CC趋化因子受体5型(CCR5)基因rs333多态性与免疫疾病的关系:来自荟萃分析的数据

F. Silva, Post Graduation Program in Basic, A. Leal, R. Koga, E. Alves, J. Lira, Humbelina Alves da Silva, K. Ayala, Paulo Roberto Carneiro Gomes, A. C. T. C. Pereira, D. Vasconcelos
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引用次数: 1

摘要

引言:炎症性肠病(IBD)、牙周炎和系统性红斑狼疮(SLE)是多因素疾病,CC趋化因子受体5型(CCR5)基因rs333多态性是导致这些疾病发生的因素之一。然而,结果仍然是矛盾的。因此,我们旨在进行荟萃分析,评估这种多态性与上述条件之间的关系。材料和方法:在不同的科学和医学数据库中搜索2020年6月22日之前发表的研究。从研究中提取数据,并通过计算统计异质性(I²)、95%置信区间(CI)的比值比(OR)和发表偏倚进行统计评估。在所有计算中,P<0.05的值被认为是显著的。结果:纳入19篇文章,21项病例/对照研究,涉及4304名病例患者和3492名对照。荟萃分析显示,在等位基因模型或任何其他计算中,rs333多态性与IBD(OR=1.05,95%CI:0.91-1.20,P=0.51)、牙周炎(OR=0.86,95%CI:0.64-1.17,P=0.34)或SLE(OR=1.00,95%CI:0.56-1.80,P=1.00)之间无显著相关性。分析中没有明显的发表偏倚。结论:总之,目前的荟萃分析证明rs333多态性与IBD、牙周炎或SLE的风险之间没有显著关系。需要进一步的研究来验证我们的数据。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Relationship between the rs333 Polymorphism in the CC Chemokine Receptor Type Five (CCR5) Gene and Immunological Disorders: Data from a Meta-Analysis
Introduction: Inflammatory Bowel Disease (IBD), periodontitis and Systemic Lupus Erythematous (SLE) are multifactorial diseases, one of the factors in the course of these diseases is the rs333 polymorphism in the CC chemokine receptor type five (CCR5) gene. However, the results remain contradictory. Therefore, we aimed to perform a meta-analysis evaluating the relation between this polymorphism and the aforementioned conditions. Material and Methods: A search in the literature was performed in diverse scientific and medical databases for studies published before June 22, 2020. The data were extracted from the studies and the statistical evaluation was performed by the calculations of statistical heterogeneity (I²), Odds Ratio (OR) with 95% of Confidence Intervals (CI) and publication bias. The values of P<0.05 were considered as significant for all calculations. Results: 19 articles with 21 case/control studies in 4,304 case patients and 3,492 controls were included. The meta-analysis showed a non-significant association among the rs333 polymorphism and IBD (OR = 1.05, 95% CI: 0.91-1.20, P = 0.51), periodontitis (OR = 0.86, 95% CI: 0.64-1.17, P = 0.34) or SLE (OR = 1.00, 95% CI: 0.56-1.80, P = 1.00) under the allelic model or for any other performed calculation. There were no obvious publication bias in the analyses. Conclusion: In conclusion, this current meta-analysis evidenced the non-significant relation among the rs333 polymorphism and the risk of IBD, periodontitis or SLE. Further studies are required to validate our data.
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