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首页> 外文期刊>Annals of epidemiology >Sexual activity and Kaposi's sarcoma among human immunodeficiency virus type 1 and human herpesvirus type 8-coinfected men.
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Sexual activity and Kaposi's sarcoma among human immunodeficiency virus type 1 and human herpesvirus type 8-coinfected men.

机译:人类免疫缺陷病毒1型和人类疱疹病毒8型合并感染的男性中的性活动和卡波济肉瘤。

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摘要

PURPOSE: There is notable heterogeneity in the progression to Kaposi's sarcoma (KS) among men coinfected with HIV-1 and human herpesvirus type 8 (HHV-8); additional determinants of KS likely exist. Here, we explore sexual activity as a proxy for a sexually transmitted determinant beyond HIV-1 and HHV-8. METHODS: The association between sexual activity and incident KS was estimated with data from 1354 HIV-1- and HHV-8-coinfected homosexual men who were followed for up to 10 years in the Multicenter AIDS Cohort Study. RESULTS: As expected, white race, low CD4 cell count, and the acquisition of HHV-8 after HIV-1 infection increased, whereas smoking decreased, the hazard of KS. The unadjusted hazard of KS among those with high sexual activity was 0.68 relative to the hazard of those with low sexual activity (95% confidence interval, 0.49-0.93) and was somewhat muted after adjustment for characteristics measured at study entry (i.e., race, smoking, CD4 cell count, infection order, history of sexual activity, and sexually transmitted diseases). However, adjustment for time-varying covariates, particularly CD4 cell count, resulted in a nullification of the association (adjusted hazard ratio = 1.06; 95% confidence interval, 0.77-1.48). CONCLUSION: Once HIV-1 and HHV-8 coinfection is established in homosexual men, progression to KS does not appear to be caused by a third pathogen transmitted by sexual activity.
机译:目的:在感染了HIV-1和人类疱疹病毒8型(HHV-8)的男性中,向卡波西氏肉瘤(KS)进展的过程中存在明显的异质性; KS的其他决定因素可能存在。在这里,我们将探讨性活动,以替代HIV-1和HHV-8以外的性传播决定因素。方法:根据多中心艾滋病队列研究中随访了长达10年的1354名HIV-1-和HHV-8合并感染同性恋男子的数据,估计了性活动与KS事件之间的相关性。结果:正如预期的那样,白人族裔,CD4细胞计数低和HIV-1感染后HHV-8的获得增加,而吸烟减少,这是KS的危害。相对于那些性活动量少的人(KS,95%的置信区间,0.49-0.93),那些具有较高性行为的人的未调整的KS危险为0.68,在调整了进入研究时所测得的特征(即种族,吸烟,CD4细胞计数,感染顺序,性活动史和性传播疾病)。但是,对随时间变化的协变量(尤其是CD4细胞计数)进行调整会导致关联无效(调整后的风险比= 1.06; 95%置信区间为0.77-1.48)。结论:一旦在同性恋男性中确立了HIV-1和HHV-8合并感染,向KS的发展似乎并不是由性活动传播的第三种病原体引起的。

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