Characterizing mild cognitive impairment in incident Parkinson disease

Alison J. Yarnall(University of Newcastle Australia), David P. Breen(Griffith University), Gordon W. Duncan(Swinburne University of Technology), Tien K. Khoo(Griffith University), Shirley Coleman(Newcastle University), Michael Firbank(Swinburne University of Technology), Cristina Nombela(Swinburne University of Technology), Sophie Winder‐Rhodes(University of Newcastle Australia), Jonathan Evans(Newcastle University), James B. Rowe(Griffith University), Brit Mollenhauer(Swinburne University of Technology), Niels Kruse(Swinburne University of Technology), Gavin Hudson(University of Newcastle Australia), Patrick F. Chinnery(Newcastle University), John T. O’Brien(Griffith University), Trevor W. Robbins(University of Newcastle Australia), Keith Wesnes(Swinburne University of Technology), David J. Brooks(University of Newcastle Australia), Roger A. Barker(Griffith University), David J. Burn(Newcastle University)
Neurology
December 21, 2013
Cited by 418Open Access
Full Text

Abstract

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 β-amyloid 1-42 levels (β standardized coefficient = 0.350; p = 0.008) after controlling for age and education in a linear regression model, with lower β-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 β-amyloid 1-42 and 1-40 levels. Future longitudinal studies should enable us to determine those measures predictive of cognitive decline.


Related Papers

No related papers found

Powered by citation graph analysis