Literature DB >> 28314753

Transethnic meta-analysis identifies GSDMA and PRDM1 as susceptibility genes to systemic sclerosis.

Chikashi Terao1,2,3,4,5, Takahisa Kawaguchi1, Philippe Dieude6, John Varga7, Masataka Kuwana8, Marie Hudson9, Yasushi Kawaguchi10, Marco Matucci-Cerinic11, Koichiro Ohmura12, Gabriela Riemekasten13,14, Aya Kawasaki15, Paolo Airo16, Tetsuya Horita17, Akira Oka18, Eric Hachulla19, Hajime Yoshifuji12, Paola Caramaschi20, Nicolas Hunzelmann21, Murray Baron9, Tatsuya Atsumi17, Paul Hassoun22, Takeshi Torii23, Meiko Takahashi1, Yasuharu Tabara1, Masakazu Shimizu1, Akiko Tochimoto10, Naho Ayuzawa24, Hidetoshi Yanagida24, Hiroshi Furukawa15,25, Shigeto Tohma25, Minoru Hasegawa26, Manabu Fujimoto27, Osamu Ishikawa28, Toshiyuki Yamamoto29, Daisuke Goto30, Yoshihide Asano31, Masatoshi Jinnin32, Hirahito Endo33, Hiroki Takahashi34, Kazuhiko Takehara35, Shinichi Sato31, Hironobu Ihn32, Soumya Raychaudhuri3,4,5,36, Katherine Liao3, Peter Gregersen37, Naoyuki Tsuchiya15, Valeria Riccieri38, Inga Melchers39, Gabriele Valentini40, Anne Cauvet41, Maria Martinez42, Tsuneyo Mimori12, Fumihiko Matsuda1, Yannick Allanore43.   

Abstract

OBJECTIVES: Systemic sclerosis (SSc) is an autoimmune disease characterised by skin and systemic fibrosis culminating in organ damage. Previous genetic studies including genome-wide association studies (GWAS) have identified 12 susceptibility loci satisfying genome-wide significance. Transethnic meta-analyses have successfully expanded the list of susceptibility genes and deepened biological insights for other autoimmune diseases.
METHODS: We performed transethnic meta-analysis of GWAS in the Japanese and European populations, followed by a two-staged replication study comprising a total of 4436 cases and 14 751 controls. Associations between significant single nuclear polymorphisms (SNPs) and neighbouring genes were evaluated. Enrichment analysis of H3K4Me3, a representative histone mark for active promoter was conducted with an expanded list of SSc susceptibility genes.
RESULTS: We identified two significant SNP in two loci, GSDMA and PRDM1, both of which are related to immune functions and associated with other autoimmune diseases (p=1.4×10-10 and 6.6×10-10, respectively). GSDMA also showed a significant association with limited cutaneous SSc. We also replicated the associations of previously reported loci including a non-GWAS locus, TNFAIP3. PRDM1 encodes BLIMP1, a transcription factor regulating T-cell proliferation and plasma cell differentiation. The top SNP in GSDMA was a missense variant and correlated with gene expression of neighbouring genes, and this could explain the association in this locus. We found different human leukocyte antigen (HLA) association patterns between the two populations. Enrichment analysis suggested the importance of CD4-naïve primary T cell.
CONCLUSIONS: GSDMA and PRDM1 are associated with SSc. These findings provide enhanced insight into the genetic and biological basis of SSc. Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://www.bmj.com/company/products-services/rights-and-licensing/.

Entities:  

Keywords:  Autoimmune Diseases; Gene Polymorphism; Systemic Sclerosis

Mesh:

Substances:

Year:  2017        PMID: 28314753      PMCID: PMC6733404          DOI: 10.1136/annrheumdis-2016-210645

Source DB:  PubMed          Journal:  Ann Rheum Dis        ISSN: 0003-4967            Impact factor:   19.103


  29 in total

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