<div><p>Background</p><p>A number of studies have examined the association between the polymorphisms of the low-density lipoprotein receptor-related protein 5 gene (LRP5), but previous results have been inconclusive. Thus we performed a meta-analysis of studies on the association between the LRP5 polymorphisms and bone mineral density (BMD) to assess their pooled effects.</p> <p>Methods</p><p>Published literature from PubMed, EMBASE and ISI web of science were searched for eligible publications. Weighted mean difference (WMD) and 95% confidence interval (CI) was calculated using fixed- or random-effects model.</p> <p>Results</p><p>A total of 19 studies with 25773 subjects were considered in this meta-analysis. Of them, 17 examined the association between the A1330V polymorphism and BMD, 8 were focused on the V667M polymorphism, and 2 analyzed the Q89R polymorphism. Individuals with the A1330V AA genotype showed significantly higher BMD than those with the AV/VV genotypes [at lumbar spine (LS): WMD = 0.02g/cm<sup>2</sup>, 95% CI = 0.01-0.03, <i>P</i> < 10<sup>-4</sup>; at femur neck (FN): WMD = 0.01g/cm<sup>2</sup>, 95% CI = 0.00-0.02, <i>P</i> = 0.01] or VV genotype (at LS: WMD = 0.02g/cm<sup>2</sup>, 95% CI = 0.01-0.04, <i>P</i> = 0.01). Significant associations were also detected in the analysis for V667M (VV vs. VM/MM: WMD at LS = 0.02g/cm<sup>2</sup>, 95% CI = 0.02-0.03, <i>P</i> < 10<sup>-5</sup>; WMD at FN = 0.01g/cm<sup>2</sup>, 95% CI = 0.01-0.02, <i>P</i> = 0.0002). As for Q89R, subjects with the QQ genotype tended to have higher BMD than those with the QR/RR genotypes at FN (WMD = 0.03g/cm<sup>2</sup>, 95% CI = 0.01-0.05, <i>P</i> = 0.005).</p> <p>Conclusion</p><p>This meta-analysis demonstrated that the <i>LRP5</i> polymorphisms may be modestly associated with BMD of LS and FN.</p> </div