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Anti-citrullinated peptide/protein antibody (ACPA)-negative RA shares a large proportion of susceptibility loci with ACPA-positive RA: a meta-analysis of genome-wide association study in a Japanese population

INTRODUCTION: Although susceptibility genes for anti-citrullinated peptide/protein antibodies (ACPA)-positive rheumatoid arthritis (RA) have been successfully discovered by genome-wide association studies (GWAS), little is known about the genetic background of ACPA-negative RA. We intended to elucid...

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Detalles Bibliográficos
Autores principales: Terao, Chikashi, Ohmura, Koichiro, Kochi, Yuta, Ikari, Katsunori, Okada, Yukinori, Shimizu, Masakazu, Nishina, Naoshi, Suzuki, Akari, Myouzen, Keiko, Kawaguchi, Takahisa, Takahashi, Meiko, Takasugi, Kiyoshi, Murasawa, Akira, Mizuki, Shinichi, Iwahashi, Mitsuhiro, Funahashi, Keiko, Natsumeda, Masamitsu, Furu, Moritoshi, Hashimoto, Motomu, Ito, Hiromu, Fujii, Takao, Ezawa, Kazuhiko, Matsubara, Tsukasa, Takeuchi, Tsutomu, Kubo, Michiaki, Yamada, Ryo, Taniguchi, Atsuo, Yamanaka, Hisashi, Momohara, Shigeki, Yamamoto, Kazuhiko, Mimori, Tsuneyo, Matsuda, Fumihiko
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4431175/
https://www.ncbi.nlm.nih.gov/pubmed/25927497
http://dx.doi.org/10.1186/s13075-015-0623-4
Descripción
Sumario:INTRODUCTION: Although susceptibility genes for anti-citrullinated peptide/protein antibodies (ACPA)-positive rheumatoid arthritis (RA) have been successfully discovered by genome-wide association studies (GWAS), little is known about the genetic background of ACPA-negative RA. We intended to elucidate genetic background of ACPA-negative RA. METHOD: We performed a meta-analysis of GWAS comprising 670 ACPA-negative RA and 16,891 controls for 1,948,138 markers, followed by a replication study of the top 35 single nucleotide polymorphisms (SNPs) using 916 cases and 3,764 controls. Inverse-variance method was applied to assess overall effects. To assess overlap of susceptibility loci between ACPA-positive and -negative RA, odds ratios (ORs) of the 21 susceptibility markers to RA in Japanese were compared between the two subsets. In addition, SNPs were stratified by the p-values in GWAS meta-analysis for either ACPA-positive RA or ACPA-negative RA to address the question whether weakly-associated genes were also shared. The correlations between ACPA-positive RA and the subpopulations of ACPA-negative RA (rheumatoid factor (RF)-positive and RF-negative subsets) were also addressed. RESULTS: Rs6904716 in LEMD2 of the human leukocyte antigen (HLA) locus showed a borderline association with ACPA-negative RA (overall p = 5.7 × 10(−8)), followed by rs6986423 in CSMD1 (p = 2.4 × 10(−6)) and rs17727339 in FCRL3 (p = 1.4 × 10(−5)). ACPA-negative RA showed significant correlations of ORs with ACPA-positive RA for the 21 susceptibility SNPs and non-HLA SNPs with p-values far from significance. These significant correlations with ACPA-positive RA were true for ACPA-negative RF-positive and ACPA-negative RF-negative RA. On the contrary, positive correlations were not observed between the ACPA-negative two subpopulations. CONCLUSION: Many of the susceptibility loci were shared between ACPA-positive and -negative RA. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13075-015-0623-4) contains supplementary material, which is available to authorized users.