@article{ATM9591,
author = {Hui Wang and Fu-Rong Sun and Lin Tan and Hui-Fu Wang and Wei Zhang and Zi-Xuan Wang and Teng Jiang and Jin-Tai Yu and Lan Tan},
title = {Association study of the PLXNA4 gene with the risk of Alzheimer’s disease},
journal = {Annals of Translational Medicine},
volume = {4},
number = {6},
year = {2016},
keywords = {},
abstract = {Background: The Plexin-A 4 (PLXNA4) gene has recently been recognized as a functional candidate gene of late-onset Alzheimer’s disease (LOAD). The single nucleotide polymorphism (SNP) rs13232207 of PLXNA4 gene has been reported to be associated with Alzheimer’s disease (AD) in Japanese cohorts. We sought to clarify whether this novel locus gains the same effect in northern Han Chinese.
Methods: To investigate the relationship between SNP rs13232207 and AD sufferers, a case-control study of unrelated individuals was conducted with a total sample size of 2,318 subjects (978 cases and 1,340 age and gender matched healthy controls) in a Northern Han Chinese population. SPSS 22.0 was applied for the statistical process.
Results: No significant difference in polymorphic distribution of rs13232207 was observed on LOAD risk independently under dominant (P=0.057), additive (P=0.233) or recessive model (P=0.392). In terms of interaction with apolipoprotein E (APOE), there is also no positive interaction in dominant (P=0.438), additive (P=0.055) or recessive model (P=0.095).
Conclusions: Replication of association between the PLXNA4 rs13232207 and AD in a Han ethnic group indicates that this link is not the result of chance.},
issn = {2305-5847}, url = {https://atm.amegroups.org/article/view/9591}
}