Imaging amyloid-β deposits in vivo

被引:83
作者
Bacskai, BJ
Klunk, WE
Mathis, CA
Hyman, BT
机构
[1] Massachusetts Gen Hosp, Alzheimers Dis Res Unit, CNY 2450, Charlestown, MA 02129 USA
[2] Univ Pittsburgh, Sch Med, Dept Psychiat, Lab Mol Neuropharmacol, Pittsburgh, PA USA
[3] Univ Pittsburgh, Sch Med, Dept Radiol, PET Facil, Pittsburgh, PA USA
关键词
Alzheimer; amyloid-beta; SPECT; PET;
D O I
10.1097/00004647-200209000-00001
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Alzheimer disease (AD) is an illness that can only be diagnosed With certainty with postmortem examination of brain tissue. Tissue samples from afflicted patients show neuronal loss, neurofibrillary tangles (NFTs), and amyloid-beta plaques. An imaging technique that permitted in vivo detection of NFTs or amyloid-beta plaques would be extremely valuable. For example, chronic imaging of senile plaques would provide a readout of the efficacy of experimental therapeutics aimed at removing these neuropathologic lesions. This review discusses the available techniques for imaging amyloid-beta deposits in the intact brain, including magnetic resonance imaging, positron emission tomography, single photon emission computed tomography, and multiphoton microscopy. A variety of agents that target amyloid-beta deposits specifically have been developed using one or several of these imaging modalities. The difficulty in developing these tools lies in the need for the agents to cross the blood-brain barrier while recognizing amyloid-beta with high sensitivity and specificity. This review describes the progress in developing reagents suitable for in vivo imaging of senile plaques.
引用
收藏
页码:1035 / 1041
页数:7
相关论文
共 51 条
[1]   Binding characteristics of radiofluorinated 6-dialkylamino-2-naphthylethylidene derivatives as positron emission tomography imaging probes for β-amyloid plaques in Alzheimer's disease [J].
Agdeppa, ED ;
Kepe, V ;
Liu, J ;
Flores-Torres, S ;
Satyamurthy, N ;
Petric, A ;
Cole, GM ;
Small, GW ;
Huang, SC ;
Barrio, JR .
JOURNAL OF NEUROSCIENCE, 2001, 21 (24) :art. no.-RC189
[2]   NEUROFIBRILLARY TANGLES BUT NOT SENILE PLAQUES PARALLEL DURATION AND SEVERITY OF ALZHEIMERS-DISEASE [J].
ARRIAGADA, PV ;
GROWDON, JH ;
HEDLEYWHYTE, ET ;
HYMAN, BT .
NEUROLOGY, 1992, 42 (03) :631-639
[3]   Imaging of amyloid-β deposits in brains of living mice permits direct observation of clearance of plaques with immunotherapy [J].
Backskai, BJ ;
Kajdasz, ST ;
Christie, RH ;
Carter, C ;
Games, D ;
Seubert, P ;
Schenk, D ;
Hyman, BT .
NATURE MEDICINE, 2001, 7 (03) :369-372
[4]   Chronic imaging of amyloid plaques in the live mouse brain using multiphoton microscopy [J].
Bacskai, BJ ;
Kajdasz, ST ;
Christie, RH ;
Zipfel, WR ;
Williams, RM ;
Kasischke, KA ;
Webb, WW ;
Hyman, BT .
MULTIPHOTON MICROSCOPY IN THE BIOMEDICAL SCIENCES, 2001, 4262 :125-133
[5]   Detection of neuritic plaques in Alzheimer's disease by magnetic resonance microscopy [J].
Benveniste, H ;
Einstein, G ;
Kim, KR ;
Hulette, C ;
Johnson, A .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (24) :14079-14084
[6]   MRI of entorhinal cortex in mild Alzheimer's disease [J].
Bobinski, M ;
de Leon, MJ ;
Convit, A ;
De Santi, S ;
Wegiel, B ;
Tarshish, CY ;
Saint Louis, LA ;
Wisniewski, HM .
LANCET, 1999, 353 (9146) :38-40
[7]  
Camargo EE, 2001, J NUCL MED, V42, P611
[8]   Trends and developments in MRI contrast agent research [J].
Cavagna, FM ;
Dapra, M ;
Castelli, PM ;
Maggioni, F ;
Kirchin, MA .
EUROPEAN RADIOLOGY, 1997, 7 (Suppl 5) :S222-S224
[9]   Growth arrest of individual senile plaques in a model of Alzheimer's disease observed by in vivo multiphoton microscopy [J].
Christie, RH ;
Bacskai, BJ ;
Zipfel, WR ;
Williams, RM ;
Kajdasz, ST ;
Webb, WW ;
Hyman, BT .
JOURNAL OF NEUROSCIENCE, 2001, 21 (03) :858-864
[10]  
de Leon M J, 1997, Int Psychogeriatr, V9 Suppl 1, P183, DOI 10.1017/S1041610297004900