TRADITIONAL POSTER - ismrm
TRADITIONAL POSTER - ismrm
TRADITIONAL POSTER - ismrm
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Poster Sessions<br />
1953. Association of White Matter Hyperintensities with White Matter Changes in Alzheimer's Disease as<br />
Studied by DTI<br />
Liya Wang 1 , Felicia C. Goldstein 2 , Hui Mao 1<br />
1 Radiology and Emory Center for Systems Imaging, Emory University School of Medicine, Atlanta, GA, United States; 2 Neurology,<br />
Emory University School of Medicine, Atlanta, GA, United States<br />
White matter hyperintensities (WMH) provide an additive effect is considered to be a risk factor of Alzheimer¡¯s disease (AD). We investigated which DTI<br />
indices: fractional anisotropy (FA), mean diffusivity (MD), radial diffusivity (DR) and axial diffusivity (DX) values were more sensitive to differentiate AD<br />
from normal control and how different levels of WMH may contribute to AD in specific areas of the white matter. FA and DR were helpful to discriminate<br />
AD with different grade of WMH. Different level WMH contributed AD in different regions and extent. The increased DR may provide measurement of<br />
demyelination of AD in pathology.<br />
1954. Reduced Regional Fractional Anisotropy in Cognitively Normal Individuals with Biochemical and<br />
Imaging Evidence of Cerebral Amyloid Deposition<br />
Joseph Mettenburg 1 , David N. Daniels 1 , Yvette I. Sheline, 12 , Beau Ances 3 , Huiling Peng 3 , Abraham Z.<br />
Snyder 1 , John C. Morris 3 , Mark A. Mintun 1 , Tammie L.S. Benzinger 4<br />
1 Mallinckrodt Institute of Radiology, Washington University in Saint Louis; 2 Psychiatry, Washington University in Saint Louis;<br />
3 Neurology, Washington University in Saint Louis; 4 Mallinckrodt Institute of Radiology, Washington University in Saint Louis, St.<br />
Louis, MO, United States<br />
Amyloid plaque deposition in the brain is one of the key pathological hallmarks of Alzheimer’s disease. Recently, CSF amyloid beta42 peptide levels and<br />
PET scans using C-11 Pittsburgh Compound B (PIB) have been established as potential biomarkers for dementia of the Alzheimer’s type (DAT). Using<br />
DTI, we evaluated white matter microstructure in subjects with and without established DAT and identified differences in both the corpus callosum and<br />
precuneus. The same white matter findings were identified in non-demented subjects with positive CSF and PIB-PET, suggesting that microstructural<br />
abnormalities in white matter integrity may precede cognitive changes in DAT.<br />
1955. White Matter Disruption and Its Relationship with Cognitive Function and Cortical Atrophy in<br />
Alzheimer’s Disease<br />
Hao Huang 1 , Xin Fan 1 , Kristin Martin-Cook 2 , Guanghua Xiao 3 , Laura Lacritz 4 , Myron Weiner 4 , Roger<br />
Rosenberg 2<br />
1 Advanced Imaging Research Center, University of Texas Southwestern Medical Center, Dallas, TX, United States; 2 Department of<br />
Neurology, University of Texas Southwestern Medical Center, Dallas, TX, United States; 3 Department of Clinical Sciences,<br />
University of Texas Southwestern Medical Center, Dallas, TX, United States; 4 Department of Psychiatry, University of Texas<br />
Southwestern Medical Center, Dallas, TX, United States<br />
The purpose of this study is to find an effective white matter biomarker of Alzheimer’s disease (AD) which may indicate disease severity and progression. In<br />
this study, DTI and T1 weighted images were acquired from 38 subjects (20 AD, 18 controls). We surveyed all white matter tracts by labeling of the ICBM-<br />
DTI-81 digital atlas and correlated FA values of individual white matter tracts with cognitive testing score and cortical atrophy map respectively. The<br />
correlation analyses show that tracts in the limbic system, namely fornix and cingulum, are the most sensitive tract to cognitive testing scores and cortical<br />
atrophy.<br />
1956. Quantitative 7T Relaxographic, Volumetric and DCE Assessment of Thalamic Changes in Early<br />
Alzheimer’s Disease<br />
Valerie C. Anderson 1 , David P. Lenar 1 , Joseph F. Quinn 2 , William J. Woodward 3 , Jeffrey A. Kaye 2 ,<br />
William D. Rooney 3<br />
1 Neurological Surgery, Oregon Health & Science University, Portland, OR, United States; 2 Neurology, Oregon Health & Science<br />
University, Portland, OR, United States; 3 Advanced Imaging Research Center, Oregon Health & Science University, Portland, OR,<br />
United States<br />
Longitudinal water proton ( 1 H 2 O) relaxation time constants (T 1 ) are strongly associated with macromolecular volume fraction. Here, we report that 1 H 2 O T 1<br />
values are increased in the thalamus of subjects with early AD compared to age-matched, cognitively normal controls. Further, we find that the increased<br />
1 H 2 O T 1 values in early AD reflect, at least in part, neurodegenerative (macromolecular loss) processes and that contributions to the increased 1 H 2 O T 1<br />
values from altered blood water content (via dilation or increased vessel density) are small.<br />
1957. Dementia Induces Correlated Reductions in White Matter Integrity and Cortical Thickness: A<br />
Multivariate Neuroimaging Study with Sparse Canonical Correlation Analysis<br />
Brian Avants 1 , Phil Cook 1 , Lyle Ungar 1 , James Gee 1 , Murray Grossman 1<br />
1 University of Pennsylvania, philadelphia, PA, United States<br />
We present a novel, unsupervised method, sparse canonical correlation analysis for neuroimaging (SCCAN), that automatically locates correlated sets of<br />
voxels in complementary imaging modalities. The method reveals significant and syndrome-specific cortical thickness-diffusion tensor imaging networks in<br />
two neurodegenerative diseases, AD and FTD. Subject diagnosis was confirmed by autopsy or CSF-biomarker ratios. The SCCAN summary correlates, in<br />
AD, with MMSE reduction and, in FTD, with reduced verbal fluency. Thus, SCCAN identifies disease-specific networks of effects in white matter and<br />
cortical thickness that appear in anatomy suspected to be involved in these diseases and that relate specifically to impaired cognitive processes.