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GWAS Study

Genetic variants in RBFOX3 are associated with sleep latency.

Amin N, Allebrandt KV, van der Spek A et al.

27142678 PubMed ID
GWAS Study Type
34619 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

AN
Amin N
AK
Allebrandt KV
VD
van der Spek A
MB
Müller-Myhsok B
HK
Hek K
TM
Teder-Laving M
HC
Hayward C
ET
Esko T
VM
van Mill JG
MH
Mbarek H
WN
Watson NF
MS
Melville SA
DG
Del Greco FM
BE
Byrne EM
OE
Oole E
KI
Kolcic I
CT
Chen TH
ED
Evans DS
CJ
Coresh J
VN
Vogelzangs N
KJ
Karjalainen J
WG
Willemsen G
GS
Gharib SA
ZL
Zgaga L
ME
Mihailov E
SK
Stone KL
CH
Campbell H
BR
Brouwer RW
DA
Demirkan A
IA
Isaacs A
DZ
Dogas Z
MK
Marciante KD
CS
Campbell S
BF
Borovecki F
LA
Luik AI
LM
Li M
HJ
Hottenga JJ
HJ
Huffman JE
VD
van den Hout MC
CS
Cummings SR
AY
Aulchenko YS
GP
Gehrman PR
UA
Uitterlinden AG
WH
Wichmann HE
MM
Müller-Nurasyid M
FR
Fehrmann RS
MG
Montgomery GW
HA
Hofman A
KW
Kao WH
OB
Oostra BA
WA
Wright AF
VJ
Vink JM
WJ
Wilson JF
PP
Pramstaller PP
HA
Hicks AA
PO
Polasek O
PN
Punjabi NM
RS
Redline S
PB
Psaty BM
HA
Heath AC
MM
Merrow M
TG
Tranah GJ
GD
Gottlieb DJ
BD
Boomsma DI
MN
Martin NG
RI
Rudan I
TH
Tiemeier H
VI
van IJcken WF
PB
Penninx BW
MA
Metspalu A
MT
Meitinger T
FL
Franke L
RT
Roenneberg T
VD
van Duijn CM
Chapter II

Abstract

Summary of the research findings

Time to fall asleep (sleep latency) is a major determinant of sleep quality. Chronic, long sleep latency is a major characteristic of sleep-onset insomnia and/or delayed sleep phase syndrome. In this study we aimed to discover common polymorphisms that contribute to the genetics of sleep latency. We performed a meta-analysis of genome-wide association studies (GWAS) including 2 572 737 single nucleotide polymorphisms (SNPs) established in seven European cohorts including 4242 individuals. We found a cluster of three highly correlated variants (rs9900428, rs9907432 and rs7211029) in the RNA-binding protein fox-1 homolog 3 gene (RBFOX3) associated with sleep latency (P-values=5.77 × 10(-08), 6.59 × 10(-)(08) and 9.17 × 10(-)(08)). These SNPs were replicated in up to 12 independent populations including 30 377 individuals (P-values=1.5 × 10(-)(02), 7.0 × 10(-)(03) and 2.5 × 10(-)(03); combined meta-analysis P-values=5.5 × 10(-07), 5.4 × 10(-07) and 1.0 × 10(-07)). A functional prediction of RBFOX3 based on co-expression with other genes shows that this gene is predominantly expressed in brain (P-value=1.4 × 10(-316)) and the central nervous system (P-value=7.5 × 10(-)(321)). The predicted function of RBFOX3 based on co-expression analysis with other genes shows that this gene is significantly involved in the release cycle of neurotransmitters including gamma-aminobutyric acid and various monoamines (P-values<2.9 × 10(-11)) that are crucial in triggering the onset of sleep. To conclude, in this first large-scale GWAS of sleep latency we report a novel association of variants in RBFOX3 gene. Further, a functional prediction of RBFOX3 supports the involvement of RBFOX3 with sleep latency.

1983 European ancestry individuals, 747 Erasmus Rucphen (founder/genetic isolate) individuals, 610 Korculan (founder/genetic isolate) individuals, 696 Tyrolean (founder/genetic isolate) individuals, 206 Orcadian (founder/genetic isolate) individuals

Chapter III

Study Statistics

Key metrics and study information

34619
Total Participants
GWAS
Study Type
Yes
Replicated
30,377 European ancestry individuals
Replication Participants
European
Ancestry
U.S., Australia, Netherlands, Croatia, Estonia, Italy, Germany, U.K.
Recruitment Country
Chapter IV

Analysis

Comprehensive review of health and genetic findings

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