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SDF1(CXCR12)基因多态性与HIV-1感染易感性及艾滋病疾病进展的关联:一项荟萃分析。

Association of gene polymorphism of SDF1(CXCR12) with susceptibility to HIV-1 infection and AIDS disease progression: A meta-analysis.

作者信息

Ding Jiwei, Zhao Jianyuan, Zhou Jinming, Li Xiaoyu, Wu Yanbin, Ge Mei, Cen Shan

机构信息

Institute of Medicinal Biotechnology, Chinese Academy of Medical Sciences and Peking Union Medical School, Beijing, PR China.

School of Pharmacy, Shanghai Jiaotong University, Shanghai, PR China.

出版信息

PLoS One. 2018 Feb 8;13(2):e0191930. doi: 10.1371/journal.pone.0191930. eCollection 2018.

Abstract

OBJECTIVES

Genetic polymorphism of viral receptors is relevant to risks of HIV-1 infection, while it is still under debated whether the polymorphism of SDF1, a unique ligand for HIV-1 coreceptor CXCR4, is associated with HIV susceptibility and AIDS disease progression. Therefore, we provided an updated quantitative assessment by meta-analysis from 16 case-control and 7 cohort studies.

METHODS

Articles reporting the relationship between SDF1 polymorphism and HIV susceptibility or AIDS progression were retrieved from PubMed, Embase and Ovid electronic databases up to Apr 2017. Data were pooled by odds ratios (ORs) for HIV-1 infection with 95% confidence intervals (CIs) and summary relative hazards (RHs) for AIDS progression with 95% CIs using 1987 Center for Disease Control (CDC) case definition of AIDS (CDC87) and 1993 Center for Disease Control (CDC) case definition of AIDS (CDC93) and death as endpoints.

RESULTS

As a result, 16 studies regarding susceptibility to HIV-1 infection with 2803 HIV-infected patients and 3697 healthy individuals and 7 studies regarding disease progression with 4239 subjects were included in the meta-analysis. For risks of infection, no evidences indicated SDF1 polymorphism was associated with the risk of HIV-1 infection in all genetic models (recessive model: OR = 0.94, 95% Cl: 0.75-1.17; homozygous model: OR = 0.89, 95% Cl: 0.70-1.15; heterozygous model: OR = 1.06, 95% Cl: 0.83-1.35; allele model: OR = 0.95, 95% Cl: 0.79-1.13), Furthermore, we failed to find an delayed AIDS progression except in some specific cohorts including MACS cohorts (RH = 0.38, 95% Cl: 0.17-0.59 for time to AIDS; RH = 0.27, 95% Cl: 0.07-0.46 for time to death at the study entry).

CONCLUSIONS

Overall, no significant association was found between SDF1 polymorphism and HIV susceptibility. A protective effect of SDF1 on AIDS progression and death was seen especially in two studies based on the same cohorts. In conclusion, SDF1 polymorphism exerts a moderate protective effect against AIDS disease deterioration in some specific populations.

摘要

目的

病毒受体的基因多态性与HIV-1感染风险相关,而作为HIV-1共受体CXCR4的唯一配体,基质细胞衍生因子1(SDF1)的多态性是否与HIV易感性及艾滋病疾病进展相关仍存在争议。因此,我们通过对16项病例对照研究和7项队列研究进行荟萃分析,提供了最新的定量评估。

方法

从PubMed、Embase和Ovid电子数据库中检索截至2017年4月报道SDF1多态性与HIV易感性或艾滋病进展关系的文章。采用1987年美国疾病控制中心(CDC)艾滋病病例定义(CDC87)和1993年美国疾病控制中心(CDC)艾滋病病例定义(CDC93)以及死亡作为终点,通过比值比(OR)及95%置信区间(CI)汇总HIV-1感染数据,并通过汇总相对风险(RH)及95%CI汇总艾滋病进展数据。

结果

结果,荟萃分析纳入了16项关于HIV-1感染易感性的研究(2803例HIV感染患者和3697名健康个体)以及7项关于疾病进展的研究(4239名受试者)。对于感染风险,在所有遗传模型中均无证据表明SDF1多态性与HIV-1感染风险相关(隐性模型:OR = 0.94,95%CI:0.75 - 1.17;纯合子模型:OR = 0.89,95%CI:0.70 - 1.15;杂合子模型:OR = 1.06,95%CI:0.83 - 1.35;等位基因模型:OR = 0.95,95%CI:0.79 - 1.13)。此外,除了一些特定队列(包括多中心艾滋病队列研究[MACS]队列)外,我们未发现艾滋病进展延迟(研究入组时,至艾滋病发生时间的RH = 0.38,95%CI:0.17 - 0.59;至死亡时间的RH = 0.27,95%CI:0.07 - 0.46)。

结论

总体而言,未发现SDF1多态性与HIV易感性之间存在显著关联。尤其在基于相同队列的两项研究中发现SDF1对艾滋病进展和死亡具有保护作用。总之,SDF1多态性在某些特定人群中对艾滋病疾病恶化具有适度的保护作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0c90/5805253/63cb49a6e827/pone.0191930.g001.jpg

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