The biphasic relationship between regional brain senile plaque and neurofibrillary tangle distributions:: Modification by age, sex, and APOE polymorphism

被引:175
作者
Corder, EH
Ghebremedhin, E
Taylor, MG
Thal, DR
Ohm, TG
Braak, H
机构
[1] Duke Univ, Ctr Demog Studies, Durham, NC 27708 USA
[2] JW Goethe Univ, Dept Clin Neuroanat, D-60590 Frankfurt, Germany
[3] Duke Univ, Dept Sociol, Durham, NC 27708 USA
[4] Univ Bonn, Ctr Med, Inst Neuropathol, D-53105 Bonn, Germany
[5] Humboldt Univ, Med Fac, Charite, Dept Anat, D-10098 Berlin, Germany
来源
STRATEGIES FOR ENGINEERED NEGLIGIBLE SENESCENCE: WHY GENUINE CONTROL OF AGING MAY BE FORESEEABLE | 2004年 / 1019卷
关键词
Alzheimer disease; gender; apolipoprotein E; aging; senile plaques; neurofibrillary tangles; neuropathology; brain;
D O I
10.1196/annals.1297.005
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
Epidemiologic studies indicate that elderly women are at higher risk for Alzheimer disease compared to men. In order to pathologically verify this result, the extent of AD brain lesions (NFY and SP) was compared for men and women at each age, that is, at each decade from 25 years to 95 years, in a large sample of >5000 routine autopsy cases. Women had more affected brain regions beginning in late middle age. They also had more extensive SP depositions throughout the brain compared to men at each early NFT stage I, II, and III. At later NFT stages IV, V, and VI both men and women had extensive SP deposits. The gender gap in SI's at early NFT stages was large and specific to women who carried the APOE4 allele (P < .001) and in addition to the acceleration in NFT stage also found for APOE4+ women.
引用
收藏
页码:24 / 28
页数:5
相关论文
共 10 条
[1]  
Braak E, 1999, EUR ARCH PSY CLIN N, V249, P14
[2]   Frequency of stages of Alzheimer-related lesions in different age categories [J].
Braak, H ;
Braak, E .
NEUROBIOLOGY OF AGING, 1997, 18 (04) :351-357
[3]   NEUROPATHOLOGICAL STAGING OF ALZHEIMER-RELATED CHANGES [J].
BRAAK, H ;
BRAAK, E .
ACTA NEUROPATHOLOGICA, 1991, 82 (04) :239-259
[4]   GENE DOSE OF APOLIPOPROTEIN-E TYPE-4 ALLELE AND THE RISK OF ALZHEIMERS-DISEASE IN LATE-ONSET FAMILIES [J].
CORDER, EH ;
SAUNDERS, AM ;
STRITTMATTER, WJ ;
SCHMECHEL, DE ;
GASKELL, PC ;
SMALL, GW ;
ROSES, AD ;
HAINES, JL ;
PERICAKVANCE, MA .
SCIENCE, 1993, 261 (5123) :921-923
[5]  
CORDER EH, 2004, UNPUB GENDER DIFFERE
[6]   Improved method facilitates reliable APOE genotyping of genomic DNA extracted from formaldehyde-fixed pathology specimens [J].
Ghebremedhin, E ;
Braak, H ;
Braak, E ;
Sahm, J .
JOURNAL OF NEUROSCIENCE METHODS, 1998, 79 (02) :229-231
[7]   Gender and age modify the association between APOE and AD-related neuropathology [J].
Ghebremedhin, E ;
Schultz, C ;
Thal, DR ;
Rüb, U ;
Ohm, TG ;
Braak, E ;
Braak, H .
NEUROLOGY, 2001, 56 (12) :1696-1701
[8]   Apolipoprotein E isoforms and the development of low and high Braak stages of Alzheimer's disease-related lesions [J].
Ohm, TG ;
Scharnagl, H ;
März, W ;
Bohl, J .
ACTA NEUROPATHOLOGICA, 1999, 98 (03) :273-280
[9]   Apolipoprotein E4 promotes the early deposition of Aβ42 and then Aβ40 in the elderly [J].
Walker, LC ;
Pahnke, J ;
Madauss, M ;
Vogelgesang, S ;
Pahnke, A ;
Herbst, EW ;
Stausske, D ;
Walther, R ;
Kessler, C ;
Warzok, RW .
ACTA NEUROPATHOLOGICA, 2000, 100 (01) :36-42
[10]   Estrogen reduces neuronal generation of Alzheimer β-amyloid peptides [J].
Xu, HX ;
Gouras, GK ;
Greenfield, JP ;
Vincent, B ;
Naslund, J ;
Mazzarelli, L ;
Fried, G ;
Jovanovic, JN ;
Seeger, M ;
Relkin, NR ;
Liao, F ;
Checler, F ;
Buxbaum, JD ;
Chait, BT ;
Thinakaran, G ;
Sisodia, SS ;
Wang, R ;
Greengard, P ;
Gandy, S .
NATURE MEDICINE, 1998, 4 (04) :447-451