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Identifying prodromal symptoms at high specificity for Parkinson’s disease

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Identifying prodromal symptoms at high specificity for Parkinson’s disease. / Jackson, Holly; Anzures-Cabrera, Judith; Simuni, Tanya et al.
In: Frontiers in Aging Neuroscience, Vol. 15, 1232387, 22.09.2023.

Research output: Contribution to Journal/MagazineJournal articlepeer-review

Harvard

Jackson, H, Anzures-Cabrera, J, Simuni, T, Postuma, RB, Marek, K & Pagano, G 2023, 'Identifying prodromal symptoms at high specificity for Parkinson’s disease', Frontiers in Aging Neuroscience, vol. 15, 1232387. https://doi.org/10.3389/fnagi.2023.1232387

APA

Jackson, H., Anzures-Cabrera, J., Simuni, T., Postuma, R. B., Marek, K., & Pagano, G. (2023). Identifying prodromal symptoms at high specificity for Parkinson’s disease. Frontiers in Aging Neuroscience, 15, Article 1232387. https://doi.org/10.3389/fnagi.2023.1232387

Vancouver

Jackson H, Anzures-Cabrera J, Simuni T, Postuma RB, Marek K, Pagano G. Identifying prodromal symptoms at high specificity for Parkinson’s disease. Frontiers in Aging Neuroscience. 2023 Sept 22;15:1232387. doi: 10.3389/fnagi.2023.1232387

Author

Jackson, Holly ; Anzures-Cabrera, Judith ; Simuni, Tanya et al. / Identifying prodromal symptoms at high specificity for Parkinson’s disease. In: Frontiers in Aging Neuroscience. 2023 ; Vol. 15.

Bibtex

@article{19e2c6d4e97b41d9bd04354f9cce20c5,
title = "Identifying prodromal symptoms at high specificity for Parkinson{\textquoteright}s disease",
abstract = "Introduction: To test drugs with the potential to prevent the onset of Parkinson{\textquoteright}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{\textquoteright}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 = "observational study, specificity, prodromal symptoms, prevalence, Parkinson{\textquoteright}s disease",
author = "Holly Jackson and Judith Anzures-Cabrera and Tanya Simuni and Postuma, {Ronald B.} and Kenneth Marek and Gennaro Pagano",
year = "2023",
month = sep,
day = "22",
doi = "10.3389/fnagi.2023.1232387",
language = "English",
volume = "15",
journal = "Frontiers in Aging Neuroscience",
issn = "1663-4365",
publisher = "Frontiers Media S.A.",

}

RIS

TY - JOUR

T1 - Identifying prodromal symptoms at high specificity for Parkinson’s disease

AU - Jackson, Holly

AU - Anzures-Cabrera, Judith

AU - Simuni, Tanya

AU - Postuma, Ronald B.

AU - Marek, Kenneth

AU - Pagano, Gennaro

PY - 2023/9/22

Y1 - 2023/9/22

N2 - 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.

AB - 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.

KW - observational study

KW - specificity

KW - prodromal symptoms

KW - prevalence

KW - Parkinson’s disease

U2 - 10.3389/fnagi.2023.1232387

DO - 10.3389/fnagi.2023.1232387

M3 - Journal article

VL - 15

JO - Frontiers in Aging Neuroscience

JF - Frontiers in Aging Neuroscience

SN - 1663-4365

M1 - 1232387

ER -