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Impaired Cognitive Modification for Estimating Time Duration in Parkinson's Disease

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Journal PLoS One
Date 2018 Dec 14
PMID 30543694
Citations 5
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Abstract

Parkinson's disease (PD) is associated with various cognitive impairments. However, the nature of cognitive modification in patients with PD remains to be elucidated. In the present study, we examined whether patients with PD could correct and maintain subjective time duration and line length estimation. After training sessions, in which participants repeatedly memorized either a duration or a length, we compared a learning performance in 20 PD patients with 20 healthy controls. In the case of duration in the PD patients, the learned durations immediately returned to baseline of pre-training within a few minutes. However, the patients' ability to learn length estimation remained unimpaired. In contrast, healthy controls were able to retain the learned duration and length estimations. Time compression in PD's internal clock may become entrained to their altered duration estimation even after learning of accurate time duration. These deficits may be associated with disrupting cognitive modification in PD.

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References
1.
Drane D, Lee G, Loring D, Meador K . Time perception following unilateral amobarbital injection in patients with temporal lobe epilepsy. J Clin Exp Neuropsychol. 1999; 21(3):385-96. DOI: 10.1076/jcen.21.3.385.922. View

2.
Salmon D, Butters N . Neurobiology of skill and habit learning. Curr Opin Neurobiol. 1995; 5(2):184-90. DOI: 10.1016/0959-4388(95)80025-5. View

3.
Raz A, Vaadia E, Bergman H . Firing patterns and correlations of spontaneous discharge of pallidal neurons in the normal and the tremulous 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine vervet model of parkinsonism. J Neurosci. 2000; 20(22):8559-71. PMC: 6773163. View

4.
Shi Z, Church R, Meck W . Bayesian optimization of time perception. Trends Cogn Sci. 2013; 17(11):556-64. DOI: 10.1016/j.tics.2013.09.009. View

5.
Hayes A, Davidson M, Keele S, Rafal R . Toward a functional analysis of the basal ganglia. J Cogn Neurosci. 1998; 10(2):178-98. DOI: 10.1162/089892998562645. View