Identification of a prospective early motor progression cluster of Parkinson's disease: Data from the PPMI study

George D Vavougios*, Triantafyllos Doskas, Constantinos Kormas, Karen A Krogfelt, Sotirios G Zarogiannis, Leonidas Stefanis

*Corresponding author for this work

Research output: Contribution to journalJournal articlepeer-review

Abstract

Aim The aim of our study is to phenotype PD motor progression, and to detect whether serum, cerebrospinal fluid (CSF), neuroimaging biomarkers and neuropsychological measures characterize PD motor progression phenotypes. Methods We defined motor progression as a difference of at least one point in the Hoehn & Yahr (H&Y) scale between the baseline (Visit 0, V0), 12 months (Visit 04, V04) and 36 months (Visit 08, V08) milestones of the Progression Markers Initiative (PPMI) study. H&Y progression events were recorded at each milestone in order to be used as cluster analysis variables, in order to produce progression phenotypes. Subsequently, cross-cluster comparisons prior to and following (pairwise) propensity score matching were performed in order to assess phenotype – defining characteristics. Results Four progression clusters where identified: SPPD: Secondarily Progressive PD, H&Y progression between V04 and V08; EPPD: Early Progressive PD. H&Y progression between V0 and V04; NPPD: Non Progressive PD, no H&Y progression; MIPD: Minimally Improving PD, i.e. Minimal H&Y improvement H&Y progression between V04 and V08;. Independent Samples Mann Whitney U tests determined CSF aSyn (p = 0.006, adj p-value = 0.036. I) and Semantic Animal fluency T-score (SFT, p = 0.003, adjusted p-value = 0.016.) as statistically significant cross-cluster characteristics. Following Propensity Score Matching, SFT, Hopkins Verbal Learning Test (Retention/Recall), Serum IGF1, CSF aSyn, DaT-SPECT binding ratios (SBRs) and the Benton Judgement of Line Orientation Test (BJLOT) were determined as statistically significant predictors of cluster differentiation (p < 0.05). Discussion SFT, Serum IGF1, CSF aSyn and DaT-SPECT-derived, basal ganglia Striatal Binding Ratios warrant further investigation as possible motor progression biomarkers.
Original languageEnglish
JournalJournal of the Neurological Sciences
Volume387
Pages (from-to)103-108
Number of pages6
ISSN0022-510X
DOIs
Publication statusPublished - 2018
Externally publishedYes

Keywords

  • Parkinson's disease
  • Progression
  • Biomarkers
  • Cluster analysis
  • Phenotypes

Cite this