Chronic hepatitis C virus infection and subsequent HIV viral load among women with HIV initiating antiretroviral therapy

被引:1
作者
Willis, Sarah J. [1 ]
Cole, Stephen R. [1 ]
Westreich, Daniel [1 ]
Edmonds, Andrew [1 ]
Hurt, Christopher B. [2 ]
Albrecht, Svenja [3 ]
Anastos, Kathryn [4 ,5 ]
Augenbraun, Michael [6 ]
Fischl, Margaret [7 ]
French, Audrey L. [8 ]
Kalapila, Aley G. [9 ]
Karim, Roksana [10 ]
Peters, Marion G. [11 ]
Plankey, Michael [12 ]
Seaberg, Eric C. [13 ]
Tien, Phyllis C. [11 ]
Adimora, Adaora A. [1 ,2 ]
机构
[1] Univ N Carolina, Gillings Sch Global Publ Hlth, Dept Epidemiol, 135 Dauer Dr,Suite 2101,McGavran Greenberg Hall, Chapel Hill, NC 27599 USA
[2] Univ N Carolina, Inst Global Hlth & Infect Dis, Chapel Hill, NC USA
[3] Univ Mississippi, Med Ctr, Div Infect Dis, Jackson, MS 39216 USA
[4] Albert Einstein Coll Med, Dept Med, Bronx, NY 10467 USA
[5] Montefiore Med Ctr, 111 E 210th St, Bronx, NY 10467 USA
[6] Suny Downstate Med Ctr, Dept Med, Brooklyn, NY 11203 USA
[7] Univ Miami, Miller Sch Med, Miami, FL 33136 USA
[8] John H Stroger Jr Hosp Cook Cty, Div Infect Dis, Chicago, IL USA
[9] Emory Univ, Sch Med, Div Infect Dis, Atlanta, GA USA
[10] Univ Southern Calif, Keck Sch Med, Dept Prevent Med, Los Angeles, CA 90033 USA
[11] Univ Calif San Francisco, Dept Med, San Francisco, CA USA
[12] Georgetown Univ, Med Ctr, Dept Med, Div Infect Dis, Washington, DC 20007 USA
[13] Johns Hopkins Univ, Bloomberg Sch Publ Hlth, Dept Epidemiol, Baltimore, MD USA
基金
美国国家卫生研究院;
关键词
antiretroviral therapy; hepatitis C virus coinfection; hepatitis C virus; HIV infection; viral load; women; HUMAN-IMMUNODEFICIENCY-VIRUS; COINFECTION; IMPACT; HCV; PROGRESSION; FIBROSIS; SEX; HEPATOTOXICITY; INDIVIDUALS; PREVALENCE;
D O I
10.1097/QAD.0000000000001745
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Objectives:One in four persons living with HIV is coinfected with hepatitis C virus (HCV). Biological and behavioral mechanisms may increase HIV viral load among coinfected persons. Therefore, we estimated the longitudinal effect of chronic HCV on HIV suppression after ART initiation among women with HIV (WWH).Design:HIV RNA was measured every 6 months among 441 WWH in the Women's Interagency HIV Study who initiated ART from 2000 to 2015.Methods:Log-binomial regression models were used to compare the proportion of study visits with detectable HIV RNA between women with and without chronic HCV. Robust sandwich variance estimators accounted for within-person correlation induced by repeated HIV RNA measurements during follow-up. We controlled for confounding and selection bias (because of loss to follow-up and death) using inverse probability-of-exposure-and-censoring weights.Results:One hundred and fourteen women (25%) had chronic HCV before ART initiation. Overall, the proportion of visits with detectable HIV RNA was similar among women with and without chronic HCV [relative risk (RR) 1.19 (95% CI 0.72, 1.95)]. Six months after ART initiation, the proportion of visits with detectable HIV RNA among women with chronic HCV was 1.88 (95% CI 1.41-2.51) times that among women without HCV, at 2 years, the ratio was 1.60 (95% CI 1.17-2.19), and by 6 years there was no difference (1.03; 95% CI 0.60-1.79).Conclusion:Chronic HCV may negatively impact early HIV viral response to ART. These findings reaffirm the need to test persons with HIV for HCV infection, and increase engagement in HIV care and access to HCV treatment among persons with HIV/HCV coinfection.
引用
收藏
页码:653 / 661
页数:9
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