Abstract:
:In an effort to analyze the genetic role of tau in Alzheimer's disease (AD), 17 polymorphisms were identified. Eleven of these polymorphisms were in complete linkage disequilibrium and segregated as two haplotypes, A and B. The A and B haplotypes were investigated in 269 AD cases and 238 controls from two different sources, a clinic-based group (mean age of onset 65+/-9 years), and a population-based group (mean age of onset 80+/-5 years). A synergistic effect between the common tau genotype AA and apolipoprotein E (APOE epsilon4) was found in the clinic-based AD group. Our study suggests that the common tau genotype AA may interact with APOE epsilon4 in increasing the risk of AD in a subgroup of the AD population.
journal_name
Neurosci Lettjournal_title
Neuroscience lettersauthors
Lilius L,Froelich Fabre S,Basun H,Forsell C,Axelman K,Mattila K,Andreadis A,Viitanen M,Winblad B,Fratiglioni L,Lannfelt Ldoi
10.1016/s0304-3940(99)00833-2keywords:
subject
Has Abstractpub_date
1999-12-17 00:00:00pages
29-32issue
1eissn
0304-3940issn
1872-7972pii
S0304-3940(99)00833-2journal_volume
277pub_type
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