PLoS ONE (Jan 2018)

Cognition among individuals along a spectrum of increased risk for Parkinson's disease.

  • Lana M Chahine,
  • Liz Urbe,
  • Chelsea Caspell-Garcia,
  • Dag Aarsland,
  • Roy Alcalay,
  • Paolo Barone,
  • David Burn,
  • Alberto J Espay,
  • Jamie L Hamilton,
  • Keith A Hawkins,
  • Shirley Lasch,
  • James B Leverenz,
  • Irene Litvan,
  • Irene Richard,
  • Andrew Siderowf,
  • Christopher S Coffey,
  • Tanya Simuni,
  • Daniel Weintraub,
  • Parkinson’s Progression Markers Initiative

DOI
https://doi.org/10.1371/journal.pone.0201964
Journal volume & issue
Vol. 13, no. 8
p. e0201964

Abstract

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INTRODUCTION:Several characteristics associated with increased risk for Parkinson's disease (PD) have been identified, including specific genotypes and various non-motor symptoms. Characterizing non-motor features, such as cognitive abilities, among individuals considered at-risk for PD is essential to improving prediction of future neurodegeneration. METHODS:Participants belonging to the following cohorts of the Parkinson Progression Markers Initiative (PPMI) study were included: de novo PD with dopamine transporter binding deficit (n = 423), idiopathic REM sleep behavior disorder (RBD, n = 39), hyposmia (n = 26) and non-PD mutation carrier (NMC; Leucine-rich repeat kinase 2 (LRRK2) G2019S (n = 88) and glucocerebrosidase (GBA) gene (n = 38) mutations)). Inclusion criteria enriched the RBD and hyposmia cohorts, but not the NMC cohort, with individuals with dopamine transporter binding deficit. Baseline neuropsychological performance was compared, and analyses were adjusted for age, sex, education, and depression. RESULTS:The RBD cohort performed significantly worse than the hyposmia and NMC cohorts on Symbol Digit Modality Test (mean (SD) 32.4 (9.16) vs. 41.8 (9.98), p = 0.002 and vs. 45.2 (10.9), p<0.001) and Judgment of Line Orientation (11.3 (2.36) vs.12.9 (1.87), p = 0.004 and vs. 12.9 (1.87), p<0.001). The RBD cohort also performed worse than the hyposmia cohort on the Montreal Cognitive Assessment (25.5 (4.13) vs. 27.3 (1.71), p = 0.02). Hyposmics did not differ from PD or NMC cohorts on any cognitive test score. CONCLUSION:Among individuals across a spectrum of risk for PD, cognitive function is worse among those with the characteristic most strongly associated with future risk of PD or dementia with Lewy bodies, namely RBD.