Genetic deficiency of plasma lipoprotein-associated phospholipase A2 (PLA2G7 V297F null mutation) and risk of Alzheimer's disease in Japan.
Détails
ID Serval
serval:BIB_45100BE4016B
Type
Article: article d'un périodique ou d'un magazine.
Collection
Publications
Institution
Titre
Genetic deficiency of plasma lipoprotein-associated phospholipase A2 (PLA2G7 V297F null mutation) and risk of Alzheimer's disease in Japan.
Périodique
Journal of Alzheimer's Disease
ISSN
1875-8908 (Electronic)
ISSN-L
1387-2877
Statut éditorial
Publié
Date de publication
2010
Peer-reviewed
Oui
Volume
21
Numéro
3
Pages
775-780
Langue
anglais
Notes
Publication types: Journal Article ; Research Support, Non-U.S. Gov't
Résumé
High plasma lipoprotein phospholipase A2 activity (Lp-PLA2) is reported to be a risk factor for dementia. A loss of function polymorphism in the Lp-PLA2 gene - PLA2G7 V279F - is found almost exclusively in Asians. In 1,952 subjects with late-onset AD and 2,079 non-demented controls recruited from Japan, the PLA2G7 null allele was not associated with risk or age at onset of AD: logistic regression OR 0.98 (95% CI 0.86-1.12, p=0.81) per additional null allele, adjusted for age/age at onset, gender, and APOE ε4. Genetic deficiency of Lp-PLA2 activity is not associated with a reduced risk of AD in the Japanese population.
Mots-clé
Alleles, Alzheimer Disease/genetics, Apolipoproteins E/genetics, Asian Continental Ancestry Group/genetics, Gene Frequency, Genetic Predisposition to Disease, Humans, Japan, Mutation, Phospholipases A2/genetics, Polymorphism, Genetic, Risk
Pubmed
Web of science
Création de la notice
21/01/2013 11:56
Dernière modification de la notice
20/08/2019 14:49
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