Department of Pulmonary and Critical Care Medicine, The First Affiliated Hospital of Chongqing Medical University, Chongqing, China; ; Department of Pulmonary and Critical Care Medicine, Fuling Central Hospital of Chongqing City, Chongqing, China.
Department of Pulmonary and Critical Care Medicine, Fuling Central Hospital of Chongqing City, Chongqing, China.
Ann Palliat Med. 2022 Feb;11(2):574-587. doi: 10.21037/apm-21-3797.
Numerous studies have reported on the genetic factors related to asthma. In recent years, the vitamin D receptor (VDR) has been identified as one of the asthma susceptibility genes that is closely associated with the pathogenesis of asthma.
Randomized controlled trials (RCTs) related to asthma and the VDR were identified from the Chinese and English databases. The following keywords were used as search terms: "asthma", "vitamin D receptor", "VDR", "polymorphism", and "mutation". Meta-analysis was performed using RevMan 5.3 and Stata 13 software provided by the Cochrane system.
A total of 7 RCTs were included in this meta-analysis, 6 of which described the correct random allocation methods, 6 described the allocation plan in detail, and 4 used the blinding method. The frequency of the CC + CA dominant genotype at the Apa I locus and the GG + GA genotype frequency at the Bsm I locus of the VDR gene were significantly higher in asthmatic patients compared to control healthy patients [odds ratio (OR) =0.81, 95% confidence interval (CI): 0.68 to 0.98, P=0.03<0.05; and OR =2.05, 95% CI: 1.23 to 3.41, P=0.006<0.05, respectively]. There were no significant differences between the CC, CT, and TT genotype frequencies at the Fok I site of the VDR gene in the experimental group and the CC, CT, TT genotype frequencies at the Taq I site and the control group (P>0.05). There was no significant difference between the genotype frequencies.
Meta-analysis confirmed that VDR gene polymorphisms are closely related to the onset of asthma, and the gene expression of the Fok I, Bsm I, Apa I, and Taq I loci directly affects the incidence of asthma.
大量研究报道了与哮喘相关的遗传因素。近年来,维生素 D 受体(VDR)被确定为哮喘易感基因之一,与哮喘的发病机制密切相关。
从中文和英文数据库中检索与哮喘和 VDR 相关的随机对照试验(RCT)。使用以下关键词作为搜索词:“哮喘”、“维生素 D 受体”、“VDR”、“多态性”和“突变”。使用 Cochrane 系统提供的 RevMan 5.3 和 Stata 13 软件进行 Meta 分析。
共有 7 项 RCT 纳入本 Meta 分析,其中 6 项描述了正确的随机分配方法,6 项详细描述了分配方案,4 项采用了盲法。VDR 基因 Apa I 位点 CC+CA 显性基因型和 Bsm I 位点 GG+GA 基因型频率在哮喘患者中明显高于对照组健康患者[比值比(OR)=0.81,95%置信区间(CI):0.68 至 0.98,P=0.03<0.05;OR=2.05,95%CI:1.23 至 3.41,P=0.006<0.05]。VDR 基因 Fok I 位点 CC、CT 和 TT 基因型频率在实验组和 Taq I 位点 CC、CT 和 TT 基因型频率在对照组之间无显著差异(P>0.05)。基因型频率无显著差异。
Meta 分析证实 VDR 基因多态性与哮喘发病密切相关,Fok I、Bsm I、Apa I 和 Taq I 位点的基因表达直接影响哮喘的发病。