An association study of the cholesteryl ester transfer protein TaqI B polymorphism with late onset Alzheimer's disease

Liana Fidani, Antonis Goulas, Richard Crook, Ronald C. Petersen, Eric Tangalos, Alexandros Kotsis, John Hardy

Research output: Contribution to journalArticlepeer-review

22 Scopus citations


Cholesteryl ester transfer protein (CETP) is reportedly able to affect the amount of cholesterol available for deposition and/or removal from peripheral tissues, in its capacity to mediate the transfer of cholesterol from high density lipoprotein (HDL) to very low density lipoprotein, in exchange for triacylglycerols from the latter. The TaqI B polymorphism of the human CETP gene has been associated with decreased CETP mass and an increase in HDL-cholesterol. While many studies have addressed the atherogenic or anti-atherogenic potential of this polymorphism, little is known about its effect on neurodegeneration, despite the fact that CETP is expressed in the brain and the disturbance of cholesterol homeostasis appears to be an important factor in the pathogenesis of Alzheimer's disease (AD). In this report, we have compared the distribution of the TaqI B polymorphism in an independent population of 102 clinically diagnosed late onset AD patients and a spousal control group of 97 individuals. We have also examined the possible interaction between this polymorphism and two other polymorphisms suspected of affecting cholesterol flux, namely apolipoprotein E APOE ε4, and lipoprotein lipase LPLS447X. No statistically significant differences have emerged with respect to either genotype or allele frequencies between the AD and control populations. CETP TaqI B did not interact significantly with either APOE ε4 or LPLS447X, in this study.

Original languageEnglish (US)
Pages (from-to)152-154
Number of pages3
JournalNeuroscience Letters
Issue number2
StatePublished - Mar 4 2004


  • Alzheimer's disease
  • Apolipoprotein E
  • Cholesteryl ester transfer protein
  • Genetics
  • Lipoprotein lipase
  • Polymorphism

ASJC Scopus subject areas

  • Neuroscience(all)


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