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Abstract Number: 226

Improved Prediction of Hip Fracture Using the Health Assessment Questionnaire-Disability Index and FRAX® in Japanese Patients with Rheumatoid Arthritis: A Prospective Observational Study

Takefumi Furuya1, Eisuke Inoue2, Kensuke Ochi1, Osamu Ishida3, Atsuo Taniguchi4, Shigeki Momohara4 and Hisashi Yamanaka1, 1Institute of Rheumatology, Tokyo Women's Medical University, Tokyo, Japan, 2Rheumatology, Institute of Rheumatology, Tokyo Women’s Medical University, Tokyo, Japan, 3Orthopedics, Institute of Rheumatology, Tokyo Women's Medical University, Tokyo, Japan, 4Institute of Rheumatology, Tokyo Women’s Medical University, Tokyo, Japan

Meeting: 2014 ACR/ARHP Annual Meeting

Keywords: fracture risk and rheumatoid arthritis (RA), Health Assessment Questionnaire, Japanese

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Session Information

Title: Osteoporosis and Metabolic Bone Disease - Clinical Aspects and Pathogenesis: Osteoporosis: Pathogenesis, Epidemiology and Diagnosis

Session Type: Abstract Submissions (ACR)

Background/Purpose: The World Health Organization Fracture Risk Assessment Tool (FRAX®) algorithm can be used to estimate 10-year probabilities of hip and major osteoporotic fractures. Previously, we and others have reported a significant association between the Health Assessment Questionnaire-Disability Index (HAQ-DI) and clinical fracture risk in patients with rheumatoid arthritis (RA). This has generated interest in the possible role the HAQ-DI could play in improving fracture risk assessment for Japanese patients with RA. The aim of this study was to evaluate the prognostic accuracy of the Japanese version of FRAX®to predict the 10-year probability of hip and major osteoporotic fractures in Japanese patients with RA, and investigate whether the HAQ-DI can further improve the prediction of hip and major osteoporotic fractures.

Methods: We analyzed the database of the Institute of Rheumatology Rheumatoid Arthritis (IORRA) study, our large prospective observational cohort study in Japanese patients with RA. IORRA study subjects included 3,095 women and 703 men with RA ranging in age from 40 to 90 years. The mean (± standard deviation) age was 60.6 ± 9.6 years. Self-reported major osteoporotic fractures of the hip, vertebrae, humerus, and wrist were verified using patient medical records. The association of FRAX® with fractures was evaluated by the Cox model, and C-statistics were used in the risk prediction model to account for censored survivaldata. The Japanese version of HAQ-DI (J-HAQ-DI) was used in the assessment in conjunction with FRAX®, without considering bone mineral density (BMD) values, and C-statistics were used for the 10-year risk calculated by the Cox model.

Results: A total of 3,789 Japanese patients with RA were followed for an average of 5.8 years. Using FRAX® without BMD, the mean 10-year predicted fracture probability for hip and major osteoporotic fractures was 5.3% and 14.5%, respectively. Among the patients, 52 (1.4%) and 216 (5.7%) presented with hip and major osteoporotic fractures (including n=52 hip, n=85 vertebral, n=41 humeral, and n=38 distal radial fractures), respectively. For hip fractures, the C-statistic was 0.735 (95% CI: 0.665, 0.804) for the statistical model prediction based on both J-HAQ-DI and FRAX®, and it was 0.688 (95% CI: 0.613, 0.762) for FRAX® alone. For major osteoporotic fractures, the C-statistic was 0.678 (95% CI: 0.636, 0.719) for both J-HAQ-DI and FRAX®, and 0.664 (95% CI: 0.624, 0.704) for FRAX®alone.

Conclusion: We evaluated the performance of FRAX® in Japanese patients with RA using our longitudinal study data. Our results were similar to those in other previously reported FRAX® studies. However, the J-HAQ-DI improved hip fracture risk assessment when used in conjunction with this conventional risk assessment tool in Japanese patients with RA.


Disclosure:

T. Furuya,
None;

E. Inoue,
None;

K. Ochi,
None;

O. Ishida,
None;

A. Taniguchi,
None;

S. Momohara,

Abbvie Japan, Chugai Parmaceutical, Eisai, Mitsubishi Tanabe Parma, Takeda Parmaceutical,

8;

H. Yamanaka,

Abbott, AbbVie, Asahikasei , Astellas, AstraZeneca, Bristol-Myers Squib, Chugai, Daiichi Sankyo, Eisai, GlaxoSmithKline, Janssen, Mitsubishi Tanabe, MSD, Nippon Kayaku, Pfizer, Santen, Taishotoyama, Takeda, Teijin,,

2,

Abbott, AbbVie, Astellas, AstraZeneca, Bristol-Myers Squib, Chugai, Daiichi Sankyo, Eisai, Mitsubishi Tanabe, Nippon Kayaku, Pfizer, Takeda, Teijin,

5,

Abbott, AbbVie, Astellas, Bristol-Myers Squib, Chugai, Eisai, Mitsubishi Tanabe, Pfizer, Takeda, Teijin,

8.

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