Jiang Hua, Qin Zhilin, Zong Shaohui, He Maolin, Zhan Xinli, Xiao Zengming, Wei Qingjun
Division of Spine Surgery, The First Affiliated Hospital of Guangxi Medical University, Nanning, China.
Department of Orthopaedic Surgery, The First Affiliated Hospital of Guangxi Medical University, Shuangyong Road No. 6, Nanning, 530021, China.
Eur Spine J. 2017 Jan;26(1):267-277. doi: 10.1007/s00586-016-4771-2. Epub 2016 Sep 9.
To examine the association between Vitamin D receptor (VDR) gene polymorphisms and lumbar disc degeneration (LDD) predisposition.
A comprehensive literature search was conducted to identify all the relevant studies. The allele/genotype frequencies were extracted from each study. We calculated the pooled odds ratios (ORs) and 95 % confidence intervals (CI) to assess the strength of the association between the VDR gene polymorphisms and LDD risk. Statistical analysis was performed using RevMan 5.31 software.
A total of 23 case-control studies (1835 cases and 1923 controls) were included in this systematic review. For the TaqI (rs731236), FokI (rs2228570) and ApaI (rs7975232) polymorphisms of VDR gene, nine studies, seven studies, and five studies, were eventually included in the meta-analysis, respectively. There was no evidence that the VDR gene polymorphisms (TaqI, FokI, ApaI) had significant associations with LDD risk.(for TaqI allelic comparison, OR = 1.07, 95 % CI 0.81-1.40, p = 0.64; for FokI allelic comparison, OR = 1.23, 95 % CI 0.83-1.82, p = 0.31; for ApaI allelic comparison, OR = 0.79, 95 % CI 0.55-1.14, p = 0.20). For stratified analyses by ethnicity and study design, no significant associations were found in Caucasian population and Asian population, as well as the population-based studies and hospital-based studies under all genetic models.
TaqI, FokI, and ApaI polymorphisms of VDR gene were not significantly associated with the predisposition of LDD. Large-scale and well-designed international studies are needed to further analyze this field.
探讨维生素D受体(VDR)基因多态性与腰椎间盘退变(LDD)易感性之间的关联。
进行全面的文献检索以识别所有相关研究。从每项研究中提取等位基因/基因型频率。我们计算合并比值比(OR)和95%置信区间(CI),以评估VDR基因多态性与LDD风险之间关联的强度。使用RevMan 5.31软件进行统计分析。
本系统评价共纳入23项病例对照研究(1835例病例和1923例对照)。对于VDR基因的TaqI(rs731236)、FokI(rs2228570)和ApaI(rs7975232)多态性,最终分别有9项研究、7项研究和5项研究纳入荟萃分析。没有证据表明VDR基因多态性(TaqI、FokI、ApaI)与LDD风险有显著关联。(TaqI等位基因比较,OR = 1.07,95% CI 0.81 - 1.40,p = 0.64;FokI等位基因比较,OR = 1.23,95% CI 0.83 - 1.82,p = 0.31;ApaI等位基因比较,OR = 0.79,95% CI 0.55 - 1.14,p = 0.20)。按种族和研究设计进行分层分析,在白种人群和亚洲人群以及所有遗传模型下的基于人群的研究和基于医院的研究中均未发现显著关联。
VDR基因的TaqI、FokI和ApaI多态性与LDD易感性无显著关联。需要大规模且设计良好的国际研究来进一步分析该领域。