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HCV RNA Levels in a Multi-Ethnic Cohort of Injection Drug Users: Human Genetic Viral and Demographic Associations

机译:HCV RNA水平在多族裔队列的注射药物中:人类遗传病毒和人口统计学协会

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摘要

In patients with chronic hepatitis C, the hepatitis C virus (HCV) RNA level is an important predictor of treatment response. To explore the relationship of HCV RNA with viral and demographic factors, as well as IL28B genotype, we examined viral levels in an ethnically diverse group of injection drug users (IDUs). Between 1998 and 2000, the Urban Health Study (UHS) recruited IDUs from street settings in San Francisco Bay area neighborhoods. Participants who were positive by HCV EIA were tested for HCV viremia by a bDNA assay. HCV genotype was determined by sequencing the HCV NS5B region. For a subset of participants, IL28B rs12979860 genotype was determined by Taqman. Among 1701 participants with HCV viremia, median age was 46 years and median duration of injection drug use was 26 years; 56.0% were African American and 34.0% were of European ancestry (non-Hispanic). HIV-1 prevalence was 13.9%. The overall median HCV RNA level was 6.45 log10 copies/ml. In unadjusted analyses, higher levels were found with older age, male gender, African American ancestry, HBV infection, HIV-1 infection and IL28B rs12979860-CC genotype; compared to participants infected with HCV genotype 1, HCV RNA was lower in participants with genotype 3 or genotype 4. In an adjusted analysis, age, gender, racial ancestry, HIV-1 infection, HCV genotype and IL28B rs12979860 genotype were all independently associated with HCV RNA. Conclusion: The level of HCV viremia is influenced by a large number of demographic, viral and human genetic factors.
机译:在慢性丙型肝炎患者中,丙型肝炎病毒(HCV)RNA水平是治疗反应的重要预测因子。为了探讨HCV RNA与病毒和人口因子的关系,以及IL28B基因型,我们检查了种族多样的注射药物(IDU)中的病毒水平。 1998年至2000年间,城市健康研究(UHS)招募了旧金山湾区街区街道环境的IDU。通过BDNA测定对HCV EIA阳性的参与者进行了HCV病毒血症。通过测序HCV NS5B区域测定HCV基因型。对于参与者的子集,由Taqman确定IL28B RS12979860基因型。在1701名与HCV病毒血症的参与者中,中位年龄为46岁,注射药物使用的中位数为26年; 56.0%是非洲裔美国人,34.0%是欧洲血统(非西班牙语)。 HIV-1患病率为13.9%。整体中位HCV RNA水平为6.45 log10拷贝/ ml。在不调整的分析中,较高的年龄,男性性别,非洲裔美国血统,HBV感染,HIV-1感染和IL28B RS12979860-CC基因型,较高水平。与感染HCV基因型1感染的参与者相比,参与者的参与者在基因型3或基因型4中较低。在调整后的分析,年龄,性别,种族血统,HIV-1感染,HCV基因型和IL28B RS12979860基因型都与之独立相关HCV RNA。结论:HCV病毒血症水平受大量人口统计学,病毒和人类遗传因素的影响。

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