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The Association Between Frailty and Parkinson’s Disease in the ReSPOnD Trial
BACKGROUND: Frailty and Parkinson’s disease (PD) are both highly prevalent in older people, but few studies have studied frailty in people with Parkinson’s. Identifying frailty in this population is vital, to target new interventions to those who would most benefit. METHODS: Data were collected as p...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Canadian Geriatrics Society
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7904322/ https://www.ncbi.nlm.nih.gov/pubmed/33680260 http://dx.doi.org/10.5770/cgj.24.437 |
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author | Smith, Natalie Gaunt, Daisy M. Whone, Alan Ben-Shlomo, Yoav Henderson, Emily J. |
author_facet | Smith, Natalie Gaunt, Daisy M. Whone, Alan Ben-Shlomo, Yoav Henderson, Emily J. |
author_sort | Smith, Natalie |
collection | PubMed |
description | BACKGROUND: Frailty and Parkinson’s disease (PD) are both highly prevalent in older people, but few studies have studied frailty in people with Parkinson’s. Identifying frailty in this population is vital, to target new interventions to those who would most benefit. METHODS: Data were collected as part of the double-blind randomised controlled rivastigmine to stabilise gait ReSPonD trial in 130 people with Hoehn and Yahr 2–3, idiopathic PD who had fallen in the year prior to enrolment. Individuals were assessed at baseline and followed up at eight months, including determination of frailty status. RESULTS: 120 patients attended for follow-up. At follow-up, the mean (SD) age was 70.2 years (8.0), MDS-UPDRS total score 91.5 (29.1), and MDS-UPDRS motor score (Part III) 42.7 (14.8). Median disease duration was 9.2 years (IQR 4.6 to 13.1), Geriatric Depression Score 4 (IQR 2 to 6). Using the Fried frailty criteria, 31 (26%) were frail and 70 (58%) pre-frail. In univariable analysis, being female, higher depression score, and MDS-UPDRS score were associated with greater frailty. Using ordinal regression, in the multivariable model, being female (odds ratio [OR] 3.10, 95%CI 1.53 to 6.26, p=.002), higher total MDS-UPDRS score (OR 2.02, 95%CI 1.42 to 2.87, p<.0001) and higher depression (OR 1.47, 95%CI 1.05 to 2.06, p=.03) were associated with higher number of frailty markers. CONCLUSION: There was a high prevalence (84%) of pre-frail and frail individuals in patients participating in this RCT. Future research should determine the optimum tool to assess frailty in this at-risk population, and delineate the association between Parkinson’s, frailty, and health outcomes. |
format | Online Article Text |
id | pubmed-7904322 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Canadian Geriatrics Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-79043222021-03-05 The Association Between Frailty and Parkinson’s Disease in the ReSPOnD Trial Smith, Natalie Gaunt, Daisy M. Whone, Alan Ben-Shlomo, Yoav Henderson, Emily J. Can Geriatr J Original Research BACKGROUND: Frailty and Parkinson’s disease (PD) are both highly prevalent in older people, but few studies have studied frailty in people with Parkinson’s. Identifying frailty in this population is vital, to target new interventions to those who would most benefit. METHODS: Data were collected as part of the double-blind randomised controlled rivastigmine to stabilise gait ReSPonD trial in 130 people with Hoehn and Yahr 2–3, idiopathic PD who had fallen in the year prior to enrolment. Individuals were assessed at baseline and followed up at eight months, including determination of frailty status. RESULTS: 120 patients attended for follow-up. At follow-up, the mean (SD) age was 70.2 years (8.0), MDS-UPDRS total score 91.5 (29.1), and MDS-UPDRS motor score (Part III) 42.7 (14.8). Median disease duration was 9.2 years (IQR 4.6 to 13.1), Geriatric Depression Score 4 (IQR 2 to 6). Using the Fried frailty criteria, 31 (26%) were frail and 70 (58%) pre-frail. In univariable analysis, being female, higher depression score, and MDS-UPDRS score were associated with greater frailty. Using ordinal regression, in the multivariable model, being female (odds ratio [OR] 3.10, 95%CI 1.53 to 6.26, p=.002), higher total MDS-UPDRS score (OR 2.02, 95%CI 1.42 to 2.87, p<.0001) and higher depression (OR 1.47, 95%CI 1.05 to 2.06, p=.03) were associated with higher number of frailty markers. CONCLUSION: There was a high prevalence (84%) of pre-frail and frail individuals in patients participating in this RCT. Future research should determine the optimum tool to assess frailty in this at-risk population, and delineate the association between Parkinson’s, frailty, and health outcomes. Canadian Geriatrics Society 2021-03-02 /pmc/articles/PMC7904322/ /pubmed/33680260 http://dx.doi.org/10.5770/cgj.24.437 Text en © 2021 Author(s). Published by the Canadian Geriatrics Society This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial No-Derivative license (http://creativecommons.org/licenses/by-nc-nd/2.5/ca/), which permits unrestricted non-commercial use and distribution, provided the original work is properly cited. |
spellingShingle | Original Research Smith, Natalie Gaunt, Daisy M. Whone, Alan Ben-Shlomo, Yoav Henderson, Emily J. The Association Between Frailty and Parkinson’s Disease in the ReSPOnD Trial |
title | The Association Between Frailty and Parkinson’s Disease in the ReSPOnD Trial |
title_full | The Association Between Frailty and Parkinson’s Disease in the ReSPOnD Trial |
title_fullStr | The Association Between Frailty and Parkinson’s Disease in the ReSPOnD Trial |
title_full_unstemmed | The Association Between Frailty and Parkinson’s Disease in the ReSPOnD Trial |
title_short | The Association Between Frailty and Parkinson’s Disease in the ReSPOnD Trial |
title_sort | association between frailty and parkinson’s disease in the respond trial |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7904322/ https://www.ncbi.nlm.nih.gov/pubmed/33680260 http://dx.doi.org/10.5770/cgj.24.437 |
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