Identifying prodromal symptoms at high specificity for Parkinson's disease.

Parkinson’s disease observational study prevalence prodromal symptoms specificity

Journal

Frontiers in aging neuroscience
ISSN: 1663-4365
Titre abrégé: Front Aging Neurosci
Pays: Switzerland
ID NLM: 101525824

Informations de publication

Date de publication:
2023
Historique:
received: 05 06 2023
accepted: 08 09 2023
medline: 9 10 2023
pubmed: 9 10 2023
entrez: 9 10 2023
Statut: epublish

Résumé

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). We aimed to identify the clinical markers at high specificity for developing PD by comparing individuals with PD or prodromal PD to healthy controls. 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. 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. 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.

Identifiants

pubmed: 37810617
doi: 10.3389/fnagi.2023.1232387
pmc: PMC10556459
doi:

Types de publication

Journal Article

Langues

eng

Pagination

1232387

Informations de copyright

Copyright © 2023 Jackson, Anzures-Cabrera, Simuni, Postuma, Marek and Pagano.

Déclaration de conflit d'intérêts

HJ was a paid intern employed through The Roche Internships for Scientific Exchange (RiSE) Programme within F. Hoffmann-La Roche Ltd. JA-C is a full-time employee of Roche Products Ltd and a shareholder of F. Hoffmann-La Roche Ltd. GP is a full-time employee of Roche Pharma Research and Early Development and a shareholder of F. Hoffmann-La Roche Ltd. The remaining authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

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Auteurs

Holly Jackson (H)

Roche Products Ltd, Welwyn Garden City, United Kingdom.
Department of Mathematics and Statistics, Lancaster University, Lancaster, United Kingdom.

Judith Anzures-Cabrera (J)

Roche Products Ltd, Welwyn Garden City, United Kingdom.

Tanya Simuni (T)

Department of Neurology, Northwestern University Feinberg School of Medicine, Chicago, IL, United States.

Ronald B Postuma (RB)

Department of Neurology, Montreal Neurological Institute, McGill University, Montreal, QC, Canada.

Kenneth Marek (K)

Institute for Neurodegenerative Disorders, New Haven, CT, United States.

Gennaro Pagano (G)

Roche Pharma Research and Early Development (pRED), Neuroscience and Rare Diseases Discovery and Translational Area, Roche Innovation Center Basel, Basel, Switzerland.
University of Exeter Medical School, London, United Kingdom.

Classifications MeSH