Magnetic Resonance (MR) imaging affords the opportunity to use safe, noninvasive techniques to identify and quantify regional brain abnormalities in living patients with psychiatric and neurological diseases. Methods We use MR structural imaging to quantify regional volumes of gray matter (comprising mostly neurons), white matter (comprising mostly neuronal tracts), and cerebral spinal fluid-filled spaces (sulci and ventricles); proton MR spectroscopy (MRS) to detect and quantify critical brain metabolites, such as N-acetylaspartate (NAA), which is a marker for living neurons; and phosphorous MR spectroscopy to measure brain cell membrane turnover. Results and Discussion We have found, for example, that: (1) Patients with Alzheimer' 5 disease have a significant cortical gray matter volume deficit that is greater in younger than older patients, relative to age norms derived from our healthy control subjects. Thus, the early onset form of this disease may be more virulent than the late onset form. (2) Patients with schizophrenia have a widespread cortical gray matter volume deficit that is most pronounced in the prefrontal and frontal-temporal regions. (3) Detoxified chronic alcoholics have cortical volume deficits that include both gray matter and white matter, and also have volume deficits of the anterior hippocampus. The alcohol-related brain volume loss appears to accelerate with age. We also found significant volume deficits in the anterior superior regions of the cerebellar vermis, which may underlie postural instability and falling even in detoxified alcoholics. (4) Recovering alcoholics show improvement in cortical gray matter, sulcal, and ventricular volumes early in the course of abstinence, and improvement in third ventricular volumes later with continued abstinence. Because of the brain dysmorphology in these patient groups is typically imperceptible to clinical review, we are excited about the advanced imaging capabilities available to quantify regional and structural brain volumes in terms of their constituent parts.

Agency
National Institute of Health (NIH)
Institute
National Center for Research Resources (NCRR)
Type
Biotechnology Resource Grants (P41)
Project #
5P41RR009784-02
Application #
5225807
Study Section
Project Start
Project End
Budget Start
Budget End
Support Year
2
Fiscal Year
1996
Total Cost
Indirect Cost
Maclaren, Julian; Aksoy, Murat; Ooi, Melvyn B et al. (2018) Prospective motion correction using coil-mounted cameras: Cross-calibration considerations. Magn Reson Med 79:1911-1921
Guo, Jia; Holdsworth, Samantha J; Fan, Audrey P et al. (2018) Comparing accuracy and reproducibility of sequential and Hadamard-encoded multidelay pseudocontinuous arterial spin labeling for measuring cerebral blood flow and arterial transit time in healthy subjects: A simulation and in vivo study. J Magn Reson Imaging 47:1119-1132
Tamir, Jonathan I; Uecker, Martin; Chen, Weitian et al. (2017) T2 shuffling: Sharp, multicontrast, volumetric fast spin-echo imaging. Magn Reson Med 77:180-195
Lai, Lillian M; Cheng, Joseph Y; Alley, Marcus T et al. (2017) Feasibility of ferumoxytol-enhanced neonatal and young infant cardiac MRI without general anesthesia. J Magn Reson Imaging 45:1407-1418
Taviani, Valentina; Alley, Marcus T; Banerjee, Suchandrima et al. (2017) High-resolution diffusion-weighted imaging of the breast with multiband 2D radiofrequency pulses and a generalized parallel imaging reconstruction. Magn Reson Med 77:209-220
Uecker, Martin; Lustig, Michael (2017) Estimating absolute-phase maps using ESPIRiT and virtual conjugate coils. Magn Reson Med 77:1201-1207
Kogan, Feliks; Hargreaves, Brian A; Gold, Garry E (2017) Volumetric multislice gagCEST imaging of articular cartilage: Optimization and comparison with T1rho. Magn Reson Med 77:1134-1141
Aksoy, Murat; Maclaren, Julian; Bammer, Roland (2017) Prospective motion correction for 3D pseudo-continuous arterial spin labeling using an external optical tracking system. Magn Reson Imaging 39:44-52
Bian, W; Tranvinh, E; Tourdias, T et al. (2016) In Vivo 7T MR Quantitative Susceptibility Mapping Reveals Opposite Susceptibility Contrast between Cortical and White Matter Lesions in Multiple Sclerosis. AJNR Am J Neuroradiol 37:1808-1815
Vos, Sjoerd B; Aksoy, Murat; Han, Zhaoying et al. (2016) Trade-off between angular and spatial resolutions in in vivo fiber tractography. Neuroimage 129:117-132

Showing the most recent 10 out of 446 publications