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Meta-Analysis
. 2016 May;95(22):e3042.
doi: 10.1097/MD.0000000000003042.

Effects of Statins on Bone Mineral Density and Fracture Risk: A PRISMA-compliant Systematic Review and Meta-Analysis

Affiliations
Meta-Analysis

Effects of Statins on Bone Mineral Density and Fracture Risk: A PRISMA-compliant Systematic Review and Meta-Analysis

Zongze Wang et al. Medicine (Baltimore). 2016 May.

Abstract

Although observational studies have identified the protective effect of statins on bone health, the effects remain controversial in randomized controlled trials (RCTs). We conducted a meta-analysis of RCTs to evaluate the effects of statins on bone mineral density (BMD) and fracture risk among adults.We searched electronic databases of Medline, Embase, and the Cochrane Central Register of Controlled Trials (CENTRAL) and conducted a bibliography review to identify articles published until May, 2015.Studies included in this meta-analysis should be randomized controlled trials conducted in adults, using statins in the intervention group. Information on changes in BMD or odds ratio, relative risk or hazard ratio (HR) for fracture risk with the corresponding 95% confidence interval (CI) was provided.Two investigators independently reviewed the title or abstract, further reviewed the full-texts and extracted information on study characteristics and study outcomes. Net change estimates of BMD and pooled HR of fracture risk comparing the intervention group with the control group were estimated across trials using random-effects models.Of the relevant 334 citations, 7 trials (including 27,900 randomized participants in total) meeting the eligibility criteria were included. Of the 7 trials, 5 were conducted to assess the association of statins use with BMD change and 2 with fracture risk. Compared with the control group, statins use was associated with significant increase in BMD of 0.03 g/cm (95% CI: 0.006, 0.053; I = 99.2%; P < 0.001), but null association with fracture risk, with the pooled HR of 1.00 (95% CI: 0.87, 1.15; I = 0; P = 0.396). Sensitivity analyses revealed that the associations were consistent and robust.The effect of statins use on bone health among subpopulation could not be identified due to limited number of trials.These findings provide evidence that statins could be used to increase BMD other than decreasing fracture risk in participant with dyslipidemia. In addition, further trials with the primary outcome of bone health-related measurements in subpopulation are warranted to ensure the effect of statins use.

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Conflict of interest statement

The authors have no funding and conflicts of interest to disclose.

Figures

FIGURE 1
FIGURE 1
Selection of eligible randomized controlled trials examining the association of statins use on bone health.
FIGURE 2
FIGURE 2
Average net change in bone mineral density in randomized controlled trials comparing statins use with control group. The size of each square is proportional to the percent weight that each study contributed in the pooled estimate. The pooled effect size is indicated by the diamond. Bars, 95% confidence interval (CI).
FIGURE 3
FIGURE 3
The association of statins use with bone fracture in randomized controlled trials comparing statin use with control group. The size of each square is proportional to the percent weight that each study contributed in the pooled estimate. The pooled effect size is indicated by the diamond. Bars, 95% confidence interval (CI).
FIGURE 4
FIGURE 4
Funnel plot of the meta-analysis on the association of statins use with bone mineral density.

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References

    1. Chung YS, Lee MD, Lee SK, et al. HMG-CoA reductase inhibitors increase BMD in type 2 diabetes mellitus patients. J Clin Endocrinol Metab 2000; 85 3:1137–1142. - PubMed
    1. Henry MJ, Pasco JA, Nicholson GC, et al. Prevalence of osteoporosis in Australian women: Geelong Osteoporosis Study. J Clin Densitom 2000; 3 3:261–268. - PubMed
    1. Jones G, Nguyen T, Sambrook PN, et al. Symptomatic fracture incidence in elderly men and women: the Dubbo Osteoporosis Epidemiology Study (DOES). Osteoporos Int 1994; 4 5:277–282. - PubMed
    1. Kanis JA, Oden A, Johnell O, et al. The components of excess mortality after hip fracture. Bone 2003; 32 5:468–473. - PubMed
    1. Johnell O, Kanis JA. An estimate of the worldwide prevalence and disability associated with osteoporotic fractures. Osteoporos Int 2006; 17 12:1726–1733. - PubMed

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