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Which neuropsychological tests? Predicting cognitive decline and dementia in Parkinson’s disease in the ICICLE-PD cohort

Lookup NU author(s): Dr Rachael LawsonORCiD, Dr Gordon Duncan, Dr Tien Kheng Khoo, Professor Lynn RochesterORCiD, Professor David Burn, Professor Alison Yarnall

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This work is licensed under a Creative Commons Attribution 4.0 International License (CC BY 4.0).


Abstract

Background Cognitive impairment is common in Parkinson’s disease (PD), with 80% cumulatively developing dementia (PDD). We sought to identify tests that are sensitive to change over time above normal ageing so as to refine the neuropsychological tests predictive of PDD. Methods Participants with newly diagnosed PD (n=211) and age-matched controls (n=99) completed a range of clinical and neuropsychological tests as part of the ICICLE-PD study at 18-month intervals over 72 months. Impairments on tests were determined using control means (<1-2SD) and median scores. Mild cognitive impairment (PD-MCI) was classified using 1-2SD below normative values. Linear mixed effects modelling assessed cognitive decline, while Cox regression identified baseline predictors of PDD. Results At 72 months, 46 (cumulative probability 33.9%) participants had developed PDD; these participants declined at a faster rate in tests of global cognition, verbal fluency, memory and attention (p<0.05) compared to those who remained dementia-free. Impaired baseline global cognition, visual memory and attention using median cut-offs were the best predictors of early PDD (area under the curve [AUC]=0.88, p<0.001) compared to control-generated cut-offs (AUC=0.76-0.84, p<0.001) and PD-MCI (AUC]=0.64-0.81, p<0.001). Impaired global cognition and semantic fluency were the most useful brief tests employable in a clinical setting (AUC=0.79, p<0.001). Conclusion Verbal fluency, attention and memory were sensitive to change in early PDD and may be suitable tests to measure therapeutic response in future interventions. Impaired global cognition, attention and visual memory were the most accurate predictors for developing a PDD. Future studies could consider adopting these tests for patient clinical trial stratification.


Publication metadata

Author(s): Lawson RA, Williams-Gray CH, Camacho M, Duncan GW, Khoo TK, Breen DP, Barker RA, Rochester L, Burn DJ, Yarnall AJ

Publication type: Article

Publication status: Published

Journal: Journal of Parkinson's Disease

Year: 2021

Volume: 11

Issue: 3

Pages: 1297-1308

Online publication date: 19/05/2021

Acceptance date: 03/05/2021

Date deposited: 27/05/2021

ISSN (print): 1877-7171

ISSN (electronic): 1877-718X

Publisher: IOS Press

URL: https://doi.org/10.3233/JPD-212581

DOI: 10.3233/JPD-212581


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Funding

Funder referenceFunder name
146281
214571/Z/18/Z
F-1801Parkinson`s UK (formerly Parkinson`s Disease Society)
G-1301
J-0802Parkinson`s UK (formerly Parkinson`s Disease Society)
G-1507
MR/R007446/1

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