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GWAS Study

Variants in MTNR1B influence fasting glucose levels.

Prokopenko I, Langenberg C, Florez JC et al.

19060907 PubMed ID
GWAS Study Type
35812 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

PI
Prokopenko I
LC
Langenberg C
FJ
Florez JC
SR
Saxena R
SN
Soranzo N
TG
Thorleifsson G
LR
Loos RJ
MA
Manning AK
JA
Jackson AU
AY
Aulchenko Y
PS
Potter SC
EM
Erdos MR
SS
Sanna S
HJ
Hottenga JJ
WE
Wheeler E
KM
Kaakinen M
LV
Lyssenko V
CW
Chen WM
AK
Ahmadi K
BJ
Beckmann JS
BR
Bergman RN
BM
Bochud M
BL
Bonnycastle LL
BT
Buchanan TA
CA
Cao A
CA
Cervino A
CL
Coin L
CF
Collins FS
CL
Crisponi L
DG
de Geus EJ
DA
Dehghan A
DP
Deloukas P
DA
Doney AS
EP
Elliott P
FN
Freimer N
GV
Gateva V
HC
Herder C
HA
Hofman A
HT
Hughes TE
HS
Hunt S
IT
Illig T
IM
Inouye M
IB
Isomaa B
JT
Johnson T
KA
Kong A
KM
Krestyaninova M
KJ
Kuusisto J
LM
Laakso M
LN
Lim N
LU
Lindblad U
LC
Lindgren CM
MO
McCann OT
MK
Mohlke KL
MA
Morris AD
NS
Naitza S
OM
Orrù M
PC
Palmer CN
PA
Pouta A
RJ
Randall J
RW
Rathmann W
SJ
Saramies J
SP
Scheet P
SL
Scott LJ
SA
Scuteri A
SS
Sharp S
SE
Sijbrands E
SJ
Smit JH
SK
Song K
SV
Steinthorsdottir V
SH
Stringham HM
TT
Tuomi T
TJ
Tuomilehto J
UA
Uitterlinden AG
VB
Voight BF
WD
Waterworth D
WH
Wichmann HE
WG
Willemsen G
WJ
Witteman JC
YX
Yuan X
ZJ
Zhao JH
ZE
Zeggini E
SD
Schlessinger D
SM
Sandhu M
BD
Boomsma DI
UM
Uda M
ST
Spector TD
PB
Penninx BW
AD
Altshuler D
VP
Vollenweider P
JM
Jarvelin MR
LE
Lakatta E
WG
Waeber G
FC
Fox CS
PL
Peltonen L
GL
Groop LC
MV
Mooser V
CL
Cupples LA
TU
Thorsteinsdottir U
BM
Boehnke M
BI
Barroso I
VD
Van Duijn C
DJ
Dupuis J
WR
Watanabe RM
SK
Stefansson K
MM
McCarthy MI
WN
Wareham NJ
MJ
Meigs JB
AG
Abecasis GR
Chapter II

Abstract

Summary of the research findings

To identify previously unknown genetic loci associated with fasting glucose concentrations, we examined the leading association signals in ten genome-wide association scans involving a total of 36,610 individuals of European descent. Variants in the gene encoding melatonin receptor 1B (MTNR1B) were consistently associated with fasting glucose across all ten studies. The strongest signal was observed at rs10830963, where each G allele (frequency 0.30 in HapMap CEU) was associated with an increase of 0.07 (95% CI = 0.06-0.08) mmol/l in fasting glucose levels (P = 3.2 x 10(-50)) and reduced beta-cell function as measured by homeostasis model assessment (HOMA-B, P = 1.1 x 10(-15)). The same allele was associated with an increased risk of type 2 diabetes (odds ratio = 1.09 (1.05-1.12), per G allele P = 3.3 x 10(-7)) in a meta-analysis of 13 case-control studies totaling 18,236 cases and 64,453 controls. Our analyses also confirm previous associations of fasting glucose with variants at the G6PC2 (rs560887, P = 1.1 x 10(-57)) and GCK (rs4607517, P = 1.0 x 10(-25)) loci.

35,812 European ancestry individuals

Chapter III

Study Statistics

Key metrics and study information

35812
Total Participants
GWAS
Study Type
No
Replicated
European
Ancestry
Chapter IV

Analysis

Comprehensive review of health and genetic findings

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