Features of brain MRI in dogs with treated and untreated mucopolysaccharidosis type I.

Journal Article (Journal Article)

The mucopolysaccharidosis type I (MPS I) dog model has been important in the development of therapies for human patients. We treated dogs with enzyme replacement therapy (ERT) by various approaches. Dogs assessed included untreated MPS I dogs, heterozygous carrier dogs, and MPS I dogs treated with intravenous ERT as adults (beginning at age 13 to 16 mo), intrathecal and intravenous ERT as adults (beginning at age 13 to 16 mo), or intrathecal ERT as juveniles (beginning at age 4 mo). We then characterized the neuroimaging findings of 32 of these dogs (age, 12 to 30 mo). Whole and midsagittal volumes of the corpus callosum, measured from brain MRI, were significantly smaller in affected dogs compared with unaffected heterozygotes. Corpus callosum volumes in dogs that were treated with intrathecal ERT from 4 mo until 21 mo of age were indistinguishable from those of age-matched carrier controls. Dogs with MPS I showed cerebral ventricular enlargement and cortical atrophy as early as 12 mo of age. Ventricular enlargement was greater in untreated MPS I dogs than in age-matched dogs treated with intrathecal ERT as juveniles or adults. However, treated dogs still showed some ventricular enlargement or cortical atrophy (or both). Understanding the progression of neuroimaging findings in dogs with MPS I and their response to brain-directed therapy may improve preclinical studies for new human-directed therapies. In particular, corpus callosum volumes may be useful quantitative neuroimaging markers for MPS-related brain disease and its response to therapy.

Full Text

Duke Authors

Cited Authors

  • Vite, CH; Nestrasil, I; Mlikotic, A; Jens, JK; Snella, EM; Gross, W; Shapiro, EG; Kovac, V; Provenzale, JM; Chen, S; Le, SQ; Kan, S-H; Banakar, S; Wang, RY; Haskins, ME; Ellinwood, NM; Dickson, PI

Published Date

  • April 2013

Published In

  • Comp Med

Volume / Issue

  • 63 / 2

Start / End Page

  • 163 - 173

PubMed ID

  • 23582423

Pubmed Central ID

  • PMC3625057

Electronic International Standard Serial Number (EISSN)

  • 2769-819X


  • eng

Conference Location

  • United States