Cerebral atrophy in myotonic dystrophy: A voxel based morphometric study

G. Antonini, C. Mainero, A. Romano, F. Giubilei, V. Ceschin, F. Gragnani, S. Marino, M. Fiorelli, F. Soscia, A. Di Pasquale, F. Caramia

Research output: Contribution to journalArticle

Abstract

Brain involvement in myotonic dystrophy type 1 (DM1) is characterised by cortical atrophy and white matter lesions. We compared the magnetic resonance imaging derived grey matter maps of 22 DM1 patients with those of matched, healthy controls using voxel based morphometry to evaluate the extension of global and regional cortical atrophy in DM1, as well as its relationships with clinical and genetic features. Patients had significantly reduced brain tissue volumes. Grey matter volume was inversely correlated with age; this inverse correlation was significantly stronger in DM1 than in controls. Neither the clinical and genetic characteristics nor white matter lesions were correlated with cortical atrophy. Grey matter atrophy was located mainly in the bilateral frontal and parietal lobes, in the bilateral middle temporal gyrus, and in the left superior temporal and occipital gyrus.

Original languageEnglish
Pages (from-to)1611-1613
Number of pages3
JournalJournal of Neurology, Neurosurgery and Psychiatry
Volume75
Issue number11
DOIs
Publication statusPublished - Nov 2004

ASJC Scopus subject areas

  • Neuropsychology and Physiological Psychology
  • Neuroscience(all)
  • Psychiatry and Mental health

Fingerprint Dive into the research topics of 'Cerebral atrophy in myotonic dystrophy: A voxel based morphometric study'. Together they form a unique fingerprint.

Cite this