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Cholinergic transmission is impaired in patients with idiopathic normal-pressure hydrocephalus: a TMS study
The pathophysiological mechanisms of cognitive and gait disturbances in subjects with normal-pressure hydrocephalus (NPH) are still unclear. Cholinergic and other neurotransmitter abnormalities have been reported in animal models of NPH. The objective of this study was to evaluate the short latency...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Springer Vienna
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6647526/ https://www.ncbi.nlm.nih.gov/pubmed/31227893 http://dx.doi.org/10.1007/s00702-019-02036-6 |
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author | Nardone, Raffaele Golaszewski, Stefan Schwenker, Kerstin Brigo, Francesco Maccarrone, Miriam Versace, Viviana Sebastianelli, Luca Saltuari, Leopold Höller, Yvonne |
author_facet | Nardone, Raffaele Golaszewski, Stefan Schwenker, Kerstin Brigo, Francesco Maccarrone, Miriam Versace, Viviana Sebastianelli, Luca Saltuari, Leopold Höller, Yvonne |
author_sort | Nardone, Raffaele |
collection | PubMed |
description | The pathophysiological mechanisms of cognitive and gait disturbances in subjects with normal-pressure hydrocephalus (NPH) are still unclear. Cholinergic and other neurotransmitter abnormalities have been reported in animal models of NPH. The objective of this study was to evaluate the short latency afferent inhibition (SAI), a transcranial magnetic stimulation protocol which gives the possibility to test an inhibitory cholinergic circuit in the human brain, in subjects with idiopathic NPH (iNPH). We applied SAI technique in twenty iNPH patients before ventricular shunt surgery. Besides SAI, also the resting motor threshold and the short intracortical inhibition to paired stimulation were assessed. A significant reduction of the SAI (p = 0.016), associated with a less pronounced decrease of the resting motor threshold and the short latency intracortical inhibition to paired stimulation, were observed in patients with iNPH at baseline evaluation. We also found significant (p < 0.001) correlations between SAI values and the gait function tests, as well as between SAI and the neuropsychological tests. These findings suggest that the impairment of cholinergic neurons markedly contributes to cognitive decline and gait impairment in subjects with iNPH. |
format | Online Article Text |
id | pubmed-6647526 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Springer Vienna |
record_format | MEDLINE/PubMed |
spelling | pubmed-66475262019-08-06 Cholinergic transmission is impaired in patients with idiopathic normal-pressure hydrocephalus: a TMS study Nardone, Raffaele Golaszewski, Stefan Schwenker, Kerstin Brigo, Francesco Maccarrone, Miriam Versace, Viviana Sebastianelli, Luca Saltuari, Leopold Höller, Yvonne J Neural Transm (Vienna) Neurology and Preclinical Neurological Studies - Original Article The pathophysiological mechanisms of cognitive and gait disturbances in subjects with normal-pressure hydrocephalus (NPH) are still unclear. Cholinergic and other neurotransmitter abnormalities have been reported in animal models of NPH. The objective of this study was to evaluate the short latency afferent inhibition (SAI), a transcranial magnetic stimulation protocol which gives the possibility to test an inhibitory cholinergic circuit in the human brain, in subjects with idiopathic NPH (iNPH). We applied SAI technique in twenty iNPH patients before ventricular shunt surgery. Besides SAI, also the resting motor threshold and the short intracortical inhibition to paired stimulation were assessed. A significant reduction of the SAI (p = 0.016), associated with a less pronounced decrease of the resting motor threshold and the short latency intracortical inhibition to paired stimulation, were observed in patients with iNPH at baseline evaluation. We also found significant (p < 0.001) correlations between SAI values and the gait function tests, as well as between SAI and the neuropsychological tests. These findings suggest that the impairment of cholinergic neurons markedly contributes to cognitive decline and gait impairment in subjects with iNPH. Springer Vienna 2019-06-21 2019 /pmc/articles/PMC6647526/ /pubmed/31227893 http://dx.doi.org/10.1007/s00702-019-02036-6 Text en © The Author(s) 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. |
spellingShingle | Neurology and Preclinical Neurological Studies - Original Article Nardone, Raffaele Golaszewski, Stefan Schwenker, Kerstin Brigo, Francesco Maccarrone, Miriam Versace, Viviana Sebastianelli, Luca Saltuari, Leopold Höller, Yvonne Cholinergic transmission is impaired in patients with idiopathic normal-pressure hydrocephalus: a TMS study |
title | Cholinergic transmission is impaired in patients with idiopathic normal-pressure hydrocephalus: a TMS study |
title_full | Cholinergic transmission is impaired in patients with idiopathic normal-pressure hydrocephalus: a TMS study |
title_fullStr | Cholinergic transmission is impaired in patients with idiopathic normal-pressure hydrocephalus: a TMS study |
title_full_unstemmed | Cholinergic transmission is impaired in patients with idiopathic normal-pressure hydrocephalus: a TMS study |
title_short | Cholinergic transmission is impaired in patients with idiopathic normal-pressure hydrocephalus: a TMS study |
title_sort | cholinergic transmission is impaired in patients with idiopathic normal-pressure hydrocephalus: a tms study |
topic | Neurology and Preclinical Neurological Studies - Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6647526/ https://www.ncbi.nlm.nih.gov/pubmed/31227893 http://dx.doi.org/10.1007/s00702-019-02036-6 |
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