921 
Impact of Hepatitis C Virus on HIV-infected Individuals in Nigeria
N Gwamzi1, C Hawkins2, S Meloni3, M Muazu1, B Badung1, R Chung4, P Kanki3, E Ekong5, J Idoko1, and Camilla Graham*6
1Jos Univ Teaching Hosp, Nigeria; 2Northwestern University, Chicago, IL, USA; 3Harvard Sch of Publ Hlth, Boston, MA, US; 4Massachusetts Gen Hosp, Boston, US; 5Military Reference Hosp, Lagos, Nigeria; and 6Beth Israel Deaconess Med Ctr, Boston, MA, US
Background: The impact of hepatitis
C virus (HCV) on HIV-related immune reconstitution and viral control after
initiation of ART is controversial. In North America and Europe,
injection drug use (IDU) is a common route of acquisition for both HIV and HCV and
may also impact HIV control and ART tolerability. We examined a cohort of
ART-naοve, non-IDU patients in Nigeria
to determine the effects of HCV on HIV parameters without IDU as a confounder.
Methods: Patients with HIV
initiating stavudine, lamivudine, and nevirapine were tested for HCV antibody (HCV+)
and hepatitis B surface antigen (HBV+). This study compared subjects
who were HCV+/HBV to those who were HCV/HBV.
Follow-up was for 6 months after ART initiation. Hepatotoxicity was defined as
ALT values 5 times the upper limit of normal (ULN; 41 IU/mL) or 3.5 times
baseline alanine aminotransferase (ALT) if ALT was above ULN at baseline. Nonparametric
tests were used to compare groups.
Results: We tested 1968
subjects for HCV and HBV: 1170 were HCV/HBV
(HIV), 271 were HCV+/HBV (HIV/HCV), and 63 were HCV+/HBV+
(excluded from further analysis). Median
age of HIV/HCV subjects was 38 years compared to 35 years for HIV (p <0.0001) and 37% vs 33% were male,
respectively (p = 0.18). Median CD4
count (cells/mm3) at baseline was 119 for HIV/HCV vs 132 for HIV,
respectively, and at months 3 and 6, CD4 counts increased to 243 vs 237 and 242
vs 247 for HIV/HCV vs HIV patients, respectively (p >0.05). Median HIV viral load (copies/mL) at baseline was
71,451 for HIV/HCV vs 53,278 for HIV (p
= 0.11) and at month 6, 72% of HIV/HCV and 76% of HIV patients had HIV viral
load <400 (p = 0.32). For patients
with baseline and month 6 ALT, mean ALT at baseline was similar (HIV/HCV ALT =
32.5 vs 31.7 in HIV) while at month 6, mean ALT was significantly higher in
HIV/HCV (ALT = 41.5) vs HIV (ALT = 30.6, p
< 0.003). For subjects with baseline and either month 3 or month 6 ALT
values, there was a 2% incidence of hepatotoxicity by month 6 in HIV/HCV
compared to 0.3% in HIV (p <0.05).
The median age of those with hepatotoxicity was 45 years for HIV/HCV vs 30
years for HIV and 33% of HIV/HCV with hepatotoxicity were females compared to
100% of HIV subjects.
Conclusions: We found few
differences in immune reconstitution or HIV virological control in this non-IDU
cohort of HIV/HCV vs HIV patients. Incidence of hepatotoxicity was low in both
groups during the first 6 months of ART, although significantly higher in
HIV/HCV patients.
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