H-1 and P-31 magnetic resonance spectroscopic imaging of white matter signal hyperintensity areas in elderly subjects

被引:0
作者
Constans, JM
Meyerhoff, DJ
Norman, D
Fein, G
Weiner, MW
机构
[1] DVA MED CTR, MAGNET RESONANCE SPECTROSCOPY UNIT, SAN FRANCISCO, CA 94121 USA
[2] UNIV CALIF SAN FRANCISCO, MAGNET RESONANCE UNIT, SAN FRANCISCO, CA 94143 USA
[3] UNIV CALIF SAN FRANCISCO, DEPT VET AFFAIRS PSYCHIAT SERV, SAN FRANCISCO, CA 94143 USA
[4] UNIV CALIF SAN FRANCISCO, DEPT RADIOL, SAN FRANCISCO, CA 94143 USA
[5] UNIV CALIF SAN FRANCISCO, DEPT MED, SAN FRANCISCO, CA USA
[6] UNIV CALIF SAN FRANCISCO, DEPT PSYCHIAT, SAN FRANCISCO, CA 94143 USA
关键词
white matter signal changes; normal aging; N-acetylaspartate; ischemia; magnetic resonance spectroscopic imaging; magnetic resonance imaging;
D O I
暂无
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
White matter signal hyperintensities (WMSH) are commonly seen on MRI of elderly subjects. The purpose of this study was to characterize metabolic changes in the white matter of elderly subjects with extensive WMSH. We used water-suppressed proton (H-1) magnetic resonance spectroscopic imag ing (MRSI) to compare six subjects with extensive WMSH with eight age-matched elderly subjects with minimal or absent WMSH, and phosphorus ((31)p) MRSI to compare nine subjects with extensive WMSH and seven age-matched elderly subjects without extensive WMSH. Relative to region-matched tissue in elderly controls, extensive WMSH were associated with increased signal from choline-containing metabolites, no significant change of signal from N-acetylaspartate, and a trend to a decreased phosphomonoester (PME) resonance. These findings suggest that WMSH may be associated with an alteration of brain my elin phospholipids in the absence of axonal damage. There were no differences in energy phosphates, consistent with lack of ongoing brain ischemia. Within the group with extensive WMSH, PME resonance measures were significantly lower in WMSH than in contralateral nor mal-appearing white matter. These results provide information on pathophysiology of WMSH and a basis for comparison with WMSH in Alzheimer's disease, vascular dementia, multiple sclerosis, and other diseases.
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收藏
页码:615 / 623
页数:9
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