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Association of large joint involvement at the start of biological disease-modifying antirheumatic drugs and Janus kinase inhibitors with disease activity and drug retention in patients with rheumatoid arthritis: The ANSWER cohort study.
Shirasugi, Iku; Onishi, Akira; Nishimura, Keisuke; Yamamoto, Wataru; Murakami, Kosaku; Onizawa, Hideo; Maeda, Yuichi; Ebina, Kosuke; Son, Yonsu; Amuro, Hideki; Katayama, Masaki; Hara, Ryota; Nagai, Koji; Hiramatsu, Yuri; Hashimoto, Motomu; Okano, Tadashi; Maeda, Toshihisa; Hayashi, Shinya; Sendo, Sho; Jinno, Sadao; Yamamoto, Yuzuru; Yamada, Hirotaka; Ueda, Yo; Saegusa, Jun.
Affiliation
  • Shirasugi I; Department of Rheumatology and Clinical Immunology, Kobe University Graduate School of Medicine, Kobe, Japan.
  • Onishi A; Department of Advanced Medicine for Rheumatic Diseases, Graduate School of Medicine, Kyoto University, Kyoto, Japan.
  • Nishimura K; Department of Rheumatology and Clinical Immunology, Kobe University Graduate School of Medicine, Kobe, Japan.
  • Yamamoto W; Department of Health Information Management, Kurashiki Sweet Hospital, Okayama, Japan.
  • Murakami K; Center for Cancer Immunotherapy and Immunobiology, Graduate School of Medicine, Kyoto University, Kyoto, Japan.
  • Onizawa H; Department of Advanced Medicine for Rheumatic Diseases, Graduate School of Medicine, Kyoto University, Kyoto, Japan.
  • Maeda Y; Department of Respiratory Medicine and Clinical Immunology, Graduate School of Medicine, Osaka University, Osaka, Japan.
  • Ebina K; Department of Orthopaedic Surgery, Graduate School of Medicine, Osaka University, Osaka, Japan.
  • Son Y; First Department of Internal Medicine, Kansai Medical University, Osaka, Japan.
  • Amuro H; First Department of Internal Medicine, Kansai Medical University, Osaka, Japan.
  • Katayama M; Department of Rheumatology, Osaka Red Cross Hospital, Osaka, Japan.
  • Hara R; Department of Orthopaedic Surgery, Nara Medical University, Nara, Japan.
  • Nagai K; Department of Internal Medicine (IV), Osaka Medical and Pharmaceutical University, Osaka, Japan.
  • Hiramatsu Y; Department of Internal Medicine (IV), Osaka Medical and Pharmaceutical University, Osaka, Japan.
  • Hashimoto M; Department of Clinical Immunology, Graduate School of Medicine, Osaka Metropolitan University, Osaka, Japan.
  • Okano T; Department of Orthopedic Surgery, Graduate School of Medicine, Osaka Metropolitan University, Osaka, Japan.
  • Maeda T; Department of Orthopaedic Surgery, Kobe University Graduate School of Medicine, Kobe, Japan.
  • Hayashi S; Department of Orthopaedic Surgery, Kobe University Graduate School of Medicine, Kobe, Japan.
  • Sendo S; Department of Rheumatology and Clinical Immunology, Kobe University Graduate School of Medicine, Kobe, Japan.
  • Jinno S; Department of Rheumatology and Clinical Immunology, Kobe University Graduate School of Medicine, Kobe, Japan.
  • Yamamoto Y; Department of Medicine, University of Hawaii, Honolulu, Hawaii, USA.
  • Yamada H; Department of Rheumatology and Clinical Immunology, Kobe University Graduate School of Medicine, Kobe, Japan.
  • Ueda Y; Department of Rheumatology and Clinical Immunology, Kobe University Graduate School of Medicine, Kobe, Japan.
  • Saegusa J; Department of Rheumatology and Clinical Immunology, Kobe University Graduate School of Medicine, Kobe, Japan.
Int J Rheum Dis ; 27(3): e15097, 2024 Mar.
Article in En | MEDLINE | ID: mdl-38439176
ABSTRACT

AIM:

To investigate the association of large joint involvement (LJI) with disease activity and drug retention in patients with rheumatoid arthritis (RA) who started receiving a biological disease-modifying antirheumatic drug or Janus kinase inhibitor.

METHODS:

Patients with RA from a Japanese multicenter observational registry were enrolled. Our definition of large joints included the shoulder, elbow, hip, knee, and ankle joints. Linear mixed-effects models were used to examine changes in the clinical disease activity index (CDAI) score at Week 24 as the primary outcome, and drug retention rates were compared between patients with and without LJI using Cox proportional hazards models. We examined the potential effect modifications of changes in the CDAI by baseline characteristics.

RESULTS:

Overall, 2507 treatment courses from 1721 patients were included (LJI, 1744; no LJI, 763). Although LJI was associated with significantly higher changes in CDAI from baseline at Week 24 (difference in change in CDAI -5.84 [-6.65 to -5.03], p < .001), CDAI was significantly higher in patients with LJI over time. Retention rates were similar in both groups. The association of LJI with changes in disease activity was more prominent in patients with a short disease duration, negative anti-citrullinated peptide antibodies, and interleukin-6 receptor inhibitor (IL-6Ri) use.

CONCLUSION:

Although LJI was associated with a greater reduction in disease activity from baseline, higher disease activity at baseline was not offset over time in patients with LJI, demonstrating that LJI is an unfavorable predictor. An early treat-to-target strategy using an IL-6Ri may be beneficial for patients with LJI.
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Full text: 1 Database: MEDLINE Main subject: Arthritis, Rheumatoid / Antirheumatic Agents / Janus Kinase Inhibitors Limits: Humans Language: En Year: 2024 Type: Article

Full text: 1 Database: MEDLINE Main subject: Arthritis, Rheumatoid / Antirheumatic Agents / Janus Kinase Inhibitors Limits: Humans Language: En Year: 2024 Type: Article