestry cases, 27,303 European ancestry controls

Chapter III

Study Statistics

Key metrics and study information

40255
Total Participants
GWAS
Study Type
Yes
Replicated
2,137 European ancestry cases, 3,168 European ancestry controls
Replication Participants
European
Ancestry
Sweden
Recruitment Country
Chapter IV

Analysis

Comprehensive review of health and genetic findings

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