PLoS ONE (Jan 2017)

Cerebellar volume as imaging outcome in progressive multiple sclerosis.

  • Matilde Inglese,
  • Maria Petracca,
  • Enricomaria Mormina,
  • Anat Achiron,
  • Rebecca Straus-Farber,
  • Shmuel Miron,
  • Michelle Fabian,
  • Stephen Krieger,
  • Aaron Miller,
  • Fred Lublin,
  • Maria Pia Sormani

DOI
https://doi.org/10.1371/journal.pone.0176519
Journal volume & issue
Vol. 12, no. 4
p. e0176519

Abstract

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To assess whether cerebellar volumes changes could represent a sensitive outcome measure in primary-progressive MS.Changes in cerebellar volumes over one-year follow-up, estimated in 26 primary-progressive MS patients and 20 controls with Freesurfer longitudinal pipeline, were assessed using Wilcoxon test and tested for their correlation with disability worsening by a logistic regression. Clinical worsening was defined as EDSS score increase or change of >20% for 25-foot walk test or 9-hole peg test scores at follow-up. Sample sizes for given treatment effects and power were calculated. The findings were validated in an independent cohort of 20 primary-progressive MS patients.Significant changes were detected in brain T1 lesion volume (p<0.01), cerebellar T2 and T1 lesion volume (p<0.01 and p<0.05), cerebellar volume, cerebellar cortex volume, and cerebellar WM volume (p<0.001). Only cerebellar volume and cerebellar cortex volume percentage change were significantly reduced in clinically progressed patients when compared to patients who did not progress (p<0.01; respectively AUC of 0.91 and 0.96). Cerebellar volume percentage changes were consistent in the exploration and validation cohorts (cerebellar volume -1.90±1.11% vs -1.47±2.30%; cerebellar cortex volume -1.68±1.41% vs -1.56±2.23%). Based on our results the numbers of patients required to detect a 30% effect are 81 per arm for cerebellar volume and 162 per arm for cerebellar cortex volume (90% power, type 1 error alpha = 0.05).Our results suggest a role for cerebellar cortex volume and cerebellar volume as potential short-term imaging metrics to monitor treatment effect in primary-progressive MS clinical trials.