Characterizing mild cognitive impairment in incident Parkinson disease The ICICLE-PD Study

被引:338
作者
Yarnall, Alison J. [1 ]
Breen, David P. [4 ]
Duncan, Gordon W. [1 ]
Khoo, Tien K. [10 ]
Coleman, Shirley Y. [2 ]
Firbank, Michael J. [1 ]
Nombela, Cristina [5 ,6 ,7 ]
Winder-Rhodes, Sophie [5 ,6 ,7 ]
Evans, Jonathan R. [4 ]
Rowe, James B. [5 ,7 ]
Mollenhauer, Brit [11 ]
Kruse, Niels [12 ]
Hudson, Gavin [3 ]
Chinnery, Patrick F. [3 ]
O'Brien, John T. [8 ]
Robbins, Trevor W. [4 ,6 ,9 ]
Wesnes, Keith [13 ]
Brooks, David J.
Barker, Roger A. [4 ]
Burn, David J. [1 ]
机构
[1] Newcastle Univ, Inst Ageing & Hlth, Newcastle Upon Tyne NE1 7RU, Tyne & Wear, England
[2] Newcastle Univ, Ind Stat Res Unit, Newcastle Upon Tyne NE1 7RU, Tyne & Wear, England
[3] Newcastle Univ, Inst Med Genet, Newcastle Upon Tyne NE1 7RU, Tyne & Wear, England
[4] Univ Cambridge, John Geest Ctr Brain Repair, Cambridge CB2 1TN, England
[5] Univ Cambridge, Dept Clin Neurosci, Cambridge CB2 1TN, England
[6] Univ Cambridge, Behav & Clin Neurosci Inst, Cambridge CB2 1TN, England
[7] Univ Cambridge, MRC, Cognit & Brain Sci Unit, Cambridge CB2 1TN, England
[8] Univ Cambridge, Dept Psychiat, Cambridge CB2 1TN, England
[9] Univ Cambridge, Dept Psychol, Cambridge CB2 1TN, England
[10] Griffith Univ, Sch Med, Nathan, Qld 4111, Australia
[11] Paracelsus Elena Klin, Kassel, Germany
[12] Univ Med Ctr Gottingen, Inst Neuropathol, Prion & Dementia Res Unit, Gottingen, Germany
[13] Swinburne Univ, Ctr Human Psychopharmacol, Melbourne, Vic, Australia
关键词
CSF AMYLOID-BETA; LEWY BODIES; CEREBROSPINAL-FLUID; ALPHA-SYNUCLEIN; DRUG-NAIVE; DEMENTIA; DECLINE; TAU; MULTICENTER; PROGRESSION;
D O I
10.1212/WNL.0000000000000066
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Objective:To describe the frequency of mild cognitive impairment (MCI) in Parkinson disease (PD) in a cohort of newly diagnosed incident PD cases and the associations with a panel of biomarkers.Methods:Between June 2009 and December 2011, 219 subjects with PD and 99 age-matched controls participated in clinical and neuropsychological assessments as part of a longitudinal observational study. Consenting individuals underwent structural MRI, lumbar puncture, and genotyping for common variants of COMT, MAPT, SNCA, BuChE, EGF, and APOE. PD-MCI was defined with reference to the new Movement Disorder Society criteria.Results:The frequency of PD-MCI was 42.5% using level 2 criteria at 1.5 SDs below normative values. Memory impairment was the most common domain affected, with 15.1% impaired at 1.5 SDs. Depression scores were significantly higher in those with PD-MCI than the cognitively normal PD group. A significant correlation was found between visual Pattern Recognition Memory and cerebrospinal -amyloid 1-42 levels ( standardized coefficient = 0.350; p = 0.008) after controlling for age and education in a linear regression model, with lower -amyloid 1-42 and 1-40 levels observed in those with PD-MCI. Voxel-based morphometry did not reveal any areas of significant gray matter loss in participants with PD-MCI compared with controls, and no specific genotype was associated with PD-MCI at the 1.5-SD threshold.Conclusions:In a large cohort of newly diagnosed PD participants, PD-MCI is common and significantly correlates with lower cerebrospinal -amyloid 1-42 and 1-40 levels. Future longitudinal studies should enable us to determine those measures predictive of cognitive decline.
引用
收藏
页码:308 / 316
页数:9
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