Effect of CLU and PICALM polymorphisms on AD risk: A study from south India

Asian J Psychiatr. 2017 Jun:27:7-11. doi: 10.1016/j.ajp.2016.12.017. Epub 2016 Dec 29.

Abstract

Objectives: To study the association of apolipoprotein E (APOE), Clusterin (CLU) and phosphatidylinositol binding clathrin assembly protein (PICALM) polymorphisms in Alzheimer's disease (AD) subjects compared to cognitively normal control subjects in an Indian population.

Methods: The study subjects included persons with AD (N=243) and age group matched healthy controls (N=164). All the AD subjects were evaluated using a standard protocol. DNA was isolated from whole blood. APOE (rs7412, rs429358), CLU (rs11136000) and PICALM (rs3851179) were genotyped. General linear model was used to test the association between the individual risk genotypes and AD.

Results: The presence of APOE ε4 was associated with AD after adjusting for age and gender (p<0.0001). There was no association observed with AD at both rs11136000 CLU (p=0.25) and rs3851179 PICALM (p=0.54).

Conclusion: Our results confirmed a significant association of APOE ε4 carrier status with AD. No association was observed for CLU and PICALM with AD. This might be due to a different genetic background. There are no previous reports of these polymorphisms in an Indian cohort. Future Indian AD studies should investigate additional SNPs in a larger sample size in these genes.

MeSH terms

  • Aged
  • Alzheimer Disease / genetics*
  • Apolipoprotein E4 / genetics
  • Clusterin / genetics*
  • Female
  • Humans
  • India
  • Male
  • Middle Aged
  • Monomeric Clathrin Assembly Proteins / genetics*
  • Polymorphism, Single Nucleotide
  • Risk

Substances

  • Apolipoprotein E4
  • CLU protein, human
  • Clusterin
  • Monomeric Clathrin Assembly Proteins
  • PICALM protein, human