Evidence map›Paper›PMID 34027120›Full record

ArticleClinical and experimental hepatology2021

Assessment of hepatitis B virus pregenomic RNA in high and low viremic chronic hepatitis B patients.

Aymen Farid Elshayeb, Mohamed Gamal Abdrabu, Sara Lotfy Asar, Mohamed Adel Abdelaziz, Hossam Abuelkheir

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Article in Clinical and experimental hepatology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Aymen Farid ElshayebDepartment of Tropical Medicine, Faculty of Medicine, Alexandria University, Egypt.
Mohamed Gamal AbdrabuDepartment of Tropical Medicine, Faculty of Medicine, Alexandria University, Egypt.
Sara Lotfy AsarDepartment of Microbiology and Immunology, Faculty of Medicine, Alexandria University, Egypt.
Mohamed Adel AbdelazizDepartment of Tropical Medicine, Faculty of Medicine, Alexandria University, Egypt.
Hossam AbuelkheirDepartment of Tropical Medicine, Faculty of Medicine, Alexandria University, Egypt.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aim of the studyIntrahepatic covalently closed circular DNA (cccDNA) is the main cause of hepatitis B virus (HBV) persistence. Therefore, a noninvasive serum biomarker that can reflect intrahepatic cccDNA is required for evaluation of HBV virological, biochemical activity and therapeutic response. Aim of the study was to assess serum hepatitis B pregenomic RNA in low viremia patients (HBV DNA < 2000 IU/ml) and high viremia (HBV DNA > 2000 IU/ml). MATERIAL AND

methodsThis study was carried out on two groups of chronic hepatitis B patients: group A - 40 patients with low viremia (HBV DNA < 2000 IU/ml); group B - 40 patients with high viremia (HBV DNA > 2000 IU/ml when diagnosed). They were assessed before treatment and after 6 months of treatment (entecavir 0.5 mg/24 h). Serum HBV pregenomic RNA was quantified using RT-PCR.

resultsPregenomic RNA (pgRNA) was significantly lower in group A than in group B (before treatment). Moreover, it was significantly lower after 6 months of treatment than before treatment in group B. A significant positive correlation was observed between pgRNA and HBV DNA in groups A and B (before treatment); however, after 6 months of treatment of group B patients, although 35 patients had undetectable HBV DNA, they showed detectable levels of serum pgRNA and pgRNA > 4000 IU/ml was associated with virological and biochemical activity.

conclusionsSerum HBV pregenomic RNA might be a promising marker for assessment of HBV virological, biochemical activity and evaluating therapeutic responses.

Indexed as

biomarkerentecavirHBV cccDNAHBV pregenomic RNAnoninvasive

Identifiers

PMID34027120
PMCPMC8122096

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