Lamivudine Treatment in Maternally Transmitted Chronic Hepatitis B Virus Infection Patients
Resource
PEDIATRICS INTERNATIONAL v.47 n.4 pp.372-377
Journal
PEDIATRICS INTERNATIONAL
Journal Volume
v.47
Journal Issue
n.4
Pages
372-377
Date Issued
2005
Date
2005
Author(s)
NI, YEN-HSUAN
HUANG, FU-CHEN
WU, TZEE-CHUNG
KONG, MAN-SHAN
JENG, YUNG-MING
CHEN, PEI-JER
TSUEI, DAW-JEN
CHEN, HUEY-LING
HSU, HONG-YUAN
CHANG, MEI-HWEI
Abstract
Background: Lamivudine treatment in chronic carriers who acquired hepatitis B virus through maternal transmission were investigated. Methods : A total of 29 subjects (Male : Female, 24:5; mean age, 14.7 ± 5.6 years ) who were hepatitis B e antigen (HBeAg) seropositive for >6 months, alanine aminotransferase (ALT) was >1.3 times of upper limit of normal value, and receiving a 52 week-long treatment, received open-label lamivudine (3 mg/kg per day, maximum 100 mg/day). Another 29 subjects matched for gender, age, liver function, and HBeAg status followed up before the introduction of lamivudine served as the control group. The control group did not receive any treatment and were evaluated at week 52 after the onset of abnormal ALT. Mothers of all study subjects were hepatitis B surface antigen (HBsAg) carriers. A successful treatment response at week 52 was defined as: (i) undetectable hepatitis B virus DNA by real time polymerase chain reaction; (ii) normal ALT; and (iii) HBeAg/ anti-HBe seroconversion. Lamivudine- resistant YMDD mutants were checked at week 52. Results: The lamivudine group did not reach a better successful treatment response rate than the control group (17 vs 10%, P = 0.44), except in patients with a baseline ALT >5 times of the upper limit of normal value. YMDD mutants developed in 34% of patients in the lamivudine group. Conclusion: Lamivudine treatment is effective for maternally transmitted subjects with high ALT.
Subjects
hepatitis
B virus
lamivudine
maternal transmision
real time polymerase chain reaction
YMDD mutant
SDGs
Type
journal article
