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Tenofovir in treatment of Iranian patients with chronic hepatitis B virus infection: An open-label case series

OBJECTIVE: Tenofovir is among the first-line treatments for chronic hepatitis B (CHB) virus infection. We evaluated the efficacy and safety of Tenofovir in treatment of Iranian patients with CHB. METHODS: Forty treatment-native patients with CHB but without concurrent hepatitis C or human immunodefi...

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Autores principales: Ataei, Behrooz, Khodadoostan, Mahsa, Pouria, Babk, Adibi, Peyman
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4966234/
https://www.ncbi.nlm.nih.gov/pubmed/27512706
http://dx.doi.org/10.4103/2279-042X.185714
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author Ataei, Behrooz
Khodadoostan, Mahsa
Pouria, Babk
Adibi, Peyman
author_facet Ataei, Behrooz
Khodadoostan, Mahsa
Pouria, Babk
Adibi, Peyman
author_sort Ataei, Behrooz
collection PubMed
description OBJECTIVE: Tenofovir is among the first-line treatments for chronic hepatitis B (CHB) virus infection. We evaluated the efficacy and safety of Tenofovir in treatment of Iranian patients with CHB. METHODS: Forty treatment-native patients with CHB but without concurrent hepatitis C or human immunodeficiency virus infections were treated with Tenobiovir(™) 300 mg/day. The hepatitis B virus (HBV) DNA load, hepatitis B e antigen (HBe Ag), anti-hepatitis B e antibody (HBe Ab), liver enzymes, and creatinine were measured before and at least 3 months after the treatment. FINDINGS: The mean age of patients was 38.1 ± 12.4 years and 65% of them were male. Seventeen (42.5%) patients were HBe Ag-positive and 15 (37.5%) patients had alanine aminotransferase (ALT) of two times above the normal. The HBV DNA load was significantly decreased after the treatment (P < 0.001). Twenty-seven (67.5%) patients had viral load of ≤2000 IU/ml and 22 (55%) patients had undetectable HBV DNA level after the treatment. Among positive HBe Ag patients, the HBe Ag became negative in 15 (88.2%) patients after the treatment and HBe Ab became positive in 3 (17.6%) patients. Liver enzymes’ levels were significantly decreased after the treatment (P <0.05) and ALT transaminase level became normalized in 86.7% (13 out of 15) of cases with baseline levels twice the normal. CONCLUSION: Treatment response rate to Tenofovir in Iranian patients with CHB was high. The virological and serological response rate and safety of Tenofovir in our population was comparable to other populations. Considering availability and costs, Tenobiovir(™) could be recommended as the first-line therapy of chronic HBV infection in Iran.
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spelling pubmed-49662342016-08-10 Tenofovir in treatment of Iranian patients with chronic hepatitis B virus infection: An open-label case series Ataei, Behrooz Khodadoostan, Mahsa Pouria, Babk Adibi, Peyman J Res Pharm Pract Original Article OBJECTIVE: Tenofovir is among the first-line treatments for chronic hepatitis B (CHB) virus infection. We evaluated the efficacy and safety of Tenofovir in treatment of Iranian patients with CHB. METHODS: Forty treatment-native patients with CHB but without concurrent hepatitis C or human immunodeficiency virus infections were treated with Tenobiovir(™) 300 mg/day. The hepatitis B virus (HBV) DNA load, hepatitis B e antigen (HBe Ag), anti-hepatitis B e antibody (HBe Ab), liver enzymes, and creatinine were measured before and at least 3 months after the treatment. FINDINGS: The mean age of patients was 38.1 ± 12.4 years and 65% of them were male. Seventeen (42.5%) patients were HBe Ag-positive and 15 (37.5%) patients had alanine aminotransferase (ALT) of two times above the normal. The HBV DNA load was significantly decreased after the treatment (P < 0.001). Twenty-seven (67.5%) patients had viral load of ≤2000 IU/ml and 22 (55%) patients had undetectable HBV DNA level after the treatment. Among positive HBe Ag patients, the HBe Ag became negative in 15 (88.2%) patients after the treatment and HBe Ab became positive in 3 (17.6%) patients. Liver enzymes’ levels were significantly decreased after the treatment (P <0.05) and ALT transaminase level became normalized in 86.7% (13 out of 15) of cases with baseline levels twice the normal. CONCLUSION: Treatment response rate to Tenofovir in Iranian patients with CHB was high. The virological and serological response rate and safety of Tenofovir in our population was comparable to other populations. Considering availability and costs, Tenobiovir(™) could be recommended as the first-line therapy of chronic HBV infection in Iran. Medknow Publications & Media Pvt Ltd 2016 /pmc/articles/PMC4966234/ /pubmed/27512706 http://dx.doi.org/10.4103/2279-042X.185714 Text en Copyright: © 2016 Journal of Research in Pharmacy Practice http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms.
spellingShingle Original Article
Ataei, Behrooz
Khodadoostan, Mahsa
Pouria, Babk
Adibi, Peyman
Tenofovir in treatment of Iranian patients with chronic hepatitis B virus infection: An open-label case series
title Tenofovir in treatment of Iranian patients with chronic hepatitis B virus infection: An open-label case series
title_full Tenofovir in treatment of Iranian patients with chronic hepatitis B virus infection: An open-label case series
title_fullStr Tenofovir in treatment of Iranian patients with chronic hepatitis B virus infection: An open-label case series
title_full_unstemmed Tenofovir in treatment of Iranian patients with chronic hepatitis B virus infection: An open-label case series
title_short Tenofovir in treatment of Iranian patients with chronic hepatitis B virus infection: An open-label case series
title_sort tenofovir in treatment of iranian patients with chronic hepatitis b virus infection: an open-label case series
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4966234/
https://www.ncbi.nlm.nih.gov/pubmed/27512706
http://dx.doi.org/10.4103/2279-042X.185714
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