Transmission and age-at-onset patterns in familial alzheimer’s disease: Evidence for heterogeneity

Academic Article


  • We evaluated age at onset and lifetime risk for Alzheimer's disease (AD) in 70 kindreds with familial AD (designated FAD) composed of 541 affected and 1,066 unaffected offspring of demented parents who were identified retrospectively. Using a survival analysis method which takes into account affected persons with unknown onset ages and unaffected persons with unknown censoring ages, we found lifetime risk of AD among at-risk offspring by age 87 to be 64%. Analysis of age at onset among kindreds showed evidence for a bimodal distribution: in this sample, families with a mean onset age of less than 58 years were designated as having early-onset, while late-onset families had a mean onset age greater than 58 years. At-risk offspring in early-onset families had an estimated lifetime risk for dementia of 53%, which is significantly less than the risk of 86% that was estimated for offspring in late-onset families. Men and women in early-onset families had equivalent risk of dementia. In late-onset families, the risk to female offspring was somewhat higher than to male offspring but this difference was marginally significant. Lifetime risk of dementia in early-onset FAD kindreds is consistent with an autosomal dominant inheritance model. Our results may suggest that late-onset FAD has at least 2 etiologies; AD in some families may be transmitted as a dominant trait, whereas a proportion of cases in these and other late-onset families may be caused by other genetic or shared environmental factors. © 1990 American Academy of Neurology.
  • Published In

  • Neurology  Journal
  • Digital Object Identifier (doi)

    Author List

  • Farrer LA; Myers RH; Cupples LA; St. George-Hyslop PH; Bird TD; Rossor MN; Mullan MJ; Polinsky R; Nee L; Heston L
  • Start Page

  • 395
  • End Page

  • 403
  • Volume

  • 40
  • Issue

  • 3