Back to Search Start Over

Lack of Implication for CALHM1 P86L Common Variation in Italian Patients with Early and Late Onset Alzheimer’s Disease

Authors :
Ersilia Lucenteforte
Andrea Tedde
Silvia Bagnoli
Laura Bracco
Valentina Bessi
Biancamaria Guarnieri
Elena Cellini
Benedetta Nacmias
Sandro Sorbi
Irene Piaceri
Publication Year :
2010

Abstract

A recent study identified a polymorphism (Pro86Leu) in the Calcium homeostasis modulator 1 (CALHM1) gene whose minor Leucine allele showed a higher frequency in Alzheimer's disease (AD) patients compared to controls (29% in AD and 22% in controls). Further studies provided conflicting results in different ethnic groups. In order to assess the involvement of the CALHM1 genetic variant on the risk of developing AD, we analyzed the genotype and allele distributions of the Pro86Leu polymorphism in 758 Italian subjects. Our results did not confirm an association between the CALHM1 variation and AD, thus suggesting a genetic heterogeneity among the various populations.

Details

Language :
English
Database :
OpenAIRE
Accession number :
edsair.doi.dedup.....0531dad278188c994dc061782e427c78