P-31 MAGNETIC-RESONANCE SPECTROSCOPY IN ALZHEIMERS AND PICKS DISEASE

被引:39
作者
SMITH, CD
GALLENSTEIN, LG
LAYTON, WJ
KRYSCIO, RJ
MARKESBERY, WR
机构
[1] UNIV KENTUCKY,COLL MED,SANDERS BROWN CTR AGING,LEXINGTON,KY 40536
[2] UNIV KENTUCKY,COLL MED,CTR MAGNET RESONANCE IMAGING & SPECT,LEXINGTON,KY 40536
[3] UNIV KENTUCKY,COLL MED,DEPT PATHOL,LEXINGTON,KY 40536
[4] UNIV KENTUCKY,COLL MED,DEPT STAT,LEXINGTON,KY 40536
关键词
PHOSPHORUS MAGNETIC RESONANCE SPECTROSCOPY; ALZHEIMERS DISEASE; PICKS DISEASE; PHOSPHOMONOESTERS; PHOSPHODIESTERS;
D O I
10.1016/0197-4580(93)90026-8
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 ; 0303 ; 100203 ;
摘要
Previous studies have suggested a defect in phosphorus metabolism in Alzheimer's disease (AD) gray matter. We have studied phosphorus metabolites in both gray and white matter in autopsy specimens of nine subjects with late-stage AD, three with Pick's disease and seven age-matched controls. Phosphorus metabolites sugar phosphate (SU), phosphomonoester (PME), phosphodiester (PD), and inorganic phosphate (PI) were quantified as mole percentages in regional neocortical specimens using nuclear magnetic resonance spectroscopy. Senile plaque (SP) and neurofibrillary tangle (NFT) counts were determined in adjacent cortical sections. In the inferior parietal lobule gray and white matter, mole percentage normalized PME, and PD were significantly greater than control values in both AD and Pick's disease. A significant correlation was found between PD and NFT in AD parietal gray matter. Our data indicates that phosphorus metabolite alterations are present in two cortical degenerative diseases and are not likely to be specific for AD.
引用
收藏
页码:85 / 92
页数:8
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