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Epidemiology, diagnosis and treatment of chronic hepatitis B in HIV-infected patients (EPIB 2005 STUDY)
- Source :
- AIDS, AIDS, Lippincott, Williams & Wilkins, 2007, 21 (10), pp.1323-1331. ⟨10.1097/QAD.0b013e32810c8bcf⟩
- Publication Year :
- 2007
- Publisher :
- HAL CCSD, 2007.
-
Abstract
- International audience; OBJECTIVE: To describe the characteristics of hepatitis B (HBV) infection in HIV-infected patients and the impact of anti-HBV treatments. PATIENTS AND METHODS: All the patients with past or present chronic HBV infection seen in October 2005 in 17 French hospitals were included. Data were retrospectively collected from their first visit in a time-dependent manner, through a detailed standardized questionnaire. RESULTS: Among 477 HBV-infected patients, 261 (55%) were co-infected with HIV. The HBV-HIV co-infected patients underwent fewer serological, virological and histological evaluations. Initial positive HBe antigenemia (HBe Ag) was more frequent in these patients (57.9 versus 28.6%; P < 10), as was cirrhosis on the initial liver biopsy (17.9 versus 7.6%; P = 0.05). Throughout the mean 5-year follow-up, HBe Ag loss was less frequent (P = 0.04), as was HBe seroconversion (incidence rate 2.6 versus 10/100 patient-years; P < 10). HBe Ag loss was associated with fibrosis improvement (METAVIR score -0.5 +/- 0.4 versus +0.2 +/- 0.6 if persistent positive HBe Ag, P = 0.01). In co-infected patients on tenofovir, adefovir or interferon, HBe seroconversions were seen in patients on combined HBV treatment, the use of which is increasing (58% in 2005). Nevertheless, no significant difference in virological, immunological or biochemical evolution was observed between these different treatments. CONCLUSIONS: In HBV-HIV co-infected patients, the assessment of HBV infection still needs to be improved, the HBV wild-type remains predominant, and HBe Ag loss is rare and associated with a better histological evolution. There is insufficient evidence of the superiority of combined HBV treatment, and this still needs be demonstrated in long term studies.
- Subjects :
- Male
HIV Infections
medicine.disease_cause
0302 clinical medicine
Orthohepadnavirus
[SDV.MHEP.MI]Life Sciences [q-bio]/Human health and pathology/Infectious diseases
HIV Seropositivity
Epidemiology
Adefovir
Immunology and Allergy
Hepatitis B e Antigens
030212 general & internal medicine
MESH: Hepatitis B e Antigens
MESH: HIV Seronegativity
biology
Reverse-transcriptase inhibitor
virus diseases
MESH: HIV Infections
Hepatitis B
3. Good health
MESH: Hepatitis B virus
Infectious Diseases
Liver
[SDV.MP.VIR]Life Sciences [q-bio]/Microbiology and Parasitology/Virology
Female
030211 gastroenterology & hepatology
France
medicine.drug
Adult
MESH: Antiviral Agents
Hepatitis B virus
medicine.medical_specialty
MESH: Hepatitis B, Chronic
Immunology
Antiviral Agents
03 medical and health sciences
Hepatitis B, Chronic
MESH: HIV Seropositivity
Acquired immunodeficiency syndrome (AIDS)
HIV Seronegativity
Internal medicine
medicine
Humans
Retrospective Studies
Hepatitis B Surface Antigens
MESH: Humans
business.industry
MESH: Adult
MESH: Retrospective Studies
medicine.disease
biology.organism_classification
[SDV.MP.BAC]Life Sciences [q-bio]/Microbiology and Parasitology/Bacteriology
digestive system diseases
MESH: Male
MESH: DNA, Viral
MESH: Hepatitis B Surface Antigens
MESH: France
Hepadnaviridae
DNA, Viral
business
MESH: Female
MESH: Liver
Subjects
Details
- Language :
- English
- ISSN :
- 02699370
- Database :
- OpenAIRE
- Journal :
- AIDS, AIDS, Lippincott, Williams & Wilkins, 2007, 21 (10), pp.1323-1331. ⟨10.1097/QAD.0b013e32810c8bcf⟩
- Accession number :
- edsair.doi.dedup.....9c83aea33b0672e462fcbac6ee60b6b8
- Full Text :
- https://doi.org/10.1097/QAD.0b013e32810c8bcf⟩