TY - JOUR
T1 - Prevalence of HBV precore/core promoter variants in the United States
AU - Chu, Chi Jen
AU - Keeffe, Emmet B.
AU - Han, Steven Huy
AU - Perrillo, Robert P.
AU - Min, Albert D.
AU - Soldevila-Pico, Consuelo
AU - Carey, William
AU - Brown, Robert S.
AU - Luketic, Velimir A.
AU - Terrault, Norah
AU - Lok, Anna S.F.
N1 - Funding Information:
Innogenetics Inc. provided Inno-Lipa kits for HBV genotyping and detection of pre-core stop codon and core promoter variants. Roche Diagnostic Systems Inc. provided Cobas HBV Amplicor Monitor kits for quantitative HBV DNA testing. No grant funding was provided by Innogenetics or Roche. GlaxoSmithKline provided an unrestricted grant for collection and shipment of samples. C.J.C. was supported by Taipei Veterans General Hospital and Research Foundation of Digestive Medicine, Republic of China, E.B.K. was supported by the Hutchison Program in Translational Medicine at Stanford University, and A.S.F.L. was supported by National Institutes of Health contract N01-DK-9-2323 and grants U01-DK-60344 and U01-DK-57577.
PY - 2003/9/1
Y1 - 2003/9/1
N2 - Variants in the precore (G1896A) and core promoter (A 1762T, G1764A) regions of hepatitis B virus (HBV) may be related to serum HBV DNA levels and severity of liver disease. The aims of this nationwide study were to determine the prevalence of HBVprecore/core promoter variants in the United States and the association between these variants and patient demographics, HBV genotypes, serum HBV DNA level, and severity of liver disease. A total of 694 consecutive chronic HBV-infected patients seen in 17 U.S. liver centers during a 1-year period were enrolled. Demographic, clinical, and laboratory data were collected. Sera were tested for HBV genotypes as well as precore and core promoter variants by line-probe assays. Quantitative HBV DNA levels were determined using Cobas Amplicor HBV Monitor kits. Precore and core promoter variants were found in 27% and 44% of patients with chronic HBV infection in the United States. Precore and core promoter variants were more common in hepatitis B e antigen (HBeAg)-negative than in HBeAg-positive patients (precore, 38% vs. 9%; core promoter, 51% vs. 36%; respectively, P < .001). The prevalence of these variants was related to ethnicity, place of birth, and HBV genotypes. Patients with core promoter variants were more likely to have hepatic decompensation. Precore and/or core promoter variants were associated with higher serum HBV DNA levels in HBeAg-negative but not in HBeAg-positive patients. In conclusion, HBV precore and core promoter variants are not rare in the United States. Physicians should be aware of the existence of HBV precore and core promoter variants and the clinical condition of "HBeAg-negative chronic hepatitis".
AB - Variants in the precore (G1896A) and core promoter (A 1762T, G1764A) regions of hepatitis B virus (HBV) may be related to serum HBV DNA levels and severity of liver disease. The aims of this nationwide study were to determine the prevalence of HBVprecore/core promoter variants in the United States and the association between these variants and patient demographics, HBV genotypes, serum HBV DNA level, and severity of liver disease. A total of 694 consecutive chronic HBV-infected patients seen in 17 U.S. liver centers during a 1-year period were enrolled. Demographic, clinical, and laboratory data were collected. Sera were tested for HBV genotypes as well as precore and core promoter variants by line-probe assays. Quantitative HBV DNA levels were determined using Cobas Amplicor HBV Monitor kits. Precore and core promoter variants were found in 27% and 44% of patients with chronic HBV infection in the United States. Precore and core promoter variants were more common in hepatitis B e antigen (HBeAg)-negative than in HBeAg-positive patients (precore, 38% vs. 9%; core promoter, 51% vs. 36%; respectively, P < .001). The prevalence of these variants was related to ethnicity, place of birth, and HBV genotypes. Patients with core promoter variants were more likely to have hepatic decompensation. Precore and/or core promoter variants were associated with higher serum HBV DNA levels in HBeAg-negative but not in HBeAg-positive patients. In conclusion, HBV precore and core promoter variants are not rare in the United States. Physicians should be aware of the existence of HBV precore and core promoter variants and the clinical condition of "HBeAg-negative chronic hepatitis".
UR - https://www.scopus.com/pages/publications/0041859593
U2 - 10.1053/jhep.2003.50352
DO - 10.1053/jhep.2003.50352
M3 - Article
C2 - 12939588
AN - SCOPUS:0041859593
SN - 0270-9139
VL - 38
SP - 619
EP - 628
JO - Hepatology
JF - Hepatology
IS - 3
ER -