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Evaluation of morning bradykinesia in Parkinson’s disease in a United States cohort using continuous objective monitoring
INTRODUCTION: Bradykinesia in Parkinson’s disease is a marker for clinical levodopa responsiveness, with persistent bradykinesia reflecting suboptimal response. We objectively measured prevalence and severity of morning bradykinesia using the Personal KinetiGraph® (PKG®). METHODS: Retrospective eval...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9127405/ https://www.ncbi.nlm.nih.gov/pubmed/35620251 http://dx.doi.org/10.1016/j.prdoa.2022.100145 |
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author | Isaacson, S.H. Pahwa, R. Pappert, E.J. Torres-Russotto, D. |
author_facet | Isaacson, S.H. Pahwa, R. Pappert, E.J. Torres-Russotto, D. |
author_sort | Isaacson, S.H. |
collection | PubMed |
description | INTRODUCTION: Bradykinesia in Parkinson’s disease is a marker for clinical levodopa responsiveness, with persistent bradykinesia reflecting suboptimal response. We objectively measured prevalence and severity of morning bradykinesia using the Personal KinetiGraph® (PKG®). METHODS: Retrospective evaluation of a large global database of de-identified PKG assessments from individuals (N=12,840) in routine clinical care in the United States (US; n=3288). Median bradykinesia scores (mBKS) and median dyskinesia scores (mDKS) were calculated using a validated algorithm and previously established targets to evaluate percent time in bradykinesia, levodopa responsiveness, and prevalence and severity (0–5; 5=highest severity) of morning bradykinesia. RESULTS: mBKS was above target (≥26) in 65% of all individuals, and mDKS was above target (≥7) in 3%. Elevated percent time in bradykinesia occurred in 79%. Among individuals where levodopa responsiveness could be evaluated (n=1933), 31% had a significant response (≥1.15 postdose decrease in severity). Morning bradykinesia was identified in 85% of individuals with available morning data (1298/1524), and 64% (954/1501) experienced continued bradykinesia after the first daily levodopa dose. Morning bradykinesia was severe (4.0–4.7) in levodopa-responsive individuals regardless of percent time spent in bradykinesia. CONCLUSION: Elevated mBKS was very common in the US. Most individuals taking levodopa had morning bradykinesia that persisted even after the first daily dose, and severity was high, indicating a need for additional treatment options. |
format | Online Article Text |
id | pubmed-9127405 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-91274052022-05-25 Evaluation of morning bradykinesia in Parkinson’s disease in a United States cohort using continuous objective monitoring Isaacson, S.H. Pahwa, R. Pappert, E.J. Torres-Russotto, D. Clin Park Relat Disord Original Article INTRODUCTION: Bradykinesia in Parkinson’s disease is a marker for clinical levodopa responsiveness, with persistent bradykinesia reflecting suboptimal response. We objectively measured prevalence and severity of morning bradykinesia using the Personal KinetiGraph® (PKG®). METHODS: Retrospective evaluation of a large global database of de-identified PKG assessments from individuals (N=12,840) in routine clinical care in the United States (US; n=3288). Median bradykinesia scores (mBKS) and median dyskinesia scores (mDKS) were calculated using a validated algorithm and previously established targets to evaluate percent time in bradykinesia, levodopa responsiveness, and prevalence and severity (0–5; 5=highest severity) of morning bradykinesia. RESULTS: mBKS was above target (≥26) in 65% of all individuals, and mDKS was above target (≥7) in 3%. Elevated percent time in bradykinesia occurred in 79%. Among individuals where levodopa responsiveness could be evaluated (n=1933), 31% had a significant response (≥1.15 postdose decrease in severity). Morning bradykinesia was identified in 85% of individuals with available morning data (1298/1524), and 64% (954/1501) experienced continued bradykinesia after the first daily levodopa dose. Morning bradykinesia was severe (4.0–4.7) in levodopa-responsive individuals regardless of percent time spent in bradykinesia. CONCLUSION: Elevated mBKS was very common in the US. Most individuals taking levodopa had morning bradykinesia that persisted even after the first daily dose, and severity was high, indicating a need for additional treatment options. Elsevier 2022-05-17 /pmc/articles/PMC9127405/ /pubmed/35620251 http://dx.doi.org/10.1016/j.prdoa.2022.100145 Text en © 2022 The Authors. Published by Elsevier Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Original Article Isaacson, S.H. Pahwa, R. Pappert, E.J. Torres-Russotto, D. Evaluation of morning bradykinesia in Parkinson’s disease in a United States cohort using continuous objective monitoring |
title | Evaluation of morning bradykinesia in Parkinson’s disease in a United States cohort using continuous objective monitoring |
title_full | Evaluation of morning bradykinesia in Parkinson’s disease in a United States cohort using continuous objective monitoring |
title_fullStr | Evaluation of morning bradykinesia in Parkinson’s disease in a United States cohort using continuous objective monitoring |
title_full_unstemmed | Evaluation of morning bradykinesia in Parkinson’s disease in a United States cohort using continuous objective monitoring |
title_short | Evaluation of morning bradykinesia in Parkinson’s disease in a United States cohort using continuous objective monitoring |
title_sort | evaluation of morning bradykinesia in parkinson’s disease in a united states cohort using continuous objective monitoring |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9127405/ https://www.ncbi.nlm.nih.gov/pubmed/35620251 http://dx.doi.org/10.1016/j.prdoa.2022.100145 |
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