Scientific article
OA Policy
English

Identifying prodromal symptoms at high specificity for Parkinson's disease

Published inFrontiers in aging neuroscience, vol. 15, 1232387
Publication date2023
First online date2023-09-22
Abstract

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.

Keywords
  • Parkinson’s disease
  • Observational study
  • Prevalence
  • Prodromal symptoms
  • Specificity
Affiliation entities Not a UNIGE publication
Citation (ISO format)
JACKSON, Holly et al. Identifying prodromal symptoms at high specificity for Parkinson’s disease. In: Frontiers in aging neuroscience, 2023, vol. 15, p. 1232387. doi: 10.3389/fnagi.2023.1232387
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Identifiers
Journal ISSN1663-4365
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Creation24/10/2023 08:21:07
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