Grey matter atrophy is associated with disability increase in natalizumab-treated patients

Ethel Ciampi, Deborah Pareto, Jaume Sastre-Garriga, Angela Vidal-Jordana, Carmen Tur, Jordi Río, Mar Tintoré, Cristina Auger, Alex Rovira, Xavier Montalban

Research output: Contribution to journalArticleResearchpeer-review

13 Citations (Scopus)

Abstract

© The Author(s), 2016. Background: Brain volume loss (BVL) is a key outcome in multiple sclerosis (MS) trials. Natalizumab is highly effective on inflammation with moderate impact on atrophy. Objective: To explore BVL in patients receiving natalizumab with an emphasis on grey matter (GM). Methods: We performed a retrospective post hoc analysis of BVL in 38 patients receiving natalizumab for 3 years using longitudinal voxel-based morphometry (VBM) and FreeSurfer. Results: Significant BVL was observed during first year: brain parenchymal fraction (BPF): -1.12% (p < 0.001); white matter fraction (WMF): -0.9% (p = 0.001); grey matter fraction (GMF): -1.28% (p = 0.002). GM loss was found using VBM in bilateral cerebellum, cingulum, left > right fronto-parietal cortex, right > left hippocampus and left caudate. FreeSurfer showed significant volume losses in subcortical GM, brainstem and cerebellum, and cortical thinning in the left insula. In the second year, only WMF decrease (-0.6%; p = 0.015) was observed with no VBM changes, although FreeSurfer detected significant volume loss in thalamus, hippocampus and cerebellum. Baseline gadolinium enhancement influenced WMF and BPF changes during the first year, but not GMF. Patients with confirmed Expanded Disability Status Scale (EDSS) worsening at 3 years had lower baseline GMF and left thalamus volume and greater BVL over follow-up. Conclusion: BVL develops mainly during the first year of natalizumab therapy. GM changes are independent of baseline inflammation and correlate with disability.
Original languageEnglish
Pages (from-to)556-566
JournalMultiple Sclerosis
Volume23
Issue number4
DOIs
Publication statusPublished - 1 Jan 2017

Keywords

  • Brain atrophy
  • Disability
  • Grey matter
  • Multiple sclerosis
  • Natalizumab

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