Beta
192795

Lamivudine: An antiviral drug with high risk factor for selection of resistance in HBV patients

Article

Last updated: 22 Jan 2023

Subjects

-

Tags

Pharmacology and toxicology

Abstract

Globally, it has been reported that nearly 257 million people suffer from chronic Hepatitis B virus (HBV). In Egypt, HBV has been classified as a moderate endemic where 4% of the population presented with chronic HBV. Long term Lamivudine (LMV) monotherapy has been found to develop resistant strains of HBV where the polymerase gene specifically is mutated (i.e., YMDD as a primary mutation). This review aimed to determine the correlation between LMV therapy and development of resistance in chronic HBV patients and to investigate the genes responsible for LMV resistance. LMV as an antiviral therapy has a fair response rate in the studied patients with 20% of the population has significant signs of mutation according to previous studies in Egypt . Unfortunately, the long duration treatment with LMV leads to development of LMV resistant mutations altering the efficacy of the drug and a rescue drug must be used immediately.

Keywords: HBV, LMV, YMDD, Mutation, Resistance.

DOI

10.21608/rpbs.2021.83271.1106

Keywords

HBV, LMV, YMDD, Mutation, resistance

Authors

First Name

Mahmoud

Last Name

Abdelaal

MiddleName

Ahmed

Affiliation

pharmacology and toxicology, faculty of pharmacy, sinai university, ismailia, egypt

Email

mahmoudahmed11099@yahoo.com

City

-

Orcid

-

Volume

5

Article Issue

Pharmacology-Pharmaceutics

Related Issue

20377

Issue Date

2021-01-01

Receive Date

2021-06-30

Publish Date

2021-01-01

Page Start

81

Page End

84

Print ISSN

2536-9857

Online ISSN

2535-2091

Link

https://rpbs.journals.ekb.eg/article_192795.html

Detail API

https://rpbs.journals.ekb.eg/service?article_code=192795

Order

10

Type

Mini-reviews

Type Code

534

Publication Type

Journal

Publication Title

Records of Pharmaceutical and Biomedical Sciences

Publication Link

https://rpbs.journals.ekb.eg/

MainTitle

-

Details

Type

Article

Created At

22 Jan 2023