ObjectivesInfection with hepatitis C virus (HCV) is a major cause of chronic liver disease. High HCV RNA levels have been associated with poor treatment response. This study aimed to examine the natural history of HCV RNA in chronically HCV/HIV-coinfected individuals.
MethodsMixed models were used to analyse the natural history of HCV RNA changes over time in HIV-positive patients with chronic HCV infection.
ResultsA total of 1541 individuals, predominantly White (91%), male (73%), from southern (35%) and western central Europe (23%) and with HCV genotype 1 (58%), were included in the analysis. The median follow-up time was 5.0 years [interquartile range (IQR) 2.8 to 8.3 years]. Among patients not on combination antiretroviral therapy (cART), HCV RNA levels increased by a mean 27.6% per year [95% confidence interval (CI) 6.1-53.5%; P = 0.0098]. Among patients receiving cART, HCV RNA levels were stable, increasing by a mean 2.6% per year (95% CI -1.1 to 6.5%; P = 0.17). Baseline HCV RNA levels were 25.5% higher (95% CI 8.8 to 39.1%; P = 0.0044) in individuals with HCV genotype 1 compared with HCV genotypes 2, 3 and 4. A 1 log HIV-1 RNA copies/mL increase in HIV RNA was associated with a 10.9% increase (95% CI 2.3 to 20.2%; P = 0.012) in HCV RNA.
ConclusionsWhile HCV RNA levels increased significantly in patients prior to receiving cART, among those treated with cART HCV RNA levels remained stable over time.Key words: combination antiretroviral therapy, hepatitis C virus, hepatitis C virus RNA, HIV, viraemia Accepted 11 February 2013
IntroductionOf the 35 million people currently living with HIV worldwide, approximately 20% have chronic hepatitis C virus (HCV) infection [1][2][3]. Coinfection with HCV is one of the most clinically important comorbidities in the HIVinfected population [1][2][3]. In recent years, mortality rates attributable to HIV infection have decreased as a result of
ORIGINAL RESEARCH 370antiretroviral therapy [4][5][6]. As a result, end-stage liver disease has assumed increasing importance as a cause of death among the coinfected population [4][5][6]. This is especially true for injecting drug users (IDUs), in whom HCV coinfection is common as a result of shared transmission routes [2,4]. Anti-HCV antibody (HCVAb) positivity has been associated with a higher rate of any-cause death and liver-related death [6][7][8][9][10], while plasma HCV RNA, along with HCV genotype and the interleukin (IL)-28B gene variant, has been shown to be one of the most important predictors of sustained virological response (SVR) to pegylated Interferon (peg-IFN) and ribavirin (RBV) in coinfected individuals [1,4,[11][12][13]. Furthermore, it has been reported that an HCV RNA measurement taken early after HIV seroconversion can predict progression to AIDS and death in individuals with high HCV viral loads [14]. Although HCV RNA has been reported to stay relatively stable over time in monoinfected individuals [4,15,16], the course of HCV RNA in coinfected individuals is less well characterized [4,17].The aim of th...