Cook Lynnette J, Ho Luk W, Wang Lin, Terrenoire Edith, Brayne Carol, Evans John Grimley, Xuereb John, Cairns Nigel J, Turic Dragana, Hollingworth Paul, Moore Pamela J, Jehu Luke, Archer Nicola, Walter Sarah, Foy Catherine, Edmondson Amanda, Powell John, Lovestone Simon, Williams Julie, Rubinsztein David C
Department of Medical Genetics, Cambridge Institute for Medical Research, Addenbrooke's Hospital, Hills Road, Cambridge, CB2 2XY, UK
Am J Med Genet B Neuropsychiatr Genet. 2005 Jan 5;132B(1):5-8. doi: 10.1002/ajmg.b.30068.
Consistent deficits in the cholinergic system are evident in the brains of Alzheimer's Disease (AD) patients, including reductions in the activities of acetylcholine, acetylcholinesterase (AChE), and choline acetyltransferase (ChAT), increased butyrylcholinesterase (BChE) activity, and a selective loss of nicotinic acetylcholine receptors (nAChRs). Accordingly, we have analyzed polymorphisms in the genes encoding AChE, ChAT, BChE, and several of the subunit genes from neuronal nAChRs, for genetic associations with late-onset AD. A significant association for disease was detected for a non-coding polymorphism in ChAT (allele chi(1) (2) = 12.84, P = 0.0003; genotype chi(2) (2) = 11.89, P = 0.0026). Although replication analysis did not confirm the significance of this finding when the replication samples were considered alone (allele chi(1) (2) = 1.02, P = 0.32; genotype chi(2) (2) = 1.101, P = 0.58) the trends were in the correct direction and a significant association remained when the two sample sets were pooled (allele chi(1) (2) = 12.37, P = 0.0004; genotype chi(2) (2) = 11.61, P = 0.003). Previous studies have reported significant disease associations for both the K-variant of BChE and the coding ChAT rs3810950 polymorphism with AD. Replication analyses of these two loci failed to detect any significant association for disease in our case-control samples.
胆碱能系统持续存在的缺陷在阿尔茨海默病(AD)患者的大脑中很明显,包括乙酰胆碱、乙酰胆碱酯酶(AChE)和胆碱乙酰转移酶(ChAT)活性降低,丁酰胆碱酯酶(BChE)活性增加,以及烟碱型乙酰胆碱受体(nAChRs)选择性丧失。因此,我们分析了编码AChE、ChAT、BChE的基因以及神经元nAChRs的几个亚基基因中的多态性,以寻找与晚发型AD的遗传关联。在ChAT基因的一个非编码多态性位点检测到与疾病的显著关联(等位基因χ²(1)(2)=12.84,P = 0.0003;基因型χ²(2)(2)=11.89,P = 0.0026)。尽管单独考虑复制样本时,复制分析未证实这一发现的显著性(等位基因χ²(1)(2)=1.02,P = 0.32;基因型χ²(2)(2)=1.101,P = 0.58),但趋势是正确的,当两个样本集合并时,仍存在显著关联(等位基因χ²(1)(2)=12.37,P = 0.0004;基因型χ²(2)(2)=11.61,P = 0.003)。先前的研究报道,BChE的K变体和编码ChAT的rs3810950多态性与AD均存在显著的疾病关联。在我们的病例对照样本中,对这两个位点的复制分析未检测到与疾病的任何显著关联。