Simao-Silva_2013_Chem.Biol.Interact_203_358

Reference

Title : Association analysis between K and -116A variants of butyrylcholinesterase and Alzheimer's disease in a Brazilian population - Simao-Silva_2013_Chem.Biol.Interact_203_358
Author(s) : Simao-Silva DP , Bertolucci PH , de Labio RW , Payao SL , Furtado-Alle L , de Souza RLR
Ref : Chemico-Biological Interactions , 203 :358 , 2013
Abstract :

In Alzheimer's disease (AD) a reduction in acetylcholinesterase (AChE) and an increase in butyrylcholinesterase (BChE) activity are observed. K variant (539T) is the most common variant of the BCHE gene and, although controversial, several studies reported association between K variant and AD. Previous results showed that the K variant alone is not capable of diminishing BChE activity, depending on the presence of the -116A variant. Considering that, we conducted a case-control association study using a clinically well defined group of AD patients (n=82) and age and sex matched control subjects (EC; n=78) in order to test the association with these variations of BCHE gene in a Brazilian population. The allele, genotype and haplotype frequencies of the K and the -116A variants of BCHE gene were not significantly different between cases and controls. Although not reaching statistical significance, the results suggested that the presence of -116A variant may have a protective effect against AD. The association of the K variant with AD in a controversial manner in different surveys is probably caused by its linkage disequilibrium with -116A that, by reducing BChE activity, potentially increases cholinergic transmission in comparison with usual genotypes.

PubMedSearch : Simao-Silva_2013_Chem.Biol.Interact_203_358
PubMedID: 23022600

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Citations formats

Simao-Silva DP, Bertolucci PH, de Labio RW, Payao SL, Furtado-Alle L, de Souza RLR (2013)
Association analysis between K and -116A variants of butyrylcholinesterase and Alzheimer's disease in a Brazilian population
Chemico-Biological Interactions 203 :358

Simao-Silva DP, Bertolucci PH, de Labio RW, Payao SL, Furtado-Alle L, de Souza RLR (2013)
Chemico-Biological Interactions 203 :358