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Abnormal ghrelin secretion contributes to gastrointestinal symptoms in multiple system atrophy patients
Patients with multiple system atrophy (MSA) often have evidence of compromised gastrointestinal motility. Ghrelin is a gut hormone that influences gastrointestinal motility in humans. The aim of this study was to determine whether ghrelin secretion is affected in MSA patients, and to investigate the...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3734593/ https://www.ncbi.nlm.nih.gov/pubmed/23652420 http://dx.doi.org/10.1007/s00415-013-6944-9 |
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author | Ozawa, Tetsutaro Tokunaga, Jun Arakawa, Musashi Ishikawa, Atsushi Takeuchi, Ryoko Mezaki, Naomi Miura, Takeshi Sakai, Naoko Hokari, Mariko Takeshima, Akari Utsumi, Kota Kondo, Takashi Yokoseki, Akio Nishizawa, Masatoyo |
author_facet | Ozawa, Tetsutaro Tokunaga, Jun Arakawa, Musashi Ishikawa, Atsushi Takeuchi, Ryoko Mezaki, Naomi Miura, Takeshi Sakai, Naoko Hokari, Mariko Takeshima, Akari Utsumi, Kota Kondo, Takashi Yokoseki, Akio Nishizawa, Masatoyo |
author_sort | Ozawa, Tetsutaro |
collection | PubMed |
description | Patients with multiple system atrophy (MSA) often have evidence of compromised gastrointestinal motility. Ghrelin is a gut hormone that influences gastrointestinal motility in humans. The aim of this study was to determine whether ghrelin secretion is affected in MSA patients, and to investigate the relation between ghrelin secretion and gastrointestinal symptoms. Plasma levels of active ghrelin and unacylated ghrelin were measured in patients with MSA (n = 30), other atypical parkinsonian disorders including progressive supranuclear palsy-Richardson syndrome and corticobasal syndrome (n = 24), and control subjects (n = 24) using enzyme-linked immunosorbent assays. Gastrointestinal symptoms were quantified in all subjects using a self-report questionnaire. The ratio of active ghrelin to total ghrelin in the plasma (active ghrelin ratio) was lower in patients with MSA (mean: 8.0 %) than in patients with other atypical parkinsonian disorders (mean: 13.7 %, P = 0.001) and control subjects (mean: 13.9 %, P = 0.001). The active ghrelin ratio was correlated with the severity of gastrointestinal symptoms in MSA (r = −0.5, P = 0.004). Our observations indicate that ghrelin secretion is affected in patients with MSA. The low active ghrelin ratio may contribute to gastrointestinal symptoms in MSA. |
format | Online Article Text |
id | pubmed-3734593 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-37345932013-08-08 Abnormal ghrelin secretion contributes to gastrointestinal symptoms in multiple system atrophy patients Ozawa, Tetsutaro Tokunaga, Jun Arakawa, Musashi Ishikawa, Atsushi Takeuchi, Ryoko Mezaki, Naomi Miura, Takeshi Sakai, Naoko Hokari, Mariko Takeshima, Akari Utsumi, Kota Kondo, Takashi Yokoseki, Akio Nishizawa, Masatoyo J Neurol Original Communication Patients with multiple system atrophy (MSA) often have evidence of compromised gastrointestinal motility. Ghrelin is a gut hormone that influences gastrointestinal motility in humans. The aim of this study was to determine whether ghrelin secretion is affected in MSA patients, and to investigate the relation between ghrelin secretion and gastrointestinal symptoms. Plasma levels of active ghrelin and unacylated ghrelin were measured in patients with MSA (n = 30), other atypical parkinsonian disorders including progressive supranuclear palsy-Richardson syndrome and corticobasal syndrome (n = 24), and control subjects (n = 24) using enzyme-linked immunosorbent assays. Gastrointestinal symptoms were quantified in all subjects using a self-report questionnaire. The ratio of active ghrelin to total ghrelin in the plasma (active ghrelin ratio) was lower in patients with MSA (mean: 8.0 %) than in patients with other atypical parkinsonian disorders (mean: 13.7 %, P = 0.001) and control subjects (mean: 13.9 %, P = 0.001). The active ghrelin ratio was correlated with the severity of gastrointestinal symptoms in MSA (r = −0.5, P = 0.004). Our observations indicate that ghrelin secretion is affected in patients with MSA. The low active ghrelin ratio may contribute to gastrointestinal symptoms in MSA. Springer Berlin Heidelberg 2013-05-08 2013 /pmc/articles/PMC3734593/ /pubmed/23652420 http://dx.doi.org/10.1007/s00415-013-6944-9 Text en © The Author(s) 2013 https://creativecommons.org/licenses/by-nc/2.0/ Open AccessThis article is distributed under the terms of the Creative Commons Attribution License which permits any use, distribution, and reproduction in any medium, provided the original author(s) and the source are credited. |
spellingShingle | Original Communication Ozawa, Tetsutaro Tokunaga, Jun Arakawa, Musashi Ishikawa, Atsushi Takeuchi, Ryoko Mezaki, Naomi Miura, Takeshi Sakai, Naoko Hokari, Mariko Takeshima, Akari Utsumi, Kota Kondo, Takashi Yokoseki, Akio Nishizawa, Masatoyo Abnormal ghrelin secretion contributes to gastrointestinal symptoms in multiple system atrophy patients |
title | Abnormal ghrelin secretion contributes to gastrointestinal symptoms in multiple system atrophy patients |
title_full | Abnormal ghrelin secretion contributes to gastrointestinal symptoms in multiple system atrophy patients |
title_fullStr | Abnormal ghrelin secretion contributes to gastrointestinal symptoms in multiple system atrophy patients |
title_full_unstemmed | Abnormal ghrelin secretion contributes to gastrointestinal symptoms in multiple system atrophy patients |
title_short | Abnormal ghrelin secretion contributes to gastrointestinal symptoms in multiple system atrophy patients |
title_sort | abnormal ghrelin secretion contributes to gastrointestinal symptoms in multiple system atrophy patients |
topic | Original Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3734593/ https://www.ncbi.nlm.nih.gov/pubmed/23652420 http://dx.doi.org/10.1007/s00415-013-6944-9 |
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