Back to Search Start Over

Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility.

Authors :
Mahajan A
Go MJ
Zhang W
Below JE
Gaulton KJ
Ferreira T
Horikoshi M
Johnson AD
Ng MC
Prokopenko I
Saleheen D
Wang X
Zeggini E
Abecasis GR
Adair LS
Almgren P
Atalay M
Aung T
Baldassarre D
Balkau B
Bao Y
Barnett AH
Barroso I
Basit A
Been LF
Beilby J
Bell GI
Benediktsson R
Bergman RN
Boehm BO
Boerwinkle E
Bonnycastle LL
Burtt N
Cai Q
Campbell H
Carey J
Cauchi S
Caulfield M
Chan JC
Chang LC
Chang TJ
Chang YC
Charpentier G
Chen CH
Chen H
Chen YT
Chia KS
Chidambaram M
Chines PS
Cho NH
Cho YM
Chuang LM
Collins FS
Cornelis MC
Couper DJ
Crenshaw AT
van Dam RM
Danesh J
Das D
de Faire U
Dedoussis G
Deloukas P
Dimas AS
Dina C
Doney AS
Donnelly PJ
Dorkhan M
van Duijn C
Dupuis J
Edkins S
Elliott P
Emilsson V
Erbel R
Eriksson JG
Escobedo J
Esko T
Eury E
Florez JC
Fontanillas P
Forouhi NG
Forsen T
Fox C
Fraser RM
Frayling TM
Froguel P
Frossard P
Gao Y
Gertow K
Gieger C
Gigante B
Grallert H
Grant GB
Grrop LC
Groves CJ
Grundberg E
Guiducci C
Hamsten A
Han BG
Hara K
Hassanali N
Hattersley AT
Hayward C
Hedman AK
Herder C
Hofman A
Holmen OL
Hovingh K
Hreidarsson AB
Hu C
Hu FB
Hui J
Humphries SE
Hunt SE
Hunter DJ
Hveem K
Hydrie ZI
Ikegami H
Illig T
Ingelsson E
Islam M
Isomaa B
Jackson AU
Jafar T
James A
Jia W
Jöckel KH
Jonsson A
Jowett JB
Kadowaki T
Kang HM
Kanoni S
Kao WH
Kathiresan S
Kato N
Katulanda P
Keinanen-Kiukaanniemi KM
Kelly AM
Khan H
Khaw KT
Khor CC
Kim HL
Kim S
Kim YJ
Kinnunen L
Klopp N
Kong A
Korpi-Hyövälti E
Kowlessur S
Kraft P
Kravic J
Kristensen MM
Krithika S
Kumar A
Kumate J
Kuusisto J
Kwak SH
Laakso M
Lagou V
Lakka TA
Langenberg C
Langford C
Lawrence R
Leander K
Lee JM
Lee NR
Li M
Li X
Li Y
Liang J
Liju S
Lim WY
Lind L
Lindgren CM
Lindholm E
Liu CT
Liu JJ
Lobbens S
Long J
Loos RJ
Lu W
Luan J
Lyssenko V
Ma RC
Maeda S
Mägi R
Männisto S
Matthews DR
Meigs JB
Melander O
Metspalu A
Meyer J
Mirza G
Mihailov E
Moebus S
Mohan V
Mohlke KL
Morris AD
Mühleisen TW
Müller-Nurasyid M
Musk B
Nakamura J
Nakashima E
Navarro P
Ng PK
Nica AC
Nilsson PM
Njølstad I
Nöthen MM
Ohnaka K
Ong TH
Owen KR
Palmer CN
Pankow JS
Park KS
Parkin M
Pechlivanis S
Pedersen NL
Peltonen L
Perry JR
Peters A
Pinidiyapathirage JM
Platou CG
Potter S
Price JF
Qi L
Radha V
Rallidis L
Rasheed A
Rathman W
Rauramaa R
Raychaudhuri S
Rayner NW
Rees SD
Rehnberg E
Ripatti S
Robertson N
Roden M
Rossin EJ
Rudan I
Rybin D
Saaristo TE
Salomaa V
Saltevo J
Samuel M
Sanghera DK
Saramies J
Scott J
Scott LJ
Scott RA
Segrè AV
Sehmi J
Sennblad B
Shah N
Shah S
Shera AS
Shu XO
Shuldiner AR
Sigurđsson G
Sijbrands E
Silveira A
Sim X
Sivapalaratnam S
Small KS
So WY
Stančáková A
Stefansson K
Steinbach G
Steinthorsdottir V
Stirrups K
Strawbridge RJ
Stringham HM
Sun Q
Suo C
Syvänen AC
Takayanagi R
Takeuchi F
Tay WT
Teslovich TM
Thorand B
Thorleifsson G
Thorsteinsdottir U
Tikkanen E
Trakalo J
Tremoli E
Trip MD
Tsai FJ
Tuomi T
Tuomilehto J
Uitterlinden AG
Valladares-Salgado A
Vedantam S
Veglia F
Voight BF
Wang C
Wareham NJ
Wennauer R
Wickremasinghe AR
Wilsgaard T
Wilson JF
Wiltshire S
Winckler W
Wong TY
Wood AR
Wu JY
Wu Y
Yamamoto K
Yamauchi T
Yang M
Yengo L
Yokota M
Young R
Zabaneh D
Zhang F
Zhang R
Zheng W
Zimmet PZ
Altshuler D
Bowden DW
Cho YS
Cox NJ
Cruz M
Hanis CL
Kooner J
Lee JY
Seielstad M
Teo YY
Boehnke M
Parra EJ
Chambers JC
Tai ES
McCarthy MI
Morris AP
Source :
Nature genetics [Nat Genet] 2014 Mar; Vol. 46 (3), pp. 234-44. Date of Electronic Publication: 2014 Feb 09.
Publication Year :
2014

Abstract

To further understanding of the genetic basis of type 2 diabetes (T2D) susceptibility, we aggregated published meta-analyses of genome-wide association studies (GWAS), including 26,488 cases and 83,964 controls of European, east Asian, south Asian and Mexican and Mexican American ancestry. We observed a significant excess in the directional consistency of T2D risk alleles across ancestry groups, even at SNPs demonstrating only weak evidence of association. By following up the strongest signals of association from the trans-ethnic meta-analysis in an additional 21,491 cases and 55,647 controls of European ancestry, we identified seven new T2D susceptibility loci. Furthermore, we observed considerable improvements in the fine-mapping resolution of common variant association signals at several T2D susceptibility loci. These observations highlight the benefits of trans-ethnic GWAS for the discovery and characterization of complex trait loci and emphasize an exciting opportunity to extend insight into the genetic architecture and pathogenesis of human diseases across populations of diverse ancestry.

Details

Language :
English
ISSN :
1546-1718
Volume :
46
Issue :
3
Database :
MEDLINE
Journal :
Nature genetics
Publication Type :
Academic Journal
Accession number :
24509480
Full Text :
https://doi.org/10.1038/ng.2897