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

Causal pathways of the effects of age and the CCR5-Delta32, CCR2-64I, and SDF-1 3'A alleles on AIDS development.

作者信息

Geskus Ronald B, Meyer Laurence, Hubert Jean-Baptiste, Schuitemaker Hanneke, Berkhout Ben, Rouzioux Christine, Theodorou Ioannis D, Delfraissy Jean-François, Prins Maria, Coutinho Roel A

机构信息

Municipal Health Service, Amsterdam, The Netherlands and Leiden University Medical Center, The Netherlands.

出版信息

J Acquir Immune Defic Syndr. 2005 Jul 1;39(3):321-6. doi: 10.1097/01.qai.0000142017.25897.06.

Abstract

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.

摘要

目的

研究年龄以及CCR5 - Delta32、CCR2 - 64I和SDF - 1 3'A等位基因影响艾滋病进展的因果途径。

设计

对两项队列研究中同性恋男性(n = 400)的随访数据进行分析,随访时间超过10年。

方法

在随机效应模型中对血清转化后这4种辅助因子对CD4和HIV - 1 RNA轨迹的影响进行建模。使用比例风险模型在校正CD4细胞计数和RNA水平后研究它们对艾滋病风险的影响。这种方法可以研究它们是通过影响CD4计数和RNA水平还是通过其他途径影响艾滋病进展。

结果

年龄较小或携带CCR2 - 64I或SDF - 1 3'A突变的人CD4水平显著更高。携带CCR5 - Delta32缺失或CCR2 - 64I突变的人RNA水平显著更低。在校正CD4计数和RNA水平后,只有SDF - 1 3'A突变显著增加艾滋病风险。

结论

年龄以及CCR5 - Delta32缺失和CCR2 - 64I突变通过影响CD4和HIV - 1 RNA来影响艾滋病进展。SDF - 1 3'A等位基因增加艾滋病风险,但其对CD4和HIV - 1 RNA水平的影响抵消了这种作用。

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