TY - JOUR
T1 - Hepatitis B virus infection in children of HBV-related chronic liver disease patients
T2 - a study of intra-familial HBV transmission
AU - Gunardi, Hartono
AU - Iskandar, Melanie Y.
AU - Turyadi,
AU - Ie, Susan I.
AU - Dwipoerwantoro, Pramita Gayatri
AU - Gani, Rino A.
AU - Muljono, David H.
N1 - Funding Information:
This study was partly supported by a research grant from the Ministry for Research and Higher Education, Republic of Indonesia.
Publisher Copyright:
© 2016, Asian Pacific Association for the Study of the Liver.
PY - 2017/1/1
Y1 - 2017/1/1
N2 - Background: HBV-infected patients are potential sources of intra-familial transmission. We studied HBV transmission and molecular characteristics within families of HBV-related chronic liver disease (CLD) patients. Methods: Family members [index cases (ICs), spouses, and 1–18-year-old children] of HBV-related CLD patients were tested for HBsAg, anti-HBc, and anti-HBs. HBsAg-positive subjects were tested for HBeAg/anti-HBe. Anti-HBc-positive children together with their family members were further investigated for HBV DNA. Sequences of positive isolates were analyzed over surface, precore (PC) and basal core promoter (BCP) regions. Results: Among 94 children of 46 ICs, the prevalence of HBsAg, anti-HBc, and anti-HBs was 10 (10.6 %), 19 (20.2 %), and 46 (48.9 %), respectively. Thirty-eight (40.4 %) children were seronegative, indicating susceptibility to HBV infection. HBV DNA was identified in all ICs, 4 spouses, and 16 children. Having both parents with HBsAg positive and at least two HBV carriers in the households were significant risk factors of intra-familial transmission. HBV genotype/subtype distributions were comparable between children and ICs/spouses, with predominance of genotype B. The majority of HBV DNA sequences found in children were identical to their corresponding ICs—particularly mothers—including mutation patterns in the surface, PC, and BCP regions. Recognized mutations associated with HBsAg detection and/or vaccination failure, T140I, T143S/M, G145R, and Y161F, were identified in 20 subjects; while mutations linked to HBeAg-defective variants, PC G1896A and BCP A1762T/G1764A, were found in 7 and 11 subjects, respectively. Conclusions: Children of HBV-related CLD patients were at increased risk of HBVinfection through multi-modal transmission routes despite negative parental HBsAg and HBeAg status.
AB - Background: HBV-infected patients are potential sources of intra-familial transmission. We studied HBV transmission and molecular characteristics within families of HBV-related chronic liver disease (CLD) patients. Methods: Family members [index cases (ICs), spouses, and 1–18-year-old children] of HBV-related CLD patients were tested for HBsAg, anti-HBc, and anti-HBs. HBsAg-positive subjects were tested for HBeAg/anti-HBe. Anti-HBc-positive children together with their family members were further investigated for HBV DNA. Sequences of positive isolates were analyzed over surface, precore (PC) and basal core promoter (BCP) regions. Results: Among 94 children of 46 ICs, the prevalence of HBsAg, anti-HBc, and anti-HBs was 10 (10.6 %), 19 (20.2 %), and 46 (48.9 %), respectively. Thirty-eight (40.4 %) children were seronegative, indicating susceptibility to HBV infection. HBV DNA was identified in all ICs, 4 spouses, and 16 children. Having both parents with HBsAg positive and at least two HBV carriers in the households were significant risk factors of intra-familial transmission. HBV genotype/subtype distributions were comparable between children and ICs/spouses, with predominance of genotype B. The majority of HBV DNA sequences found in children were identical to their corresponding ICs—particularly mothers—including mutation patterns in the surface, PC, and BCP regions. Recognized mutations associated with HBsAg detection and/or vaccination failure, T140I, T143S/M, G145R, and Y161F, were identified in 20 subjects; while mutations linked to HBeAg-defective variants, PC G1896A and BCP A1762T/G1764A, were found in 7 and 11 subjects, respectively. Conclusions: Children of HBV-related CLD patients were at increased risk of HBVinfection through multi-modal transmission routes despite negative parental HBsAg and HBeAg status.
KW - Hepatitis B in children
KW - Hepatitis B virus
KW - Intra-familial transmission
KW - Mutation
KW - Transmission modes of HBV
UR - http://www.scopus.com/inward/record.url?scp=84987681459&partnerID=8YFLogxK
U2 - 10.1007/s12072-016-9764-z
DO - 10.1007/s12072-016-9764-z
M3 - Article
C2 - 27624502
AN - SCOPUS:84987681459
SN - 1936-0533
VL - 11
SP - 96
EP - 104
JO - Hepatology International
JF - Hepatology International
IS - 1
ER -