期刊
EXPERT REVIEW OF CLINICAL IMMUNOLOGY
卷 18, 期 10, 页码 1083-1090出版社
TAYLOR & FRANCIS LTD
DOI: 10.1080/1744666X.2022.2117160
关键词
Tumor necrosis factor-alpha; tumor necrosis factor-beta; meta-analysis; interferon-gamma; polymorphism; multiple sclerosis
类别
资金
- Health Research Talents Project of Jilin Province [2019sc2018, 20201SCI06]
- Project of Development and Reform Commission of Jilin Province
This meta-analysis found a marginally significant association between the IFNG +874AT genotype and high risk of MS, but no significant association between TNFA and TNFB gene polymorphisms and MS risk. Further studies with larger samples are needed for more conclusive results about the contribution of other polymorphisms to the risk of MS.
Background Epidemiological studies about the association between genetic polymorphisms in TNFA, TNFB, and IFNG and the risk for multiple sclerosis (MS) have been performed extensively. However, the results are inconclusive. The purpose of this meta-analysis was to evaluate the contribution of the polymorphisms in TNFA, TNFB, and IFNG to the susceptibility of MS. Methods The PubMed, Web of Science, and China National Knowledge Infrastructure databases were searched to identify relevant studies up to October 2021. A meta-analysis was performed, and pooled odds ratios (OR) and confidence intervals (CI) were computed using fixed or random effects models. Results A marginally significant association of the IFNG +874AT genotype with high risk of MS was observed in a heterozygous comparison (OR = 1.51, 95% CI, 1.02-2.23). However, no significant association between the TNFA (-308 G/A, - 238 G/A, and - 376 G/A) and TNFB +252A/G polymorphisms and MS risk was observed both in overall analysis and in subgroup analysis. Conclusion This meta-analysis provides evidence that the TNFA (-308 G/A, - 238 G/A, and - 376 G/A) and TNFB +252A/G polymorphisms were not risk factors for the occurrence of MS. Further studies with larger samples are necessary to reach the concise results about the contribution of other polymorphisms to the risk of MS.
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