Prevalence and Associated Factors of Sarcopenia and Frailty in Parkinson's Disease: A Cross-Sectional Study.


Journal

Gerontology
ISSN: 1423-0003
Titre abrégé: Gerontology
Pays: Switzerland
ID NLM: 7601655

Informations de publication

Date de publication:
2019
Historique:
received: 02 05 2018
accepted: 31 07 2018
pubmed: 11 9 2018
medline: 3 1 2020
entrez: 11 9 2018
Statut: ppublish

Résumé

Sarcopenia and frailty are found in up to one-third of the general elderly population. Both are associated with major adverse health outcomes such as nursing home placement, disability, decreased quality of life, and death. Data on the frequency of both syndromes in Parkinson's disease (PD), however, are very limited. We aimed to screen for sarcopenia and frailty in PD patients and to assess potential associations of both geriatric syndromes with demographic and clinical parameters as well as quality of life. In this observational, cross-sectional study, we included 104 PD patients from a tertiary center and 330 non-PD controls from a population-based cohort aged > 65 years. All groups were screened for sarcopenia using the SARC-F score and for frailty using the Clinical Frailty Scale of the Canadian Study of Health and Aging (CSHA CFS). Prevalence rates of sarcopenia and frailty were also assessed in 18 PD patients from a population-based cohort aged > 65 years. Moreover, PD patients from the tertiary center were evaluated for motor and non-motor symptoms, quality of life, and dependency. The prevalence of sarcopenia was 55.8% (95% CI: 46.2-64.9%) in PD patients from the tertiary center and 8.2% (5.7-11.7%; p < 0.001) in non-PD controls. Frailty was detected in 35.6% (27.0-45.2%) and 5.2% (3.2-8.1%; p < 0.001). Prevalence rates for sarcopenia and frailty were 33.3% (16.1-56.4%; p = 0.004) and 22.2% (8.5-45.8%; p = 0.017) in the community-based PD sample. Both sarcopenia and frailty were significantly associated with longer disease duration, higher motor impairment, higher Hoehn and Yahr stages, decreased quality of life, higher frequency of falls, a higher non-motor symptom burden, institutionalization, and higher care levels in PD patients from a tertiary center compared to not affected PD patients (all p < 0.05). Both frailty and sarcopenia are more common in PD patients than in the general community and are associated with a more adverse course of the disease. Future studies should look into underlying risk factors for the occurrence of sarcopenia and frailty in PD patients and into adequate management to prevent and mitigate them.

Sections du résumé

BACKGROUND
Sarcopenia and frailty are found in up to one-third of the general elderly population. Both are associated with major adverse health outcomes such as nursing home placement, disability, decreased quality of life, and death. Data on the frequency of both syndromes in Parkinson's disease (PD), however, are very limited.
OBJECTIVE
We aimed to screen for sarcopenia and frailty in PD patients and to assess potential associations of both geriatric syndromes with demographic and clinical parameters as well as quality of life.
METHODS
In this observational, cross-sectional study, we included 104 PD patients from a tertiary center and 330 non-PD controls from a population-based cohort aged > 65 years. All groups were screened for sarcopenia using the SARC-F score and for frailty using the Clinical Frailty Scale of the Canadian Study of Health and Aging (CSHA CFS). Prevalence rates of sarcopenia and frailty were also assessed in 18 PD patients from a population-based cohort aged > 65 years. Moreover, PD patients from the tertiary center were evaluated for motor and non-motor symptoms, quality of life, and dependency.
RESULTS
The prevalence of sarcopenia was 55.8% (95% CI: 46.2-64.9%) in PD patients from the tertiary center and 8.2% (5.7-11.7%; p < 0.001) in non-PD controls. Frailty was detected in 35.6% (27.0-45.2%) and 5.2% (3.2-8.1%; p < 0.001). Prevalence rates for sarcopenia and frailty were 33.3% (16.1-56.4%; p = 0.004) and 22.2% (8.5-45.8%; p = 0.017) in the community-based PD sample. Both sarcopenia and frailty were significantly associated with longer disease duration, higher motor impairment, higher Hoehn and Yahr stages, decreased quality of life, higher frequency of falls, a higher non-motor symptom burden, institutionalization, and higher care levels in PD patients from a tertiary center compared to not affected PD patients (all p < 0.05).
CONCLUSIONS
Both frailty and sarcopenia are more common in PD patients than in the general community and are associated with a more adverse course of the disease. Future studies should look into underlying risk factors for the occurrence of sarcopenia and frailty in PD patients and into adequate management to prevent and mitigate them.

Identifiants

pubmed: 30199864
pii: 000492572
doi: 10.1159/000492572
doi:

Types de publication

Journal Article Observational Study Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

216-228

Informations de copyright

© 2018 S. Karger AG, Basel.

Auteurs

Marina Peball (M)

Department of Neurology, Innsbruck Medical University, Innsbruck, Austria.

Philipp Mahlknecht (P)

Department of Neurology, Innsbruck Medical University, Innsbruck, Austria.

Mario Werkmann (M)

Department of Neurology, Innsbruck Medical University, Innsbruck, Austria.

Kathrin Marini (K)

Department of Neurology, Innsbruck Medical University, Innsbruck, Austria.

Franziska Murr (F)

Department of Neurology, Innsbruck Medical University, Innsbruck, Austria.

Helga Herzmann (H)

Department of Neurology, Innsbruck Medical University, Innsbruck, Austria.

Heike Stockner (H)

Department of Neurology, Innsbruck Medical University, Innsbruck, Austria.

Roberto de Marzi (R)

Department of Neurology, Innsbruck Medical University, Innsbruck, Austria.

Beatrice Heim (B)

Department of Neurology, Innsbruck Medical University, Innsbruck, Austria.

Atbin Djamshidian (A)

Department of Neurology, Innsbruck Medical University, Innsbruck, Austria.

Peter Willeit (P)

Department of Neurology, Innsbruck Medical University, Innsbruck, Austria.

Johann Willeit (J)

Department of Neurology, Innsbruck Medical University, Innsbruck, Austria.

Stefan Kiechl (S)

Department of Neurology, Innsbruck Medical University, Innsbruck, Austria.

Dora Valent (D)

Department of Neurology, Innsbruck Medical University, Innsbruck, Austria.

Florian Krismer (F)

Department of Neurology, Innsbruck Medical University, Innsbruck, Austria.

Gregor Karl Wenning (GK)

Department of Neurology, Innsbruck Medical University, Innsbruck, Austria.

Michael Nocker (M)

Department of Neurology, Innsbruck Medical University, Innsbruck, Austria.

Katherina Mair (K)

Department of Neurology, Innsbruck Medical University, Innsbruck, Austria.

Werner Poewe (W)

Department of Neurology, Innsbruck Medical University, Innsbruck, Austria.

Klaus Seppi (K)

Department of Neurology, Innsbruck Medical University, Innsbruck, Austria, klaus.seppi@tirol-kliniken.at.

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