Hippocampal atrophy and disconnection in incipient and mild Alzheimer's disease

被引:63
作者
deToledo-Morrell, Leyla [1 ]
Stoub, Travis R. [1 ]
Wang, Changsheng [1 ]
机构
[1] Rush Univ, Med Ctr, Dept Neurol Sci, Chicago, IL 60612 USA
来源
DENTATE GYRUS: A COMPHREHENSIVE GUIDE TO STRUCTURE, FUNCTION, AND CLINICAL IMPLICATIONS | 2007年 / 163卷
关键词
entorhinal cortex; perforant path; imaging; aging; memory;
D O I
10.1016/S0079-6123(07)63040-4
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Quantitative imaging techniques allow the in vivo investigation of age and disease related changes in the brain and their relation to cognitive function. In this chapter we review imaging evidence indicating that the entorhinal cortex and hippocampus show atrophy very early in Alzheimer's disease (AD) and in individuals who are at risk of developing AD compared to age appropriate controls. Furthermore, the extent and rate of atrophy of the entorhinal cortex, a brain region pathologically involved very early in the disease process, can predict who among the elderly will develop AD. Techniques that assess the integrity of white matter further demonstrate that alterations in the parahippocampal white matter in the region that includes the perforant path could partially disconnect the dentate gyrus and other hippocampal subfields from incoming sensory information. Such partial disconnection and degradation in transmission of sensory information in people at risk of AD and in patients with very mild AD could contribute to the memory dysfunction associated with the early stages of the disease.
引用
收藏
页码:741 / +
页数:14
相关论文
共 65 条
[1]   USE OF BRIEF COGNITIVE TESTS TO IDENTIFY INDIVIDUALS IN THE COMMUNITY WITH CLINICALLY DIAGNOSED ALZHEIMERS-DISEASE [J].
ALBERT, M ;
SMITH, LA ;
SCHERR, PA ;
TAYLOR, JO ;
EVANS, DA ;
FUNKENSTEIN, HH .
INTERNATIONAL JOURNAL OF NEUROSCIENCE, 1991, 57 (3-4) :167-178
[2]   THE ENTORHINAL CORTEX OF THE MONKEY .1. CYTOARCHITECTONIC ORGANIZATION [J].
AMARAL, DG ;
INSAUSTI, R ;
COWAN, WM .
JOURNAL OF COMPARATIVE NEUROLOGY, 1987, 264 (03) :326-355
[3]  
[Anonymous], POLICY STUDIES
[4]   Apolipoprotein E ε4 allele, AD pathology, and the clinical expression of Alzheimer's disease [J].
Bennett, DA ;
Wilson, RS ;
Schneider, JA ;
Evans, DA ;
Aggarwal, NT ;
Arnold, SE ;
Cochran, EJ ;
Berry-Kravis, E ;
Bienias, JL .
NEUROLOGY, 2003, 60 (02) :246-252
[5]  
Braak H, 1998, J NEURAL TRANSM-SUPP, P97
[6]   STAGING OF ALZHEIMERS-DISEASE-RELATED NEUROFIBRILLARY CHANGES [J].
BRAAK, H ;
BRAAK, E .
NEUROBIOLOGY OF AGING, 1995, 16 (03) :271-278
[7]   NEUROPATHOLOGICAL STAGING OF ALZHEIMER-RELATED CHANGES [J].
BRAAK, H ;
BRAAK, E .
ACTA NEUROPATHOLOGICA, 1991, 82 (04) :239-259
[8]   Comparison of methods for measuring longitudinal brain change in cognitive impairment and dementia [J].
Cardenas, VA ;
Du, AT ;
Hardin, D ;
Ezekiel, F ;
Weber, P ;
Jagust, WJ ;
Chui, HC ;
Schuff, N ;
Weiner, MW .
NEUROBIOLOGY OF AGING, 2003, 24 (04) :537-544
[9]   Specific hippocampal volume reductions in individuals at risk for Alzheimer's disease [J].
Convit, A ;
DeLeon, MJ ;
Tarshish, C ;
DeSanti, S ;
Tsui, W ;
Rusinek, H ;
George, A .
NEUROBIOLOGY OF AGING, 1997, 18 (02) :131-138
[10]   Prediction of cognitive decline in normal elderly subjects with 2-[18F]fluoro-2-deoxy-D-glucose/positron-emission tomography (FDG/PET) [J].
de Leon, MJ ;
Convit, A ;
Wolf, OT ;
Tarshish, CY ;
DeSanti, S ;
Rusinek, H ;
Tsui, W ;
Kandil, E ;
Scherer, AJ ;
Roche, A ;
Imossi, A ;
Thorn, E ;
Bobinski, M ;
Caraos, C ;
Lesbre, P ;
Schlyer, D ;
Poirier, J ;
Reisberg, B ;
Fowler, J .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (19) :10966-10971