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

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 associat...

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Autores principales: Terao, Chikashi, Ohmura, Koichiro, Ikari, Katsunori, Kochi, Yuta, Maruya, Etsuko, Katayama, Masaki, Yurugi, Kimiko, Shimada, Kota, Murasawa, Akira, Honjo, Shigeru, Takasugi, Kiyoshi, Matsuo, Keitaro, Tajima, Kazuo, Suzuki, Akari, Yamamoto, Kazuhiko, Momohara, Shigeki, Yamanaka, Hisashi, Yamada, Ryo, Saji, Hiroo, Matsuda, Fumihiko, Mimori, Tsuneyo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3391228/
https://www.ncbi.nlm.nih.gov/pubmed/22792215
http://dx.doi.org/10.1371/journal.pone.0040067
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author Terao, Chikashi
Ohmura, Koichiro
Ikari, Katsunori
Kochi, Yuta
Maruya, Etsuko
Katayama, Masaki
Yurugi, Kimiko
Shimada, Kota
Murasawa, Akira
Honjo, Shigeru
Takasugi, Kiyoshi
Matsuo, Keitaro
Tajima, Kazuo
Suzuki, Akari
Yamamoto, Kazuhiko
Momohara, Shigeki
Yamanaka, Hisashi
Yamada, Ryo
Saji, Hiroo
Matsuda, Fumihiko
Mimori, Tsuneyo
author_facet Terao, Chikashi
Ohmura, Koichiro
Ikari, Katsunori
Kochi, Yuta
Maruya, Etsuko
Katayama, Masaki
Yurugi, Kimiko
Shimada, Kota
Murasawa, Akira
Honjo, Shigeru
Takasugi, Kiyoshi
Matsuo, Keitaro
Tajima, Kazuo
Suzuki, Akari
Yamamoto, Kazuhiko
Momohara, Shigeki
Yamanaka, Hisashi
Yamada, Ryo
Saji, Hiroo
Matsuda, Fumihiko
Mimori, Tsuneyo
author_sort Terao, Chikashi
collection PubMed
description 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.
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spelling pubmed-33912282012-07-12 ACPA-Negative RA Consists of Two Genetically Distinct Subsets Based on RF Positivity in Japanese Terao, Chikashi Ohmura, Koichiro Ikari, Katsunori Kochi, Yuta Maruya, Etsuko Katayama, Masaki Yurugi, Kimiko Shimada, Kota Murasawa, Akira Honjo, Shigeru Takasugi, Kiyoshi Matsuo, Keitaro Tajima, Kazuo Suzuki, Akari Yamamoto, Kazuhiko Momohara, Shigeki Yamanaka, Hisashi Yamada, Ryo Saji, Hiroo Matsuda, Fumihiko Mimori, Tsuneyo PLoS One Research Article 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. Public Library of Science 2012-07-06 /pmc/articles/PMC3391228/ /pubmed/22792215 http://dx.doi.org/10.1371/journal.pone.0040067 Text en Terao et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Terao, Chikashi
Ohmura, Koichiro
Ikari, Katsunori
Kochi, Yuta
Maruya, Etsuko
Katayama, Masaki
Yurugi, Kimiko
Shimada, Kota
Murasawa, Akira
Honjo, Shigeru
Takasugi, Kiyoshi
Matsuo, Keitaro
Tajima, Kazuo
Suzuki, Akari
Yamamoto, Kazuhiko
Momohara, Shigeki
Yamanaka, Hisashi
Yamada, Ryo
Saji, Hiroo
Matsuda, Fumihiko
Mimori, Tsuneyo
ACPA-Negative RA Consists of Two Genetically Distinct Subsets Based on RF Positivity in Japanese
title ACPA-Negative RA Consists of Two Genetically Distinct Subsets Based on RF Positivity in Japanese
title_full ACPA-Negative RA Consists of Two Genetically Distinct Subsets Based on RF Positivity in Japanese
title_fullStr ACPA-Negative RA Consists of Two Genetically Distinct Subsets Based on RF Positivity in Japanese
title_full_unstemmed ACPA-Negative RA Consists of Two Genetically Distinct Subsets Based on RF Positivity in Japanese
title_short ACPA-Negative RA Consists of Two Genetically Distinct Subsets Based on RF Positivity in Japanese
title_sort acpa-negative ra consists of two genetically distinct subsets based on rf positivity in japanese
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3391228/
https://www.ncbi.nlm.nih.gov/pubmed/22792215
http://dx.doi.org/10.1371/journal.pone.0040067
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