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Association between bleomycin hydrolase and Alzheimer's disease in caucasians.

Abstract
A recent study showed modest evidence for an increased frequency of the bleomycin hydrolase (BH) V/V genotype in Alzheimer's disease (AD) patients compared with non-demented controls. To test this hypothesis, we examined this polymorphism in 621 rigorously evaluated patients and 502 control subjects (all caucasian) but were unable to detect an association between BH and AD even after controlling for age, gender, and apolipoprotein E (ApoE) genotype. We conclude that this polymorphism does not account for inherited susceptibility to AD in the populations represented in this sample.
AuthorsL A Farrer, C R Abraham, J L Haines, E A Rogaeva, Y Song, W T McGraw, N Brindle, S Premkumar, W K Scott, L H Yamaoka, A M Saunders, A D Roses, S A Auerbach, S Sorbi, R Duara, M A Pericak-Vance, P H St George-Hyslop
JournalAnnals of neurology (Ann Neurol) Vol. 44 Issue 5 Pg. 808-11 (Nov 1998) ISSN: 0364-5134 [Print] United States
PMID9818937 (Publication Type: Comparative Study, Journal Article, Research Support, Non-U.S. Gov't, Research Support, U.S. Gov't, P.H.S.)
Chemical References
  • Apolipoproteins E
  • Cysteine Endopeptidases
  • bleomycin hydrolase
Topics
  • Aged
  • Alleles
  • Alzheimer Disease (genetics)
  • Apolipoproteins E (genetics)
  • Boston
  • Cysteine Endopeptidases (genetics)
  • Female
  • Gene Frequency
  • Genotype
  • Humans
  • Male
  • North Carolina
  • Polymorphism, Genetic
  • Reference Values
  • White People (genetics)

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