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1.
PLoS One ; 17(4): e0266134, 2022.
Article in English | MEDLINE | ID: mdl-35390033

ABSTRACT

BACKGROUND: Chronic hepatitis B virus (CHB) infection is a major health problem and leading cause of hepatocellular carcinoma (HCC) worldwide. Several point and deletion mutations on the PreS/S gene have been intensively considered associated with HCC. This study aimed to describe the characteristics of HBV PreS/S mutations in Vietnamese CHB-infected patients and their association with HCC. METHODS: This cross-sectional study was conducted from 02/2020 to 03/2021, recruited Vietnamese CHB-infected patients with HBV-DNA >3 log10-copies/mL and successful PreS/S gene sequencing. Mutations were detected by direct Sanger sequencing. RESULTS: 247 CHB-infected patients were recruited, characterized by 68.8% males, 54.7% HBV genotype B, 57.5% HBeAg positive, 23.1% fibrosis score ≥F3 and 19.8% HCC. 61.8% amino acid replacements were detected throughout the PreS1/PreS2/S genes. The most common point-mutations included N/H51Y/T/S/Q/P (30.4%), V68T/S/I (44.9%), T/N87S/T/P (46.2%) on PreS1 gene; T125S/N/P (30.8%), I150T (42.5%) on PreS2 gene; S53L (37.7%), A184V/G (39.3%), S210K/N/R/S (39.3%) on S gene. The rates of case(s) with any point-mutation on the Major Hydrophylic Region (MHR) and the "a" determinant region were 63.6% and 39.7%, respectively. Most of S point-mutations were presented with low rates such as T47A/E/V/K (9.3%), P120S/T (8.5%), G145R (2%). On multivariable analysis, males (OR = 4.51, 95%CI 1.78-11.4, p = 0.001), age≥40 (OR = 5.5, 95%CI 2.06-14.68, p = 0.001), W4P/R/Y on PreS1 (OR = 11.56, 95%CI 1.99-67.05, p = 0.006) and 4 S point-mutations as: T47A/E/V/K (OR = 3.67, 95%CI 1.19-11.29, p = 0.023), P120S/T (OR = 3.38, 95%CI 1.09-10.49, p = 0.035), S174N (OR = 29.73, 95%CI 2.12-417.07, p = 0.012), P203R (OR = 8.45, 95%CI 1.43-50.06, p = 0.019) were associated with HCC. CONCLUSIONS: We detected 61% amino acid changes on PreS/S regions in Vietnamese CHB patients. One point-mutation at amino acid 4 on PreS1 gene and 4 point-mutations at amino acids 47, 120, 174, and 203 on S gene were associated with HCC. Further investigations are recommended to further clarify the relationship and interaction between mutations in HBV genome and HCC progression.


Subject(s)
Carcinoma, Hepatocellular , Hepatitis B virus , Hepatitis B, Chronic , Liver Neoplasms , Viral Envelope Proteins , Adult , Amino Acids/genetics , Carcinoma, Hepatocellular/pathology , Carcinoma, Hepatocellular/virology , Cross-Sectional Studies , DNA, Viral/genetics , Female , Genotype , Hepatitis B Surface Antigens/genetics , Hepatitis B virus/genetics , Hepatitis B, Chronic/complications , Hepatitis B, Chronic/pathology , Humans , Liver Neoplasms/pathology , Liver Neoplasms/virology , Male , Mutation , Vietnam , Viral Envelope Proteins/genetics
2.
Sci Total Environ ; 743: 140741, 2020 Nov 15.
Article in English | MEDLINE | ID: mdl-32758837

ABSTRACT

In recent years, the impacts of biomass energy consumption on the environment have attracted the attention of policymakers and scholars. Although empirical studies have been conducted on this topic, the relationship between biomass energy production and the ecological footprint has been overlooked in the literature. This study seeks to fill this gap by investigating the effects of biomass energy production on the ecological footprint of the G7 countries for the period 1980-2016. For this purpose, we use a set of methods, that help overcome the problem of cross-sectional dependence in panel data analysis. The findings from dynamic seemingly unrelated regression (DSUR) estimation show that biomass energy production increases the ecological footprint of the G7 countries. Meanwhile, a Dumitrescu-Hurlin causality test provides evidence that unidirectional causality runs from biomass energy production to the ecological footprint. Based on these empirical results, several policy recommendations are proposed for the G7 countries.

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