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肿瘤坏死因子-α -308多态性与登革热感染的关联:一项系统评价和荟萃分析

Associations of tumor necrosis factor-α-308 polymorphism with dengue infection: A systematic review and meta-analysis.

作者信息

Pabalan Noel, Chaisri Suwit, Tabunhan Sompong, Tarasuk Mayuri, Jarjanazi Hamdi, Steiner Theodore

机构信息

Chulabhorn International College of Medicine, Thammasat University, Pathum Thani, Thailand.

Chulabhorn International College of Medicine, Thammasat University, Pathum Thani, Thailand.

出版信息

Acta Trop. 2017 Sep;173:17-22. doi: 10.1016/j.actatropica.2017.05.007. Epub 2017 May 8.

DOI:10.1016/j.actatropica.2017.05.007
PMID:28495402
Abstract

Inconsistency of reported associations between the tumor necrosis factor-alpha-308 (TNFα-308) polymorphism (rs1800629) and dengue virus infection prompted a meta-analysis, to obtain more precise estimates. A literature search yielded 14 case-control studies. We calculated pooled odds ratios (OR) and 95% confidence intervals in three groups according to severity, dengue fever (DF), dengue hemorrhagic fever (DHF) and dengue (DEN) using standard genetic models. Pooled ORs were subjected to modifier treatment where re-analysis was confined to Hardy-Weinberg compliant (HWC) studies. Heterogeneity of outcomes warranted examining their sources with outlier treatment. In subgroup analysis, we compared Asian and South/Central American (SCA)/Brazilian effects. Overall pooled outcomes yielded no significant effects (OR 0.66-1.44, P=0.08-0.96). In the dominant-codominant model, pooled effects were heterogeneous (I=47%-71%) which was lost/reduced (I=0%-43%) when outlier treatment was applied. This also yielded significant associations (OR 0.68-0.77, P=0.02-0.05). Our results are best seen in the Asian subgroup, which in itself already yielded significant effects in DEN (OR 0.62-0.67, P=0.01-0.02). These reduced risk findings were significant from the tests of interaction (P=0.001-0.02) which highlights the protective effects of TNFα-308 among Asians. TNFα-308 effects on dengue are based on significance and non-heterogeneity of the post-outlier outcomes in the dominant and codominant models. Here, pooled effects may also be ethnic specific, where Asians are protected but not SCA. Both modified and Asian effects are up to 38% protective.

摘要

肿瘤坏死因子-α-308(TNFα-308)基因多态性(rs1800629)与登革病毒感染之间已报道关联的不一致性促使进行一项荟萃分析,以获得更精确的估计值。文献检索得到14项病例对照研究。我们根据严重程度将其分为三组,即登革热(DF)、登革出血热(DHF)和登革热(DEN),使用标准遗传模型计算合并优势比(OR)和95%置信区间。合并的OR值进行了修正处理,重新分析仅限于符合哈迪-温伯格平衡(HWC)的研究。结果的异质性需要通过异常值处理来检查其来源。在亚组分析中,我们比较了亚洲和南美洲/中美洲(SCA)/巴西的效应。总体合并结果未产生显著效应(OR 0.66 - 1.44,P = 0.08 - 0.96)。在显性-共显性模型中,合并效应具有异质性(I = 47% - 71%),应用异常值处理后这种异质性消失/降低(I = 0% - 43%)。这也产生了显著关联(OR 0.68 - 0.77,P = 0.02 - 0.05)。我们的结果在亚洲亚组中最为明显,亚洲亚组本身在登革热(DEN)中已产生显著效应(OR 0.62 - 0.67,P = 0.01 - 0.02)。这些风险降低的发现从交互作用检验中具有显著性(P = 0.001 - 0.02),这突出了TNFα-308在亚洲人中的保护作用。TNFα-308对登革热的影响基于显性和共显性模型中异常值处理后的结果的显著性和非异质性。在此,合并效应也可能具有种族特异性,亚洲人受到保护而南美洲/中美洲人则不然。修正效应和亚洲效应的保护作用均高达38%。

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TNFA -308G>A and IL10 -1082A>G polymorphisms seem to be predictive biomarkers of chronic HCV infection.肿瘤坏死因子-α -308G>A 和白细胞介素 10-1082A>G 多态性似乎是慢性 HCV 感染的预测生物标志物。
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Association of tumour necrosis factor-α (TNF-α) gene polymorphisms (-308 G>A and -238 G>A) and the risk of severe dengue: A meta-analysis and trial sequential analysis.肿瘤坏死因子-α(TNF-α)基因多态性(-308 G>A 和 -238 G>A)与重症登革热风险的关联:Meta 分析和试验序贯分析。
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