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Illicit Stimulant Use Is Associated with Abnormal Substantia Nigra Morphology in Humans

Use of illicit stimulants such as methamphetamine, cocaine, and ecstasy is an increasing health problem. Chronic use can cause neurotoxicity in animals and humans but the long-term consequences are not well understood. The aim of the current study was to investigate the long-term effect of stimulant...

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Autores principales: Todd, Gabrielle, Noyes, Carolyn, Flavel, Stanley C., Della Vedova, Chris B., Spyropoulos, Peter, Chatterton, Barry, Berg, Daniela, White, Jason M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3572078/
https://www.ncbi.nlm.nih.gov/pubmed/23418568
http://dx.doi.org/10.1371/journal.pone.0056438
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author Todd, Gabrielle
Noyes, Carolyn
Flavel, Stanley C.
Della Vedova, Chris B.
Spyropoulos, Peter
Chatterton, Barry
Berg, Daniela
White, Jason M.
author_facet Todd, Gabrielle
Noyes, Carolyn
Flavel, Stanley C.
Della Vedova, Chris B.
Spyropoulos, Peter
Chatterton, Barry
Berg, Daniela
White, Jason M.
author_sort Todd, Gabrielle
collection PubMed
description Use of illicit stimulants such as methamphetamine, cocaine, and ecstasy is an increasing health problem. Chronic use can cause neurotoxicity in animals and humans but the long-term consequences are not well understood. The aim of the current study was to investigate the long-term effect of stimulant use on the morphology of the human substantia nigra. We hypothesised that history of illicit stimulant use is associated with an abnormally bright and enlarged substantia nigra (termed ‘hyperechogenicity’) when viewed with transcranial sonography. Substantia nigra morphology was assessed in abstinent stimulant users (n = 36; 31±9 yrs) and in two groups of control subjects: non-drug users (n = 29; 24±5 yrs) and cannabis users (n = 12; 25±7 yrs). Substantia nigra morphology was viewed with transcranial sonography and the area of echogenicity at the anatomical site of the substantia nigra was measured at its greatest extent. The area of substantia nigra echogenicity was significantly larger in the stimulant group (0.273±0.078 cm(2)) than in the control (0.201±0.054 cm(2); P<0.001) and cannabis (0.202±0.045 cm(2); P<0.007) groups. 53% of stimulant users exhibited echogenicity that exceeded the 90(th) percentile for the control group. The results of the current study suggest that individuals with a history of illicit stimulant use exhibit abnormal substantia nigra morphology. Substantia nigra hyperechogenicity is a strong risk factor for developing Parkinson's disease later in life and further research is required to determine if the observed abnormality in stimulant users is associated with a functional deficit of the nigro-striatal system.
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spelling pubmed-35720782013-02-15 Illicit Stimulant Use Is Associated with Abnormal Substantia Nigra Morphology in Humans Todd, Gabrielle Noyes, Carolyn Flavel, Stanley C. Della Vedova, Chris B. Spyropoulos, Peter Chatterton, Barry Berg, Daniela White, Jason M. PLoS One Research Article Use of illicit stimulants such as methamphetamine, cocaine, and ecstasy is an increasing health problem. Chronic use can cause neurotoxicity in animals and humans but the long-term consequences are not well understood. The aim of the current study was to investigate the long-term effect of stimulant use on the morphology of the human substantia nigra. We hypothesised that history of illicit stimulant use is associated with an abnormally bright and enlarged substantia nigra (termed ‘hyperechogenicity’) when viewed with transcranial sonography. Substantia nigra morphology was assessed in abstinent stimulant users (n = 36; 31±9 yrs) and in two groups of control subjects: non-drug users (n = 29; 24±5 yrs) and cannabis users (n = 12; 25±7 yrs). Substantia nigra morphology was viewed with transcranial sonography and the area of echogenicity at the anatomical site of the substantia nigra was measured at its greatest extent. The area of substantia nigra echogenicity was significantly larger in the stimulant group (0.273±0.078 cm(2)) than in the control (0.201±0.054 cm(2); P<0.001) and cannabis (0.202±0.045 cm(2); P<0.007) groups. 53% of stimulant users exhibited echogenicity that exceeded the 90(th) percentile for the control group. The results of the current study suggest that individuals with a history of illicit stimulant use exhibit abnormal substantia nigra morphology. Substantia nigra hyperechogenicity is a strong risk factor for developing Parkinson's disease later in life and further research is required to determine if the observed abnormality in stimulant users is associated with a functional deficit of the nigro-striatal system. Public Library of Science 2013-02-13 /pmc/articles/PMC3572078/ /pubmed/23418568 http://dx.doi.org/10.1371/journal.pone.0056438 Text en © 2013 Todd et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Todd, Gabrielle
Noyes, Carolyn
Flavel, Stanley C.
Della Vedova, Chris B.
Spyropoulos, Peter
Chatterton, Barry
Berg, Daniela
White, Jason M.
Illicit Stimulant Use Is Associated with Abnormal Substantia Nigra Morphology in Humans
title Illicit Stimulant Use Is Associated with Abnormal Substantia Nigra Morphology in Humans
title_full Illicit Stimulant Use Is Associated with Abnormal Substantia Nigra Morphology in Humans
title_fullStr Illicit Stimulant Use Is Associated with Abnormal Substantia Nigra Morphology in Humans
title_full_unstemmed Illicit Stimulant Use Is Associated with Abnormal Substantia Nigra Morphology in Humans
title_short Illicit Stimulant Use Is Associated with Abnormal Substantia Nigra Morphology in Humans
title_sort illicit stimulant use is associated with abnormal substantia nigra morphology in humans
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3572078/
https://www.ncbi.nlm.nih.gov/pubmed/23418568
http://dx.doi.org/10.1371/journal.pone.0056438
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