Chest
Volume 156, Issue 6, December 2019, Pages 1092-1110
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Original Research: COPD
Prevalence and Risk Factors for Osteoporosis in Individuals With COPD: A Systematic Review and Meta-analysis

The abstract of this systematic review has been presented at the American Thoracic Society 2018 International Conference, May 18-23, 2018, San Diego, CA. Part of this article has been presented in abstract form (Chen YW, Ramsook AH, Coxson HO, Bon J, Reid WD. Am J Respir Crit Care Med. 2018;197:A1720).
https://doi.org/10.1016/j.chest.2019.06.036Get rights and content

Background

Osteoporosis is prevalent in individuals with COPD. Updated evidence is required to complement the previous systematic review on this topic to provide best practice. The aim of this systematic review and meta-analysis was to quantitatively synthesize data from studies with respect to the prevalence and risk factors for osteoporosis among individuals with COPD.

Methods

EMBASE, CINAHL, MEDLINE, and PubMed databases were searched for articles containing the key words “COPD,” “osteoporosis,” “prevalence,” and “risk factor.” Eligibility screening, data extraction, and quality assessment of the retrieved articles were conducted independently by two reviewers. Meta-analyses were performed to determine osteoporosis prevalence and risk factors in individuals with COPD. Meta-regression analyses were conducted to explore the sources of heterogeneity.

Results

The pooled global prevalence from 58 studies was 38% (95% CI, 34-43). The presence of COPD increased the likelihood of having osteoporosis (OR, 2.83). Other significant risk factors for osteoporosis in COPD patients were BMI < 18.5 kg/m2 (OR, 4.26) and the presence of sarcopenia (OR, 3.65).

Conclusions

Osteoporosis is prevalent in individuals with COPD, and the prevalence seems to be high and similar in many countries. Patients with COPD should be screened for osteoporosis and contributing risk factors.

Section snippets

Search Strategy

The protocol for this systematic review was registered on PROSPERO (CRD42017067485). Four databases (EMBASE, CINAHL, MEDLINE, and PubMed) were searched from their inception to January 22, 2018. To define the population, “chronic obstructive pulmonary disease” was combined by the Boolean operator “AND” with terms that potentially evaluated osteoporosis; that is, “osteoporosis,” “bone mineral density,” “dual-energy X-ray absorptiometry,” and “computed tomography.” To determine the prevalence and

Study Selection

The initial search produced 4,957 articles. After excluding duplicates, the titles and abstracts of 1,926 articles were screened for eligibility. Of these, the full-text of 116 articles was screened for eligibility, resulting in the identification of 58 studies that were reported in 64 publications13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30, 31, 32, 33, 34, 35, 36, 37, 38, 39, 40, 41, 42, 43, 44, 45, 46, 47, 48, 49, 50, 51, 52, 53, 54, 55, 56, 57, 58, 59, 60, 61, 62,

Discussion

This review quantitatively synthesized the current evidence on the prevalence and risk factors for osteoporosis in COPD in 58 studies with 8,753 participants with COPD to demonstrate a pooled global prevalence of 38%. The prevalence of osteoporosis did not significantly differ (P = .49) among the five regions in the world. In addition to COPD, significant risk factors were BMI < 18.5 kg/m2, decreased FFMI values, and the presence of sarcopenia.

This study found that patients with COPD have a

Conclusions

This systematic review and meta-analysis revealed that osteoporosis is a prevalent comorbidity worldwide in patients with COPD. Low BMI and low muscle mass are associated with this increased prevalence. Individuals with COPD at high risk for osteoporosis should be identified early through screening, and strategies aimed at improving or controlling risk factors for osteoporosis should be implemented in the early stages of lung disease.

Acknowledgments

Author contributions: Y.-W. C. is the guarantor of the content of the manuscript, including the data and analysis. Y.-W. C., H. O. C., and W. D. R. conceived and designed the research questions. Y.-W. C. and A. H. R. performed the search, quality assessment, and extraction of the data. Y.-W. C. analyzed the data and drafted the manuscript, and all the authors interpreted the data. A. H. R., J. B., H. O. C., and W. D. R. edited and provided critical revision of the manuscript. All the authors

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    FUNDING/SUPPORT: The authors have reported to CHEST that no funding was received for this study.

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