Genetic evidence for the involvement of τ in progressive supranuclear palsy

C Conrad, A Andreadis, JQ Trojanowski… - Annals of Neurology …, 1997 - Wiley Online Library
C Conrad, A Andreadis, JQ Trojanowski, DW Dickson, D Kang, X Chen, W Wiederholt…
Annals of Neurology: Official Journal of the American Neurological …, 1997Wiley Online Library
A dinucleotide repeat polymorphism in a τ intron was identified and used in a case‐control
study to analyze the genetic association of τ with several neurodegenerative disease with τ
pathology. Subjects with the homozygous τ AO alleles were excessively represented in the
progressive supranuclear palsy (PSP) group, compared with the age‐matched healthy
control group. Consequently, this allele is more frequently found in PSP than in a group of
healthy subjects. This trend was not found in Alzheimer's disease or parkinsonism‐dementia …
Abstract
A dinucleotide repeat polymorphism in a τ intron was identified and used in a case‐control study to analyze the genetic association of τ with several neurodegenerative disease with τ pathology. Subjects with the homozygous τ AO alleles were excessively represented in the progressive supranuclear palsy (PSP) group, compared with the age‐matched healthy control group. Consequently, this allele is more frequently found in PSP than in a group of healthy subjects. This trend was not found in Alzheimer's disease or parkinsonism‐dementia complex of Guam, both of which are accompanied by major τ pathology. The result suggests τ possible involvement of τ in the pathogenesis of PSP.
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