TY - JOUR
T1 - Clinical characteristics of patients with spondyloarthritis and inflammatory bowel disease versus inflammatory bowel disease-related arthritis
AU - Ono, Keisuke
AU - Kishimoto, Mitsumasa
AU - Deshpande, Gautam A.
AU - Fukui, Sho
AU - Kawaai, Satoshi
AU - Sawada, Haruki
AU - Matsuura, Minoru
AU - Rodriguez, Valeria Rios
AU - Proft, Fabian
AU - Tada, Kurisu
AU - Tamura, Naoto
AU - Taniguchi, Yoshinori
AU - Hirata, Ayako
AU - Kameda, Hideto
AU - Tsuji, Shigeyoshi
AU - Kaneko, Yuko
AU - Dobashi, Hiroaki
AU - Okano, Tadashi
AU - Haji, Yoichiro
AU - Morita, Akimichi
AU - Okada, Masato
AU - Komagata, Yoshinori
AU - Medina, Clementina López
AU - Molto, Anna
AU - Dougados, Maxime
AU - Hisamatsu, Tadakazu
AU - Tomita, Tetsuya
AU - Kaname, Shinya
N1 - Funding Information:
This study was conducted under the umbrella of ASAS with unrestricted grant of AbbVie, Pfizer, Lilly, Novartis, UCB, Janssen and Merck. The funders did not have any role in the design and conduct of the study; collection, management, analysis and interpretation of the data; preparation, review or approval of the manuscript and decision to submit the manuscript for publication.
Publisher Copyright:
© 2022, The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.
PY - 2022/10
Y1 - 2022/10
N2 - The purpose of this study was to clarify the clinical characteristics of spondyloarthritis (SpA) patients with inflammatory bowel disease (IBD) compared to those without IBD. Furthermore, among patients with SpA and IBD, we aimed to clarify what clinical characteristics lead rheumatologists to diagnose “IBD-related arthritis.” Utilizing SpA and psoriatic arthritis (PsA) patients’ data from an international, cross-sectional, observational study, we analyzed information on demographics and disease characteristics, dichotomizing patients by IBD status. The presence or absence of IBD was determined based on data collection of treating rheumatologists. Patients with SpA (including PsA) and IBD were also categorized based on treating rheumatologists’ definitive diagnosis in regard to SpA type, and compared by whether the patients had IBD-related arthritis or not. Among 4465 SpA patients, 287 (6.4%, 95%CI 5.7–7.2%) were identified with IBD. Compared to SpA patients without IBD, patients with SpA and IBD had a longer diagnostic delay (5.1 vs. 2.9 years, p < 0.001). In patients with SpA and IBD, 111 (38.7%, 95%CI 33.0–44.6%) were diagnosed with IBD-related arthritis. Multivariable analyses showed that HLA-B27 positivity [OR = 0.35, (95%CI 0.15–0.80)], psoriasis [OR = 0.14, (95%CI 0.04–0.50)], IBD as first symptom of SpA [OR = 3.32, (95%CI 1.84–6.01)], and need for IBD-specific treatment [OR = 5.41, (95%CI 2.02–14.50)] were independently associated with the definitive diagnosis of IBD-related arthritis. Collaboration with gastroenterologists is needed to shorten the diagnostic delay in patients with SpA and IBD. The recognition of the factors for the diagnosis of “IBD-related arthritis” may lead to the elucidation of the pathogenesis.
AB - The purpose of this study was to clarify the clinical characteristics of spondyloarthritis (SpA) patients with inflammatory bowel disease (IBD) compared to those without IBD. Furthermore, among patients with SpA and IBD, we aimed to clarify what clinical characteristics lead rheumatologists to diagnose “IBD-related arthritis.” Utilizing SpA and psoriatic arthritis (PsA) patients’ data from an international, cross-sectional, observational study, we analyzed information on demographics and disease characteristics, dichotomizing patients by IBD status. The presence or absence of IBD was determined based on data collection of treating rheumatologists. Patients with SpA (including PsA) and IBD were also categorized based on treating rheumatologists’ definitive diagnosis in regard to SpA type, and compared by whether the patients had IBD-related arthritis or not. Among 4465 SpA patients, 287 (6.4%, 95%CI 5.7–7.2%) were identified with IBD. Compared to SpA patients without IBD, patients with SpA and IBD had a longer diagnostic delay (5.1 vs. 2.9 years, p < 0.001). In patients with SpA and IBD, 111 (38.7%, 95%CI 33.0–44.6%) were diagnosed with IBD-related arthritis. Multivariable analyses showed that HLA-B27 positivity [OR = 0.35, (95%CI 0.15–0.80)], psoriasis [OR = 0.14, (95%CI 0.04–0.50)], IBD as first symptom of SpA [OR = 3.32, (95%CI 1.84–6.01)], and need for IBD-specific treatment [OR = 5.41, (95%CI 2.02–14.50)] were independently associated with the definitive diagnosis of IBD-related arthritis. Collaboration with gastroenterologists is needed to shorten the diagnostic delay in patients with SpA and IBD. The recognition of the factors for the diagnosis of “IBD-related arthritis” may lead to the elucidation of the pathogenesis.
KW - Inflammatory bowel disease
KW - Inflammatory bowel disease-related arthritis
KW - Psoriatic arthritis
KW - Spondyloarthritis
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U2 - 10.1007/s00296-022-05117-0
DO - 10.1007/s00296-022-05117-0
M3 - Article
C2 - 35532790
AN - SCOPUS:85129741927
SN - 0172-8172
VL - 42
SP - 1751
EP - 1766
JO - Rheumatology International
JF - Rheumatology International
IS - 10
ER -