Bone mineral density of postmenopausal women with rheumatoid arthritis depends on disease duration regardless of treatment

Yu Mori, Yoshiyuki Kuwahara, Shinpei Chiba, Atsushi Kogre, Kazuyoshi Baba, Masayuki Kamimura, Eiji Itoi

Research output: Contribution to journalArticlepeer-review

11 Citations (Scopus)

Abstract

The aim of this study was to determine the associations of disease activity and disease duration with the bone mineral density (BMD) in rheumatoid arthritis (RA) patients. We also evaluated the associations of biological drugs with bone loss. A total of 138 postmenopausal RA patients were retrospectively assessed to identify the associations of disease activity, disease duration, and biological drug use with BMD. We assessed the associations of disease duration, a C-reactive protein based disease activity score in 28 joints (DAS28), simplified disease activity index, clinical disease activity index, health assessment questionnaire scores, and the use of biological drugs with the lumbar spine, total hip, and femoral neck BMDs using univariate and multivariate linear regression analyses in bisphosphonate treatment and non-bisphosphonate treatment groups at 1 year of follow-up. The multivariate linear regression analyses showed that disease duration was significantly related to the BMD of the femoral neck and total hip regardless of bisphosphonate treatment. The use of biological drugs was not significantly associated with BMD. Hip BMD in postmenopausal women with RA depends on the disease duration regardless of bisphosphonate use. Biological drugs for RA treatment were not negatively associated with general bone loss.

Original languageEnglish
Pages (from-to)52-57
Number of pages6
JournalJournal of Bone and Mineral Metabolism
Volume35
Issue number1
DOIs
Publication statusPublished - 2017 Jan 1

Keywords

  • Biologics
  • Bisphosphonates
  • Disease activity
  • Osteoporosis
  • Rheumatoid arthritis

ASJC Scopus subject areas

  • Endocrinology, Diabetes and Metabolism
  • Orthopedics and Sports Medicine
  • Endocrinology

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