Yu Meng, Chen Guo-Qiang, Yu Fang
Department of Orthopedics, Beijing Shijitan Hospital Affiliated to Capital Medical University, Beijing, China.
Department of Orthopedics, Beijing Shijitan Hospital Affiliated to Capital Medical University, Beijing, China.
Kaohsiung J Med Sci. 2016 Dec;32(12):599-606. doi: 10.1016/j.kjms.2016.10.002. Epub 2016 Nov 14.
In this study, we aimed to assess the relationship between vitamin D receptor gene polymorphisms and osteoporosis in the Han Chinese population. Articles regarding associations between vitamin D receptor polymorphisms (ApaI rs7975232 and BsmI rs1544410) and osteoporosis were retrieved from databases in November 2014. Eligible studies were tested by the Hardy-Weinberg equilibrium. The odds ratio and 95% confidence interval (95% CI) were analyzed to evaluate the strength of the associations. Pooled effect estimates were derived using a fixed-effect model and a random-effect model according to the heterogeneity of the test results. A subgroup analysis by study type and a sensitivity analysis based on studies that conform to the Hardy-Weinberg equilibrium and studies with postmenopausal women as participants were performed. This meta-analysis involved 15 eligible studies including 1580 cases and 1389 controls. The pooled estimated odds ratios in the dominant and additive genetic models were 0.73 (95% CI: 0.46-1.14, p=0.17) and 1.01 (95% CI: 0.77-1.33, p=0.81), respectively, for rs7975232 and 1.01 (95% CI: 0.81-1.26, p=0.91) and 1.01 (95% CI: 0.77-1.33, p=0.92), respectively, for rs1544410. The subgroup analysis showed that regardless of the dominant or additive genetic model, the effect of pooled odds ratios for rs7975232 and rs1544410 was insignificant. The sensitivity analysis also showed that the pooled effect was not significantly changed. In conclusion, no evidence of association is apparent between polymorphisms of vitamin D receptor genes and osteoporosis risk in the Han Chinese population.
在本研究中,我们旨在评估汉族人群中维生素D受体基因多态性与骨质疏松症之间的关系。于2014年11月从数据库中检索有关维生素D受体多态性(ApaI rs7975232和BsmI rs1544410)与骨质疏松症关联的文章。符合条件的研究采用哈迪-温伯格平衡检验。分析比值比和95%置信区间(95%CI)以评估关联强度。根据检验结果的异质性,使用固定效应模型和随机效应模型得出合并效应估计值。按研究类型进行亚组分析,并基于符合哈迪-温伯格平衡的研究以及以绝经后女性为参与者的研究进行敏感性分析。该荟萃分析纳入了15项符合条件的研究,包括1580例病例和1389例对照。对于rs7975232,在显性和加性遗传模型中合并估计比值比分别为0.73(95%CI:0.46 - 1.14,p = 0.17)和1.01(95%CI:0.77 - 1.33,p = 0.81);对于rs1544410,分别为1.01(95%CI:0.81 - 1.26,p = 0.91)和1.01(95%CI:0.77 - 1.33,p = 0.92)。亚组分析表明,无论显性还是加性遗传模型,rs7975232和rs1544410的合并比值比效应均不显著。敏感性分析也表明合并效应无显著变化。总之,在汉族人群中,没有明显证据表明维生素D受体基因多态性与骨质疏松症风险之间存在关联。