Profiling cognitive and neuropsychiatric heterogeneity in Parkinson's disease

被引:15
|
作者
van Balkom, Tim D. [1 ,2 ,3 ]
Vriend, Chris [1 ,2 ,3 ,4 ]
Berendse, Henk W. [3 ,4 ]
Foncke, Elisabeth M. J. [4 ]
van der Werf, Ysbrand D. [2 ,3 ]
van den Heuvel, Odile A. [1 ,2 ,3 ]
Klein, Martin [5 ]
机构
[1] Vrije Univ Amsterdam, Med Ctr, Dept Psychiat, POB 7057, NL-1007 MB Amsterdam, Netherlands
[2] Vrije Univ Amsterdam, Med Ctr, Dept Anat & Neurosci, POB 7057, NL-1007 MB Amsterdam, Netherlands
[3] Vrije Univ Amsterdam, Med Ctr, Neurosci Campus Amsterdam, Amsterdam, Netherlands
[4] Vrije Univ Amsterdam, Med Ctr, Dept Neurol, POB 7057, NL-1007 MB Amsterdam, Netherlands
[5] Vrije Univ Amsterdam, Med Ctr, Dept Med Psychol, De Boelelaan 1117, NL-1081 HV Amsterdam, Netherlands
关键词
Parkinson's disease; Cognition; Neuropsychiatry; Profiling; Cluster analysis; DATA-DRIVEN APPROACH; SUBTYPES; IMPAIRMENT; DEMENTIA; COHORT; IDENTIFICATION; DISTURBANCES; DISORDERS; CAMPAIGN;
D O I
10.1016/j.parkreldis.2016.05.014
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background: Parkinson's disease (PD) is a highly heterogeneous disease, in which motor symptom subtypes are often-described. While it is recognized that motor, cognitive and affective neuropsychiatric symptoms negatively influence the patients' quality of life, it is currently unknown how these symptoms contribute to phenotypic subtypes. The objective of this study was to assess subtypes of motor, cognitive and affective symptoms in PD. Methods: A hierarchical cluster analysis was conducted on clinical data of 226 PD patients screened at the VU University Medical Center using comprehensive assessment of cognitive, affective and motor symptoms. Subsequent linear discriminant analyses were conducted to investigate discriminating constructs between clusters. Results: The cluster analysis yielded four clusters: (1) a young-age (59.9 years), mildly affected cluster (N = 86), (2) an old-age (72.3 years) cluster with severe motor and non-motor symptoms (N = 15), (3) a cluster (age 64.7 years) with mild motor symptoms, below-average executive functioning and affective symptoms (N = 46) and (4) a cluster (age 64.8 years) with severe motor symptoms, affective symptoms and below-average verbal memory (N = 79). Conclusions: Cluster 1 and 2 seem to represent opposite ends of the PD disease stages. Patients in clusters 3 and 4 had similar age, educational level and disease duration but different symptom profiles we therefore suggest that these clusters represent different pathways of disease progression, presumably with distinct underlying pathology localization. Future research on the neuropathophysiological characteristics of these two clusters and monitoring of disease progression is required. (C) 2016 Elsevier Ltd. All rights reserved.
引用
收藏
页码:130 / 136
页数:7
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