Magnetic resonance spectroscopic imaging (MRS imaging) is a promising new approach for the in vivo study of degenerative brain disorders. The major MRS-visible components of a water-suppressed brain proton spectrum are N-acetyl aspartate (NAA) (observed primarily in living neurons), creatine (an energy metabolite), and choline (a precursor to acetylcholine and also a constituent of cell membrane synthesis). We have recently used proton MRS to produce axial images of regional brain distribution of NAA, choline and creatine. In this project, we propose to further develop a system for proton spectroscopic imaging of all parts of the human brain which will be robust to the problems of inhomogeneity and susceptibility and will produce metabolic images that can be readily interpreted. In addition we will develop a method for quantification of spectroscopic data which will provide reliable regional concentration measurements. MRS imaging will be used to develop normative values for NAA, choline and creatine concentrations and distributions found across the age range of 50-80 in healthy community members and to examine alterations in metabolite concentrations and distributions in Alzheimer's disease (AD) patients. All subjects will be retested after a 2-year interval to determine change with normal aging and disease progression. An age-regression model will be used to identify heterogeneity within the AD group based on age of disease onset. In addition, we will investigate hypothesized associations between metabolite concentrations, volumes of white and grey matter in defined regions of interest, and performance on tests of specific cognitive functions.

Agency
National Institute of Health (NIH)
Institute
National Institute on Aging (NIA)
Type
Research Project (R01)
Project #
5R01AG011427-03
Application #
2052617
Study Section
Neurology A Study Section (NEUA)
Project Start
1993-07-01
Project End
1998-06-30
Budget Start
1995-07-15
Budget End
1996-06-30
Support Year
3
Fiscal Year
1995
Total Cost
Indirect Cost
Name
Stanford University
Department
Psychiatry
Type
Schools of Medicine
DUNS #
800771545
City
Stanford
State
CA
Country
United States
Zip Code
94305
Sullivan, E V; Deshmukh, A; Desmond, J E et al. (2000) Cerebellar volume decline in normal aging, alcoholism, and Korsakoff's syndrome: relation to ataxia. Neuropsychology 14:341-52
Adalsteinsson, E; Sullivan, E V; Kleinhans, N et al. (2000) Longitudinal decline of the neuronal marker N-acetyl aspartate in Alzheimer's disease. Lancet 355:1696-7
Fama, R; Sullivan, E V; Shear, P K et al. (2000) Extent, pattern, and correlates of remote memory impairment in Alzheimer's disease and Parkinson's disease. Neuropsychology 14:265-76
Pfefferbaum, A; Adalsteinsson, E; Spielman, D et al. (1999) In vivo spectroscopic quantification of the N-acetyl moiety, creatine, and choline from large volumes of brain gray and white matter: effects of normal aging. Magn Reson Med 41:276-84
Pfefferbaum, A; Adalsteinsson, E; Spielman, D et al. (1999) In vivo brain concentrations of N-acetyl compounds, creatine, and choline in Alzheimer disease. Arch Gen Psychiatry 56:185-92
Faull, K F; Rafie, R; Pascoe, N et al. (1999) N-acetylaspartic acid (NAA) and N-acetylaspartylglutamic acid (NAAG) in human ventricular, subarachnoid, and lumbar cerebrospinal fluid. Neurochem Res 24:1249-61
Adalsteinsson, E; Star-Lack, J; Meyer, C H et al. (1999) Reduced spatial side lobes in chemical-shift imaging. Magn Reson Med 42:314-23
Adalsteinsson, E; Spielman, D M (1999) Spatially resolved two-dimensional spectroscopy. Magn Reson Med 41:8-12
Cahn, D A; Sullivan, E V; Shear, P K et al. (1998) Structural MRI correlates of recognition memory in Alzheimer's disease. J Int Neuropsychol Soc 4:106-14
Lim, K O; Adalsteinsson, E; Spielman, D et al. (1998) Proton magnetic resonance spectroscopic imaging of cortical gray and white matter in schizophrenia. Arch Gen Psychiatry 55:346-52

Showing the most recent 10 out of 16 publications