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维生素 D 结合蛋白(DBP)基因多态性(rs7041 和 rs4588)与多发性硬化症和 1 型糖尿病无关:一项荟萃分析。

No association between the vitamin D-binding protein (DBP) gene polymorphisms (rs7041 and rs4588) and multiple sclerosis and type 1 diabetes mellitus: A meta-analysis.

机构信息

Department of Neurology, Shenyang First People's Hospital, Shenyang, Liaoning Province, China.

Department of Nerve Function, Shengjing Hospital of China Medical University, Shenyang, Liaoning Province, China.

出版信息

PLoS One. 2020 Nov 12;15(11):e0242256. doi: 10.1371/journal.pone.0242256. eCollection 2020.

Abstract

BACKGROUND

The association between polymorphisms in vitamin D-binding protein (DBP) gene and the risk of multiple sclerosis (MS) and type 1 diabetes mellitus (T1DM) has been investigated in many studies, but the studies showed controversial results. The rationale for this meta-analysis was to determine whether DBP polymorphisms increases the risk of MS and T1DM by pooling data.

METHODS

Potentially relevant studies were searched using GWAS Catalog, PubMed, Embase, CNKI and WANFANG databases up to November 2019. The pooled odds ratios (ORs) and corresponding 95% confidence intervals (CIs) were performed to estimate the associations in a fixed-effects or random-effects model.

RESULTS

A total of 13 studies were enrolled in this meta-analysis, including eight studies for MS and five for T1DM. The overall results showed that there was no significant association of DBP rs7041 and rs4588 polymorphisms with the risk of MS and T1DM under any genetic model. Similarly, subgroup analysis by ethnicity revealed that no significant association of rs7041 and rs4588 polymorphisms with the risk of MS and T1DM was observed in white or non-white racial groups.

CONCLUSIONS

This meta-analysis provides evidence that DBP rs7041 and rs4588 polymorphisms may not be associated with an increased risk in MS and T1DM. However, these findings need further validation by larger-scale epidemiological studies and genome-wide association studies (GWASs) in different populations.

摘要

背景

维生素 D 结合蛋白(DBP)基因多态性与多发性硬化症(MS)和 1 型糖尿病(T1DM)的风险之间的关联已在许多研究中进行了探讨,但研究结果存在争议。进行这项荟萃分析的基本原理是通过汇总数据来确定 DBP 多态性是否会增加 MS 和 T1DM 的风险。

方法

使用 GWAS 目录、PubMed、Embase、中国知网和万方数据库检索了截至 2019 年 11 月的潜在相关研究。使用固定效应或随机效应模型进行荟萃分析,以评估关联的合并优势比(OR)和相应的 95%置信区间(CI)。

结果

共有 13 项研究纳入了这项荟萃分析,其中 8 项研究针对 MS,5 项研究针对 T1DM。总体结果表明,DBP rs7041 和 rs4588 多态性与 MS 和 T1DM 的风险之间没有显著的关联,无论是在任何遗传模型下。同样,按种族进行的亚组分析表明,rs7041 和 rs4588 多态性与 MS 和 T1DM 的风险之间也没有明显的关联,无论是在白种人或非白种人群中。

结论

这项荟萃分析提供的证据表明,DBP rs7041 和 rs4588 多态性可能与 MS 和 T1DM 的风险增加无关。然而,这些发现需要在不同人群中进行更大规模的流行病学研究和全基因组关联研究(GWAS)来进一步验证。

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