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Multi-ancestry genome-wide association analyses identify novel genetic mechanisms in rheumatoid arthritis

Authors :
Ishigaki, Kazuyoshi
Sakaue, Saori
Terao, Chikashi
Luo, Yang
Sonehara, Kyuto
Yamaguchi, Kensuke
Amariuta, Tiffany
Too, Chun Lai
Laufer, Vincent A.
Scott, Ian C.
Viatte, Sebastien
Takahashi, Meiko
Ohmura, Koichiro
Murasawa, Akira
Hashimoto, Motomu
Ito, Hiromu
Hammoudeh, Mohammed
Emadi, Samar Al
Masri, Basel K.
Halabi, Hussein
Badsha, Humeira
Uthman, Imad W.
Wu, Xin
Lin, Li
Li, Ting
Plant, Darren
Barton, Anne
Orozco, Gisela
Verstappen, Suzanne M. M.
Bowes, John
MacGregor, Alexander J.
Honda, Suguru
Koido, Masaru
Tomizuka, Kohei
Kamatani, Yoichiro
Tanaka, Hiroaki
Tanaka, Eiichi
Suzuki, Akari
Maeda, Yuichi
Yamamoto, Kenichi
Miyawaki, Satoru
Xie, Gang
Zhang, Jinyi
Amos, Christopher I.
Keystone, Edward
Wolbink, Gertjan
van der Horst-Bruinsma, Irene
Cui, Jing
Liao, Katherine P.
Carroll, Robert J.
Lee, Hye-Soon
Bang, So-Young
Siminovitch, Katherine A.
de Vries, Niek
Alfredsson, Lars
Rantapää-Dahlqvist, Solbritt
Karlson, Elizabeth W.
Bae, Sang-Cheol
Kimberly, Robert P.
Edberg, Jeffrey C.
Mariette, Xavier
Huizinga, Tom
Dieudé, Philippe
Schneider, Matthias
Kerick, Martin
Denny, Joshua C.
Matsuda, Koichi
Matsuo, Keitaro
Mimori, Tsuneyo
Matsuda, Fumihiko
Fujio, Keishi
Tanaka, Yoshiya
Kumanogoh, Atsushi
Traylor, Matthew
Lewis, Cathryn M.
Eyre, Stephen
Xu, Huji
Saxena, Richa
Arayssi, Thurayya
Kochi, Yuta
Ikari, Katsunori
Harigai, Masayoshi
Gregersen, Peter K.
Yamamoto, Kazuhiko
Louis Bridges, S.
Padyukov, Leonid
Martin, Javier
Klareskog, Lars
Okada, Yukinori
Raychaudhuri, Soumya
Source :
Nature Genetics; November 2022, Vol. 54 Issue: 11 p1640-1651, 12p
Publication Year :
2022

Abstract

Rheumatoid arthritis (RA) is a highly heritable complex disease with unknown etiology. Multi-ancestry genetic research of RA promises to improve power to detect genetic signals, fine-mapping resolution and performances of polygenic risk scores (PRS). Here, we present a large-scale genome-wide association study (GWAS) of RA, which includes 276,020 samples from five ancestral groups. We conducted a multi-ancestry meta-analysis and identified 124 loci (P< 5 × 10−8), of which 34 are novel. Candidate genes at the novel loci suggest essential roles of the immune system (for example, TNIP2and TNFRSF11A) and joint tissues (for example, WISP1) in RA etiology. Multi-ancestry fine-mapping identified putatively causal variants with biological insights (for example, LEF1). Moreover, PRS based on multi-ancestry GWAS outperformed PRS based on single-ancestry GWAS and had comparable performance between populations of European and East Asian ancestries. Our study provides several insights into the etiology of RA and improves the genetic predictability of RA.

Details

Language :
English
ISSN :
10614036 and 15461718
Volume :
54
Issue :
11
Database :
Supplemental Index
Journal :
Nature Genetics
Publication Type :
Periodical
Accession number :
ejs61097172
Full Text :
https://doi.org/10.1038/s41588-022-01213-w