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Focus on the Brain: HIV Infection and Alcoholism: Comorbidity Effects on Brain Structure and Function

Both HIV infection and alcohol abuse have negative effects on the brain, with some unique to each condition and others shared by both conditions. Investigators have used magnetic resonance imaging to study the size and integrity of various brain structures in participants with alcoholism, HIV infect...

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Autores principales: Rosenbloom, Margaret J., Sullivan, Edith V., Pfefferbaum, Adolf
Formato: Online Artículo Texto
Lenguaje:English
Publicado: National Institute on Alcohol Abuse and Alcoholism 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3860510/
https://www.ncbi.nlm.nih.gov/pubmed/23584066
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author Rosenbloom, Margaret J.
Sullivan, Edith V.
Pfefferbaum, Adolf
author_facet Rosenbloom, Margaret J.
Sullivan, Edith V.
Pfefferbaum, Adolf
author_sort Rosenbloom, Margaret J.
collection PubMed
description Both HIV infection and alcohol abuse have negative effects on the brain, with some unique to each condition and others shared by both conditions. Investigators have used magnetic resonance imaging to study the size and integrity of various brain structures in participants with alcoholism, HIV infection, or both conditions and in healthy control subjects. In these studies, alcoholics exhibited enlarged, cerebrospinal fluid-filled spaces (i.e., ventricles) as well as tissue shrinkage in various brain regions (e.g., the corpus callosum and frontal cortex), whereas study participants with asymptomatic HIV infection showed few abnormalities. Those with both HIV infection and alcoholism also had these volume abnormalities, particularly if they had experienced an AIDS-defining event. Diffusion tensor imaging, which measures the integrity of white matter fibers, has identified abnormalities of constituents of these fibers in both diseases. Again, people with HIV infection plus alcoholism show the greatest abnormalities, particularly those with a history of an AIDS-defining event. Magnetic resonance spectroscopy, which assesses the levels of brain metabolites and selective neurotransmitters, has revealed different patterns of deficits in biochemical markers of brain integrity in individuals singly affected and a compounding of effects in individuals with both HIV infection and alcoholism. Finally, neuropsychological studies have revealed impairment in selective functions involving working memory, visuospatial abilities, and movement speed that are especially likely to occur in people with comorbid HIV infection and alcoholism. Thus, alcoholism is a major risk factor for development of neuropathology and its functional sequelae in HIV-infected people.
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spelling pubmed-38605102014-01-13 Focus on the Brain: HIV Infection and Alcoholism: Comorbidity Effects on Brain Structure and Function Rosenbloom, Margaret J. Sullivan, Edith V. Pfefferbaum, Adolf Alcohol Res Health Special Section: Modeling HIV and Alcohol’s Effects Both HIV infection and alcohol abuse have negative effects on the brain, with some unique to each condition and others shared by both conditions. Investigators have used magnetic resonance imaging to study the size and integrity of various brain structures in participants with alcoholism, HIV infection, or both conditions and in healthy control subjects. In these studies, alcoholics exhibited enlarged, cerebrospinal fluid-filled spaces (i.e., ventricles) as well as tissue shrinkage in various brain regions (e.g., the corpus callosum and frontal cortex), whereas study participants with asymptomatic HIV infection showed few abnormalities. Those with both HIV infection and alcoholism also had these volume abnormalities, particularly if they had experienced an AIDS-defining event. Diffusion tensor imaging, which measures the integrity of white matter fibers, has identified abnormalities of constituents of these fibers in both diseases. Again, people with HIV infection plus alcoholism show the greatest abnormalities, particularly those with a history of an AIDS-defining event. Magnetic resonance spectroscopy, which assesses the levels of brain metabolites and selective neurotransmitters, has revealed different patterns of deficits in biochemical markers of brain integrity in individuals singly affected and a compounding of effects in individuals with both HIV infection and alcoholism. Finally, neuropsychological studies have revealed impairment in selective functions involving working memory, visuospatial abilities, and movement speed that are especially likely to occur in people with comorbid HIV infection and alcoholism. Thus, alcoholism is a major risk factor for development of neuropathology and its functional sequelae in HIV-infected people. National Institute on Alcohol Abuse and Alcoholism 2010 /pmc/articles/PMC3860510/ /pubmed/23584066 Text en http://creativecommons.org/publicdomain/mark/1.0/ Unless otherwise noted in the text, all material appearing in this journal is in the public domain and may be reproduced without permission. Citation of the source is appreciated.
spellingShingle Special Section: Modeling HIV and Alcohol’s Effects
Rosenbloom, Margaret J.
Sullivan, Edith V.
Pfefferbaum, Adolf
Focus on the Brain: HIV Infection and Alcoholism: Comorbidity Effects on Brain Structure and Function
title Focus on the Brain: HIV Infection and Alcoholism: Comorbidity Effects on Brain Structure and Function
title_full Focus on the Brain: HIV Infection and Alcoholism: Comorbidity Effects on Brain Structure and Function
title_fullStr Focus on the Brain: HIV Infection and Alcoholism: Comorbidity Effects on Brain Structure and Function
title_full_unstemmed Focus on the Brain: HIV Infection and Alcoholism: Comorbidity Effects on Brain Structure and Function
title_short Focus on the Brain: HIV Infection and Alcoholism: Comorbidity Effects on Brain Structure and Function
title_sort focus on the brain: hiv infection and alcoholism: comorbidity effects on brain structure and function
topic Special Section: Modeling HIV and Alcohol’s Effects
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3860510/
https://www.ncbi.nlm.nih.gov/pubmed/23584066
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