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Identifying prodromal symptoms at high specificity for Parkinson’s disease
INTRODUCTION: To test drugs with the potential to prevent the onset of Parkinson’s disease (PD), it is key to identify individuals in the general population at high risk of developing PD. This is often difficult because most of the clinical markers are non-specific, common in PD but also common in o...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10556459/ https://www.ncbi.nlm.nih.gov/pubmed/37810617 http://dx.doi.org/10.3389/fnagi.2023.1232387 |
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author | Jackson, Holly Anzures-Cabrera, Judith Simuni, Tanya Postuma, Ronald B. Marek, Kenneth Pagano, Gennaro |
author_facet | Jackson, Holly Anzures-Cabrera, Judith Simuni, Tanya Postuma, Ronald B. Marek, Kenneth Pagano, Gennaro |
author_sort | Jackson, Holly |
collection | PubMed |
description | INTRODUCTION: To test drugs with the potential to prevent the onset of Parkinson’s disease (PD), it is key to identify individuals in the general population at high risk of developing PD. This is often difficult because most of the clinical markers are non-specific, common in PD but also common in older adults (e.g., sleep problems). OBJECTIVE: We aimed to identify the clinical markers at high specificity for developing PD by comparing individuals with PD or prodromal PD to healthy controls. METHODS: We investigated motor and non-motor symptoms (Movement Disorder Society Unified Parkinson’s Disease Rating Scale Part 1 and 2 items) in 64 prodromal PD and 422 PD individuals calculating the odds ratios, adjusting for age and gender, for PD and prodromal PD versus 195 healthy controls. Symptoms at high specificity were defined as having an adjusted odds ratio ≥ 6. RESULTS: Constipation had an adjusted odds ratio, 6.14 [95% CI: 2.94–12.80] showing high specificity for prodromal PD, and speech difficulties had an adjusted odds ratio, 9.61 [95% CI: 7.88–48.81] showing high specificity for PD. The proportion of participants showing these specific markers was moderate (e.g., prevalence of constipation was 43.75% in prodromal PD, and speech difficulties was 33.89% in PD), suggesting these symptoms may make robust predictors of prodromal PD and PD, respectively. DISCUSSION: Clinical markers at high specificity for developing PD could be used as tools in the screening of general populations to identify individuals at higher risk of developing PD. |
format | Online Article Text |
id | pubmed-10556459 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-105564592023-10-07 Identifying prodromal symptoms at high specificity for Parkinson’s disease Jackson, Holly Anzures-Cabrera, Judith Simuni, Tanya Postuma, Ronald B. Marek, Kenneth Pagano, Gennaro Front Aging Neurosci Aging Neuroscience INTRODUCTION: To test drugs with the potential to prevent the onset of Parkinson’s disease (PD), it is key to identify individuals in the general population at high risk of developing PD. This is often difficult because most of the clinical markers are non-specific, common in PD but also common in older adults (e.g., sleep problems). OBJECTIVE: We aimed to identify the clinical markers at high specificity for developing PD by comparing individuals with PD or prodromal PD to healthy controls. METHODS: We investigated motor and non-motor symptoms (Movement Disorder Society Unified Parkinson’s Disease Rating Scale Part 1 and 2 items) in 64 prodromal PD and 422 PD individuals calculating the odds ratios, adjusting for age and gender, for PD and prodromal PD versus 195 healthy controls. Symptoms at high specificity were defined as having an adjusted odds ratio ≥ 6. RESULTS: Constipation had an adjusted odds ratio, 6.14 [95% CI: 2.94–12.80] showing high specificity for prodromal PD, and speech difficulties had an adjusted odds ratio, 9.61 [95% CI: 7.88–48.81] showing high specificity for PD. The proportion of participants showing these specific markers was moderate (e.g., prevalence of constipation was 43.75% in prodromal PD, and speech difficulties was 33.89% in PD), suggesting these symptoms may make robust predictors of prodromal PD and PD, respectively. DISCUSSION: Clinical markers at high specificity for developing PD could be used as tools in the screening of general populations to identify individuals at higher risk of developing PD. Frontiers Media S.A. 2023-09-22 /pmc/articles/PMC10556459/ /pubmed/37810617 http://dx.doi.org/10.3389/fnagi.2023.1232387 Text en Copyright © 2023 Jackson, Anzures-Cabrera, Simuni, Postuma, Marek and Pagano. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Aging Neuroscience Jackson, Holly Anzures-Cabrera, Judith Simuni, Tanya Postuma, Ronald B. Marek, Kenneth Pagano, Gennaro Identifying prodromal symptoms at high specificity for Parkinson’s disease |
title | Identifying prodromal symptoms at high specificity for Parkinson’s disease |
title_full | Identifying prodromal symptoms at high specificity for Parkinson’s disease |
title_fullStr | Identifying prodromal symptoms at high specificity for Parkinson’s disease |
title_full_unstemmed | Identifying prodromal symptoms at high specificity for Parkinson’s disease |
title_short | Identifying prodromal symptoms at high specificity for Parkinson’s disease |
title_sort | identifying prodromal symptoms at high specificity for parkinson’s disease |
topic | Aging Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10556459/ https://www.ncbi.nlm.nih.gov/pubmed/37810617 http://dx.doi.org/10.3389/fnagi.2023.1232387 |
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