Progression of regional neuropathology in Alzheimer disease and normal elderly: Findings from the Nun Study

被引:96
作者
Wolf, DS
Gearing, M
Snowdon, DA
Mori, H
Markesbery, WR
Mirra, SS
机构
[1] SUNY Hlth Sci Ctr, Dept Pathol, Brooklyn, NY 11203 USA
[2] Vet Adm Med Ctr, Dept Pathol & Lab Med, Atlanta, GA 30033 USA
[3] Emory Univ, Sch Med, Atlanta, GA USA
[4] Univ Kentucky, Dept Prevent Med, Lexington, KY USA
[5] Univ Kentucky, Dept Pathol & Neurol, Lexington, KY USA
[6] Tokyo Inst Psychiat, Tokyo, Japan
关键词
amyloid; cerebellum; diffuse plaque; striatum;
D O I
10.1097/00002093-199910000-00009
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Although diffuse plaques in the neocortex may represent an early stage in the evolution of neuritic plaques, plaques in the striatum and cerebellum retain their predominantly diffuse nature in Alzheimer disease (AD), regardless of disease duration. We had the opportunity to explore the progression of these regional features by using autopsy brain specimens from 15 cognitively normal and five AD subjects, all Catholic sisters enrolled in the Nun Study, a longitudinal study on aging and AD. Neuropathologic changes were assessed in the temporal cortex, striatum, and cerebellum without knowledge of clinical status. We found diffuse plaques in the striatum in six (40%) and cerebellar plaques in none of the brains from the non-demented subjects. Striatal plaques were present in all five and cerebellar plaques in four of the five AD cases. In the 20 cases overall, the presence of striatal plaques generally paralleled the occurrence of neuritic plaques in neocortex and correlated with lower scores on several neuropsychologic tests assessing memory. Our findings suggest that striatal diffuse plaques occur relatively early in the progression of AD pathology and coincide with neocortical pathology and cognitive changes. Thus, it is unlikely that temporal factors alone account for regional differences in progression of AD neuropathology.
引用
收藏
页码:226 / 231
页数:6
相关论文
共 26 条
[1]   NEUROPATHOLOGICAL STAGING OF ALZHEIMER-RELATED CHANGES [J].
BRAAK, H ;
BRAAK, E .
ACTA NEUROPATHOLOGICA, 1991, 82 (04) :239-259
[2]  
FUKOMOTO H, 1996, AM J PATHOL, V148, P259
[3]   A beta-peptide length and apolipoprotein E genotype in Alzheimer's disease [J].
Gearing, M ;
Mori, H ;
Mirra, SS .
ANNALS OF NEUROLOGY, 1996, 39 (03) :395-399
[4]   AMYLOID PRECURSOR PROTEIN (APP) IN THE STRIATUM IN ALZHEIMERS-DISEASE - AN IMMUNOHISTOCHEMICAL STUDY [J].
GEARING, M ;
WILSON, RW ;
UNGER, ER ;
SHELTON, ER ;
CHAN, HW ;
MASTERS, CL ;
BEYREUTHER, K ;
MIRRA, SS .
JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY, 1993, 52 (01) :22-30
[5]   ALZHEIMERS-DISEASE WITH AND WITHOUT COEXISTING PARKINSONS-DISEASE CHANGES - APOLIPOPROTEIN-E GENOTYPE AND NEUROPATHOLOGIC CORRELATES [J].
GEARING, M ;
SCHNEIDER, JA ;
REBECK, GW ;
HYMAN, BT ;
MIRRA, SS .
NEUROLOGY, 1995, 45 (11) :1985-1990
[6]   REGIONAL VARIATION IN THE DISTRIBUTION OF APOLIPOPROTEIN-E AND A-BETA IN ALZHEIMERS-DISEASE [J].
GEARING, M ;
SCHNEIDER, JA ;
ROBINS, RS ;
HOLLISTER, RD ;
MORI, H ;
GAMES, D ;
HYMAN, BT ;
MIRRA, SS .
JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY, 1995, 54 (06) :833-841
[7]   A beta(40) is a major form of beta-amyloid in nonhuman primates [J].
Gearing, M ;
Tigges, J ;
Mori, H ;
Mirra, SS .
NEUROBIOLOGY OF AGING, 1996, 17 (06) :903-908
[8]  
HIXSON JE, 1990, J LIPID RES, V31, P545
[9]   VISUALIZATION OF A-BETA-42(43) AND A-BETA-40 IN SENILE PLAQUES WITH END-SPECIFIC A-BETA MONOCLONALS - EVIDENCE THAT AN INITIALLY DEPOSITED SPECIES IS A-BETA-42(43) [J].
IWATSUBO, T ;
ODAKA, A ;
SUZUKI, N ;
MIZUSAWA, H ;
NUKINA, N ;
IHARA, Y .
NEURON, 1994, 13 (01) :45-53
[10]   AMYLOID-BETA PROTEIN (A-BETA) DEPOSITION - A-BETA-42(43) PRECEDES A-BETA-40 IN DOWN-SYNDROME [J].
IWATSUBO, T ;
MANN, DMA ;
ODAKA, A ;
SUZUKI, N ;
IHARA, Y .
ANNALS OF NEUROLOGY, 1995, 37 (03) :294-299