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干扰素诱导跨膜蛋白 3 基因多态性与 COVID-19 易感性和严重程度相关:一项荟萃分析。

Interferon-induced transmembrane protein 3 gene polymorphisms are associated with COVID-19 susceptibility and severity: A meta-analysis.

机构信息

Rehabilitation Therapy Center, Luoyang Orthopedic Hospital of Henan Province, Orthopedic Hospital of Henan Province, Luoyang, China.

Inspection and Monitoring Center, Luoyang Center for Disease Control and Prevention, Luoyang, China.

出版信息

J Infect. 2022 Jun;84(6):825-833. doi: 10.1016/j.jinf.2022.04.029. Epub 2022 Apr 21.

Abstract

BACKGROUND

Recent evidence has linked the interferon-induced transmembrane protein 3 gene (IFITM3) to coronavirus disease 2019 (COVID-19) outcomes, but the results are inconsistent. The purpose of this meta-analysis was to evaluate the association of IFITM3 gene polymorphisms with COVID-19 susceptibility and severity.

METHOD

A systematic search was performed with PubMed, Web of Science, Cochrane Library, and Embase from the date of inception to 20 December 2021. The results were analyzed with pooled odds ratios (ORs) and 95% confidence intervals (95% CIs). The robustness was performed using the method of sequential removal for each trial.

RESULTS

Four studies involving 1989 subjects were included, from which 1114 patients were positive for COVID-19. For IFITM3 rs12252, the pooled OR showed that there was a significant association between the genotype frequencies and infection with COVID-19 in any of the gene models, i.e., the allelic model (OR = 1.91, 95% CI, 1.36-2.68), the dominant model (OR = 1.80, 95% CI, 1.27-2.56), the recessive model (OR = 5.67, 95% CI, 1.01-31.77), the heterozygous model (OR = 1.65, 95% CI, 1.16-2.36) and the homozygous model (OR = 5.88, 95% CI, 1.05-32.98). The results stratified by severity showed that there was a significant correlation only between the allelic (OR = 0.69, 95% CI, 0.49-0.97) and recessive (OR = 0.43, 95% CI, 0.20-0.93) models. Our results did not support the associations between the IFITM3 rs34481144 gene polymorphism and COVID-19 susceptibility or severity in any of the gene models.

CONCLUSIONS

The findings indicated that IFITM3 rs12252 gene polymorphisms were associated with COVID-19 susceptibility and that the rs12252-C variant was particularly critical for severity. Genetic factors should be considered in future vaccine development.

摘要

背景

最近的证据表明,干扰素诱导跨膜蛋白 3 基因(IFITM3)与 2019 年冠状病毒病(COVID-19)结局有关,但结果不一致。本荟萃分析的目的是评估 IFITM3 基因多态性与 COVID-19 易感性和严重程度的关系。

方法

从研究开始到 2021 年 12 月 20 日,通过 PubMed、Web of Science、Cochrane Library 和 Embase 进行系统检索。使用合并优势比(OR)和 95%置信区间(95%CI)进行分析。使用逐个试验的逐步剔除法进行稳健性分析。

结果

纳入了四项共涉及 1989 名受试者的研究,其中 1114 名患者 COVID-19 检测呈阳性。对于 IFITM3 rs12252,在任何基因模型中,基因型频率与 COVID-19 感染的相关性均有统计学意义,即等位基因模型(OR=1.91,95%CI,1.36-2.68)、显性模型(OR=1.80,95%CI,1.27-2.56)、隐性模型(OR=5.67,95%CI,1.01-31.77)、杂合模型(OR=1.65,95%CI,1.16-2.36)和纯合模型(OR=5.88,95%CI,1.05-32.98)。按严重程度分层的结果显示,仅在等位基因(OR=0.69,95%CI,0.49-0.97)和隐性(OR=0.43,95%CI,0.20-0.93)模型中存在显著相关性。我们的结果不支持 IFITM3 rs34481144 基因多态性与 COVID-19 易感性或严重程度之间的任何基因模型的关联。

结论

研究结果表明,IFITM3 rs12252 基因多态性与 COVID-19 易感性有关,rs12252-C 变异对严重程度尤其重要。在未来的疫苗开发中应考虑遗传因素。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a825/9022375/a37e076022a5/gr1_lrg.jpg

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