|
|
||||||||
From the Departments of Neurology (Drs. Rosas, Kennedy, Makris, Beal, and Koroshetz) and Psychiatry (Dr. Seidman) and the Center for Morphometric Analyses (Drs. Kennedy and Makris and M. Patti), Massachusetts General Hospital and Harvard Medical School; the Department of Psychiatry, Massachusetts Mental Health Center (Dr. Seidman), Boston; and the MGH-NMR Center, Department of Radiology, Massachusetts General Hospital and Harvard Medical School (Drs. Rosas, Goodman, Chen, and Jenkins), Charlestown.
Address correspondence and reprint requests to Dr. H.D. Rosas, Neurology Service, Massachusetts General Hospital, Warren 408, 32 Fruit St., Boston, MA 02114; e-mail: rosas{at}helix.mgh.harvard.edu
Background: Huntingtons disease (HD) is an autosomal dominant neurodegenerative disease that results from the expansion of a trinucleotide (CAG) repeat on chromosome 4. Progressive degeneration of the striatum is the pathologic hallmark of the disease. Little is known about the regional selectivity of the neurodegeneration and its relationship to the genetic expansion.
Methods: The authors used high-resolution MRI to determine the relationship between the genetic expansion and the degree of striatal degeneration. Morphometric analyses of the striatum from high-resolution MR images from 27 subjects with HD were compared with those of 24 healthy control subjects.
Results and conclusions: Striatal volumes were reduced in subjects with HD as compared with control subjects, in agreement with previously published reports. Left-sided volumes were smaller than right-sided volumes in subjects with HD; in healthy subjects, right-sided volumes were smaller. Finally, volume loss was significantly correlated with CAG repeat number. These results have potential implications for the design and assessment of therapeutic agents in the future.
This article has been cited by other articles:
![]() |
N. A. Aziz, J.M.M. van der Burg, G. B. Landwehrmeyer, P. Brundin, T. Stijnen, EHDI Study Group, and R. A.C. Roos Weight loss in Huntington disease increases with higher CAG repeat number Neurology, November 4, 2008; 71(19): 1506 - 1513. [Abstract] [Full Text] [PDF] |
||||
![]() |
W. J. Powers, T. O. Videen, J. Markham, L. McGee-Minnich, J. V. Antenor-Dorsey, T. Hershey, and J. S. Perlmutter Selective defect of in vivo glycolysis in early Huntington's disease striatum PNAS, February 20, 2007; 104(8): 2945 - 2949. [Abstract] [Full Text] [PDF] |
||||
![]() |
K. Finke, P. Bublak, M. Dose, H. J. Muller, and W. X. Schneider Parameter-based assessment of spatial and non-spatial attentional deficits in Huntington's disease Brain, May 1, 2006; 129(5): 1137 - 1151. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. Mascalchi, F. Lolli, R. D. Nave, C. Tessa, R. Petralli, C. Gavazzi, L. S. Politi, M. Macucci, M. Filippi, and S. Piacentini Huntington Disease: Volumetric, Diffusion-weighted, and Magnetization Transfer MR Imaging of Brain Radiology, September 1, 2004; 232(3): 867 - 873. [Abstract] [Full Text] [PDF] |
||||
![]() |
J Kassubek, F D Juengling, T Kioschies, K Henkel, J Karitzky, B Kramer, D Ecker, J Andrich, C Saft, P Kraus, et al. Topography of cerebral atrophy in early Huntington's disease: a voxel based morphometric MRI study J. Neurol. Neurosurg. Psychiatry, February 1, 2004; 75(2): 213 - 220. [Abstract] [Full Text] [PDF] |
||||
![]() |
E. J. Slow, J. van Raamsdonk, D. Rogers, S. H. Coleman, R. K. Graham, Y. Deng, R. Oh, N. Bissada, S. M. Hossain, Y.-Z. Yang, et al. Selective striatal neuronal loss in a YAC128 mouse model of Huntington disease Hum. Mol. Genet., July 1, 2003; 12(13): 1555 - 1567. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. R. Aron, F. Schlaghecken, P. C. Fletcher, E. T. Bullmore, M. Eimer, R. Barker, B. J. Sahakian, and T. W. Robbins Inhibition of subliminally primed responses is mediated by the caudate and thalamus: evidence from functional MRI and Huntington's disease Brain, March 1, 2003; 126(3): 713 - 723. [Abstract] [Full Text] [PDF] |
||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |