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首页> 外文期刊>Hematology >The relationship between interferon-gamma (INF-γ) single nucleotide polymorphism +874(T/A) and occurrence risk of aplastic anemia: a meta-analysis
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The relationship between interferon-gamma (INF-γ) single nucleotide polymorphism +874(T/A) and occurrence risk of aplastic anemia: a meta-analysis

机译:干扰素 - γ(INF-γ)单核苷酸多态性+874(T / A)与血栓性贫血的发生风险:META分析

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div class="hlFld-Abstract test" Objective: This meta-analysis was designed to investigate the association between interferon-gamma (IFN-γ) polymorphisms and occurrence risk of aplastic anemia. Methods: Literature search was conducted in PubMed, Embase and Cochrane Library up to April 2018. The pooled odds ratios (ORs) and 95% confidence interval (CI) were calculated by R 3.12. Results: Total five studies with 304 aplastic anemia patients and 588 controls were included. The statistically significant results were found in the following models: allele genetic model (T vs A: OR?=?2.1749, 95% CI?=?1.6825–2.8114, P ?0.01), additive genetic model (TA vs AA: OR?=?2.1071, 95% CI?=?1.3962–3.1799, P ?0.01; TT vs AA: OR?=?4.5788, 95% CI?=?2.6606–7.8797, P ?0.01), recessive genetic model (TT vs AA?+?TA: OR?=?2.5579, 95%?=?1.6680–3.9226, P ?0.01), dominant genetic model (TT?+?TA vs AA: OR?=?2.5599, 95%?=?1.7424–3.7611, P ?0.01), the results suggested that the increased occurrence risk of aplastic anemia is significantly associated with the IFN-γ polymorphism. Conclusions: Patients with IFN-γ genotype carrying allele T have higher occurrence risk of aplastic anemia.
机译:DIV类=“HLFLD-摘要测试”>目的:该元分析旨在探讨干扰素-γ(IFN-γ)多态性与营养性贫血的发生风险。方法:在2018年4月,在PubMed,Embase和Cochrane图书馆进行文献搜索。通过R 3.12计算汇集的赔率比(ORS)和95%置信区间(CI)。结果:包括304例血栓性贫血患者的五项研究,包括588例。在以下模型中发现了统计学上显着的结果:等位基因遗传模型(T VS A:或?= 2.1249,95%CI?=?1.6825-2.8114,P <0.01),添加遗传模型(TA VS AA:或?=?2.1071,95%ci?=?1.3962-3.1799,p <0.01; tt vs aa:或?= 4.5788,95%ci?=?2.6606-7.8797,p <0.01),隐性遗传模型( tt vs aa?+?ta:或?=?2.5579,95%?=?1.6680-3.9226,p <0.01),显性遗传模型(tt?+?ta vs vs aa:或?=?2.5599,95%? =?1.7424-3.7611,P <0.01),结果表明,增强血症的发生风险增加与IFN-γ多态性显着相关。结论:IFN-γ基因型携带等位基因T的患者具有较高的血糖性贫血的出现风险。

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