Genetic variations in the CLU and PICALM genes are associated with cognitive function in the oldest old

Neurobiol Aging. 2011 Mar;32(3):554.e7-11. doi: 10.1016/j.neurobiolaging.2010.07.016. Epub 2010 Aug 23.

Abstract

Recently, two large, and independent genome wide association studies of late-onset Alzheimer's disease (AD) established association with the same rs11136000 variation in the clusterin (CLU) gene. In addition, one variation, rs3851179, in the phosphatidylinositol binding clathrin assembly protein (PICALM) gene and one variation, rs6656401, in the complement component (3b/4b) receptor 1 (CR) gene were associated with AD. Here, we replicate these associations with cognitive functioning in 1380 individuals from the Danish (1905) birth cohort study of the oldest old (92-93 years at intake) using measures of Mini Mental State Examination (MMSE) and a cognitive composite score. We found a significant association between the highly frequent CLU rs11136000 T allele (38%) and better performance on the cognitive composite score (p = 0.016) explaining 0.5% of the mean variation in cognitive composite score, and for men a significant association between the highly frequent PICALM rs3851179 A allele (38%). Better performance was found (p = 0.024), explaining 1.4% of the mean variation in cognitive composite score in men. These alleles correspond to the minor alleles initially found more frequent in controls than in cases of AD.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amyotrophic Lateral Sclerosis / genetics*
  • Cohort Studies
  • DNA Mutational Analysis / methods
  • DNA-Binding Proteins / genetics*
  • Female
  • Humans
  • Male
  • Mutation / genetics*
  • Polymorphism, Single Nucleotide / genetics*
  • RNA-Binding Protein FUS / genetics*
  • Superoxide Dismutase / genetics*
  • Superoxide Dismutase-1
  • Taiwan / epidemiology
  • Taiwan / ethnology

Substances

  • DNA-Binding Proteins
  • RNA-Binding Protein FUS
  • SOD1 protein, human
  • Superoxide Dismutase
  • Superoxide Dismutase-1