POSITRON EMISSION TOMOGRAPHY IN FAMILIAL ALZHEIMER-DISEASE

被引:28
作者
KENNEDY, AM
ROSSOR, MN
FRACKOWIAK, RSJ
机构
[1] HAMMERSMITH HOSP,MRC,CYCLOTRON UNIT,LONDON W12 0HS,ENGLAND
[2] NATL HOSP NEUROL & NEUROSURG,LONDON WC1N 3BG,ENGLAND
关键词
POSITRON EMISSION TOMOGRAPHY; FAMILIAL ALZHEIMER DISEASE; AMYLOID PRECURSOR PROTEIN; CHROMOSOME; 14; LINKAGE;
D O I
10.1097/00002093-199505000-00005
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
There is increasing evidence for genetic heterogeneity in Alzheimer disease. A longitudinal clinical and imaging study had been established in order to determine whether specific phenotypic profiles are present in aetiologically distinct familial Alzheimer disease (FAD) pedigrees. [F-18]fluorodeoxyglucose positron emission tomography has been used in conjunction with statistical parametric mapping to determine the relative distribution of hypometabolism. A parietotemporal deficit has been observed in individuals from both amyloid precursor protein mutation and chromosome 14 linked FAD families. Preliminary data from asymptomatic individuals at risk of FAD shows similar, although a less extensive pattern of deficit.
引用
收藏
页码:17 / 20
页数:4
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