Youthful Memory Capacity in Old Brains: Anatomic and Genetic Clues from the Northwestern SuperAging Project

被引:131
作者
Rogalski, Emily J. [1 ]
Gefen, Tamar [1 ]
Shi, Junzi [1 ]
Samimi, Mehrnoosh [1 ]
Bigio, Eileen [1 ]
Weintraub, Sandra [1 ]
Geula, Changiz [1 ]
Mesulam, M. -Marsel [1 ]
机构
[1] Northwestern Univ, Cognit Neurol & Alzheimers Dis Ctr, Feinberg Sch Med, Chicago, IL 60611 USA
关键词
ALZHEIMERS-DISEASE; APOLIPOPROTEIN-E; CEREBRAL-CORTEX; ALLELE; TANGLES; RISK;
D O I
10.1162/jocn_a_00300
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The Northwestern University SuperAging Project recruits community dwellers over the age of 80 who have unusually high performance on tests of episodic memory. In a previous report, a small cohort of SuperAgers was found to have higher cortical thickness on structural MRI than a group of age-matched but cognitively average peers. SuperAgers also displayed a patch of ACC where cortical thickness was higher than in 50- to 60-year-old younger cognitively healthy adults. In additional analyses, some SuperAgers had unusually low densities of age-related Alzheimer pathology and unusually high numbers of von Economo neurons in the anterior cingulate gyrus. SuperAgers were also found to have a lower frequency of the epsilon 4 allele of apolipoprotein E than the general population. These preliminary results show that above-average memory capacity can be encountered in advanced age. They also offer clues to potential biological factors that may promote resistance to age-related involutional changes in the structure and function of the brain.
引用
收藏
页码:29 / 36
页数:8
相关论文
共 34 条
[21]   THE CONSORTIUM TO ESTABLISH A REGISTRY FOR ALZHEIMERS-DISEASE (CERAD) .1. CLINICAL AND NEUROPSYCHOLOGICAL ASSESSMENT OF ALZHEIMERS-DISEASE [J].
MORRIS, JC ;
HEYMAN, A ;
MOHS, RC ;
HUGHES, JP ;
VANBELLE, G ;
FILLENBAUM, G ;
MELLITS, ED ;
CLARK, C .
NEUROLOGY, 1989, 39 (09) :1159-1165
[22]   DIFFERENTIAL-EFFECTS OF APOLIPOPROTEINS E3 AND E4 ON NEURONAL GROWTH IN-VITRO [J].
NATHAN, BP ;
BELLOSTA, S ;
SANAN, DA ;
WEISGRABER, KH ;
MAHLEY, RW ;
PITAS, RE .
SCIENCE, 1994, 264 (5160) :850-852
[23]   AGED HETEROGENEITY - FACT OR FICTION - THE FATE OF DIVERSITY IN GERONTOLOGICAL RESEARCH [J].
NELSON, EA ;
DANNEFER, D .
GERONTOLOGIST, 1992, 32 (01) :17-23
[24]   A neuronal morphologic type unique to humans and great apes [J].
Nimchinsky, EA ;
Gilissen, E ;
Allman, JM ;
Perl, DP ;
Erwin, JM ;
Hof, PR .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (09) :5268-5273
[25]   APOLIPOPROTEIN-E POLYMORPHISM AND ALZHEIMERS-DISEASE [J].
POIRIER, J ;
DAVIGNON, J ;
BOUTHILLIER, D ;
KOGAN, S ;
BERTRAND, P ;
GAUTHIER, S .
LANCET, 1993, 342 (8873) :697-699
[26]  
Price JL, 1999, ANN NEUROL, V45, P358, DOI 10.1002/1531-8249(199903)45:3<358::AID-ANA12>3.0.CO
[27]  
2-X
[28]   Preclinical evidence of Alzheimer's disease in persons homozygous for the epsilon 4 allele for apolipoprotein E [J].
Reiman, EM ;
Caselli, RJ ;
Yun, LS ;
Chen, KW ;
Bandy, D ;
Minoshima, S ;
Thibodeau, SN ;
Osborne, D .
NEW ENGLAND JOURNAL OF MEDICINE, 1996, 334 (12) :752-758
[29]  
Roses AD, 1997, ALZHEIMER'S DISEASE: BIOLOGY, DIAGNOSIS AND THERAPEUTICS, P85
[30]   Normative data on the Boston Naming Test and two equivalent 30-item short forms [J].
Saxton, J ;
Ratcliff, G ;
Munro, CA ;
Coffey, CE ;
Becker, JT ;
Fried, L ;
Kuller, L .
CLINICAL NEUROPSYCHOLOGIST, 2000, 14 (04) :526-534