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Evaluation of antiretroviral effect on mitochondrial DNA depletion among HIV-infected patients in Bali
BACKGROUND: Nucleoside reverse transcriptase inhibitors (NRTIs) are the cornerstone of highly active antiretroviral therapy combination regimens for HIV infection. Unfortunately, NRTIs have been noticeably associated with many adverse effects related to mitochondrial toxicity leading to mitochondria...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6072679/ https://www.ncbi.nlm.nih.gov/pubmed/30104903 http://dx.doi.org/10.2147/HIV.S166245 |
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author | Masyeni, Sri Sintya, Erly Megawati, Dewi Sukmawati, Ni Made Hegard Budiyasa, Dewa GA Aryastuti, Sri Agung Khairunisa, Siti Qamariyah Arijana, IGKN Nasronudin, N |
author_facet | Masyeni, Sri Sintya, Erly Megawati, Dewi Sukmawati, Ni Made Hegard Budiyasa, Dewa GA Aryastuti, Sri Agung Khairunisa, Siti Qamariyah Arijana, IGKN Nasronudin, N |
author_sort | Masyeni, Sri |
collection | PubMed |
description | BACKGROUND: Nucleoside reverse transcriptase inhibitors (NRTIs) are the cornerstone of highly active antiretroviral therapy combination regimens for HIV infection. Unfortunately, NRTIs have been noticeably associated with many adverse effects related to mitochondrial toxicity leading to mitochondrial deoxyribonucleic acid (mtDNA) depletion. However, similar mitochondrial dysfunction has recently been found even in antiretroviral therapy-naïve patients, suggesting HIV itself could contribute to this abnormality. In this study, we determine whether mtDNA depletion was present in either antiretroviral therapy-naïve or NRTI-treated patients at Sanjiwani Hospital, Bali, Indonesia. PATIENTS AND METHODS: A cross-sectional study was conducted from the peripheral blood mononuclear cells of HIV patients. Specifically, the relative content of mtDNA (mtRNR1 gene) to nuclear DNA (ASPOLG gene) was determined by real-time polymerase chain reaction. Data were analyzed with SPSS 16.0 software and GraphPad Prism 7.02. RESULTS: A total of 84 samples (67 on NRTIs and 17 HIV-naïve) were suitable for analysis. We identified 21.4% of the samples (18/84) with mtDNA:nDNA ratio <1. Although it was not significant (P=0.121), the median mtDNA:nDNA ratio of HIV-naïve group was slightly higher (median 1.8; interquartile range [IQR]: 1.1–2.1) than NRTI-treated patients (median 1.5; IQR: 1.3–2.85). Tenofovir-based NRTI was more frequently used (73.13%) than zidovudine-based NRTI (26.86%). The period for which NRTI was used probably contributed to the ratio of mtDNA:nDNA. The median ratio of mtDNA:nDNA zidovudine-treated patients was slightly lower (median 1.2; IQR: 1.08–1.98) when compared to tenofovir-based NRTI (median 1.6; IQR: 1.05–2.10), with the median period of former treatment being significantly longer (P<0.001). Although these data overall indicate that NRTI treatment had no effect on mtDNA:nDNA ratios, patients who undergo more than 12 months of NRTIs treatment show a decrease in the ratio; however, further study is required. CONCLUSION: Almost one-fourth of the samples showed a lower mtDNA:nDNA ratio. The decreasing of the ratio mtDNA:nDNA was most likely present after 12 months of NRTI treatment. |
format | Online Article Text |
id | pubmed-6072679 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-60726792018-08-13 Evaluation of antiretroviral effect on mitochondrial DNA depletion among HIV-infected patients in Bali Masyeni, Sri Sintya, Erly Megawati, Dewi Sukmawati, Ni Made Hegard Budiyasa, Dewa GA Aryastuti, Sri Agung Khairunisa, Siti Qamariyah Arijana, IGKN Nasronudin, N HIV AIDS (Auckl) Original Research BACKGROUND: Nucleoside reverse transcriptase inhibitors (NRTIs) are the cornerstone of highly active antiretroviral therapy combination regimens for HIV infection. Unfortunately, NRTIs have been noticeably associated with many adverse effects related to mitochondrial toxicity leading to mitochondrial deoxyribonucleic acid (mtDNA) depletion. However, similar mitochondrial dysfunction has recently been found even in antiretroviral therapy-naïve patients, suggesting HIV itself could contribute to this abnormality. In this study, we determine whether mtDNA depletion was present in either antiretroviral therapy-naïve or NRTI-treated patients at Sanjiwani Hospital, Bali, Indonesia. PATIENTS AND METHODS: A cross-sectional study was conducted from the peripheral blood mononuclear cells of HIV patients. Specifically, the relative content of mtDNA (mtRNR1 gene) to nuclear DNA (ASPOLG gene) was determined by real-time polymerase chain reaction. Data were analyzed with SPSS 16.0 software and GraphPad Prism 7.02. RESULTS: A total of 84 samples (67 on NRTIs and 17 HIV-naïve) were suitable for analysis. We identified 21.4% of the samples (18/84) with mtDNA:nDNA ratio <1. Although it was not significant (P=0.121), the median mtDNA:nDNA ratio of HIV-naïve group was slightly higher (median 1.8; interquartile range [IQR]: 1.1–2.1) than NRTI-treated patients (median 1.5; IQR: 1.3–2.85). Tenofovir-based NRTI was more frequently used (73.13%) than zidovudine-based NRTI (26.86%). The period for which NRTI was used probably contributed to the ratio of mtDNA:nDNA. The median ratio of mtDNA:nDNA zidovudine-treated patients was slightly lower (median 1.2; IQR: 1.08–1.98) when compared to tenofovir-based NRTI (median 1.6; IQR: 1.05–2.10), with the median period of former treatment being significantly longer (P<0.001). Although these data overall indicate that NRTI treatment had no effect on mtDNA:nDNA ratios, patients who undergo more than 12 months of NRTIs treatment show a decrease in the ratio; however, further study is required. CONCLUSION: Almost one-fourth of the samples showed a lower mtDNA:nDNA ratio. The decreasing of the ratio mtDNA:nDNA was most likely present after 12 months of NRTI treatment. Dove Medical Press 2018-07-30 /pmc/articles/PMC6072679/ /pubmed/30104903 http://dx.doi.org/10.2147/HIV.S166245 Text en © 2018 Masyeni et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. |
spellingShingle | Original Research Masyeni, Sri Sintya, Erly Megawati, Dewi Sukmawati, Ni Made Hegard Budiyasa, Dewa GA Aryastuti, Sri Agung Khairunisa, Siti Qamariyah Arijana, IGKN Nasronudin, N Evaluation of antiretroviral effect on mitochondrial DNA depletion among HIV-infected patients in Bali |
title | Evaluation of antiretroviral effect on mitochondrial DNA depletion among HIV-infected patients in Bali |
title_full | Evaluation of antiretroviral effect on mitochondrial DNA depletion among HIV-infected patients in Bali |
title_fullStr | Evaluation of antiretroviral effect on mitochondrial DNA depletion among HIV-infected patients in Bali |
title_full_unstemmed | Evaluation of antiretroviral effect on mitochondrial DNA depletion among HIV-infected patients in Bali |
title_short | Evaluation of antiretroviral effect on mitochondrial DNA depletion among HIV-infected patients in Bali |
title_sort | evaluation of antiretroviral effect on mitochondrial dna depletion among hiv-infected patients in bali |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6072679/ https://www.ncbi.nlm.nih.gov/pubmed/30104903 http://dx.doi.org/10.2147/HIV.S166245 |
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