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Kinetics and prediction of HBsAg loss during therapy with analogues in patients affected by chronic hepatitis B HBeAg negative and genotype D
- Source :
- Liver international : official journal of the International Association for the Study of the Liver. 33(4)
- Publication Year :
- 2012
-
Abstract
- Background & Aims In patients affected by chronic hepatitis because of HBV infection, long-term suppressive therapy with nucleos(t)ides analogues in the HBeAg− patients has shown low effects on HBsAg titre (qHBsAg) decrease, and HBsAg loss is difficult to achieve. Thus, in this type of patients the main goals of antiviral therapy is the suppression of HBV-DNA and ALT normalization. Methods We retrospectively evaluated different qHBsAg kinetics in 134 treatment-naive patients having the same characteristics: HBeAg-, infection sustained by HBV genotype D and persistently undetectable HBV-DNA. Patients were treated with NAs therapy (lamivudine, adefovir, telbivudine, entecavir and tenofovir) for at least 2 years. qHBsAg was performed every 6 months. Results Our results showed a significantly greater qHBsAg decline after 2 years in patients treated with tenofovir (0.45 logIU/ml) than in patients treated with telbivudine (0.12 logIU/ml; P
- Subjects :
- Male
HBsAg
medicine.medical_specialty
Hepatitis B virus
Guanine
Genotype
Organophosphonates
medicine.disease_cause
Gastroenterology
Antiviral Agents
Hepatitis B, Chronic
Telbivudine
Internal medicine
Adefovir
medicine
Humans
Hepatitis B e Antigens
Tenofovir
Aged
Retrospective Studies
Chi-Square Distribution
Hepatitis B Surface Antigens
Hepatology
business.industry
Adenine
virus diseases
Lamivudine
Entecavir
Hepatitis B
Middle Aged
medicine.disease
Virology
digestive system diseases
Kinetics
Treatment Outcome
HBeAg
DNA, Viral
Female
business
Biomarkers
medicine.drug
Thymidine
Subjects
Details
- ISSN :
- 14783231
- Volume :
- 33
- Issue :
- 4
- Database :
- OpenAIRE
- Journal :
- Liver international : official journal of the International Association for the Study of the Liver
- Accession number :
- edsair.doi.dedup.....eddb7a62fa5e9102f1086b2a0a4612cc