Quantitative MRI assessment of Alzheimer's disease

被引:15
作者
Helpern, JA
Jensen, J
Lee, SP
Falangola, MF
机构
[1] NYU, Sch Med, Dept Radiol, Ctr Biomed Imaging, New York, NY 10016 USA
[2] Nathan S Kline Inst Psychiat Res, Ctr Adv Brain Imaging, Orangeburg, NY 10962 USA
关键词
MRI; imaging; transgenic mice; Alzheimer's disease; beta-amyloid;
D O I
10.1385/JMN:24:1:045
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The development of a noninvasive method to detect early, subtle changes in the brains of patients with Alzheimer's disease (AD) would have considerable clinical value as therapy. This therapy is most likely to be successful if intervention could occur before neurons were irreversibly damaged or lost. An ideal biological neuroimaging marker would be an early, sensitive, and valid indicator of brain changes, capable of discriminating the effects of normal aging. The introduction of high field-strength clinical magnetic resonance imaging (MRI) systems now offer a powerful new noninvasive tool that may be capable of detecting brain pathology resulting from AD. Here we present results from high field-strength MRI in transgenic mice along with a new MRI technique for imaging brain iron. The successful translation of this research to the clinic could prove important to both the early diagnosis and monitoring of the efficacy of potential therapies in humans.
引用
收藏
页码:45 / 48
页数:4
相关论文
共 19 条
[1]   In vivo evaluation of brain iron in Alzheimer disease using magnetic resonance imaging [J].
Bartzokis, G ;
Sultzer, D ;
Cummings, J ;
Holt, LE ;
Hance, DB ;
Henderson, VW ;
Mintz, J .
ARCHIVES OF GENERAL PSYCHIATRY, 2000, 57 (01) :47-53
[2]   Endocytic pathway abnormalities precede amyloid β deposition in sporadic Alzheimer's disease and Down syndrome -: Differential effects of APOE genotype and presenilin mutations [J].
Cataldo, AM ;
Peterhoff, CM ;
Troncosco, JC ;
Gomez-Isla, T ;
Hyman, BT ;
Nixon, RA .
AMERICAN JOURNAL OF PATHOLOGY, 2000, 157 (01) :277-286
[3]   CELLULAR-DISTRIBUTION OF TRANSFERRIN, FERRITIN, AND IRON IN NORMAL AND AGED HUMAN BRAINS [J].
CONNOR, JR ;
MENZIES, SL ;
STMARTIN, SM ;
MUFSON, EJ .
JOURNAL OF NEUROSCIENCE RESEARCH, 1990, 27 (04) :595-611
[4]   A HISTOCHEMICAL-STUDY OF IRON, TRANSFERRIN, AND FERRITIN IN ALZHEIMERS DISEASED BRAINS [J].
CONNOR, JR ;
MENZIES, SL ;
STMARTIN, SM ;
MUFSON, EJ .
JOURNAL OF NEUROSCIENCE RESEARCH, 1992, 31 (01) :75-83
[5]  
FALANGOLA M, 2003, INT SOC MAGN RES MED, P2037
[6]  
Gröhn OHJ, 2000, J CEREBR BLOOD F MET, V20, P316
[7]   Regional distribution of neuritic plaques in the nondemented elderly and subjects with very mild Alzheimer disease [J].
Haroutunian, V ;
Perl, DP ;
Purohit, DP ;
Marin, D ;
Khan, K ;
Lantz, M ;
Davis, KL ;
Mohs, RC .
ARCHIVES OF NEUROLOGY, 1998, 55 (09) :1185-1191
[8]   HISTOPATHOLOGICAL CORRELATIONS OF NUCLEAR-MAGNETIC-RESONANCE IMAGING PARAMETERS IN EXPERIMENTAL CEREBRAL-ISCHEMIA [J].
HELPERN, JA ;
DERESKI, MO ;
KNIGHT, RA ;
ORDIDGE, RJ ;
CHOPP, M ;
QING, ZX .
MAGNETIC RESONANCE IMAGING, 1993, 11 (02) :241-246
[9]   Accelerated Alzheimer-type phenotype in transgenic mice carrying both mutant amyloid precursor protein and presenilin 1 transgenes [J].
Holcomb, L ;
Gordon, MN ;
McGowan, E ;
Yu, X ;
Benkovic, S ;
Jantzen, P ;
Wright, K ;
Saad, I ;
Mueller, R ;
Morgan, D ;
Sanders, S ;
Zehr, C ;
O'Campo, K ;
Hardy, J ;
Prada, CM ;
Eckman, C ;
Younkin, S ;
Hsiao, K ;
Duff, K .
NATURE MEDICINE, 1998, 4 (01) :97-100
[10]  
Jensen JH, 2000, MAGN RESON MED, V44, P144, DOI 10.1002/1522-2594(200007)44:1<144::AID-MRM21>3.0.CO