GENETIC-LINKAGE ANALYSIS OF NERVE GROWTH-FACTOR (BETA) IN FAMILIAL ALZHEIMERS-DISEASE

被引:4
作者
ALBERTS, MJ
PERICAKVANCE, MA
ROYAL, V
BEBOUT, J
GASKELL, P
THOMAS, J
HUNG, WY
CLARK, C
EARL, N
ROSES, AD
机构
[1] DUKE UNIV,MED CTR,DEPT MED NEUROL,DURHAM,NC 27710
[2] DUKE UNIV,MED CTR,DEPT NEUROBIOL,DURHAM,NC 27710
关键词
D O I
10.1002/ana.410300217
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Recent studies have not shown linkage of late-onset (mean age, > 60 years) familial Alzheimer's disease (FAD) to the chromosome 21 locus reported linked to early-onset FAD. Beta nerve growth factor (beta-NGF) has been considered a candidate gene in the pathogenesis and therapy of FAD, based on its localization in the cortex and hippocampus and its ability to enhance the growth and survival of cholinergic neurons. A 1.5-kb fragment of the beta-NGF gene was used to detect a Bgl II restriction fragment length polymorphism, which was then used for linkage analysis. A total of 30 families (27 late onset) with 147 affected members were studied. Close linkage (0 less-than-or-equal-to 0.03, z less-than-or-equal-to -2.00) of late-onset FAD with beta-NGF was excluded. Two apparent obligate crossovers between affected members were detected in different autopsy-confirmed families. Based on these results, beta-NGF is not the gene responsible for late-onset FAD in the families analyzed.
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页码:216 / 219
页数:4
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