
Genetic linkage analysis of nerve growth factor (beta) in familial Alzheimer's disease.
Recent studies have not shown linkage of late-onset (mean age, greater than 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 BglII 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 (theta 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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Related Subject Headings
- Polymorphism, Restriction Fragment Length
- Pedigree
- Neurology & Neurosurgery
- Nerve Growth Factors
- Male
- Humans
- Genetic Linkage
- Female
- Crossing Over, Genetic
- Alzheimer Disease
Citation

Published In
DOI
ISSN
Publication Date
Volume
Issue
Start / End Page
Location
Related Subject Headings
- Polymorphism, Restriction Fragment Length
- Pedigree
- Neurology & Neurosurgery
- Nerve Growth Factors
- Male
- Humans
- Genetic Linkage
- Female
- Crossing Over, Genetic
- Alzheimer Disease