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Peripheral and Central Iron Measures in Alcohol Use Disorder and Aging: A Quantitative Susceptibility Mapping Pilot Study
Chronic excessive alcohol use has neurotoxic effects, which may contribute to cognitive decline and the risk of early-onset dementia. Elevated peripheral iron levels have been reported in individuals with alcohol use disorder (AUD), but its association with brain iron loading has not been explored....
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10002495/ https://www.ncbi.nlm.nih.gov/pubmed/36901892 http://dx.doi.org/10.3390/ijms24054461 |
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author | Adams, Aiden R. Li, Xinyi Byanyima, Juliana I. Vesslee, Sianneh A. Nguyen, Thanh D. Wang, Yi Moon, Brianna Pond, Timothy Kranzler, Henry R. Witschey, Walter R. Shi, Zhenhao Wiers, Corinde E. |
author_facet | Adams, Aiden R. Li, Xinyi Byanyima, Juliana I. Vesslee, Sianneh A. Nguyen, Thanh D. Wang, Yi Moon, Brianna Pond, Timothy Kranzler, Henry R. Witschey, Walter R. Shi, Zhenhao Wiers, Corinde E. |
author_sort | Adams, Aiden R. |
collection | PubMed |
description | Chronic excessive alcohol use has neurotoxic effects, which may contribute to cognitive decline and the risk of early-onset dementia. Elevated peripheral iron levels have been reported in individuals with alcohol use disorder (AUD), but its association with brain iron loading has not been explored. We evaluated whether (1) serum and brain iron loading are higher in individuals with AUD than non-dependent healthy controls and (2) serum and brain iron loading increase with age. A fasting serum iron panel was obtained and a magnetic resonance imaging scan with quantitative susceptibility mapping (QSM) was used to quantify brain iron concentrations. Although serum ferritin levels were higher in the AUD group than in controls, whole-brain iron susceptibility did not differ between groups. Voxel-wise QSM analyses revealed higher susceptibility in a cluster in the left globus pallidus in individuals with AUD than controls. Whole-brain iron increased with age and voxel-wise QSM indicated higher susceptibility with age in various brain areas including the basal ganglia. This is the first study to analyze both serum and brain iron loading in individuals with AUD. Larger studies are needed to examine the effects of alcohol use on iron loading and its associations with alcohol use severity, structural and functional brain changes, and alcohol-induced cognitive impairments. |
format | Online Article Text |
id | pubmed-10002495 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-100024952023-03-11 Peripheral and Central Iron Measures in Alcohol Use Disorder and Aging: A Quantitative Susceptibility Mapping Pilot Study Adams, Aiden R. Li, Xinyi Byanyima, Juliana I. Vesslee, Sianneh A. Nguyen, Thanh D. Wang, Yi Moon, Brianna Pond, Timothy Kranzler, Henry R. Witschey, Walter R. Shi, Zhenhao Wiers, Corinde E. Int J Mol Sci Article Chronic excessive alcohol use has neurotoxic effects, which may contribute to cognitive decline and the risk of early-onset dementia. Elevated peripheral iron levels have been reported in individuals with alcohol use disorder (AUD), but its association with brain iron loading has not been explored. We evaluated whether (1) serum and brain iron loading are higher in individuals with AUD than non-dependent healthy controls and (2) serum and brain iron loading increase with age. A fasting serum iron panel was obtained and a magnetic resonance imaging scan with quantitative susceptibility mapping (QSM) was used to quantify brain iron concentrations. Although serum ferritin levels were higher in the AUD group than in controls, whole-brain iron susceptibility did not differ between groups. Voxel-wise QSM analyses revealed higher susceptibility in a cluster in the left globus pallidus in individuals with AUD than controls. Whole-brain iron increased with age and voxel-wise QSM indicated higher susceptibility with age in various brain areas including the basal ganglia. This is the first study to analyze both serum and brain iron loading in individuals with AUD. Larger studies are needed to examine the effects of alcohol use on iron loading and its associations with alcohol use severity, structural and functional brain changes, and alcohol-induced cognitive impairments. MDPI 2023-02-24 /pmc/articles/PMC10002495/ /pubmed/36901892 http://dx.doi.org/10.3390/ijms24054461 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Adams, Aiden R. Li, Xinyi Byanyima, Juliana I. Vesslee, Sianneh A. Nguyen, Thanh D. Wang, Yi Moon, Brianna Pond, Timothy Kranzler, Henry R. Witschey, Walter R. Shi, Zhenhao Wiers, Corinde E. Peripheral and Central Iron Measures in Alcohol Use Disorder and Aging: A Quantitative Susceptibility Mapping Pilot Study |
title | Peripheral and Central Iron Measures in Alcohol Use Disorder and Aging: A Quantitative Susceptibility Mapping Pilot Study |
title_full | Peripheral and Central Iron Measures in Alcohol Use Disorder and Aging: A Quantitative Susceptibility Mapping Pilot Study |
title_fullStr | Peripheral and Central Iron Measures in Alcohol Use Disorder and Aging: A Quantitative Susceptibility Mapping Pilot Study |
title_full_unstemmed | Peripheral and Central Iron Measures in Alcohol Use Disorder and Aging: A Quantitative Susceptibility Mapping Pilot Study |
title_short | Peripheral and Central Iron Measures in Alcohol Use Disorder and Aging: A Quantitative Susceptibility Mapping Pilot Study |
title_sort | peripheral and central iron measures in alcohol use disorder and aging: a quantitative susceptibility mapping pilot study |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10002495/ https://www.ncbi.nlm.nih.gov/pubmed/36901892 http://dx.doi.org/10.3390/ijms24054461 |
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