This project significantly extends the power of MRI and diffusion tensor imaging (DTI) at ultra-high magnetic field strengths (7T) to resolve previously unseen features of brain structure and fiber properties, providing unique power to investigate disease. We will exploit the extreme spatial resolution and signal contrast at 7T, to compute sensitive biomarkers of aging, mild cognitive impairment (MCI), and Alzheimer's disease (AD). Combining data from 80 human subjects scanned at both 7T and 3T, we will compute the profile of cortical gray matter thickness (Aim 1), a measure sensitive to subtle changes in aging, development and a key target of drug trials in dementia and neuropsychiatric research. Extending DTI to 7T, we will assess white matter microstructure and fiber integrity with unprecedented power (Aim 2), and how it changes with aging and dementia. We will quantify how much 7T (versus 3T) boosts the detection sensitivity, signal to noise, stability and effect size of these key biomarkers of brain disease. Uniting the UCLA/University of Minnesota imaging centers, we will develop novel signal processing computations and mathematics to extract maximal information from the 7T images, advancing their current resolution and detection limits. New denoising, registration, and statistical techniques will detect individual and group differences in cortical thickness and fiber integrity. Advances in the mathematics of partial differential equations (PDEs), harmonic maps, and Riemannian manifolds, will provide unique power to denoise tensor- and vector-valued imaging signals (DTI). New statistics will detect disease-sensitive changes in the brain's fiber pathways. We will quantify how much effect sizes increase at 7T versus 3T, and what benefits our novel algorithms yield. In the first high- field study of AD and MCI, we will exploit the higher contrast and resolution at 7T to map key brain changes, undetected at 3T. We will unravel the geometry of cortical surfaces in the brain, and map how cortical thickness changes in aging (Aim 3), AD and MCI (Aim 4). We will map individuals and populations, encoding group patterns of cortical thinning and fiber architecture to detect local or diffuse brain changes. These gains will immediately advance clinical trials of anti-dementia and anti-psychotic drugs that depend on MRI for their power. Validated on unique data, our tools will help monitor disease progression, and map how brain diseases begin and spread in human populations. We will share all images, protocols, and algorithms with our network of 100+ collaborating laboratories. ? ? ?

Agency
National Institute of Health (NIH)
Institute
National Institute of Biomedical Imaging and Bioengineering (NIBIB)
Type
Research Project (R01)
Project #
5R01EB007813-02
Application #
7470616
Study Section
Medical Imaging Study Section (MEDI)
Program Officer
Cohen, Zohara
Project Start
2007-08-01
Project End
2011-04-30
Budget Start
2008-05-01
Budget End
2009-04-30
Support Year
2
Fiscal Year
2008
Total Cost
$321,953
Indirect Cost
Name
University of California Los Angeles
Department
Neurology
Type
Schools of Medicine
DUNS #
092530369
City
Los Angeles
State
CA
Country
United States
Zip Code
90095
Dennis, Emily L; Rashid, Faisal; Faskowitz, Josh et al. (2017) MAPPING AGE EFFECTS ALONG FIBER TRACTS IN YOUNG ADULTS. Proc IEEE Int Symp Biomed Imaging 2017:101-104
Hibar, Derrek P; Stein, Jason L; Jahanshad, Neda et al. (2015) Genome-wide interaction analysis reveals replicated epistatic effects on brain structure. Neurobiol Aging 36 Suppl 1:S151-8
Jahanshad, Neda; Couture, Marie-Claude; Prasitsuebsai, Wasana et al. (2015) Brain Imaging and Neurodevelopment in HIV-uninfected Thai Children Born to HIV-infected Mothers. Pediatr Infect Dis J 34:e211-6
Kochunov, Peter; Jahanshad, Neda; Marcus, Daniel et al. (2015) Heritability of fractional anisotropy in human white matter: a comparison of Human Connectome Project and ENIGMA-DTI data. Neuroimage 111:300-11
Prestia, Annapaola; Cavedo, Enrica; Boccardi, Marina et al. (2015) Hippocampal and amygdalar local structural differences in elderly patients with schizophrenia. Am J Geriatr Psychiatry 23:47-58
Warstadt, Nicholus M; Dennis, Emily L; Jahanshad, Neda et al. (2014) Serum cholesterol and variant in cholesterol-related gene CETP predict white matter microstructure. Neurobiol Aging 35:2504-2513
Nir, Talia M; Jahanshad, Neda; Busovaca, Edgar et al. (2014) Mapping white matter integrity in elderly people with HIV. Hum Brain Mapp 35:975-92
Dennis, Emily L; Jahanshad, Neda; Braskie, Meredith N et al. (2014) Obesity gene NEGR1 associated with white matter integrity in healthy young adults. Neuroimage 102 Pt 2:548-57
Kochunov, Peter; Jahanshad, Neda; Sprooten, Emma et al. (2014) Multi-site study of additive genetic effects on fractional anisotropy of cerebral white matter: Comparing meta and megaanalytical approaches for data pooling. Neuroimage 95:136-50
Dennis, Emily L; Thompson, Paul M (2014) Reprint of: Mapping connectivity in the developing brain. Int J Dev Neurosci 32:41-57

Showing the most recent 10 out of 98 publications