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TNF-α 基因启动子多态性与乙型肝炎病毒感染结局的关系:荟萃分析。

Relationship between TNF-<alpha> gene promoter polymorphisms and outcomes of hepatitis B virus infections: a meta-analysis.

机构信息

State Key Laboratory of Infectious Disease Diagnosis and Treatment, College of Medicine, First Affiliated Hospital, Zhejiang University, Zhejiang, China.

出版信息

PLoS One. 2011 May 10;6(5):e19606. doi: 10.1371/journal.pone.0019606.

Abstract

BACKGROUND

The clearance of hepatitis B virus (HBV) is a complex process which may be influenced by many factors including polymorphisms in the tumor necrosis factor (TNF-) gene promoter. However, previous reports regarding the relationship between polymorphisms in the TNF- promoter and HBV clearance have been inconsistent. Therefore, we performed a meta-analysis on a large population to address this inconsistency.

METHODS

A meta-analysis was performed to examine the association between TNF- promoter polymorphisms (-1031T/C, -863C/A, -857C/T, -308G/A and-238G/A) and chronic hepatitis B infection. Odds ratio (OR) and its 95 % confidence interval (CI) were used.

RESULTS

Twelve studies were chosen in our meta-analysis, involving 2,754 chronic HBV infection cases and 1,630 HBV clearance cases. The data showed that TNF--863 CC genotype was significantly associated with HBV clearance (-863 CC vs. AA: OR, 0.64; 95% CI, [0.42, 0.97]; p = 0.04) while patients carrying -308 GG genotype had a significantly increased risk of HBV persistence compared with those with GA or AA genotype (GG vs. GA+AA: OR, 1.35; 95% CI, [1.08, 1.70]; p = 0.01). For the other polymorphisms, no association with HBV infection outcome was found.

CONCLUSIONS

The data showed that polymorphisms -863 A and -308 G in the TNF- gene promoter region might be risk factors for HBV persistence. Furthermore, ethnicity might play an important role in HBV infection outcome, leading to conflicting results. More studies on individuals from various ethnic groups will be necessary to determine the role of TNF- promoter polymorphisms in the outcome of HBV infection.

摘要

背景

乙型肝炎病毒(HBV)的清除是一个复杂的过程,可能受到许多因素的影响,包括肿瘤坏死因子-α(TNF-α)基因启动子多态性。然而,先前关于 TNF-α 启动子多态性与 HBV 清除之间关系的报告并不一致。因此,我们对大量人群进行了荟萃分析以解决这一不一致性。

方法

进行荟萃分析以检查 TNF-α 启动子多态性(-1031T/C、-863C/A、-857C/T、-308G/A 和-238G/A)与慢性乙型肝炎感染之间的关联。使用比值比(OR)及其 95%置信区间(CI)。

结果

荟萃分析共纳入 12 项研究,涉及 2754 例慢性 HBV 感染病例和 1630 例 HBV 清除病例。数据显示,TNF-α-863 CC 基因型与 HBV 清除显著相关(-863 CC 与 AA:OR,0.64;95%CI,[0.42,0.97];p=0.04),而携带-308 GG 基因型的患者与 GA 或 AA 基因型相比,HBV 持续存在的风险显著增加(GG 与 GA+AA:OR,1.35;95%CI,[1.08,1.70];p=0.01)。对于其他多态性,与 HBV 感染结果无关联。

结论

数据表明 TNF-α 基因启动子区域的多态性-863 A 和-308 G 可能是 HBV 持续存在的危险因素。此外,种族可能在 HBV 感染结果中起重要作用,导致结果相互矛盾。需要对来自不同种族的个体进行更多的研究,以确定 TNF-α 启动子多态性在 HBV 感染结果中的作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b837/3091871/faca23441ab0/pone.0019606.g001.jpg

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