932
Increased Progression to Liver Disease and Death in HIV/HCV than in HBV-co-infected Patients
Colette Smit*1, L Gras1, A van Sighem1, T Ruys2, J Lange2, F de Wolf1,3, and F de Wolf1,3
1HIV Monitoring Fndn, Academic Med Ctr, Univ of Amsterdam, The Netherlands; 2Ctr for Immunity and Infection, Academic Med Ctr, Univ of Amsterdam, The Netherlands; and 3Imperial Coll Sch of Med, London, UK
Background:
Hepatitis B (HBV) and C (HCV) are
associated with liver fibrosis, cirrhosis, and hepatocellular
carcinoma (HCC) and progression is accelerated in the presence of HIV. We
studied differences in liver disease progression between HCV and HBV co-infected
HIV+ patients.
Methods: All
HIV-1-infected patients co-infected with HBV or HCV were selected from the
Netherlands ATHENA national observational HIV cohort. Patients positive for HBsAg were defined as HBV-co-infected. Patients positive for
HCV antibodies or HCV RNA were defined as HCV-co-infected. Liver disease was
defined as having liver fibrosis, cirrhosis, or HCC. Time to liver disease was
analyzed using a Cox proportional hazard model for those patients who initiated
HAART, adjusted for age, gender, transmission risk group, and baseline CD4 cell
count. Time was from HAART initiation until liver disease, death, or closure of
the database (January 1, 2006). Data on liver disease was systematically
collected from January 1, 2001 onward, left entry was
used when HAART initiation was before January 1, 2001. Kaplan Meier method was
used to compare the time from HAART initiation until death HBV-, HCV-coinfected, and both HBV- and HCV-co-infected patients.
Results: Of the 12257 HIV-infected patients in the
ATHENA cohort, 1129 (9%) patients were HCV-co-infected and 815 (7%) were HBV-co-infected;
31(0.3%) patients co-infected with both HBV and HCV were excluded from the
analyses, because this number was too small. Among the co-infected patients, 31(2%)
developed liver fibrosis, 71(4%) liver cirrhoses, and 5 (0.3%) HCC between 2001 and 2006. Of the HBV or HCV co-infected
patients, 1651 (85%) initiated HAART and 246 (13%) died during follow-up.
The adjusted risk of
liver disease was 1.93 (95% confidence interval (CI) 0.85 to 4.42) in HCV/HIV-co-infected
patients compared to HBV/HIV-co-infected patients. By 5 years after HAART
initiation, 7% (95%CI 5 to 10) of the HBV-, 14% (95%CI 11 to 16) of the HCV-, and
7% (95%CI 6 to 7) of the non-co-infected had died. HCV-co-infected patients
died significantly faster than HBV-co-infected (p log rank test = 0.0001), time to death did not differ between HBV-
and non-co-infected patients (p = 0.23).
Conclusions:
HCV-co-infected HAART-treated patients
have a faster progression to hepatitis-related liver disease and to death than
HBV/HIV-co-infected patients, suggesting that progression to liver-related
disease may be faster in HCV-co-infected patients.
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