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Session 162 Poster Abstracts
Impact of HBV or HCV on Disease Progression in HIV-Infected Persons
Session Day and Time: Tuesday, 1 - 4 pm
Poster Hall


920    
Hepatitis B Virus Co-infection Affects Baseline HIV Parameters and HAART-related Hepatotoxicity Risk in an HIV-infected Nigerian Cohort
J Idoko1, S Meloni2, M Muazu1, C Hawkins3, B Badung1, N Gwamzi1, P Kanki2, R Murphy3, E Ekong4, and Chloe Thio*5
1Jos Univ Teaching Hosp, Plateau State, Nigeria; 2Harvard Sch of Publ Hlth, Boston, MA, US; 3Northwestern University, Chicago, IL, USA; 4Harvard-PEPFAR Prgm, Lagos, Nigeria; and 5Johns Hopkins Univ, Baltimore, MD, US

Background:  Hepatitis B virus (HBV) co-infection is common in HIV-infected persons, especially in countries with high HBV endemicity. As ART is introduced into such countries, it is imperative to understand how HBV affects HIV and ART-related outcomes. We hypothesized that HBV would increase the risk for ART-related hepatotoxicity and decrease the response to ART.

Methods:  We tested our hypothesis in persons participating in the PEPFAR program in Nigeria who initiated ART with stavudine, lamivudine, and nevirapine and who were negative for HCV antibody. We compared subjects who were co-infected with HBV (HBsAg+) to those who were HIV mono-infected (HBsAg) with regards to HIV parameters and ALT at baseline and after months 3 and 6 of ART. Hepatotoxicity was defined as ALT > 5x the ULN (41 IU/mL) or >3.5x baseline ALT if ALT was above ULN at baseline. Nonparametric tests were used to compare groups for continuous variables and χ2 tests were used for categorical variables.

Results:  Of the 1968 subjects tested, 229 (11.6%) were co-infected with HBV (HIV/HBV), 1170 were mono-infected with HIV (HIV), and the remainder, who were excluded from this study, were HIV/HCV or HIV/HBV/HCV-infected. The mean age was 35 years in both the HIV/HBV and HIV groups. Median CD4 count (cells/mm3) at baseline was lower in the HIV/HBV group compared to the HIV group (99 vs 132, p <0.0001). The baseline HIV RNA was significantly higher in the HIV/HBV group (91,529 copies/mL vs 53,278 copies/mL, p = 0.0001). Despite these differences, the percent of patients with a HIV viral load <400 copies/mL at months 3 or 6 was similar. CD4 counts increased to 220 vs 247 in HIV/HBV vs HIV groups, respectively (p = 0.02), but the number with a CD4 increase >50 did not differ (73% and 70%). For patients with baseline and month 6 ALT, mean baseline ALT was higher in HIV/HBV group (42.9 vs 31.7, p = 0.001). At month 6, the same ALT difference remained and the cumulative hepatotoxicity was higher in the HIV/HBV group (4.3%) compared to the HIV group (0.4%, p = 0.007).

Conclusions:  HBV co-infection is common in HIV-infected persons in Nigeria. Prior to ART, the HIV/HBV group had lower CD4 counts and higher HIV RNA levels, but with 6 months of ART, their immunological and virological responses were not impaired. The ART-related hepatotoxicity rates are low, but are increased in HBV co-infection. Further follow-up is needed to determine longer term effects of HBV on ART response in this cohort.