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Biogenic amine metabolism in juvenile neurocardiogenic syncope with dysautonomia
OBJECTIVE: Biogenic amine brain levels and their cerebral metabolism are frequently studied by quantitation of biogenic amine metabolites in cerebrospinal fluid (CSF) compared to age-matched controls. There is a paucity of studies in adolescents and young adults investigating the potential role of d...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Blackwell Publishing Ltd
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4292742/ https://www.ncbi.nlm.nih.gov/pubmed/25590038 http://dx.doi.org/10.1002/acn3.49 |
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author | Butler, Ian J Lankford, Jeremy E Hashmi, Syed Shahrukh Numan, Mohammed T |
author_facet | Butler, Ian J Lankford, Jeremy E Hashmi, Syed Shahrukh Numan, Mohammed T |
author_sort | Butler, Ian J |
collection | PubMed |
description | OBJECTIVE: Biogenic amine brain levels and their cerebral metabolism are frequently studied by quantitation of biogenic amine metabolites in cerebrospinal fluid (CSF) compared to age-matched controls. There is a paucity of studies in adolescents and young adults investigating the potential role of disordered cerebral biogenic amine metabolism in young patients who have dysautonomia based on abnormal head-up tilt table (HUTT). METHODS: In a cohort of juvenile patients with neurocardiogenic syncope and dysautonomia documented by abnormal HUTT, biogenic amine metabolites of dopamine and serotonin were quantitated in 18 patients (15 females). HUTT testing is an effective clinical method to evaluate posturally induced physiological events in patients suspected of neurocardiogenic syncope with dysautonomia. RESULTS: Levels of the dopamine metabolite (homovanillic acid: HVA) and/or the serotonin metabolite (5-hydroxyindoleacetic acid: 5HIAA) were significantly reduced in 13 patients compared to age-matched controls. INTERPRETATION: Peripheral biogenic amines and their metabolites have been extensively studied in adults with dysautonomia due to various neurodegenerative disorders (Parkinson disease, multiple system atrophy, primary autonomic failure). Our findings indicate that more than two-thirds of this cohort of young patients with dysautonomia of variable severity have a defect in cerebral biogenic amines, particularly in dopamine and serotonin metabolism. |
format | Online Article Text |
id | pubmed-4292742 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Blackwell Publishing Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-42927422015-01-14 Biogenic amine metabolism in juvenile neurocardiogenic syncope with dysautonomia Butler, Ian J Lankford, Jeremy E Hashmi, Syed Shahrukh Numan, Mohammed T Ann Clin Transl Neurol Research Papers OBJECTIVE: Biogenic amine brain levels and their cerebral metabolism are frequently studied by quantitation of biogenic amine metabolites in cerebrospinal fluid (CSF) compared to age-matched controls. There is a paucity of studies in adolescents and young adults investigating the potential role of disordered cerebral biogenic amine metabolism in young patients who have dysautonomia based on abnormal head-up tilt table (HUTT). METHODS: In a cohort of juvenile patients with neurocardiogenic syncope and dysautonomia documented by abnormal HUTT, biogenic amine metabolites of dopamine and serotonin were quantitated in 18 patients (15 females). HUTT testing is an effective clinical method to evaluate posturally induced physiological events in patients suspected of neurocardiogenic syncope with dysautonomia. RESULTS: Levels of the dopamine metabolite (homovanillic acid: HVA) and/or the serotonin metabolite (5-hydroxyindoleacetic acid: 5HIAA) were significantly reduced in 13 patients compared to age-matched controls. INTERPRETATION: Peripheral biogenic amines and their metabolites have been extensively studied in adults with dysautonomia due to various neurodegenerative disorders (Parkinson disease, multiple system atrophy, primary autonomic failure). Our findings indicate that more than two-thirds of this cohort of young patients with dysautonomia of variable severity have a defect in cerebral biogenic amines, particularly in dopamine and serotonin metabolism. Blackwell Publishing Ltd 2014-04 2014-03-26 /pmc/articles/PMC4292742/ /pubmed/25590038 http://dx.doi.org/10.1002/acn3.49 Text en © 2014 The Authors. Annals of Clinical and Translational Neurology published by Wiley Periodicals, Inc on behalf of American Neurological Association. http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an open access article under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made. |
spellingShingle | Research Papers Butler, Ian J Lankford, Jeremy E Hashmi, Syed Shahrukh Numan, Mohammed T Biogenic amine metabolism in juvenile neurocardiogenic syncope with dysautonomia |
title | Biogenic amine metabolism in juvenile neurocardiogenic syncope with dysautonomia |
title_full | Biogenic amine metabolism in juvenile neurocardiogenic syncope with dysautonomia |
title_fullStr | Biogenic amine metabolism in juvenile neurocardiogenic syncope with dysautonomia |
title_full_unstemmed | Biogenic amine metabolism in juvenile neurocardiogenic syncope with dysautonomia |
title_short | Biogenic amine metabolism in juvenile neurocardiogenic syncope with dysautonomia |
title_sort | biogenic amine metabolism in juvenile neurocardiogenic syncope with dysautonomia |
topic | Research Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4292742/ https://www.ncbi.nlm.nih.gov/pubmed/25590038 http://dx.doi.org/10.1002/acn3.49 |
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