Capturing Trial-by-Trial Variability in Behaviour: People with Parkinson's Disease Exhibit a Greater Rate of Short-Term Fluctuations in Response Times

Abstract

Average response time is frequently used to reflect executive function. Less often studied is intra-individual variability in response times (IIVRT) which reflects within-person consistency. Higher IIVRT in Parkinson's disease (PD) has been associated with poor executive function but almost exclusively studied using standard deviations. Such linear measures cannot capture rapid and spontaneous changes in biological systems such as dopaminergic bursting activity. Therefore, nonlinear measures may provide important complementary insights into dopamine-related neurocognition. Our primary aim was to investigate nonlinear IIVRT measures in PD using graph theory, constituting the first use of this approach on RT data. As hypothesized, PD was associated with a greater rate of trial-by-trial IIVRT compared to healthy older adults. These novel results indicate that a similarity graph algorithm may be a useful tool to capture the more rapidly varying and spontaneous changes in RT behavior that result from the dysfunctional dopamine bursting dynamics present in PD.

Competing Interest Statement

The authors have declared no competing interest.

Funding Statement

Open access funding provided by the University of Bergen.

Author Declarations

I confirm all relevant ethical guidelines have been followed, and any necessary IRB and/or ethics committee approvals have been obtained.

Yes

The details of the IRB/oversight body that provided approval or exemption for the research described are given below:

All data was collected in studies which received approval from local ethics boards: University of Auckland Human Participant Ethics Committee ID: 10083; Health and Disability Ethics Committee ID: 13/NTA/215; University of Birmingham Ethical Review Committee ID: ERN_18-2077AP1A.

I confirm that all necessary patient/participant consent has been obtained and the appropriate institutional forms have been archived, and that any patient/participant/sample identifiers included were not known to anyone (e.g., hospital staff, patients or participants themselves) outside the research group so cannot be used to identify individuals.

Yes

I understand that all clinical trials and any other prospective interventional studies must be registered with an ICMJE-approved registry, such as ClinicalTrials.gov. I confirm that any such study reported in the manuscript has been registered and the trial registration ID is provided (note: if posting a prospective study registered retrospectively, please provide a statement in the trial ID field explaining why the study was not registered in advance).

Yes

I have followed all appropriate research reporting guidelines, such as any relevant EQUATOR Network research reporting checklist(s) and other pertinent material, if applicable.

Yes

留言 (0)

沒有登入
gif