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Does the CD33 rs3865444 Polymorphism Confer Susceptibility to Alzheimer’s Disease?

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Autor
Siokas V., Aslanidou P., Aloizou A.-M., Peristeri E., Stamati P., Liampas I., Arseniou S., Drakoulis N., Aschner M., Tsatsakis A., Mitsias P.D., Bogdanos D.P., Hadjigeorgiou G.M., Dardiotis E.
Datum
2020
Language
en
DOI
10.1007/s12031-020-01507-w
Schlagwort
CD33 antigen
CD33 antigen
aged
Alzheimer disease
Article
Caucasian
cohort analysis
controlled study
DNA isolation
DNA polymorphism
ethnicity
female
gene frequency
gene interaction
genetic association
genetic model
genetic susceptibility
genotype
human
inheritance
major clinical study
male
Alzheimer disease
genetics
single nucleotide polymorphism
very elderly
Aged
Aged, 80 and over
Alzheimer Disease
Female
Humans
Male
Polymorphism, Single Nucleotide
Sialic Acid Binding Ig-like Lectin 3
Humana Press Inc.
Zur Langanzeige
Zusammenfassung
Alzheimer’s disease (AD) is a complex genetic disorder. To date, published data have reported conflicting results on the role of CD33 rs3865444 polymorphism in AD. The present study aimed at evaluating the effect of rs3865444 on AD in a large cohort of Greek native patients with AD. We also conducted a meta-analysis by pooling information from different studies on the same topic. Patients with AD (n = 327) and healthy controls (n = 327) were analyzed and genotyped for rs3865444. Single locus analyses were run to explore possible associations between CD33 rs3865444 polymorphism and AD. Our analysis yielded no significant interaction between AD and the CD33 rs3865444 polymorphism. The lack of interaction between the two variables persisted even after a pooled meta-analysis of 8 studies (with 13 datasets), with 4015 AD cases and 7981 controls. The overall results do not support the hypothesis that CD33 rs3865444 polymorphism increases the risk of AD. The results also suggest that the identification of functional variants in CD33 that are indisputably correlated with AD may be an important factor to investigate in future genetic screening studies. © 2020, Springer Science+Business Media, LLC, part of Springer Nature.
URI
http://hdl.handle.net/11615/79029
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