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Short- and Long-term Risks of Highly Active Antiretroviral Treatment with Incident Opportunistic Infections among People Living with HIV/AIDS

Highly active antiretroviral therapy (HAART) causes a rapid increase of CD4 + T cells counts during the first 3–6 months of treatment and may enhance the development of opportunistic infections (OIs). However, the short- and long-term effects of HAART exposure on the development of incident OIs has...

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Autores principales: Yen, Yung-Feng, Chen, Marcelo, Jen, I.-An, Chuang, Pei-Hung, Lee, Chun-Yuan, Lin, Su-I., Chen, Yi-Ming Arthur
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6400900/
https://www.ncbi.nlm.nih.gov/pubmed/30837537
http://dx.doi.org/10.1038/s41598-019-39665-6
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author Yen, Yung-Feng
Chen, Marcelo
Jen, I.-An
Chuang, Pei-Hung
Lee, Chun-Yuan
Lin, Su-I.
Chen, Yi-Ming Arthur
author_facet Yen, Yung-Feng
Chen, Marcelo
Jen, I.-An
Chuang, Pei-Hung
Lee, Chun-Yuan
Lin, Su-I.
Chen, Yi-Ming Arthur
author_sort Yen, Yung-Feng
collection PubMed
description Highly active antiretroviral therapy (HAART) causes a rapid increase of CD4 + T cells counts during the first 3–6 months of treatment and may enhance the development of opportunistic infections (OIs). However, the short- and long-term effects of HAART exposure on the development of incident OIs has not been extensively studied. This nationwide longitudinal study followed up a total of 26,258 people living with HIV/AIDS (PLWHA) to ascertain the short- and long-term effects of HAART on incident OIs. During 150,196 person-years of follow-up, 6,413 (24.4%) PLWHA had new onset of OIs. After adjusting for demographics, comorbidities, and AIDS status, PLWHA who received HAART were more likely to develop OIs than those who did not receive HAART. Considering the short- and long-term effects of HAART on the development of OIs, HAART was found to be a risk factor for developing OIs during the first 90 days of treatment, but a protective factor against OIs after 180 days of HAART use. The risk for the development of active OIs significantly decreased as the duration of HAART increased (P < 0.001). Our study suggests that HAART is a risk factor for developing OIs in the short term, but is a protective factor in the long term.
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spelling pubmed-64009002019-03-07 Short- and Long-term Risks of Highly Active Antiretroviral Treatment with Incident Opportunistic Infections among People Living with HIV/AIDS Yen, Yung-Feng Chen, Marcelo Jen, I.-An Chuang, Pei-Hung Lee, Chun-Yuan Lin, Su-I. Chen, Yi-Ming Arthur Sci Rep Article Highly active antiretroviral therapy (HAART) causes a rapid increase of CD4 + T cells counts during the first 3–6 months of treatment and may enhance the development of opportunistic infections (OIs). However, the short- and long-term effects of HAART exposure on the development of incident OIs has not been extensively studied. This nationwide longitudinal study followed up a total of 26,258 people living with HIV/AIDS (PLWHA) to ascertain the short- and long-term effects of HAART on incident OIs. During 150,196 person-years of follow-up, 6,413 (24.4%) PLWHA had new onset of OIs. After adjusting for demographics, comorbidities, and AIDS status, PLWHA who received HAART were more likely to develop OIs than those who did not receive HAART. Considering the short- and long-term effects of HAART on the development of OIs, HAART was found to be a risk factor for developing OIs during the first 90 days of treatment, but a protective factor against OIs after 180 days of HAART use. The risk for the development of active OIs significantly decreased as the duration of HAART increased (P < 0.001). Our study suggests that HAART is a risk factor for developing OIs in the short term, but is a protective factor in the long term. Nature Publishing Group UK 2019-03-05 /pmc/articles/PMC6400900/ /pubmed/30837537 http://dx.doi.org/10.1038/s41598-019-39665-6 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Yen, Yung-Feng
Chen, Marcelo
Jen, I.-An
Chuang, Pei-Hung
Lee, Chun-Yuan
Lin, Su-I.
Chen, Yi-Ming Arthur
Short- and Long-term Risks of Highly Active Antiretroviral Treatment with Incident Opportunistic Infections among People Living with HIV/AIDS
title Short- and Long-term Risks of Highly Active Antiretroviral Treatment with Incident Opportunistic Infections among People Living with HIV/AIDS
title_full Short- and Long-term Risks of Highly Active Antiretroviral Treatment with Incident Opportunistic Infections among People Living with HIV/AIDS
title_fullStr Short- and Long-term Risks of Highly Active Antiretroviral Treatment with Incident Opportunistic Infections among People Living with HIV/AIDS
title_full_unstemmed Short- and Long-term Risks of Highly Active Antiretroviral Treatment with Incident Opportunistic Infections among People Living with HIV/AIDS
title_short Short- and Long-term Risks of Highly Active Antiretroviral Treatment with Incident Opportunistic Infections among People Living with HIV/AIDS
title_sort short- and long-term risks of highly active antiretroviral treatment with incident opportunistic infections among people living with hiv/aids
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6400900/
https://www.ncbi.nlm.nih.gov/pubmed/30837537
http://dx.doi.org/10.1038/s41598-019-39665-6
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