Clinical classification systems and long-term outcome in mid- and late-stage Parkinson’s disease
Abstract Parkinson’s disease shows a heterogeneous course and different clinical subtyping systems have been described. To compare the capabilities of two clinical classification systems, motor-phenotypes, and a simplified clinical motor-nonmotor subtyping system, a cohort was included at mean 7.9 ±...
Guardado en:
Autores principales: | , |
---|---|
Formato: | article |
Lenguaje: | EN |
Publicado: |
Nature Portfolio
2021
|
Materias: | |
Acceso en línea: | https://doaj.org/article/893524f5226b4872a5f3c4e30b1a4eee |
Etiquetas: |
Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
|
id |
oai:doaj.org-article:893524f5226b4872a5f3c4e30b1a4eee |
---|---|
record_format |
dspace |
spelling |
oai:doaj.org-article:893524f5226b4872a5f3c4e30b1a4eee2021-12-02T17:06:26ZClinical classification systems and long-term outcome in mid- and late-stage Parkinson’s disease10.1038/s41531-021-00208-42373-8057https://doaj.org/article/893524f5226b4872a5f3c4e30b1a4eee2021-08-01T00:00:00Zhttps://doi.org/10.1038/s41531-021-00208-4https://doaj.org/toc/2373-8057Abstract Parkinson’s disease shows a heterogeneous course and different clinical subtyping systems have been described. To compare the capabilities of two clinical classification systems, motor-phenotypes, and a simplified clinical motor-nonmotor subtyping system, a cohort was included at mean 7.9 ± 5.3 years of disease duration, classified using both clinical systems, and reexamined and reclassified at the end of an observation period. Time-points were retrospectively extracted for five major disease milestones: death, dementia, Hoehn and Yahr stage 5, nursing home living, and walking aid use. Eighty-nine patients were observed for 8.1 ± 2.7 years after inclusion. Dementia developed in 32.9% of the patients and 36.0–67.4% reached the other milestones. Motor-phenotypes were unable to stratify risks during this period, but the worst compared with the more favorable groups in the motor-nonmotor system conveyed hazard ratios between 2.6 and 63.6 for all milestones. A clear separation of risks for dying, living at the nursing home, and reaching motor end-stage was also shown when using only postural instability and gait disorder symptoms, without weighing them against the severity of the tremor. At reexamination, 29.4% and 64.7% of patients had changed classification groups in the motor-phenotype and motor-nonmotor systems, respectively. The motor-nonmotor system thus stratified risks of reaching crucial outcomes in mid–late Parkinson’s disease far better than the well-studied motor-phenotypes. Removing the tremor aspect of motor-phenotypes clearly improved this system, however. Classifications in both systems became unstable over time. The simplification of the motor-nonmotor system was easily applicable and showed potential as a prognostic marker during a large part of Parkinson’s disease.Emil Ygland RödströmAndreas PuschmannNature PortfolioarticleNeurology. Diseases of the nervous systemRC346-429ENnpj Parkinson's Disease, Vol 7, Iss 1, Pp 1-9 (2021) |
institution |
DOAJ |
collection |
DOAJ |
language |
EN |
topic |
Neurology. Diseases of the nervous system RC346-429 |
spellingShingle |
Neurology. Diseases of the nervous system RC346-429 Emil Ygland Rödström Andreas Puschmann Clinical classification systems and long-term outcome in mid- and late-stage Parkinson’s disease |
description |
Abstract Parkinson’s disease shows a heterogeneous course and different clinical subtyping systems have been described. To compare the capabilities of two clinical classification systems, motor-phenotypes, and a simplified clinical motor-nonmotor subtyping system, a cohort was included at mean 7.9 ± 5.3 years of disease duration, classified using both clinical systems, and reexamined and reclassified at the end of an observation period. Time-points were retrospectively extracted for five major disease milestones: death, dementia, Hoehn and Yahr stage 5, nursing home living, and walking aid use. Eighty-nine patients were observed for 8.1 ± 2.7 years after inclusion. Dementia developed in 32.9% of the patients and 36.0–67.4% reached the other milestones. Motor-phenotypes were unable to stratify risks during this period, but the worst compared with the more favorable groups in the motor-nonmotor system conveyed hazard ratios between 2.6 and 63.6 for all milestones. A clear separation of risks for dying, living at the nursing home, and reaching motor end-stage was also shown when using only postural instability and gait disorder symptoms, without weighing them against the severity of the tremor. At reexamination, 29.4% and 64.7% of patients had changed classification groups in the motor-phenotype and motor-nonmotor systems, respectively. The motor-nonmotor system thus stratified risks of reaching crucial outcomes in mid–late Parkinson’s disease far better than the well-studied motor-phenotypes. Removing the tremor aspect of motor-phenotypes clearly improved this system, however. Classifications in both systems became unstable over time. The simplification of the motor-nonmotor system was easily applicable and showed potential as a prognostic marker during a large part of Parkinson’s disease. |
format |
article |
author |
Emil Ygland Rödström Andreas Puschmann |
author_facet |
Emil Ygland Rödström Andreas Puschmann |
author_sort |
Emil Ygland Rödström |
title |
Clinical classification systems and long-term outcome in mid- and late-stage Parkinson’s disease |
title_short |
Clinical classification systems and long-term outcome in mid- and late-stage Parkinson’s disease |
title_full |
Clinical classification systems and long-term outcome in mid- and late-stage Parkinson’s disease |
title_fullStr |
Clinical classification systems and long-term outcome in mid- and late-stage Parkinson’s disease |
title_full_unstemmed |
Clinical classification systems and long-term outcome in mid- and late-stage Parkinson’s disease |
title_sort |
clinical classification systems and long-term outcome in mid- and late-stage parkinson’s disease |
publisher |
Nature Portfolio |
publishDate |
2021 |
url |
https://doaj.org/article/893524f5226b4872a5f3c4e30b1a4eee |
work_keys_str_mv |
AT emilyglandrodstrom clinicalclassificationsystemsandlongtermoutcomeinmidandlatestageparkinsonsdisease AT andreaspuschmann clinicalclassificationsystemsandlongtermoutcomeinmidandlatestageparkinsonsdisease |
_version_ |
1718381623146184704 |