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The effect of different combination therapies on oxidative stress markers in HIV infected patients in cameroon

The study assessed the effect of some highly active antiretroviral therapies (HAART), used in the management of HIV/AIDS in Cameroon, on oxidative stress markers such as malondialdehyde (as TBARs), albumin, protein carbonyl content and protein sulfhydryls groups. 85 HIV positive patients (34.8 ± 9.3...

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Autores principales: Ngondi, Judith L, Oben, Julius, Forkah, David Musoro, Etame, Lucten Honore, Mbanya, Dora
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2006
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1557529/
https://www.ncbi.nlm.nih.gov/pubmed/16859567
http://dx.doi.org/10.1186/1742-6405-3-19
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author Ngondi, Judith L
Oben, Julius
Forkah, David Musoro
Etame, Lucten Honore
Mbanya, Dora
author_facet Ngondi, Judith L
Oben, Julius
Forkah, David Musoro
Etame, Lucten Honore
Mbanya, Dora
author_sort Ngondi, Judith L
collection PubMed
description The study assessed the effect of some highly active antiretroviral therapies (HAART), used in the management of HIV/AIDS in Cameroon, on oxidative stress markers such as malondialdehyde (as TBARs), albumin, protein carbonyl content and protein sulfhydryls groups. 85 HIV positive patients (34.8 ± 9.3 years) were on three different highly active antiretroviral therapies (HAART patients). 65 HIV positive patients (32.2 ± 10.9 years) on no treatment (Pre-HAART patients), and 90 non-HIV infected patients (32.6 ± 9.3 years), were the control groups. Plasma TBARs as well as carbonyl levels were significantly higher in HIV patients on HAART compared to pre-HAART patients or non-HIV infected controls. On the other hand, the protein sulfhydryl group content was not different for patients on HAART compared to pre-HAART patients, but both were significantly lower than non-HIV infected controls (P < 0.0001, 0.001). The combination treatment Therapy I [stavudin (80 mg) + Lamivudin (600 mg) + Nevirapin + (400 mg) zidovudin (600 mg)] brought about a significant (p < 0.05) reduction in the plasma concentration of protein sulfhydrl groups as well as TBARs compared to Therapy II [stavudin (80 mg) + Lamivudin (300 mg) + nevirapin (400 mg)] or with combination Therapy III of [zidovudine (600 mg) + lamivudin(300 mg) with efavirenz (600 mg)] (P < 0.05). The content of the antioxidant, Vitamin C was lower in the plasma of patients on Therapy I compared to those on Therapy II (P < 0.01) and Therapy III (P < 0.001). HIV infection therefore increases the oxidative stress process, while antiretroviral combination therapy increased protein oxidation as well as the level of oxidative stress already present in HIV infection.
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spelling pubmed-15575292006-08-30 The effect of different combination therapies on oxidative stress markers in HIV infected patients in cameroon Ngondi, Judith L Oben, Julius Forkah, David Musoro Etame, Lucten Honore Mbanya, Dora AIDS Res Ther Research The study assessed the effect of some highly active antiretroviral therapies (HAART), used in the management of HIV/AIDS in Cameroon, on oxidative stress markers such as malondialdehyde (as TBARs), albumin, protein carbonyl content and protein sulfhydryls groups. 85 HIV positive patients (34.8 ± 9.3 years) were on three different highly active antiretroviral therapies (HAART patients). 65 HIV positive patients (32.2 ± 10.9 years) on no treatment (Pre-HAART patients), and 90 non-HIV infected patients (32.6 ± 9.3 years), were the control groups. Plasma TBARs as well as carbonyl levels were significantly higher in HIV patients on HAART compared to pre-HAART patients or non-HIV infected controls. On the other hand, the protein sulfhydryl group content was not different for patients on HAART compared to pre-HAART patients, but both were significantly lower than non-HIV infected controls (P < 0.0001, 0.001). The combination treatment Therapy I [stavudin (80 mg) + Lamivudin (600 mg) + Nevirapin + (400 mg) zidovudin (600 mg)] brought about a significant (p < 0.05) reduction in the plasma concentration of protein sulfhydrl groups as well as TBARs compared to Therapy II [stavudin (80 mg) + Lamivudin (300 mg) + nevirapin (400 mg)] or with combination Therapy III of [zidovudine (600 mg) + lamivudin(300 mg) with efavirenz (600 mg)] (P < 0.05). The content of the antioxidant, Vitamin C was lower in the plasma of patients on Therapy I compared to those on Therapy II (P < 0.01) and Therapy III (P < 0.001). HIV infection therefore increases the oxidative stress process, while antiretroviral combination therapy increased protein oxidation as well as the level of oxidative stress already present in HIV infection. BioMed Central 2006-07-22 /pmc/articles/PMC1557529/ /pubmed/16859567 http://dx.doi.org/10.1186/1742-6405-3-19 Text en Copyright © 2006 Judith L et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Ngondi, Judith L
Oben, Julius
Forkah, David Musoro
Etame, Lucten Honore
Mbanya, Dora
The effect of different combination therapies on oxidative stress markers in HIV infected patients in cameroon
title The effect of different combination therapies on oxidative stress markers in HIV infected patients in cameroon
title_full The effect of different combination therapies on oxidative stress markers in HIV infected patients in cameroon
title_fullStr The effect of different combination therapies on oxidative stress markers in HIV infected patients in cameroon
title_full_unstemmed The effect of different combination therapies on oxidative stress markers in HIV infected patients in cameroon
title_short The effect of different combination therapies on oxidative stress markers in HIV infected patients in cameroon
title_sort effect of different combination therapies on oxidative stress markers in hiv infected patients in cameroon
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1557529/
https://www.ncbi.nlm.nih.gov/pubmed/16859567
http://dx.doi.org/10.1186/1742-6405-3-19
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