α -1-抗凝乳胰蛋白酶基因启动子区域多态性影响阿尔茨海默病的生存和突触丧失。

F Licastro, M Chiappelli, L J Thal, E Masliah
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引用次数: 7

摘要

对130例经神经病理学证实的阿尔茨海默病(AD)患者进行了载脂蛋白Eepsilon (APOE)多态性区域和α -1抗凝乳胰蛋白酶(ACT)基因启动子区域新多态性的基因分型。ACT TT基因型与AD患者较长的生存期相关,并且在APOE ε 4等位基因患者中,该基因型增加了疾病的持续时间。ACT TT基因型也与没有APOE ε 4等位基因的患者发病年龄较晚和死亡年龄较晚相关。后一组患者也表现出中额叶(MF)皮层突触素水平的增加。ACT似乎在AD中发挥着复杂的、多重的作用,并影响没有APOE - epsilon4等位基因的AD患者大脑中的突触可塑性。
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alpha-1-Antichymotrypsin polymorphism in the gene promoter region affects survival and synapsis loss in Alzheimer's disease.

One-hundred-thirty-tree patients with neuropathologically confirmed Alzheimer's disease (AD) were genotyped for the polymorphic regions in the apolipoprotein Eepsilon (APOE)and a new polymorphism in the promoter region of the alpha-1-antichymotrypsin (ACT) gene. The ACT TT genotype was associated with a longer survival of AD patients, and among patients with the APOE epsilon4 allele, this genotype increased the duration of the disease. The ACT TT genotype was also associated with a late age at onset of the disease and a delayed age at death in patients without the APOE epsilon4 allele. This latter group of patients also showed increased levels of synaptophysin from the mid-frontal (MF) cortex area. ACT appears to play complex, multiple roles on AD and to affect synaptic plasticity in the AD brain of patients without the allele APOE epsilon4 allele.

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