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Salivary caffeine in Parkinson’s disease
We aimed to investigate salivary caffeine content, caffeine absorption and metabolism in Parkinson’s disease (PD) and verify whether salivary caffeine can be used as a biomarker of PD. We enrolled 98 PD patients and 92 healthy subjects. Caffeine and its major metabolite, paraxanthine, were measured...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8110998/ https://www.ncbi.nlm.nih.gov/pubmed/33972579 http://dx.doi.org/10.1038/s41598-021-89168-6 |
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author | Leodori, Giorgio De Bartolo, Maria Ilenia Belvisi, Daniele Ciogli, Alessia Fabbrini, Andrea Costanzo, Matteo Manetto, Simone Conte, Antonella Villani, Claudio Fabbrini, Giovanni Berardelli, Alfredo |
author_facet | Leodori, Giorgio De Bartolo, Maria Ilenia Belvisi, Daniele Ciogli, Alessia Fabbrini, Andrea Costanzo, Matteo Manetto, Simone Conte, Antonella Villani, Claudio Fabbrini, Giovanni Berardelli, Alfredo |
author_sort | Leodori, Giorgio |
collection | PubMed |
description | We aimed to investigate salivary caffeine content, caffeine absorption and metabolism in Parkinson’s disease (PD) and verify whether salivary caffeine can be used as a biomarker of PD. We enrolled 98 PD patients and 92 healthy subjects. Caffeine and its major metabolite, paraxanthine, were measured in saliva samples collected before and 4 h after the oral intake of caffeine (100 mg). We measured caffeine absorption as the normalized increase in caffeine levels, and caffeine metabolism as the paraxanthine/caffeine ratio. The Movement Disorder Society Unified Parkinson's Disease Rating Scale part III, the Hoehn & Yahr, the presence of motor complications, and levodopa equivalent dose (LED) were assessed and correlated with caffeine levels, absorption, and metabolism. The effects of demographic and environmental features possibly influencing caffeine levels were also investigated. Caffeine levels were decreased in patients with moderate/advanced PD, while caffeine levels were normal in patients with early and de-novo PD, unrelated to caffeine intake. Caffeine absorption and metabolism were normal in PD. Decreased salivary caffeine levels in PD were associated with higher disease severity, longer duration, and the presence of motor complications, no significant association was found with LED. Salivary caffeine decrease correlates with PD progression. |
format | Online Article Text |
id | pubmed-8110998 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-81109982021-05-12 Salivary caffeine in Parkinson’s disease Leodori, Giorgio De Bartolo, Maria Ilenia Belvisi, Daniele Ciogli, Alessia Fabbrini, Andrea Costanzo, Matteo Manetto, Simone Conte, Antonella Villani, Claudio Fabbrini, Giovanni Berardelli, Alfredo Sci Rep Article We aimed to investigate salivary caffeine content, caffeine absorption and metabolism in Parkinson’s disease (PD) and verify whether salivary caffeine can be used as a biomarker of PD. We enrolled 98 PD patients and 92 healthy subjects. Caffeine and its major metabolite, paraxanthine, were measured in saliva samples collected before and 4 h after the oral intake of caffeine (100 mg). We measured caffeine absorption as the normalized increase in caffeine levels, and caffeine metabolism as the paraxanthine/caffeine ratio. The Movement Disorder Society Unified Parkinson's Disease Rating Scale part III, the Hoehn & Yahr, the presence of motor complications, and levodopa equivalent dose (LED) were assessed and correlated with caffeine levels, absorption, and metabolism. The effects of demographic and environmental features possibly influencing caffeine levels were also investigated. Caffeine levels were decreased in patients with moderate/advanced PD, while caffeine levels were normal in patients with early and de-novo PD, unrelated to caffeine intake. Caffeine absorption and metabolism were normal in PD. Decreased salivary caffeine levels in PD were associated with higher disease severity, longer duration, and the presence of motor complications, no significant association was found with LED. Salivary caffeine decrease correlates with PD progression. Nature Publishing Group UK 2021-05-10 /pmc/articles/PMC8110998/ /pubmed/33972579 http://dx.doi.org/10.1038/s41598-021-89168-6 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Leodori, Giorgio De Bartolo, Maria Ilenia Belvisi, Daniele Ciogli, Alessia Fabbrini, Andrea Costanzo, Matteo Manetto, Simone Conte, Antonella Villani, Claudio Fabbrini, Giovanni Berardelli, Alfredo Salivary caffeine in Parkinson’s disease |
title | Salivary caffeine in Parkinson’s disease |
title_full | Salivary caffeine in Parkinson’s disease |
title_fullStr | Salivary caffeine in Parkinson’s disease |
title_full_unstemmed | Salivary caffeine in Parkinson’s disease |
title_short | Salivary caffeine in Parkinson’s disease |
title_sort | salivary caffeine in parkinson’s disease |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8110998/ https://www.ncbi.nlm.nih.gov/pubmed/33972579 http://dx.doi.org/10.1038/s41598-021-89168-6 |
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