Abstract

BACKGROUND In Brazil, few studies have investigated the prevalence of infection with the precore (PC) and basal core promoter (BCP) mutants of the hepatitis B virus (HBV).OBJECTIVES This study aimed to analyse the frequency of PC and BCP mutations among patients infected with HBV and to evaluate the association between the variants and advanced hepatic disease.METHODS A total of 161 patients infected with HBV were studied. To identify PC and BCP mutations, a 501-bp fragment of HBV DNA was amplified and sequenced.FINDINGS PC and BCP regions from HBV strains were successfully amplified and sequenced in 129 and 118 cases, respectively. PC and BCP mutations were detected in 61.0% and 80.6% of the cases, respectively. The A1762T/G1764A variant was identified in 36.7% of the patients with grade 1 and 2 liver fibrosis (29/79) and in 81.8% of the patients with grade 3 and 4 liver fibrosis (9/11) (p < 0.01); in 76.9% of the patients with cirrhosis (10/13) and in 38.1% of the patients without cirrhosis (40/105) (p = 0.01); and in 77.8% of the patients with hepatocellular carcinoma (HCC) (7/9) and in 39.4% of the patients without HCC (43/109) (p = 0.03).MAIN CONCLUSIONS A high prevalence of HBV PC and BCP mutants was found. The A1762T/G1764A variant was independently associated with advanced forms of liver fibrosis, hepatic cirrhosis, and HCC.

Highlights

  • In Brazil, few studies have investigated the prevalence of infection with the precore (PC) and basal core promoter (BCP) mutants of the hepatitis B virus (HBV)

  • The natural course of chronic hepatitis B virus (HBV) infection involves varied forms ranging from inactive carriers to patients with cirrhosis, hepatocellular carcinoma (HCC), or liver failure (Chang 2010, McMahon 2010, Dandri & Locarnini 2012)

  • The viral load was used to aid in the distribution of patients into groups according to the evolutionary stage of chronic HBV infection, and was determined through absolute quantitation of HBV DNA by real-time polymerase chain reaction (PCR) using TaqMan® (Applied Biosystems), with primers and probes annealing to the regions of the S gene conserved in all HBV genotypes (Sitnik et al 2010)

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Summary

METHODS

A total of 161 patients infected with HBV were studied. To identify PC and BCP mutations, a 501-bp fragment of HBV DNA was amplified and sequenced. The natural course of chronic hepatitis B virus (HBV) infection involves varied forms ranging from inactive carriers to patients with cirrhosis, hepatocellular carcinoma (HCC), or liver failure (Chang 2010, McMahon 2010, Dandri & Locarnini 2012). Due to such a broad spectrum of clinical presentations, the search for factors predictive of the disease evolution has proved to be highly valuable for deciding the strategy to monitor and treat the infected patients (McMahon 2010). Precore and BCP HBV mutations in Brazil Silvana Gama Florencio Chachá et al 627

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