Multi-trait and cross-population genome-wide association studies across autoimmune and allergic diseases identify shared and distinct genetic component

Author:

Shirai Yuya,Nakanishi Yoshimitsu,Suzuki Akari,Konaka Hachirou,Nishikawa Rika,Sonehara Kyuto,Namba Shinichi,Tanaka Hiroaki,Masuda Tatsuo,Yaga Moto,Satoh Shingo,Izumi Mayuko,Mizuno Yumiko,Jo Tatsunori,Maeda YuichiORCID,Nii Takuro,Oguro-Igashira EriORCID,Morisaki Takayuki,Kamatani Yoichiro,Nakayamada Shingo,Nishigori Chikako,Tanaka YoshiyaORCID,Takeda Yoshito,Yamamoto KazuhikoORCID,Kumanogoh Atsushi,Okada YukinoriORCID,

Abstract

ObjectivesAutoimmune and allergic diseases are outcomes of the dysregulation of the immune system. Our study aimed to elucidate differences or shared components in genetic backgrounds between autoimmune and allergic diseases.MethodsWe estimated genetic correlation and performed multi-trait and cross-population genome-wide association study (GWAS) meta-analysis of six immune-related diseases: rheumatoid arthritis, Graves’ disease, type 1 diabetes for autoimmune diseases and asthma, atopic dermatitis and pollinosis for allergic diseases. By integrating large-scale biobank resources (Biobank Japan and UK biobank), our study included 105 721 cases and 433 663 controls. Newly identified variants were evaluated in 21 778 cases and 712 767 controls for two additional autoimmune diseases: psoriasis and systemic lupus erythematosus. We performed enrichment analyses of cell types and biological pathways to highlight shared and distinct perspectives.ResultsAutoimmune and allergic diseases were not only mutually classified based on genetic backgrounds but also they had multiple positive genetic correlations beyond the classifications. Multi-trait GWAS meta-analysis newly identified six allergic disease-associated loci. We identified four loci shared between the six autoimmune and allergic diseases (rs10803431 atPRDM2, OR=1.07, p=2.3×10−8, rs2053062 atG3BP1, OR=0.90, p=2.9×10−8, rs2210366 atHBS1L, OR=1.07, p=2.5×10−8in Japanese and rs4529910 atPOU2AF1, OR=0.96, p=1.9×10−10across ancestries). Associations of rs10803431 and rs4529910 were confirmed at the two additional autoimmune diseases. Enrichment analysis demonstrated link to T cells, natural killer cells and various cytokine signals, including innate immune pathways.ConclusionOur multi-trait and cross-population study should elucidate complex pathogenesis shared components across autoimmune and allergic diseases.

Funder

Japan Society for the Promotion of Science (JSPS) KAKENHI

Japan Agency for Medical Research and Development

Takeda Science Foundation

JST Moonshot R&D

Bioinformatics Initiative of Osaka University Graduate School of Medicine

Publisher

BMJ

Subject

General Biochemistry, Genetics and Molecular Biology,Immunology,Immunology and Allergy,Rheumatology

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