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Incongruent reduction of dopamine transporter availability in different subgroups of alcohol dependence

The dopamine transporter (DAT) plays a crucial role in the pathogenesis of alcohol dependence (AD) and major depression (MD), and males have more risk factors for the development of AD. However, imaging studies on brain DAT availability in males with AD comorbid with MD (AD/MD) are limited, and the...

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Autores principales: Yen, Che-Hung, Shih, Mei-Chen, Cheng, Cheng-Yi, Ma, Kuo-Hsing, Lu, Ru-Band, Huang, San-Yuan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5370777/
https://www.ncbi.nlm.nih.gov/pubmed/27537550
http://dx.doi.org/10.1097/MD.0000000000004048
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author Yen, Che-Hung
Shih, Mei-Chen
Cheng, Cheng-Yi
Ma, Kuo-Hsing
Lu, Ru-Band
Huang, San-Yuan
author_facet Yen, Che-Hung
Shih, Mei-Chen
Cheng, Cheng-Yi
Ma, Kuo-Hsing
Lu, Ru-Band
Huang, San-Yuan
author_sort Yen, Che-Hung
collection PubMed
description The dopamine transporter (DAT) plays a crucial role in the pathogenesis of alcohol dependence (AD) and major depression (MD), and males have more risk factors for the development of AD. However, imaging studies on brain DAT availability in males with AD comorbid with MD (AD/MD) are limited, and the association of DAT availability with cognitive function and depressive scores in patients with AD/MD has not been analyzed. Hence, this study examined the relationship between brain DAT availability, cognitive function, and depressive symptoms in different subgroups of males with AD. Single-photon emission computed tomography imaging with (99m)Tc-TRODAT-1 as a ligand was used to measure striatal DAT availability in 49 patients with AD (28 pure AD and 21 AD/MD) and 24 age- and sex-matched healthy volunteers. The Wisconsin Card Sorting Test (WCST) and 17-item Hamilton Depression Rating Scale were used to assess neurocognitive function and depressive scores, respectively. Patients with AD showed a significant reduction of DAT availability in 3 brain regions (P < 0.001), and this reduction was more pronounced in the patients with pure AD compared to healthy controls. The patients with AD showed significantly poorer performance on the WCST, but only in the control group was DAT availability significantly negatively correlated with total errors and perseverative errors (P < 0.001). These preliminary findings suggest that DAT availability is associated with neurocognitive function, and incongruent reduction of DAT may play a pathophysiological role in different subgroups of AD. In addition, decreased DAT availability may be associated with the severity of depressive symptoms in patients with AD/MD.
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spelling pubmed-53707772017-03-31 Incongruent reduction of dopamine transporter availability in different subgroups of alcohol dependence Yen, Che-Hung Shih, Mei-Chen Cheng, Cheng-Yi Ma, Kuo-Hsing Lu, Ru-Band Huang, San-Yuan Medicine (Baltimore) 5300 The dopamine transporter (DAT) plays a crucial role in the pathogenesis of alcohol dependence (AD) and major depression (MD), and males have more risk factors for the development of AD. However, imaging studies on brain DAT availability in males with AD comorbid with MD (AD/MD) are limited, and the association of DAT availability with cognitive function and depressive scores in patients with AD/MD has not been analyzed. Hence, this study examined the relationship between brain DAT availability, cognitive function, and depressive symptoms in different subgroups of males with AD. Single-photon emission computed tomography imaging with (99m)Tc-TRODAT-1 as a ligand was used to measure striatal DAT availability in 49 patients with AD (28 pure AD and 21 AD/MD) and 24 age- and sex-matched healthy volunteers. The Wisconsin Card Sorting Test (WCST) and 17-item Hamilton Depression Rating Scale were used to assess neurocognitive function and depressive scores, respectively. Patients with AD showed a significant reduction of DAT availability in 3 brain regions (P < 0.001), and this reduction was more pronounced in the patients with pure AD compared to healthy controls. The patients with AD showed significantly poorer performance on the WCST, but only in the control group was DAT availability significantly negatively correlated with total errors and perseverative errors (P < 0.001). These preliminary findings suggest that DAT availability is associated with neurocognitive function, and incongruent reduction of DAT may play a pathophysiological role in different subgroups of AD. In addition, decreased DAT availability may be associated with the severity of depressive symptoms in patients with AD/MD. Wolters Kluwer Health 2016-08-19 /pmc/articles/PMC5370777/ /pubmed/27537550 http://dx.doi.org/10.1097/MD.0000000000004048 Text en Copyright © 2016 the Author(s). Published by Wolters Kluwer Health, Inc. All rights reserved. http://creativecommons.org/licenses/by/4.0 This is an open access article distributed under the Creative Commons Attribution License 4.0, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. http://creativecommons.org/licenses/by/4.0
spellingShingle 5300
Yen, Che-Hung
Shih, Mei-Chen
Cheng, Cheng-Yi
Ma, Kuo-Hsing
Lu, Ru-Band
Huang, San-Yuan
Incongruent reduction of dopamine transporter availability in different subgroups of alcohol dependence
title Incongruent reduction of dopamine transporter availability in different subgroups of alcohol dependence
title_full Incongruent reduction of dopamine transporter availability in different subgroups of alcohol dependence
title_fullStr Incongruent reduction of dopamine transporter availability in different subgroups of alcohol dependence
title_full_unstemmed Incongruent reduction of dopamine transporter availability in different subgroups of alcohol dependence
title_short Incongruent reduction of dopamine transporter availability in different subgroups of alcohol dependence
title_sort incongruent reduction of dopamine transporter availability in different subgroups of alcohol dependence
topic 5300
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5370777/
https://www.ncbi.nlm.nih.gov/pubmed/27537550
http://dx.doi.org/10.1097/MD.0000000000004048
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