Cognitive impairment in Parkinson's disease

被引:177
作者
Verbaan, D.
Marinus, J.
Visser, M.
van Rooden, S. M.
Stiggelbout, A. M.
Middelkoop, H. A. M.
van Hilten, J. J.
机构
[1] Leiden Univ, Ctr Med, Dept Neurol, NL-2300 RC Leiden, Netherlands
[2] Leiden Univ, Med Ctr, Dept Med Decis Making, Leiden, Netherlands
[3] Leiden Univ, Med Ctr, Dept Neuropsychol, Leiden, Netherlands
关键词
D O I
10.1136/jnnp.2006.112367
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background: Cognitive impairment plays a role in Parkinson's disease (PD) and has important consequences for patient management. However, many aspects of cognitive impairment in PD remain unclear because of the use of different and often invalid measurement instruments. In this study, a reliable and valid instrument, the SCales for Outcomes in PArkinson's disease-COGnition (SCOPA-COG), was used. Aim: To evaluate cognitive functioning in a large cohort of patients with Parkinson's disease and to assess the relations with demographic, disease related and clinical variables. Methods: A cohort of 400 patients with PD was evaluated for cognition, motor and non-motor domains, as well as for demographic and disease related characteristics. Results were compared with 150 controls matched for overall age, sex and education distribution. Results: Patients with PD scored significantly lower on all cognitive subdomains compared with controls, with the largest differences for executive functioning and memory. After correction for age and years of education, 22% of patients had impaired cognition, as measured by the total SCOPA-COG score, compared with controls. Across all patients, more severe cognitive impairment was associated with significantly more impairment in motor, autonomic, depressive and psychotic domains. Patients with the postural instability gait difficulty (PIGD) dominant phenotype showed more cognitive impairment compared with patients with the tremor dominant phenotype. Contrary to tremor scores, PIGD scores significantly worsened with increasing disease severity. Conclusions: Cognition is an important domain of the clinical spectrum of PD and poorer cognitive performance is associated with greater impairment in motor and non-motor domains in PD. The difference in cognitive scores between PIGD dominant patients and tremor dominant patients likely reflects more advanced disease.
引用
收藏
页码:1182 / 1187
页数:6
相关论文
共 37 条
[1]   The rate of cognitive decline in Parkinson disease [J].
Aarsland, D ;
Andersen, K ;
Larsen, JP ;
Perry, R ;
Wentzel-Larsen, T ;
Lolk, A ;
Kragh-Sorensen, P .
ARCHIVES OF NEUROLOGY, 2004, 61 (12) :1906-1911
[2]   A systematic review of prevalence studies of dementia in Parkinson's disease [J].
Aarsland, D ;
Zaccai, J ;
Brayne, C .
MOVEMENT DISORDERS, 2005, 20 (10) :1255-1263
[3]   Risk of dementia in Parkinson's disease - A community-based, prospective study [J].
Aarsland, D ;
Andersen, K ;
Larsen, JP ;
Lolk, A ;
Nielsen, H ;
Kragh-Sorensen, P .
NEUROLOGY, 2001, 56 (06) :730-736
[4]   Prevalence and characteristics of dementia in Parkinson disease - An 8-year prospective study [J].
Aarsland, D ;
Andersen, K ;
Larsen, JP ;
Lolk, A ;
Kragh-Sorensen, P .
ARCHIVES OF NEUROLOGY, 2003, 60 (03) :387-392
[5]   Changes in motor subtype and risk for incident dementia in Parkinson's disease [J].
Alves, Guido ;
Petter Larsen, Jan ;
Emre, Murat ;
Wentzel-Larsen, Tore ;
Aarsland, Dag .
MOVEMENT DISORDERS, 2006, 21 (08) :1123-1130
[6]   Dementia in Parkinson's disease [J].
Anderson K.E. .
Current Treatment Options in Neurology, 2004, 6 (3) :201-207
[7]   AN INVENTORY FOR MEASURING DEPRESSION [J].
BECK, AT ;
ERBAUGH, J ;
WARD, CH ;
MOCK, J ;
MENDELSOHN, M .
ARCHIVES OF GENERAL PSYCHIATRY, 1961, 4 (06) :561-&
[8]   Cognitive status correlates with neuropathologic stage in Parkinson disease [J].
Braak, H ;
Rüb, U ;
Steur, ENHJ ;
Del Tredici, K ;
de Vos, RAI .
NEUROLOGY, 2005, 64 (08) :1404-1410
[9]  
Braak H, 2002, J NEUROL S3, V249, P1, DOI DOI 10.1007/S00415-002-1301-4
[10]   Non-motor symptoms of Parkinson's disease: diagnosis and management [J].
Chaudhuri, KR ;
Healy, DG ;
Schapira, AHV .
LANCET NEUROLOGY, 2006, 5 (03) :235-245