Skip to main content
Top
Published in: Journal of Neurology 9/2015

01-09-2015 | Original Communication

Longitudinal changes in cerebellar and subcortical volumes in adult-onset Niemann–Pick disease type C patients treated with miglustat

Authors: Elizabeth A. Bowman, Mark Walterfang, Larry Abel, Patricia Desmond, Michael Fahey, Dennis Velakoulis

Published in: Journal of Neurology | Issue 9/2015

Login to get access

Abstract

Niemann–Pick disease type C (NPC) is a rare neurovisceral disorder resulting in impaired intracellular lipid trafficking. The only disease-modifying treatment available to date is miglustat, an iminosugar inhibiting the accumulation of lipid by-products in neurons. This study explored how changes in cerebellar grey and white matter volumes, and in subcortical volumes, related to patient treatment status and disability and ataxia ratings. Nine adult-onset NPC patients and 17 matched controls underwent T1-weighted MRI. One patient was not receiving miglustat, and pre-treatment data were available for a further patient. Semi-automated cerebellar and subcortical segmentation was undertaken, and the rates of change in putamen, hippocampal, thalamic and caudal volumes, and grey and white matter cerebellar volumes, were compared to rates of change in Iturriaga disability score, Brief Ataxia Rating Scale (BARS), and horizontal saccadic gain. Untreated NPC patients appeared to lose cerebellar grey and white matter, bilateral thalamic volume, and right caudate volume faster than treated patients. Cerebellar grey matter volume loss and volume loss in the left thalamus were significantly correlated with Iturriaga disability scale changes. Change in both cerebellar grey and white matter was correlated with decrease in horizontal saccadic gain, but not with change in BARS. This is the first study to examine longitudinal treatment effects of miglustat on cerebellar and subcortical volumes in patients with adult-onset NPC, and is evidence that miglustat may have a protective effect on cerebellar and subcortical structure and function.
Literature
2.
3.
go back to reference Zervas M, Dobrenis K, Walkley SU (2001) Neurons in Niemann–Pick disease type C accumulate gangliosides as well as unesterified cholesterol and undergo dendritic and axonal alterations. J Neuropathol Exp Neurol 60(1):49–64PubMed Zervas M, Dobrenis K, Walkley SU (2001) Neurons in Niemann–Pick disease type C accumulate gangliosides as well as unesterified cholesterol and undergo dendritic and axonal alterations. J Neuropathol Exp Neurol 60(1):49–64PubMed
4.
go back to reference Suzuki K, Parker CC, Pentchev PG, Katz D, Ghetti B, D’Agostino AN, Carstea ED (1995) Neurofibrillary tangles in Niemann–Pick disease type C. Acta Neuropathol 89(3):227–238CrossRefPubMed Suzuki K, Parker CC, Pentchev PG, Katz D, Ghetti B, D’Agostino AN, Carstea ED (1995) Neurofibrillary tangles in Niemann–Pick disease type C. Acta Neuropathol 89(3):227–238CrossRefPubMed
5.
go back to reference Taniguchi M, Shinoda Y, Ninomiya H, Vanier MT, Ohno K (2001) Sites and temporal changes of gangliosides GM1/GM2 storage in the Niemann–Pick disease type C mouse brain. Brain Dev 23(6):414–421CrossRefPubMed Taniguchi M, Shinoda Y, Ninomiya H, Vanier MT, Ohno K (2001) Sites and temporal changes of gangliosides GM1/GM2 storage in the Niemann–Pick disease type C mouse brain. Brain Dev 23(6):414–421CrossRefPubMed
7.
go back to reference Walterfang M, Fahey M, Desmond P, Wood A, Seal ML, Steward C, Adamson C, Kokkinos C, Fietz M, Velakoulis D (2010) White and gray matter alterations in adults with Niemann–Pick disease type C: a cross-sectional study. Neurology 75(1):49–56. doi:10.1212/WNL.0b013e3181e6210e CrossRefPubMed Walterfang M, Fahey M, Desmond P, Wood A, Seal ML, Steward C, Adamson C, Kokkinos C, Fietz M, Velakoulis D (2010) White and gray matter alterations in adults with Niemann–Pick disease type C: a cross-sectional study. Neurology 75(1):49–56. doi:10.​1212/​WNL.​0b013e3181e6210e​ CrossRefPubMed
9.
go back to reference Stein VM, Crooks A, Ding W, Prociuk M, O’Donnell P, Bryan C, Sikora T, Dingemanse J, Vanier MT, Walkley SU, Vite CH (2012) Miglustat improves purkinje cell survival and alters microglial phenotype in feline Niemann–Pick disease type C. J Neuropathol Exp Neurol 71(5):434–448. doi:10.1097/NEN.0b013e31825414a6 PubMedCentralCrossRefPubMed Stein VM, Crooks A, Ding W, Prociuk M, O’Donnell P, Bryan C, Sikora T, Dingemanse J, Vanier MT, Walkley SU, Vite CH (2012) Miglustat improves purkinje cell survival and alters microglial phenotype in feline Niemann–Pick disease type C. J Neuropathol Exp Neurol 71(5):434–448. doi:10.​1097/​NEN.​0b013e31825414a6​ PubMedCentralCrossRefPubMed
10.
go back to reference Zervas M, Somers KL, Thrall MA, Walkley SU (2001) Critical role for glycosphingolipids in Niemann–Pick disease type C. Curr Biol 11(16):1283–1287CrossRefPubMed Zervas M, Somers KL, Thrall MA, Walkley SU (2001) Critical role for glycosphingolipids in Niemann–Pick disease type C. Curr Biol 11(16):1283–1287CrossRefPubMed
14.
17.
go back to reference Free SL, Bergin PS, Fish DR, Cook MJ, Shorvon SD, Stevens JM (1995) Methods for normalization of hippocampal volumes measured with MR. AJNR Am J Neuroradiol 16(4):637–643PubMed Free SL, Bergin PS, Fish DR, Cook MJ, Shorvon SD, Stevens JM (1995) Methods for normalization of hippocampal volumes measured with MR. AJNR Am J Neuroradiol 16(4):637–643PubMed
19.
go back to reference Platt FM, Neises GR, Dwek RA, Butters TD (1994) N-butyldeoxynojirimycin is a novel inhibitor of glycolipid biosynthesis. J Biol Chem 269(11):8362–8365PubMed Platt FM, Neises GR, Dwek RA, Butters TD (1994) N-butyldeoxynojirimycin is a novel inhibitor of glycolipid biosynthesis. J Biol Chem 269(11):8362–8365PubMed
20.
go back to reference Walterfang M, Fahey M, Abel L, Fietz M, Wood A, Bowman E, Reutens D, Velakoulis D (2011) Size and shape of the corpus callosum in adult Niemann–Pick type C reflects state and trait illness variables. AJNR Am J Neuroradiol 32(7):1340–1346. doi:10.3174/ajnr.A2490 CrossRefPubMed Walterfang M, Fahey M, Abel L, Fietz M, Wood A, Bowman E, Reutens D, Velakoulis D (2011) Size and shape of the corpus callosum in adult Niemann–Pick type C reflects state and trait illness variables. AJNR Am J Neuroradiol 32(7):1340–1346. doi:10.​3174/​ajnr.​A2490 CrossRefPubMed
21.
go back to reference Walterfang M, Patenaude B, Abel LA, Kluenemann H, Bowman EA, Fahey MC, Desmond P, Kelso W, Velakoulis D (2012) Subcortical volumetric reductions in adult Niemann–Pick Disease type C: a cross-sectional study. AJNR Am J Neuroradiol. doi:10.3174/ajnr.A3356 PubMed Walterfang M, Patenaude B, Abel LA, Kluenemann H, Bowman EA, Fahey MC, Desmond P, Kelso W, Velakoulis D (2012) Subcortical volumetric reductions in adult Niemann–Pick Disease type C: a cross-sectional study. AJNR Am J Neuroradiol. doi:10.​3174/​ajnr.​A3356 PubMed
23.
go back to reference Zaaraoui W, Crespy L, Rico A, Faivre A, Soulier E, Confort-Gouny S, Cozzone PJ, Pelletier J, Ranjeva JP, Kaphan E, Audoin B (2011) In vivo quantification of brain injury in adult Niemann–Pick Disease type C. Mol Genet Metab 103(2):138–141. doi:10.1016/j.ymgme.2011.02.013 CrossRefPubMed Zaaraoui W, Crespy L, Rico A, Faivre A, Soulier E, Confort-Gouny S, Cozzone PJ, Pelletier J, Ranjeva JP, Kaphan E, Audoin B (2011) In vivo quantification of brain injury in adult Niemann–Pick Disease type C. Mol Genet Metab 103(2):138–141. doi:10.​1016/​j.​ymgme.​2011.​02.​013 CrossRefPubMed
24.
go back to reference Galanaud D, Tourbah A, Lehericy S, Leveque N, Heron B, Billette de Villemeur T, Guffon N, Feillet F, Baumann N, Vanier MT, Sedel F (2009) 24 month-treatment with miglustat of three patients with Niemann–Pick disease type C: follow up using brain spectroscopy. Mol Genet Metab 96(2):55–58. doi:10.1016/j.ymgme.2008.10.002 CrossRefPubMed Galanaud D, Tourbah A, Lehericy S, Leveque N, Heron B, Billette de Villemeur T, Guffon N, Feillet F, Baumann N, Vanier MT, Sedel F (2009) 24 month-treatment with miglustat of three patients with Niemann–Pick disease type C: follow up using brain spectroscopy. Mol Genet Metab 96(2):55–58. doi:10.​1016/​j.​ymgme.​2008.​10.​002 CrossRefPubMed
25.
26.
27.
go back to reference Rottach KG, von Maydell RD, Das VE, Zivotofsky AZ, Discenna AO, Gordon JL, Landis DM, Leigh RJ (1997) Evidence for independent feedback control of horizontal and vertical saccades from Niemann–Pick type C disease. Vision Res 37(24):3627–3638. doi:10.1016/S0042-6989(96)00066-1 CrossRefPubMed Rottach KG, von Maydell RD, Das VE, Zivotofsky AZ, Discenna AO, Gordon JL, Landis DM, Leigh RJ (1997) Evidence for independent feedback control of horizontal and vertical saccades from Niemann–Pick type C disease. Vision Res 37(24):3627–3638. doi:10.​1016/​S0042-6989(96)00066-1 CrossRefPubMed
28.
go back to reference Takagi M, Zee DS, Tamargo RJ (1998) Effects of lesions of the oculomotor vermis on eye movements in primate: saccades. J Neurophysiol 80(4):1911–1931PubMed Takagi M, Zee DS, Tamargo RJ (1998) Effects of lesions of the oculomotor vermis on eye movements in primate: saccades. J Neurophysiol 80(4):1911–1931PubMed
29.
go back to reference Elleder M, Jirasek A (1981) Neuropathology of various types of Niemann–Pick disease. Acta Neuropathol Suppl 7:201–203CrossRefPubMed Elleder M, Jirasek A (1981) Neuropathology of various types of Niemann–Pick disease. Acta Neuropathol Suppl 7:201–203CrossRefPubMed
30.
go back to reference German DC, Quintero EM, Liang CL, Ng B, Punia S, Xie C, Dietschy JM (2001) Selective neurodegeneration, without neurofibrillary tangles, in a mouse model of Niemann–Pick C disease. J Comp Neurol 433(3):415–425PubMedCentralCrossRefPubMed German DC, Quintero EM, Liang CL, Ng B, Punia S, Xie C, Dietschy JM (2001) Selective neurodegeneration, without neurofibrillary tangles, in a mouse model of Niemann–Pick C disease. J Comp Neurol 433(3):415–425PubMedCentralCrossRefPubMed
31.
go back to reference Fusco C, Russo A, Galla D, Hladnik U, Frattini D, Giustina ED (2013) New Niemann–Pick type C1 gene mutation associated with very severe disease course and marked early cerebellar vermis atrophy. J Child Neurol 28(12):1694–1697. doi:10.1177/0883073812462765 CrossRefPubMed Fusco C, Russo A, Galla D, Hladnik U, Frattini D, Giustina ED (2013) New Niemann–Pick type C1 gene mutation associated with very severe disease course and marked early cerebellar vermis atrophy. J Child Neurol 28(12):1694–1697. doi:10.​1177/​0883073812462765​ CrossRefPubMed
Metadata
Title
Longitudinal changes in cerebellar and subcortical volumes in adult-onset Niemann–Pick disease type C patients treated with miglustat
Authors
Elizabeth A. Bowman
Mark Walterfang
Larry Abel
Patricia Desmond
Michael Fahey
Dennis Velakoulis
Publication date
01-09-2015
Publisher
Springer Berlin Heidelberg
Published in
Journal of Neurology / Issue 9/2015
Print ISSN: 0340-5354
Electronic ISSN: 1432-1459
DOI
https://doi.org/10.1007/s00415-015-7819-z

Other articles of this Issue 9/2015

Journal of Neurology 9/2015 Go to the issue