Biologic and Targeted Synthetic Disease-Modifying Antirheumatic Drugs Do Not Arrest Bone Loss in Patients With Rheumatoid Arthritis: A Long-Term Multicenter Observational Study - Summary - MDSpire
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Long-Term Multicenter Observational Study Reveals No Impact of Biologic and Targeted Synthetic DMARDs on Bone Loss in Rheumatoid Arthritis Patients

  • By

  • Takafumi Aritomi

  • Koshiro Sonomoto

  • Shingo Nakayamada

  • Hiroaki Tanaka

  • Atsushi Nagayasu

  • Satoshi Kubo

  • Ippei Miyagawa

  • Ayako Yamaguchi

  • Naoaki Ohkubo

  • Yasuyuki Todoroki

  • Yurie Satoh-Kanda

  • Masanobu Ueno

  • Ryuichiro Kanda

  • Yuya Fujita

  • Masashi Funada

  • Hidenori Sakai

  • Satsuki Matsunaga

  • Masayuki Shinojima

  • Hiroki Kawamura

  • Kazuki Takahashi

  • Miyabi Ando

  • Kazuki Haru

  • Yusuke Miyazaki

  • Kentaro Hanami

  • Masao Nawata

  • Shunsuke Fukuyo

  • Keisuke Nakatsuka

  • Mikiko Tokunaga

  • Kazuyoshi Saito

  • Yoshiya Tanaka

  • April 21, 2026

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Objective:

To investigate the long-term effects of biologic and targeted synthetic DMARDs on bone metabolism in patients with rheumatoid arthritis.

Approach:
  • Study Design: A multicenter prospective observational study was conducted as part of the FIRST registry, enrolling patients with active RA initiating their first b/tsDMARD from August 2013 to July 2022.
  • Participants: Consecutive patients fulfilling the 2010 RA classification criteria were included. Participants provided informed consent and were followed for up to five years.
  • BMD Measurement: Bone mineral density (BMD) was measured at the femoral neck and one-third radius at specified intervals, with assessments conducted at the Hospital of the University of Occupational and Environmental Health.
Key Findings:
  • Despite treatment with b/tsDMARDs, bone mineral density at the femoral neck and radius decreased significantly over five years.
  • The study included 1,164 patients with active RA, showing marked disease activity decline but no improvement in systemic osteoporosis.
  • Treatment rates for osteoporosis remain low among RA patients, particularly those using glucocorticoids.
Interpretation:

The findings suggest that b/tsDMARD therapy and inflammation control may not be sufficient to manage osteoporosis in RA patients.

Limitations:
  • The study did not assess lumbar spine BMD due to potential overestimation from degenerative disease.
  • Censored cases were handled for participants who did not attend annual assessments.
Conclusion:

The study emphasizes the need for ongoing attention to bone health in RA patients, as treatment with b/tsDMARDs alone does not halt osteoporosis progression.

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