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1.
Gut ; 46(5): 715-8, 2000 May.
Article in English | MEDLINE | ID: mdl-10764718

ABSTRACT

BACKGROUND/AIMS: The purpose of this study was to better define the long term prognosis of infection and disease in children with chronic hepatitis B treated with interferon (IFN) alpha. PATIENTS: A total of 107 children with chronic hepatitis B who received IFN alpha for three or six months in two clinical trials were followed for a mean period of 69 (17) months. Response to treatment was defined as loss of hepatitis B e antigen (HBeAg) within 12 months after stopping treatment. A control group of 59 patients was also followed for a shorter mean time (46 (19) months). RESULTS: Sixteen (15%) treated children responded during therapy and 18 (17%) during post-treatment follow up; 31 (29%) non-responders lost HBeAg during subsequent years. High pretreatment levels of transaminases and a greater histological activity index were predictors of response. Kaplan-Meier estimates of cumulative HBeAg clearance rates at five years were similar between treated patients (60%) and controls (65%). After HBeAg clearance, all cases lost hepatitis B virus DNA and 94% had normal transaminase levels. Loss of hepatitis B surface antigen (HBsAg) occurred in four (25%) patients who responded during treatment but in none of the other treated or untreated patients. CONCLUSIONS: After five years' observation, the proportion of treated children with sustained HBeAg clearance comprised an equal number of responders and non-responders and did not differ from that observed in untreated controls, suggesting that IFN simply accelerated a spontaneous event. However, IFN significantly improved the rate of HBsAg loss in cases with more prominent disease activity who were early responders, and may be particularly useful in this type of patient.


Subject(s)
Antiviral Agents/therapeutic use , Hepatitis B e Antigens/analysis , Hepatitis B, Chronic/drug therapy , Interferon-alpha/therapeutic use , Adolescent , Alanine Transaminase/blood , Aspartate Aminotransferases/blood , Case-Control Studies , Child , Child, Preschool , Female , Follow-Up Studies , Hepatitis B, Chronic/enzymology , Hepatitis B, Chronic/immunology , Humans , Long-Term Care , Male , Multicenter Studies as Topic , Prognosis , Randomized Controlled Trials as Topic , Treatment Outcome
2.
Acta Gastroenterol Belg ; 61(2): 198-201, 1998.
Article in English | MEDLINE | ID: mdl-9658608

ABSTRACT

Chronic Hepatitis B virus (HBV) infection in children is commonly associated with Hepatitis B e antigen (HBeAg) seropositivity and histologic features of minimal to moderate hepatitis. Remission of liver disease is the rule following HBeAg to antiHBe seroconversion and clearance of HBV DNA from serum. In intermediate and low endemicity areas chronic HBV infection is usually acquired postnatally, and more than 80% of children are likely to achieve stable remission during the pediatric age. Severe sequelae, namely cirrhosis and HCC, have been observed only in less than 4% of children followed over two decades. In all cases cirrhosis was an early complication. Chronic HCV infection is usually silent in children. The chronicity rate seems to be high (50-80%) in post-transfusion hepatitis C as well as in perinatally acquired infection. HCV-associated liver disease is characterized by fluctuations of ALT which remain below two times the normal in about half of the cases. Liver histology shows minimal to mild hepatitis in the large majority of patients and cirrhosis is rare. Few patients achieve spontaneous remission and progression to a more severe liver disease might occur in adult life.


Subject(s)
Hepatitis B, Chronic/diagnosis , Hepatitis C, Chronic/diagnosis , Hepatitis D, Chronic/diagnosis , Age Factors , Child , Child, Preschool , Female , Hepatitis B, Chronic/epidemiology , Hepatitis B, Chronic/physiopathology , Hepatitis C, Chronic/epidemiology , Hepatitis C, Chronic/physiopathology , Hepatitis D, Chronic/epidemiology , Hepatitis D, Chronic/physiopathology , Humans , Infant , Italy/epidemiology , Male , Prevalence , Risk Factors
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