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Examining Relationships between Metabolism and Persistent Inflammation in HIV Patients on Antiretroviral Therapy

With the advent of antiretroviral therapy (ART), HIV-infected individuals are now living longer and healthier lives. However, ART does not completely restore health and treated individuals are experiencing increased rates of noncommunicable diseases such as dyslipidemia, insulin resistance, type 2 d...

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Detalles Bibliográficos
Autores principales: Ahmed, Duale, Roy, David, Cassol, Edana
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6181007/
https://www.ncbi.nlm.nih.gov/pubmed/30363715
http://dx.doi.org/10.1155/2018/6238978
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author Ahmed, Duale
Roy, David
Cassol, Edana
author_facet Ahmed, Duale
Roy, David
Cassol, Edana
author_sort Ahmed, Duale
collection PubMed
description With the advent of antiretroviral therapy (ART), HIV-infected individuals are now living longer and healthier lives. However, ART does not completely restore health and treated individuals are experiencing increased rates of noncommunicable diseases such as dyslipidemia, insulin resistance, type 2 diabetes, cardiovascular disease, and nonalcoholic fatty liver disease. While it is well known that persistent immune activation and inflammation contribute to the development of these comorbid diseases, the mechanisms underlying this chronic activation remain incompletely understood. In this review, we will discuss emerging evidence that suggests that alterations in cellular metabolism may play a central role in driving this immune dysfunction in HIV patients on ART.
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spelling pubmed-61810072018-10-24 Examining Relationships between Metabolism and Persistent Inflammation in HIV Patients on Antiretroviral Therapy Ahmed, Duale Roy, David Cassol, Edana Mediators Inflamm Review Article With the advent of antiretroviral therapy (ART), HIV-infected individuals are now living longer and healthier lives. However, ART does not completely restore health and treated individuals are experiencing increased rates of noncommunicable diseases such as dyslipidemia, insulin resistance, type 2 diabetes, cardiovascular disease, and nonalcoholic fatty liver disease. While it is well known that persistent immune activation and inflammation contribute to the development of these comorbid diseases, the mechanisms underlying this chronic activation remain incompletely understood. In this review, we will discuss emerging evidence that suggests that alterations in cellular metabolism may play a central role in driving this immune dysfunction in HIV patients on ART. Hindawi 2018-09-27 /pmc/articles/PMC6181007/ /pubmed/30363715 http://dx.doi.org/10.1155/2018/6238978 Text en Copyright © 2018 Duale Ahmed et al. http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Ahmed, Duale
Roy, David
Cassol, Edana
Examining Relationships between Metabolism and Persistent Inflammation in HIV Patients on Antiretroviral Therapy
title Examining Relationships between Metabolism and Persistent Inflammation in HIV Patients on Antiretroviral Therapy
title_full Examining Relationships between Metabolism and Persistent Inflammation in HIV Patients on Antiretroviral Therapy
title_fullStr Examining Relationships between Metabolism and Persistent Inflammation in HIV Patients on Antiretroviral Therapy
title_full_unstemmed Examining Relationships between Metabolism and Persistent Inflammation in HIV Patients on Antiretroviral Therapy
title_short Examining Relationships between Metabolism and Persistent Inflammation in HIV Patients on Antiretroviral Therapy
title_sort examining relationships between metabolism and persistent inflammation in hiv patients on antiretroviral therapy
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6181007/
https://www.ncbi.nlm.nih.gov/pubmed/30363715
http://dx.doi.org/10.1155/2018/6238978
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