TY - JOUR
T1 - Hepatitis C virus coinfection and HIV load, CD4+ cell percentage, and clinical progression to AIDS or death among HIV-infected women
T2 - Women and infants transmission study
AU - Hershow, Ronald C.
AU - O'Driscoll, Peter T.
AU - Handelsman, Ed
AU - Pitt, Jane
AU - Hillyer, George
AU - Serchuck, Leslie
AU - Lu, Ming
AU - Chen, Katherine T.
AU - Yawetz, Sigal
AU - Pacheco, Susan
AU - Davenny, Katherine
AU - Adeniyi-Jones, Samuel
AU - Thomas, David L.
N1 - Funding Information:
Financial support. National Institute of Allergy and Infectious Diseases, the National Institute of Child Health, and Human Development and the National Institute on Drug Abuse. Study sites received the following financial support: University of Puerto Rico, grant U01 AI 34858; Boston/ Worcester Site, grant 9U01 DA 15054; Columbia Presbyterian Hospital, grant U01 DA 15053; State University of New York, grant U01 HD 36117; University of Illinois at Chicago, grant U01 AI 34841; Baylor College of Medicine, grant U01 HD 41983; Clinical Trials & Surveys, grants N01 AI 85339 and 1 U01 AI 50274-01. Additional support has been provided by local Clinical Research Centers to Baylor College of Medicine (grant NIH GCRC RR00188) and Columbia University (grant NIH GCRC RR00645). Potential conflicts of interest. All authors: no conflicts.
PY - 2005/3/15
Y1 - 2005/3/15
N2 - Background. Despite previous study, it remains unclear whether hepatitis C virus (HCV) coinfection affects the progression of human immunodeficiency virus (HIV) type 1 infection. The Women and Infants Transmission Study provided an opportunity to assess this issue. Methods. Longitudinal data on 652 HIV-1-infected women enrolled in the study before the availability of highly active antiretroviral therapy (HAART; 1989-1995) were analyzed. Random effects models were used to determine whether HCV coinfection was associated with different CD4+ cell percentages and HIV-1 RNA levels over time, and Cox proportional hazards models were used to compare the rates of clinical progression to acquired immunodeficiency syndrome (AIDS) or death. Results. Of 652 women, 190 (29%) were HCV infected. During follow-up, 19% of women were exposed to HAART. After controlling for indicators of disease progression (CD4+ cell percentages and HIV-1 RNA levels determined closest to the time of delivery in pregnant women), ongoing drug use, receipt of antiretroviral therapy, and other important covariates, no differences were detected in the HIV-1 RNA levels, but the CD4+ cell percentages were slightly higher in HCV-infected women than in HCV-uninfected women. During follow-up, 48 women had progression to a first clinical AIDS-defining illness (ADI), and 26 died with no documented antecedent ADI. In multivariable analyses, HCV-infected participants did not have faster progression to a first class C AIDS-defining event or death (relative hazard, 0.75; 95% confidence interval, 0.37-1.53). Conclusions. In this cohort, the rate of clinical progression of HIV-1 infection was not greater for HCV-infected women.
AB - Background. Despite previous study, it remains unclear whether hepatitis C virus (HCV) coinfection affects the progression of human immunodeficiency virus (HIV) type 1 infection. The Women and Infants Transmission Study provided an opportunity to assess this issue. Methods. Longitudinal data on 652 HIV-1-infected women enrolled in the study before the availability of highly active antiretroviral therapy (HAART; 1989-1995) were analyzed. Random effects models were used to determine whether HCV coinfection was associated with different CD4+ cell percentages and HIV-1 RNA levels over time, and Cox proportional hazards models were used to compare the rates of clinical progression to acquired immunodeficiency syndrome (AIDS) or death. Results. Of 652 women, 190 (29%) were HCV infected. During follow-up, 19% of women were exposed to HAART. After controlling for indicators of disease progression (CD4+ cell percentages and HIV-1 RNA levels determined closest to the time of delivery in pregnant women), ongoing drug use, receipt of antiretroviral therapy, and other important covariates, no differences were detected in the HIV-1 RNA levels, but the CD4+ cell percentages were slightly higher in HCV-infected women than in HCV-uninfected women. During follow-up, 48 women had progression to a first clinical AIDS-defining illness (ADI), and 26 died with no documented antecedent ADI. In multivariable analyses, HCV-infected participants did not have faster progression to a first class C AIDS-defining event or death (relative hazard, 0.75; 95% confidence interval, 0.37-1.53). Conclusions. In this cohort, the rate of clinical progression of HIV-1 infection was not greater for HCV-infected women.
UR - http://www.scopus.com/inward/record.url?scp=20144380691&partnerID=8YFLogxK
U2 - 10.1086/428121
DO - 10.1086/428121
M3 - Article
C2 - 15736020
AN - SCOPUS:20144380691
SN - 1058-4838
VL - 40
SP - 859
EP - 867
JO - Clinical Infectious Diseases
JF - Clinical Infectious Diseases
IS - 6
ER -