High specificity of MMSE pentagon scoring for diagnosis of prodromal dementia with Lewy bodies

Parkinsonism Relat Disord. 2015 Mar;21(3):303-5. doi: 10.1016/j.parkreldis.2014.12.007. Epub 2014 Dec 16.

Abstract

Background: Patients with dementia with Lewy bodies (DLB) may display a different cognitive pattern from Alzheimer's disease (AD) with more severe impairment performing visuospatial/visuoconstructive tasks. The aim of this study was to investigate whether the analysis of the MMSE pentagon copy could be a useful diagnostic screening tool in prodromal DLB.

Methods: Fifty-three patients with Mild Cognitive Impairment (MCI) were followed over 3-years until a diagnosis of DLB (MCI-DLB: n = 30) and AD (MCI-AD: n = 23) were made according to standard criteria. At the first assessment patients underwent a thorough cognitive assessment including the Qualitative Scoring MMSE Pentagon Test (QSPT), the NPI, the UPDRS as well as questionnaires to determine fluctuations and sleep disorders.

Results: The percentage of subjects who were unable to determine the correct number of angles in the pentagon copy test was 45.1% of MCI-DLB and 8.3% of MCI-AD patients (sensitivity 41.1%; specificity 91%). Attentive/executive functions and visual-spatial abilities were worse in the MCI-DLB group, while episodic memory impairment was greater in MCI-AD. Subtle extrapyramidal signs (63%) and RBD symptoms (56%) were the most frequent clinical features supporting the diagnosis of MCI-DLB.

Conclusions: We suggest that a poor performance in determining the number of angles when performing the pentagon copying test, together with the presence of subtle extrapyramidal signs and symptoms of RBD may serve as a predictive tool for early DLB.

Keywords: Cognitive impairment; Dementia with Lewy bodies; Mini-Mental State Examination; Visuo-constructional abilities.

MeSH terms

  • Aged
  • Aged, 80 and over
  • Alzheimer Disease / diagnosis*
  • Cognitive Dysfunction / physiopathology
  • Disease Progression
  • Female
  • Humans
  • Lewy Body Disease / diagnosis*
  • Longitudinal Studies
  • Male
  • Mental Status Schedule*
  • Middle Aged
  • Neuropsychological Tests
  • Prodromal Symptoms*
  • Psychomotor Performance
  • Sensitivity and Specificity