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首页> 外文期刊>JAIDS: Journal of acquired immune deficiency syndromes >Causal pathways of the effects of age and the CCR5-Delta32, CCR2-64I, and SDF-1 3'A alleles on AIDS development.
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Causal pathways of the effects of age and the CCR5-Delta32, CCR2-64I, and SDF-1 3'A alleles on AIDS development.

机译:年龄以及CCR5-Delta32,CCR2-64I和SDF-1 3'A等位基因对艾滋病发展的影响的因果途径。

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摘要

OBJECTIVE: To investigate the causal pathways by which age and the CCR5-Delta32, CCR2-64I, and SDF-1 3'A alleles influence progression to AIDS. DESIGN: Analysis of follow-up data from 2 cohort studies among homosexual men (n=400), having >10 years of follow-up. METHODS: The effects of the 4 cofactors on the CD4 and HIV-1 RNA trajectories after seroconversion were modeled in a random-effects model. A proportional hazards model was used to investigate their effect on the risk of AIDS after correction for CD4 cell count and RNA level. This approach allows investigation as to whether they influence AIDS progression by affecting CD4 count and RNA level or by other pathways. RESULTS: Persons of younger age or having the CCR2-64I or SDF-1 3'A mutation have significantly higher CD4 levels. Persons with the CCR5-Delta32 deletion or CCR2-64I mutation have significantly lower RNA levels. After correction for both CD4 count and RNA level, only the SDF-1 3'A mutation significantly increases the AIDS risk. CONCLUSIONS: Age and the CCR5-Delta32 deletion and CCR2-64I mutation influence AIDS progression by affecting CD4 and HIV-1 RNA. The SDF-1 3'A allele increases the AIDS risk, but this effect is countered by its effect on CD4 and HIV-1 RNA level.
机译:目的:探讨年龄和CCR5-Delta32,CCR2-64I和SDF-1 3'A等位基因影响艾滋病进展的原因。设计:对两项随访超过10年的同性恋者(n = 400)进行的队列研究分析。方法:在随机效应模型中,模拟了血清转化后这4种辅助因子对CD4和HIV-1 RNA轨迹的影响。在校正CD4细胞计数和RNA水平后,使用比例风险模型研究其对艾滋病风险的影响。这种方法可以研究它们是否通过影响CD4计数和RNA水平或通过其他途径影响艾滋病的进展。结果:年龄较小或患有CCR2-64I或SDF-1 3'A突变的人的CD4水平明显升高。具有CCR5-Delta32缺失或CCR2-64I突变的人的RNA水平明显降低。校正CD4计数和RNA水平后,仅SDF-1 3'A突变会显着增加AIDS风险。结论:年龄和CCR5-Delta32缺失和CCR2-64I突变通过影响CD4和HIV-1 RNA影响艾滋病的进展。 SDF-1 3'A等位基因会增加AIDS的风险,但是这种作用被其对CD4和HIV-1 RNA水平的影响所抵消。

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