Literature DB >> 18423577

Polymorphisms at the beta2-adrenergic receptor gene influence Alzheimer's disease susceptibility.

Jin-Tai Yu1, Lan Tan, Jiang-Rong Ou, Jun-Xia Zhu, Kun Liu, Jing-Hui Song, Yan-Ping Sun.   

Abstract

Increasing evidence indicates that the beta2-adrenergic receptor (beta2-AR) may play an important role in Alzheimer's disease (AD). We investigated the effect of two polymorphisms in the beta2-AR gene: Gly16Arg and Gln27Glu for the risk of sporadic Late Onset Alzheimer's Disease (LOAD) in 109 patients and 109 healthy controls matched for sex and age in a Han Chinese population. Results revealed that both the 16Gly allele and the 27Glu allele of the beta2-AR gene were associated with an increased risk of LOAD (P=0.009, OR=1.652 and P=0.002, OR=2.846, respectively), and they also showed a highly significant interaction with the Apolipoprotein E gene (APOE) epsilon4 allele (OR=4.200 and 9.441, respectively). Examination of the haplotypes identified the Gly16Glu27 haplotype to increase the risk of LOAD (P=0.004). Our results suggest that variations in the beta2-AR gene play an important role in the pathogenesis of sporadic LOAD, and interact with the epsilon4 allele to markedly increase the LOAD risk.

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Year:  2008        PMID: 18423577     DOI: 10.1016/j.brainres.2008.03.019

Source DB:  PubMed          Journal:  Brain Res        ISSN: 0006-8993            Impact factor:   3.252


  28 in total

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Review 8.  β-Arrestins as potential therapeutic targets for Alzheimer's disease.

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10.  SAMP8 mice have altered hippocampal gene expression in long term potentiation, phosphatidylinositol signaling, and endocytosis pathways.

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Journal:  Neurobiol Aging       Date:  2013-08-19       Impact factor: 4.673

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