Liu Yao, Guo Xin, Huang Shao-Yan, Gong Luan, Cui Jin-Hui, Shen Hu-Wei, Ye Xiang-Hua, He Xiao-Feng
Changzhi Medical College, No. 161, JieFangDong Street.
Department of Endocrinology, Heping Hospital Affiliated to Changzhi Medical College, Shanxi, Changzhi city.
Medicine (Baltimore). 2021 Jul 16;100(28):e25934. doi: 10.1097/MD.0000000000025934.
Numerous original studies and 4 published meta-analyses have reported the association between the Vitamin D receptor (VDR) BsmI, FokI, ApaI, and TaqI polymorphisms and type 2 diabetes mellitus (T2DM) risk. However, the results were inconsistent. Therefore, an updated meta-analysis was performed to further explore these issues.To further explore the association between the VDR BsmI, FokI, ApaI, and TaqI polymorphisms and T2DM risk.PubMed, EMBASE, Scopus, and Wanfang databases were searched. The following search strategy were used: (VDR OR vitamin D receptor) AND (polymorphism OR variant OR mutation) AND (diabetes OR mellitus OR diabetes mellitus). Pooled crude odds ratios with 95% confidence intervals were applied to evaluate the strength of association in 5 genetic models. Statistical heterogeneity, the test of publication bias, and sensitivity analysis were carried out using the STATA software (Version 12.0). To evaluate the credibility of statistically significant associations, we applied the false-positive report probabilities (FPRP) and Bayesian false discovery probability (BFDP) test.Overall, the VDR BsmI polymorphism was associated with a significantly decreased T2DM risk in Asians; the VDR FokI polymorphism was associated with a significantly decreased T2DM risk in Asians, African countries, and Asian countries; the VDR ApaI polymorphism was associated with a significantly decreased T2DM risk in Caucasians and North American countries.On the VDR ApaI polymorphism, a significantly increased T2DM risk was found in a mixed population. However, when we further performed a sensitivity analysis, FPRP, and BFDP test, less-credible positive results were identified (all FPRP > 0.2 and BFDP > 0.8) in any significant association.In summary, this study strongly indicates that all significant associations were less credible positive results, rather than from true associations.
众多原创研究及4项已发表的荟萃分析报告了维生素D受体(VDR)的BsmI、FokI、ApaI和TaqI基因多态性与2型糖尿病(T2DM)风险之间的关联。然而,结果并不一致。因此,进行了一项更新的荟萃分析以进一步探究这些问题。为进一步探究VDR的BsmI、FokI、ApaI和TaqI基因多态性与T2DM风险之间的关联。检索了PubMed、EMBASE、Scopus和万方数据库。采用了以下检索策略:(VDR或维生素D受体)与(多态性或变体或突变)与(糖尿病或糖尿病 mellitus)。应用合并的粗比值比及95%置信区间来评估5种遗传模型中的关联强度。使用STATA软件(版本12.0)进行统计异质性、发表偏倚检验和敏感性分析。为评估具有统计学意义的关联的可信度,我们应用了假阳性报告概率(FPRP)和贝叶斯假发现概率(BFDP)检验。总体而言,VDR的BsmI基因多态性与亚洲人T2DM风险显著降低相关;VDR的FokI基因多态性与亚洲、非洲国家及亚洲国家的T2DM风险显著降低相关;VDR的ApaI基因多态性与白种人和北美国家的T2DM风险显著降低相关。在VDR的ApaI基因多态性方面,在混合人群中发现T2DM风险显著增加。然而,当我们进一步进行敏感性分析、FPRP和BFDP检验时,在任何显著关联中均发现可信度较低的阳性结果(所有FPRP>0.2且BFDP>0.8)。总之,本研究强烈表明,所有显著关联均为可信度较低的阳性结果,而非真实关联。