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The Aging Brain With HIV Infection: Effects of Alcoholism or Hepatitis C Comorbidity

As successfully treated individuals with Human Immunodeficiency Virus (HIV)-infected age, cognitive and health challenges of normal aging ensue, burdened by HIV, treatment side effects, and high prevalence comorbidities, notably, Alcohol Use Disorders (AUD) and Hepatitis C virus (HCV) infection. In...

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Autor principal: Zahr, Natalie M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5874324/
https://www.ncbi.nlm.nih.gov/pubmed/29623036
http://dx.doi.org/10.3389/fnagi.2018.00056
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author Zahr, Natalie M.
author_facet Zahr, Natalie M.
author_sort Zahr, Natalie M.
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description As successfully treated individuals with Human Immunodeficiency Virus (HIV)-infected age, cognitive and health challenges of normal aging ensue, burdened by HIV, treatment side effects, and high prevalence comorbidities, notably, Alcohol Use Disorders (AUD) and Hepatitis C virus (HCV) infection. In 2013, people over 55 years old accounted for 26% of the estimated number of people living with HIV (~1.2 million). The aging brain is increasingly vulnerable to endogenous and exogenous insult which, coupled with HIV infection and comorbid risk factors, can lead to additive or synergistic effects on cognitive and motor function. This paper reviews the literature on neuropsychological and in vivo Magnetic Resonance Imaging (MRI) evaluation of the aging HIV brain, while also considering the effects of comorbidity for AUD and HCV.
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spelling pubmed-58743242018-04-05 The Aging Brain With HIV Infection: Effects of Alcoholism or Hepatitis C Comorbidity Zahr, Natalie M. Front Aging Neurosci Neuroscience As successfully treated individuals with Human Immunodeficiency Virus (HIV)-infected age, cognitive and health challenges of normal aging ensue, burdened by HIV, treatment side effects, and high prevalence comorbidities, notably, Alcohol Use Disorders (AUD) and Hepatitis C virus (HCV) infection. In 2013, people over 55 years old accounted for 26% of the estimated number of people living with HIV (~1.2 million). The aging brain is increasingly vulnerable to endogenous and exogenous insult which, coupled with HIV infection and comorbid risk factors, can lead to additive or synergistic effects on cognitive and motor function. This paper reviews the literature on neuropsychological and in vivo Magnetic Resonance Imaging (MRI) evaluation of the aging HIV brain, while also considering the effects of comorbidity for AUD and HCV. Frontiers Media S.A. 2018-03-22 /pmc/articles/PMC5874324/ /pubmed/29623036 http://dx.doi.org/10.3389/fnagi.2018.00056 Text en Copyright © 2018 Zahr. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neuroscience
Zahr, Natalie M.
The Aging Brain With HIV Infection: Effects of Alcoholism or Hepatitis C Comorbidity
title The Aging Brain With HIV Infection: Effects of Alcoholism or Hepatitis C Comorbidity
title_full The Aging Brain With HIV Infection: Effects of Alcoholism or Hepatitis C Comorbidity
title_fullStr The Aging Brain With HIV Infection: Effects of Alcoholism or Hepatitis C Comorbidity
title_full_unstemmed The Aging Brain With HIV Infection: Effects of Alcoholism or Hepatitis C Comorbidity
title_short The Aging Brain With HIV Infection: Effects of Alcoholism or Hepatitis C Comorbidity
title_sort aging brain with hiv infection: effects of alcoholism or hepatitis c comorbidity
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5874324/
https://www.ncbi.nlm.nih.gov/pubmed/29623036
http://dx.doi.org/10.3389/fnagi.2018.00056
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