Hayley J MacDonald, Ole Bernt Fasmer, Olav T Jønsi, Lin Sørensen
{"title":"捕捉每次试验的行为差异:帕金森病患者在反应时间上表现出更大的短期波动率。","authors":"Hayley J MacDonald, Ole Bernt Fasmer, Olav T Jønsi, Lin Sørensen","doi":"10.1038/s41398-025-03516-y","DOIUrl":null,"url":null,"abstract":"<p><p>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 deviation (SD). SD provides a standardised measure of inconsistency in RTs but is necessarily calculated as an average measure, precluding any trial-level investigation. Such linear measures cannot capture rapid and spontaneous changes in biological systems such as dopaminergic bursting activity. Therefore, nonlinear measures provide important complementary insights into dopamine-related neurocognition. The nonlinear method of graph theory is one viable approach to capture the complex biological changes in PD and their effect on behaviour. Our primary aim was to increase the understanding of RT fluctuations in PD beyond the use of SD by investigating nonlinear IIVRT measures 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. The difference between groups could not be explained simply by worse overall RT performance, as average RT was comparable between groups. Instead, the IIVRT findings reflected impaired consistency in performance for people with PD and specifically a greater rate of short-term fluctuations in behaviour. These novel results indicate that a similarity graph algorithm may be a sensitive tool to capture the rapidly varying changes in behaviour that result from dysfunctional dopamine bursting activity in PD.</p>","PeriodicalId":23278,"journal":{"name":"Translational Psychiatry","volume":"15 1","pages":"300"},"PeriodicalIF":6.2000,"publicationDate":"2025-08-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12368238/pdf/","citationCount":"0","resultStr":"{\"title\":\"Capturing trial-by-trial variability in behaviour: people with Parkinson's disease exhibit a greater rate of short-term fluctuations in response times.\",\"authors\":\"Hayley J MacDonald, Ole Bernt Fasmer, Olav T Jønsi, Lin Sørensen\",\"doi\":\"10.1038/s41398-025-03516-y\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>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 deviation (SD). SD provides a standardised measure of inconsistency in RTs but is necessarily calculated as an average measure, precluding any trial-level investigation. Such linear measures cannot capture rapid and spontaneous changes in biological systems such as dopaminergic bursting activity. Therefore, nonlinear measures provide important complementary insights into dopamine-related neurocognition. The nonlinear method of graph theory is one viable approach to capture the complex biological changes in PD and their effect on behaviour. Our primary aim was to increase the understanding of RT fluctuations in PD beyond the use of SD by investigating nonlinear IIVRT measures 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. The difference between groups could not be explained simply by worse overall RT performance, as average RT was comparable between groups. Instead, the IIVRT findings reflected impaired consistency in performance for people with PD and specifically a greater rate of short-term fluctuations in behaviour. These novel results indicate that a similarity graph algorithm may be a sensitive tool to capture the rapidly varying changes in behaviour that result from dysfunctional dopamine bursting activity in PD.</p>\",\"PeriodicalId\":23278,\"journal\":{\"name\":\"Translational Psychiatry\",\"volume\":\"15 1\",\"pages\":\"300\"},\"PeriodicalIF\":6.2000,\"publicationDate\":\"2025-08-20\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12368238/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Translational Psychiatry\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1038/s41398-025-03516-y\",\"RegionNum\":1,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"PSYCHIATRY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Translational Psychiatry","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1038/s41398-025-03516-y","RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"PSYCHIATRY","Score":null,"Total":0}
Capturing trial-by-trial variability in behaviour: people with Parkinson's disease exhibit a greater rate of short-term fluctuations in response times.
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 deviation (SD). SD provides a standardised measure of inconsistency in RTs but is necessarily calculated as an average measure, precluding any trial-level investigation. Such linear measures cannot capture rapid and spontaneous changes in biological systems such as dopaminergic bursting activity. Therefore, nonlinear measures provide important complementary insights into dopamine-related neurocognition. The nonlinear method of graph theory is one viable approach to capture the complex biological changes in PD and their effect on behaviour. Our primary aim was to increase the understanding of RT fluctuations in PD beyond the use of SD by investigating nonlinear IIVRT measures 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. The difference between groups could not be explained simply by worse overall RT performance, as average RT was comparable between groups. Instead, the IIVRT findings reflected impaired consistency in performance for people with PD and specifically a greater rate of short-term fluctuations in behaviour. These novel results indicate that a similarity graph algorithm may be a sensitive tool to capture the rapidly varying changes in behaviour that result from dysfunctional dopamine bursting activity in PD.
期刊介绍:
Psychiatry has suffered tremendously by the limited translational pipeline. Nobel laureate Julius Axelrod''s discovery in 1961 of monoamine reuptake by pre-synaptic neurons still forms the basis of contemporary antidepressant treatment. There is a grievous gap between the explosion of knowledge in neuroscience and conceptually novel treatments for our patients. Translational Psychiatry bridges this gap by fostering and highlighting the pathway from discovery to clinical applications, healthcare and global health. We view translation broadly as the full spectrum of work that marks the pathway from discovery to global health, inclusive. The steps of translation that are within the scope of Translational Psychiatry include (i) fundamental discovery, (ii) bench to bedside, (iii) bedside to clinical applications (clinical trials), (iv) translation to policy and health care guidelines, (v) assessment of health policy and usage, and (vi) global health. All areas of medical research, including — but not restricted to — molecular biology, genetics, pharmacology, imaging and epidemiology are welcome as they contribute to enhance the field of translational psychiatry.