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Real‐World Driving Data Indexes Dopaminergic Treatment Effects in Parkinson's Disease
BACKGROUND: Driving is a complex, everyday task that impacts patient agency, safety, mobility, social connections, and quality of life. Digital tools can provide comprehensive real‐world (RW) data on driver behavior in patients with Parkinson's disease (PD), providing critical data on disease s...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley & Sons, Inc.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10525064/ https://www.ncbi.nlm.nih.gov/pubmed/37772286 http://dx.doi.org/10.1002/mdc3.13803 |
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author | Chang, Jun Ha Bhatti, Danish Rizzo, Matthew Uc, Ergun Y. Bertoni, John Merickel, Jennifer |
author_facet | Chang, Jun Ha Bhatti, Danish Rizzo, Matthew Uc, Ergun Y. Bertoni, John Merickel, Jennifer |
author_sort | Chang, Jun Ha |
collection | PubMed |
description | BACKGROUND: Driving is a complex, everyday task that impacts patient agency, safety, mobility, social connections, and quality of life. Digital tools can provide comprehensive real‐world (RW) data on driver behavior in patients with Parkinson's disease (PD), providing critical data on disease status and treatment efficacy in the patient's own environment. OBJECTIVE: This pilot study examined the use of driving data as a RW digital biomarker of PD symptom severity and dopaminergic therapy effectiveness. METHODS: Naturalistic driving data (3974 drives) were collected for 1 month from 30 idiopathic PD drivers treated with dopaminergic medications. Prescriptions data were used to calculate levodopa equivalent daily dose (LEDD). The association between LEDD and driver mobility (number of drives) was assessed across PD severity, measured by the Movement Disorder Society Unified Parkinson's Disease Rating Scale (MDS‐UPDRS). RESULTS: PD drivers with worse motor symptoms based on self‐report (Part II: P = 0.02) and clinical examination (Part III: P < 0.001) showed greater decrements in driver mobility. LEDD levels >400 mg/day were associated with higher driver mobility than those with worse PD symptoms (Part I: P = 0.02, Part II: P < 0.001, Part III: P < 0.001). CONCLUSIONS: Results suggest that comprehensive RW driving data on PD patients may index disease status and treatment effectiveness to improve patient symptoms, safety, mobility, and independence. Higher dopaminergic treatment may enhance safe driver mobility in PD patients with worse symptom severity. |
format | Online Article Text |
id | pubmed-10525064 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | John Wiley & Sons, Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-105250642023-09-28 Real‐World Driving Data Indexes Dopaminergic Treatment Effects in Parkinson's Disease Chang, Jun Ha Bhatti, Danish Rizzo, Matthew Uc, Ergun Y. Bertoni, John Merickel, Jennifer Mov Disord Clin Pract Research Articles BACKGROUND: Driving is a complex, everyday task that impacts patient agency, safety, mobility, social connections, and quality of life. Digital tools can provide comprehensive real‐world (RW) data on driver behavior in patients with Parkinson's disease (PD), providing critical data on disease status and treatment efficacy in the patient's own environment. OBJECTIVE: This pilot study examined the use of driving data as a RW digital biomarker of PD symptom severity and dopaminergic therapy effectiveness. METHODS: Naturalistic driving data (3974 drives) were collected for 1 month from 30 idiopathic PD drivers treated with dopaminergic medications. Prescriptions data were used to calculate levodopa equivalent daily dose (LEDD). The association between LEDD and driver mobility (number of drives) was assessed across PD severity, measured by the Movement Disorder Society Unified Parkinson's Disease Rating Scale (MDS‐UPDRS). RESULTS: PD drivers with worse motor symptoms based on self‐report (Part II: P = 0.02) and clinical examination (Part III: P < 0.001) showed greater decrements in driver mobility. LEDD levels >400 mg/day were associated with higher driver mobility than those with worse PD symptoms (Part I: P = 0.02, Part II: P < 0.001, Part III: P < 0.001). CONCLUSIONS: Results suggest that comprehensive RW driving data on PD patients may index disease status and treatment effectiveness to improve patient symptoms, safety, mobility, and independence. Higher dopaminergic treatment may enhance safe driver mobility in PD patients with worse symptom severity. John Wiley & Sons, Inc. 2023-06-12 /pmc/articles/PMC10525064/ /pubmed/37772286 http://dx.doi.org/10.1002/mdc3.13803 Text en © 2023 The Authors. Movement Disorders Clinical Practice published by Wiley Periodicals LLC on behalf of International Parkinson and Movement Disorder Society. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Articles Chang, Jun Ha Bhatti, Danish Rizzo, Matthew Uc, Ergun Y. Bertoni, John Merickel, Jennifer Real‐World Driving Data Indexes Dopaminergic Treatment Effects in Parkinson's Disease |
title | Real‐World Driving Data Indexes Dopaminergic Treatment Effects in Parkinson's Disease |
title_full | Real‐World Driving Data Indexes Dopaminergic Treatment Effects in Parkinson's Disease |
title_fullStr | Real‐World Driving Data Indexes Dopaminergic Treatment Effects in Parkinson's Disease |
title_full_unstemmed | Real‐World Driving Data Indexes Dopaminergic Treatment Effects in Parkinson's Disease |
title_short | Real‐World Driving Data Indexes Dopaminergic Treatment Effects in Parkinson's Disease |
title_sort | real‐world driving data indexes dopaminergic treatment effects in parkinson's disease |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10525064/ https://www.ncbi.nlm.nih.gov/pubmed/37772286 http://dx.doi.org/10.1002/mdc3.13803 |
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