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Increased osteoporosis risk in dermatomyositis or polymyositis independent of the treatments: a population-based cohort study with propensity score

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Abstract

We investigated the relationship between dermatomyositis/polymyositis (DM/PM) and the risk of subsequent osteoporosis development. A population-based retrospective cohort analysis was conducted using the National Health Insurance Research Database and the Catastrophic Illness Patients Database of Taiwan. We included 1179 patients and 4716 patients from 1999 to 2008 as the DM/PM cohort and the comparison cohort, respectively, and calculated the incidence rates of newly diagnosed osteoporosis. We used Cox proportional hazards models stratified on matched pair to assess the effect of DM/PM. The Kaplan–Meier method was applied to estimate the cumulative osteoporosis incidence curves. Patients with DM/PM were 2.99 times more likely to experience osteoporosis than those without DM/PM. The risk for osteoporosis in DM/PM patients was higher than comparisons in different propensity score quartiles. DM/PM cohort, no matter treated with or without corticosteroids and immunosuppressant, had a higher risk than the comparison cohort. The incidence of osteoporosis in Taiwan is associated with a priori DM/PM history. This risk was independent of the corticosteroids and immunosuppressant treatment.

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Abbreviations

BMD:

Bone mineral density

BNHI:

Bureau of National Health Insurance

CIPD:

Catastrophic Illness Patients Database

COPD:

Chronic obstructive pulmonary disease

DM:

Dermatomyositis

DXA:

Dual energy X-ray absorptiometry

IHD:

Ischemic heart disease

IIMs:

Idiopathic inflammatory myopathies

LHID:

Longitudinal Health Insurance Database

NHIRD:

National Health Insurance Research Database

OPD:

Outpatient department

PM:

Polymyositis

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Acknowledgments

This study is supported in part by Taiwan Ministry of Health and Welfare Clinical Trial and Research Center of Excellence (MOHW104-TDU-B-212-113002); China Medical University Hospital, Academia Sinica Taiwan Biobank, Stroke Biosignature Project (BM104010092); NRPB Stroke Clinical Trial Consortium (MOST 103-2325-B-039 -006); Tseng-Lien Lin Foundation, Taichung, Taiwan; Taiwan Brain Disease Foundation, Taipei, Taiwan; Katsuzo and Kiyo Aoshima Memorial Funds, Japan; and CMU under the Aim for Top University Plan of the Ministry of Education, Taiwan.

Author contributions

The individual contributions of the authors are listed as follows. Conception and design: Cynthia Wei-Sheng Lee and Chia-Hung Kao. Administrative support: Chih-Hsin Muo and Fung-Chang Sung. Data collection and assembly: Cynthia Wei-Sheng Lee, Ji-An Liang, and Chia-Hung Kao. Data analysis and interpretation: Cynthia Wei-Sheng Lee and Chia-Hung Kao. Manuscript writing and final approval of the manuscript: All authors. The guarantor of the paper assumes responsibility for the integrity of the work as a whole: Chia-Hung Kao.

Funding

The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript. No additional external funding was received for this study.

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Correspondence to Chia-Hung Kao.

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Lee, C.WS., Muo, CH., Liang, JA. et al. Increased osteoporosis risk in dermatomyositis or polymyositis independent of the treatments: a population-based cohort study with propensity score. Endocrine 52, 86–92 (2016). https://doi.org/10.1007/s12020-015-0756-x

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  • DOI: https://doi.org/10.1007/s12020-015-0756-x

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