THE APOLIPOPROTEIN-E-EPSILON-4 ALLELE DOES NOT INFLUENCE THE CLINICAL EXPRESSION OF THE AMYLOID PRECURSOR PROTEIN GENE CODON-693 OR CODON-692 MUTATIONS

被引:46
作者
HAAN, J
VAN BROECKHOVEN, C
VANDUIJN, CM
VOORHOEVE, E
VANHARSKAMP, F
VANSWIETEN, JC
MAATSCHIEMAN, MLC
ROOS, RAC
BAKKER, E
机构
[1] RIJNLAND HOSP, DEPT NEUROL, LEIDERDORP, NETHERLANDS
[2] UNIV ANTWERP, BORN BUNGE INST, NEUROGENET LAB, B-2020 ANTWERP, BELGIUM
[3] ERASMUS UNIV ROTTERDAM, DEPT EPIDEMIOL & BIOSTAT, 3000 DR ROTTERDAM, NETHERLANDS
[4] SYLVIUS LAB, DEPT HUMAN GENET, LEIDEN, NETHERLANDS
[5] UNIV HOSP DIJKZIGT, DEPT NEUROL, 3015 GD ROTTERDAM, NETHERLANDS
关键词
D O I
10.1002/ana.410360315
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
In 31 symptomatic and 5 asymptomatic carriers of the amyloid precursor protein (APP) gene codon 693 mutation, 10 family members without mutation, and 5 carriers of the APP gene codon 692 mutation (3 with early-onset Alzheimer dementia, 2 with cerebral hemorrhage), a high frequency of the apolipoprotein E epsilon 4 allele was found. Age at onset, age at death, occurrence of dementia, and number of strokes did not differ between APP gene mutation carriers with or without epsilon 4 allele, showing that the clinical expression of these APP mutations is not influenced by the apolipoprotein E gene.
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页码:434 / 437
页数:4
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