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Deficits in cortical, diencephalic and midbrain gray matter in alcoholism measured by VBM: Effects of co-morbid substance abuse()()()
OBJECTIVE: Alcoholism has been associated with a widespread pattern of gray matter atrophy. This study sought to investigate the spectrum of volume alterations in a population of alcoholics with only alcohol dependence, polysubstance abusing alcoholics, and a comparison population of healthy control...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3777684/ https://www.ncbi.nlm.nih.gov/pubmed/24179800 http://dx.doi.org/10.1016/j.nicl.2013.03.013 |
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author | Grodin, Erica N. Lin, Henry Durkee, Caitlin A. Hommer, Daniel W. Momenan, Reza |
author_facet | Grodin, Erica N. Lin, Henry Durkee, Caitlin A. Hommer, Daniel W. Momenan, Reza |
author_sort | Grodin, Erica N. |
collection | PubMed |
description | OBJECTIVE: Alcoholism has been associated with a widespread pattern of gray matter atrophy. This study sought to investigate the spectrum of volume alterations in a population of alcoholics with only alcohol dependence, polysubstance abusing alcoholics, and a comparison population of healthy controls. METHOD: Thirty-seven ‘pure’ alcoholics, 93 polysubstance abusing alcoholics, and 69 healthy controls underwent structural T1 MRI scans. Voxel-based morphometry was performed to investigate gray matter alterations. RESULTS: Alcoholic dependent inpatients (both with and without a history of DSM-IV substance abuse/dependence diagnosis) displayed significant gray matter differences in the mesial region of the frontal lobe and right temporal lobe. ‘Pure’ alcoholics exhibited a pattern of subcortical changes similar to that seen in Wernicke–Korsakoff Syndrome when compared to polysubstance abusing alcoholics. ‘Pure’ alcoholics and polysubstance abusing alcoholics did not differ significantly in measures of cortical gray matter, liver function, or nutrition. CONCLUSIONS: These findings reinforce the accepted literature in regards to frontal lobe gray matter atrophy in alcohol dependence. This study calls for additional research in order to investigate the spectrum from uncomplicated alcoholism to Wernicke–Korsakoff Syndrome. Further research is needed to elucidate the exact cause of this pattern of differences and to determine what factors are responsible for the patterns of gray matter reduction or difference in ‘pure’ and polysubstance abusing alcoholics. |
format | Online Article Text |
id | pubmed-3777684 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-37776842013-10-31 Deficits in cortical, diencephalic and midbrain gray matter in alcoholism measured by VBM: Effects of co-morbid substance abuse()()() Grodin, Erica N. Lin, Henry Durkee, Caitlin A. Hommer, Daniel W. Momenan, Reza Neuroimage Clin Regular Articles OBJECTIVE: Alcoholism has been associated with a widespread pattern of gray matter atrophy. This study sought to investigate the spectrum of volume alterations in a population of alcoholics with only alcohol dependence, polysubstance abusing alcoholics, and a comparison population of healthy controls. METHOD: Thirty-seven ‘pure’ alcoholics, 93 polysubstance abusing alcoholics, and 69 healthy controls underwent structural T1 MRI scans. Voxel-based morphometry was performed to investigate gray matter alterations. RESULTS: Alcoholic dependent inpatients (both with and without a history of DSM-IV substance abuse/dependence diagnosis) displayed significant gray matter differences in the mesial region of the frontal lobe and right temporal lobe. ‘Pure’ alcoholics exhibited a pattern of subcortical changes similar to that seen in Wernicke–Korsakoff Syndrome when compared to polysubstance abusing alcoholics. ‘Pure’ alcoholics and polysubstance abusing alcoholics did not differ significantly in measures of cortical gray matter, liver function, or nutrition. CONCLUSIONS: These findings reinforce the accepted literature in regards to frontal lobe gray matter atrophy in alcohol dependence. This study calls for additional research in order to investigate the spectrum from uncomplicated alcoholism to Wernicke–Korsakoff Syndrome. Further research is needed to elucidate the exact cause of this pattern of differences and to determine what factors are responsible for the patterns of gray matter reduction or difference in ‘pure’ and polysubstance abusing alcoholics. Elsevier 2013-04-01 /pmc/articles/PMC3777684/ /pubmed/24179800 http://dx.doi.org/10.1016/j.nicl.2013.03.013 Text en © 2013 The Authors https://creativecommons.org/licenses/by/3.0/This work is licensed under a Creative Commons Attribution 3.0 Unported License (https://creativecommons.org/licenses/by/3.0/) . |
spellingShingle | Regular Articles Grodin, Erica N. Lin, Henry Durkee, Caitlin A. Hommer, Daniel W. Momenan, Reza Deficits in cortical, diencephalic and midbrain gray matter in alcoholism measured by VBM: Effects of co-morbid substance abuse()()() |
title | Deficits in cortical, diencephalic and midbrain gray matter in alcoholism measured by VBM: Effects of co-morbid substance abuse()()() |
title_full | Deficits in cortical, diencephalic and midbrain gray matter in alcoholism measured by VBM: Effects of co-morbid substance abuse()()() |
title_fullStr | Deficits in cortical, diencephalic and midbrain gray matter in alcoholism measured by VBM: Effects of co-morbid substance abuse()()() |
title_full_unstemmed | Deficits in cortical, diencephalic and midbrain gray matter in alcoholism measured by VBM: Effects of co-morbid substance abuse()()() |
title_short | Deficits in cortical, diencephalic and midbrain gray matter in alcoholism measured by VBM: Effects of co-morbid substance abuse()()() |
title_sort | deficits in cortical, diencephalic and midbrain gray matter in alcoholism measured by vbm: effects of co-morbid substance abuse()()() |
topic | Regular Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3777684/ https://www.ncbi.nlm.nih.gov/pubmed/24179800 http://dx.doi.org/10.1016/j.nicl.2013.03.013 |
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