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ACPA-Negative RA Consists of Two Genetically Distinct Subsets Based on RF Positivity in Japanese

Author

Listed:
  • Chikashi Terao
  • Koichiro Ohmura
  • Katsunori Ikari
  • Yuta Kochi
  • Etsuko Maruya
  • Masaki Katayama
  • Kimiko Yurugi
  • Kota Shimada
  • Akira Murasawa
  • Shigeru Honjo
  • Kiyoshi Takasugi
  • Keitaro Matsuo
  • Kazuo Tajima
  • Akari Suzuki
  • Kazuhiko Yamamoto
  • Shigeki Momohara
  • Hisashi Yamanaka
  • Ryo Yamada
  • Hiroo Saji
  • Fumihiko Matsuda
  • Tsuneyo Mimori

Abstract

HLA-DRB1, especially the shared epitope (SE), is strongly associated with rheumatoid arthritis (RA). However, recent studies have shown that SE is at most weakly associated with RA without anti-citrullinated peptide/protein antibody (ACPA). We have recently reported that ACPA-negative RA is associated with specific HLA-DRB1 alleles and diplotypes. Here, we attempted to detect genetically different subsets of ACPA-negative RA by classifying ACPA-negative RA patients into two groups based on their positivity for rheumatoid factor (RF). HLA-DRB1 genotyping data for totally 954 ACPA-negative RA patients and 2,008 healthy individuals in two independent sets were used. HLA-DRB1 allele and diplotype frequencies were compared among the ACPA-negative RF-positive RA patients, ACPA-negative RF-negative RA patients, and controls in each set. Combined results were also analyzed. A similar analysis was performed in 685 ACPA-positive RA patients classified according to their RF positivity. As a result, HLA-DRB1*04:05 and *09:01 showed strong associations with ACPA-negative RF-positive RA in the combined analysis (p = 8.8×10−6 and 0.0011, OR: 1.57 (1.28–1.91) and 1.37 (1.13–1.65), respectively). We also found that HLA-DR14 and the HLA-DR8 homozygote were associated with ACPA-negative RF-negative RA (p = 0.00022 and 0.00013, OR: 1.52 (1.21–1.89) and 3.08 (1.68–5.64), respectively). These association tendencies were found in each set. On the contrary, we could not detect any significant differences between ACPA-positive RA subsets. As a conclusion, ACPA-negative RA includes two genetically distinct subsets according to RF positivity in Japan, which display different associations with HLA-DRB1. ACPA-negative RF-positive RA is strongly associated with HLA-DRB1*04:05 and *09:01. ACPA-negative RF-negative RA is associated with DR14 and the HLA-DR8 homozygote.

Suggested Citation

  • Chikashi Terao & Koichiro Ohmura & Katsunori Ikari & Yuta Kochi & Etsuko Maruya & Masaki Katayama & Kimiko Yurugi & Kota Shimada & Akira Murasawa & Shigeru Honjo & Kiyoshi Takasugi & Keitaro Matsuo & , 2012. "ACPA-Negative RA Consists of Two Genetically Distinct Subsets Based on RF Positivity in Japanese," PLOS ONE, Public Library of Science, vol. 7(7), pages 1-8, July.
  • Handle: RePEc:plo:pone00:0040067
    DOI: 10.1371/journal.pone.0040067
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    1. Chikashi Terao & Koichiro Ohmura & Masaki Katayama & Meiko Takahashi & Miki Kokubo & Gora Diop & Yoshinobu Toda & Natsuki Yamamoto & Human Disease Genomics Working Group & Rheumatoid Arthritis (RA) Cl, 2011. "Myelin Basic Protein as a Novel Genetic Risk Factor in Rheumatoid Arthritis—A Genome-Wide Study Combined with Immunological Analyses," PLOS ONE, Public Library of Science, vol. 6(6), pages 1-10, June.
    2. Gary S. Firestein, 2003. "Evolving concepts of rheumatoid arthritis," Nature, Nature, vol. 423(6937), pages 356-361, May.
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    1. Shomi Oka & Hiroshi Furukawa & Aya Kawasaki & Kota Shimada & Shoji Sugii & Atsushi Hashimoto & Akiko Komiya & Naoshi Fukui & Satoshi Ito & Tadashi Nakamura & Koichiro Saisho & Masao Katayama & Shinich, 2014. "Protective Effect of the HLA-DRB1*13:02 Allele in Japanese Rheumatoid Arthritis Patients," PLOS ONE, Public Library of Science, vol. 9(6), pages 1-12, June.

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