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The absence of an apolipoprotem ε4 allele is associated with a more aggressive form of Alzheimer's disease

  • Yaakov Stern
  • , Jason Brandt
  • , Marilyn Albert
  • , Diane M. Jacobs
  • , Xinhua Liu
  • , Karen Bell
  • , Karen Marder
  • , Mary Sano
  • , Steven Albert
  • , Caridad Del-Castillo Castenada
  • , Fred Bylsma
  • , Ben Tycko
  • , Richard Mayeux

Research output: Contribution to journalArticlepeer-review

Abstract

We investigated the relationship between APOE genotype and rate of disease progression and survival in 99 patients with probable Alzheimer's disease (AD) who were followed biannually for up to 6 years. Patients were stratified into two groups, those with and without at least one APOE ε4 allele. The rate of decline in modified Mini-Mental State Examination scores was slower, the presence of extrapyramidal signs was decreased, and the development of myoclonus occurred later among patients with APOE ε4 alleles compared with patients with other genotypes. Compared with patients without an APOE ε4 allele, the risk of mortality was also decreased in patients with at least one ε4 allele (RR = 0.38; CI = 0.17-0.84, p < 0.02). Because the decline in mental ability as well as the development of myoclonus and extrapyramidal signs are consistent manifestations of disease progression, our results imply that APOE ε4 is associated with a less aggressive form of AD.

Original languageEnglish (US)
Pages (from-to)615-620
Number of pages6
JournalAnnals of neurology
Volume41
Issue number5
DOIs
StatePublished - May 1997

ASJC Scopus subject areas

  • Neurology
  • Clinical Neurology

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