944
Hepatitis B Surface Antigen Seroreversion in HIV Patients in the Era of HAART: A Population Profile
S Aitchison, Anne Mijch*, J Yu, and K Watson
Victorian HIV Svc, Alfred Hosp, Prahran, Victoria, Australia
Background: This study examines a population of patients with
HIV/hepatitis B virus (HBV) co-infection, where the hepatitis B surface antigen
(HBsAg) is positive for 6 months or more and then becomes
HBsAg negative (HB seroreversion). This group of
patients is compared with HIV/HBV-co-infected patients who have not undergone seroreversion. The main comparisons being investigated are ART,
liver function, hepatitis- and HIV-related factors, such as CD4 counts and plasma
HIV RNA.
Methods: A retrospective matched case-control design was
used to investigate this issue. Cases
and 2 matched controls were selected from the Victorian HIV Service database at
the Alfred Hospital
in Melbourne, Australia. All controls were HBsAg+ at the time of selection. Matching was
based on date of birth and whether the patient was first seen at the Victorian
HIV Service pre-HAART or within the era of HAART.
Result: This investigation has found that 8.5% (20 of 236)
of individuals with chronic HBV infection underwent seroreversion in the era of
HAART, 95% of whom (n = 19, 95%) were
male compared to 92.5% (n = 37) of
the controls. Mean age was 40.6 (SD 7.7) vs 35.1 (SD
6.2) for the controls. And, 95% (n = 19)
of the cases and 90% (n = 38) of the
controls were on HAART. No significant difference was found in CD4 or plasma
HIV RNA at nadir/peak, commencement of HAART, or at 3, 6, or 12 months prior to
HBV seroreversion; 15% (n = 3) of cases and 45% (n
= 18) of controls were HBeAg+ during
follow-up; 25% (n = 3) and 8% (n = 3) of the case and controls tested
positive for HCV antibody. Alanine aminotransferase was significantly lower in cases than in
controls at time of seroreversion and 3, 6, and 12 months prior (24 vs 50 cells/µL).
Conclusions: Our study provides preliminary evidence that
potent HIV and HBV antiviral treatment is associated with seroreversion of HBV.
Ongoing prospective studies will further elucidate predictive factors and long-term
outcome.
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|
Cases
|
Controls
|
|
|
n=20
|
n=40
|
|
Duration
of known HBsAg (years [SD])
|
8.8
[6.3]
|
2.3
[4.2]**
|
|
CD4
at seroreversion (median cells/µL [IQR^])
|
334
[180, 507]
|
199
[130, 299]
|
|
Plasma HIV RNA at seroreversion (median copies/mL
[IQR^])
|
500
[50, 32500]
|
1250
[230, 51100]
|
|
Time
on HAART (mean years [SD])
|
7.4
[4.3]
|
5.7
[3.5]
|
|
Time
on lamivudine (median years [IQR^])
|
2.5
[1.1, 4.5]
|
1.4
[0.51, 2]*
|
|
Time
on lamivudine + tenofovir
(median [IQR^])
|
2.9
[2.58, 3.1]
|
1.3
[0.7, 1.9]*
|
*p<0.05; **p<0.01; ^interquartile
range
|