Huntington's disease (HD) is a devastating autosomal dominant progressive neurodegenerative disorder. New therapies are being developed to slow disease progression or to delay its onset. Testing these compounds clinically is a major challenge because there are limited numbers of potential subjects either genetically at-risk for HD or already symptomatic. Currently, therapeutic trials in HD rely on clinical measures of diagnosis and progression, which are quite variable and also change relatively slowly and thus require large numbers of subjects and long periods of follow-up. There is a critical need to develop surrogate markers, such as neuroanatomic measures, which more precisely correlate with progression than variable clinical measures or which may be predictive of onset. Neuroimaging technology provides a way to prospectively examine the HD brain in vivo. We have developed novel neuro-imaging technologies that enable us to obtain highly accurate, reliable, and rapid morphometric measurements of progressive regional atrophy occurring in the entire brain. We have preliminary evidence that regional brain atrophy occurs in gene-positive presymptomatic individuals, permitting its detection and longitudinal assessment even before HD can be diagnosed clinically. By the time of diagnosis, atrophy is apparent in many cortical and subcortical regions and appears to occur in particular patterns, which likely correspond to the appearance of specific clinical features of the disease. Our data challenges the traditional focus on basal ganglia degeneration in HD, provides evidence for earlier and more extensive involvement of many additional brain regions, and greatly enriches the potential for brain imaging to help elucidate the structural basis of symptoms while providing relevant biological markers for response to neuroprotective therapies that can be tested in both symptomatic and presymptomatic patients. We propose to perform a prospective, longitudinal neuro-imaging study of presymptomatic and symptomatic individuals with HD to fully characterize the regional and progressive changes that occur throughout the disease. We will determine the sensitivity and reliability of our morphometric measures as surrogate markers of disease onset and disease progression in comparison to standard clinical measures to determine their potential as surrogate markers.

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Research Project (R01)
Project #
5R01NS042861-03
Application #
6924624
Study Section
Brain Disorders and Clinical Neuroscience 5 (BDCN)
Program Officer
Oliver, Eugene J
Project Start
2003-09-30
Project End
2008-06-30
Budget Start
2005-07-01
Budget End
2006-06-30
Support Year
3
Fiscal Year
2005
Total Cost
$410,875
Indirect Cost
Name
Massachusetts General Hospital
Department
Type
DUNS #
073130411
City
Boston
State
MA
Country
United States
Zip Code
02199
Rosas, H D; Wilkens, P; Salat, D H et al. (2018) Complex spatial and temporally defined myelin and axonal degeneration in Huntington disease. Neuroimage Clin 20:236-242
Coutinho, Artur Martins; Coutu, Jean-Philippe; Lindemer, Emily Rose et al. (2017) Differential associations between systemic markers of disease and cortical thickness in healthy middle-aged and older adults. Neuroimage 146:19-27
Konukoglu, Ender; Coutu, Jean-Philippe; Salat, David H et al. (2016) Multivariate statistical analysis of diffusion imaging parameters using partial least squares: Application to white matter variations in Alzheimer's disease. Neuroimage 134:573-586
Coutu, Jean-Philippe; Goldblatt, Alison; Rosas, H Diana et al. (2016) White Matter Changes are Associated with Ventricular Expansion in Aging, Mild Cognitive Impairment, and Alzheimer's Disease. J Alzheimers Dis 49:329-42
Lee, S-H; Coutu, J-P; Wilkens, P et al. (2015) Tract-based analysis of white matter degeneration in Alzheimer's disease. Neuroscience 301:79-89
Rosas, Herminia D; Doros, Gheorghe; Bhasin, Swati et al. (2015) A systems-level ""misunderstanding"": the plasma metabolome in Huntington's disease. Ann Clin Transl Neurol 2:756-68
Ryu, Seon Young; Coutu, Jean-Philippe; Rosas, H Diana et al. (2014) Effects of insulin resistance on white matter microstructure in middle-aged and older adults. Neurology 82:1862-70
Adriaanse, Sofie M; van Dijk, Koene R A; Ossenkoppele, Rik et al. (2014) The effect of amyloid pathology and glucose metabolism on cortical volume loss over time in Alzheimer's disease. Eur J Nucl Med Mol Imaging 41:1190-8
Sabuncu, Mert R; Bernal-Rusiel, Jorge L; Reuter, Martin et al. (2014) Event time analysis of longitudinal neuroimage data. Neuroimage 97:9-18
Rosas, Herminia D; Doros, Gheorghe; Gevorkian, Sona et al. (2014) PRECREST: a phase II prevention and biomarker trial of creatine in at-risk Huntington disease. Neurology 82:850-7

Showing the most recent 10 out of 35 publications