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Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation.

Authors :
Mahajan A
Spracklen CN
Zhang W
Ng MCY
Petty LE
Kitajima H
Yu GZ
Rüeger S
Speidel L
Kim YJ
Horikoshi M
Mercader JM
Taliun D
Moon S
Kwak SH
Robertson NR
Rayner NW
Loh M
Kim BJ
Chiou J
Miguel-Escalada I
Della Briotta Parolo P
Lin K
Bragg F
Preuss MH
Takeuchi F
Nano J
Guo X
Lamri A
Nakatochi M
Scott RA
Lee JJ
Huerta-Chagoya A
Graff M
Chai JF
Parra EJ
Yao J
Bielak LF
Tabara Y
Hai Y
Steinthorsdottir V
Cook JP
Kals M
Grarup N
Schmidt EM
Pan I
Sofer T
Wuttke M
Sarnowski C
Gieger C
Nousome D
Trompet S
Long J
Sun M
Tong L
Chen WM
Ahmad M
Noordam R
Lim VJY
Tam CHT
Joo YY
Chen CH
Raffield LM
Lecoeur C
Prins BP
Nicolas A
Yanek LR
Chen G
Jensen RA
Tajuddin S
Kabagambe EK
An P
Xiang AH
Choi HS
Cade BE
Tan J
Flanagan J
Abaitua F
Adair LS
Adeyemo A
Aguilar-Salinas CA
Akiyama M
Anand SS
Bertoni A
Bian Z
Bork-Jensen J
Brandslund I
Brody JA
Brummett CM
Buchanan TA
Canouil M
Chan JCN
Chang LC
Chee ML
Chen J
Chen SH
Chen YT
Chen Z
Chuang LM
Cushman M
Das SK
de Silva HJ
Dedoussis G
Dimitrov L
Doumatey AP
Du S
Duan Q
Eckardt KU
Emery LS
Evans DS
Evans MK
Fischer K
Floyd JS
Ford I
Fornage M
Franco OH
Frayling TM
Freedman BI
Fuchsberger C
Genter P
Gerstein HC
Giedraitis V
González-Villalpando C
González-Villalpando ME
Goodarzi MO
Gordon-Larsen P
Gorkin D
Gross M
Guo Y
Hackinger S
Han S
Hattersley AT
Herder C
Howard AG
Hsueh W
Huang M
Huang W
Hung YJ
Hwang MY
Hwu CM
Ichihara S
Ikram MA
Ingelsson M
Islam MT
Isono M
Jang HM
Jasmine F
Jiang G
Jonas JB
Jørgensen ME
Jørgensen T
Kamatani Y
Kandeel FR
Kasturiratne A
Katsuya T
Kaur V
Kawaguchi T
Keaton JM
Kho AN
Khor CC
Kibriya MG
Kim DH
Kohara K
Kriebel J
Kronenberg F
Kuusisto J
Läll K
Lange LA
Lee MS
Lee NR
Leong A
Li L
Li Y
Li-Gao R
Ligthart S
Lindgren CM
Linneberg A
Liu CT
Liu J
Locke AE
Louie T
Luan J
Luk AO
Luo X
Lv J
Lyssenko V
Mamakou V
Mani KR
Meitinger T
Metspalu A
Morris AD
Nadkarni GN
Nadler JL
Nalls MA
Nayak U
Nongmaithem SS
Ntalla I
Okada Y
Orozco L
Patel SR
Pereira MA
Peters A
Pirie FJ
Porneala B
Prasad G
Preissl S
Rasmussen-Torvik LJ
Reiner AP
Roden M
Rohde R
Roll K
Sabanayagam C
Sander M
Sandow K
Sattar N
Schönherr S
Schurmann C
Shahriar M
Shi J
Shin DM
Shriner D
Smith JA
So WY
Stančáková A
Stilp AM
Strauch K
Suzuki K
Takahashi A
Taylor KD
Thorand B
Thorleifsson G
Thorsteinsdottir U
Tomlinson B
Torres JM
Tsai FJ
Tuomilehto J
Tusie-Luna T
Udler MS
Valladares-Salgado A
van Dam RM
van Klinken JB
Varma R
Vujkovic M
Wacher-Rodarte N
Wheeler E
Whitsel EA
Wickremasinghe AR
van Dijk KW
Witte DR
Yajnik CS
Yamamoto K
Yamauchi T
Yengo L
Yoon K
Yu C
Yuan JM
Yusuf S
Zhang L
Zheng W
Raffel LJ
Igase M
Ipp E
Redline S
Cho YS
Lind L
Province MA
Hanis CL
Peyser PA
Ingelsson E
Zonderman AB
Psaty BM
Wang YX
Rotimi CN
Becker DM
Matsuda F
Liu Y
Zeggini E
Yokota M
Rich SS
Kooperberg C
Pankow JS
Engert JC
Chen YI
Froguel P
Wilson JG
Sheu WHH
Kardia SLR
Wu JY
Hayes MG
Ma RCW
Wong TY
Groop L
Mook-Kanamori DO
Chandak GR
Collins FS
Bharadwaj D
Paré G
Sale MM
Ahsan H
Motala AA
Shu XO
Park KS
Jukema JW
Cruz M
McKean-Cowdin R
Grallert H
Cheng CY
Bottinger EP
Dehghan A
Tai ES
Dupuis J
Kato N
Laakso M
Köttgen A
Koh WP
Palmer CNA
Liu S
Abecasis G
Kooner JS
Loos RJF
North KE
Haiman CA
Florez JC
Saleheen D
Hansen T
Pedersen O
Mägi R
Langenberg C
Wareham NJ
Maeda S
Kadowaki T
Lee J
Millwood IY
Walters RG
Stefansson K
Myers SR
Ferrer J
Gaulton KJ
Meigs JB
Mohlke KL
Gloyn AL
Bowden DW
Below JE
Chambers JC
Sim X
Boehnke M
Rotter JI
McCarthy MI
Morris AP
Source :
Nature genetics [Nat Genet] 2022 May; Vol. 54 (5), pp. 560-572. Date of Electronic Publication: 2022 May 12.
Publication Year :
2022

Abstract

We assembled an ancestrally diverse collection of genome-wide association studies (GWAS) of type 2 diabetes (T2D) in 180,834 affected individuals and 1,159,055 controls (48.9% non-European descent) through the Diabetes Meta-Analysis of Trans-Ethnic association studies (DIAMANTE) Consortium. Multi-ancestry GWAS meta-analysis identified 237 loci attaining stringent genome-wide significance (P < 5 × 10 <superscript>-9</superscript> ), which were delineated to 338 distinct association signals. Fine-mapping of these signals was enhanced by the increased sample size and expanded population diversity of the multi-ancestry meta-analysis, which localized 54.4% of T2D associations to a single variant with >50% posterior probability. This improved fine-mapping enabled systematic assessment of candidate causal genes and molecular mechanisms through which T2D associations are mediated, laying the foundations for functional investigations. Multi-ancestry genetic risk scores enhanced transferability of T2D prediction across diverse populations. Our study provides a step toward more effective clinical translation of T2D GWAS to improve global health for all, irrespective of genetic background.<br /> (© 2022. The Author(s), under exclusive licence to Springer Nature America, Inc.)

Details

Language :
English
ISSN :
1546-1718
Volume :
54
Issue :
5
Database :
MEDLINE
Journal :
Nature genetics
Publication Type :
Academic Journal
Accession number :
35551307
Full Text :
https://doi.org/10.1038/s41588-022-01058-3