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补体成分C1r中的一种多态性与散发性阿尔茨海默病无关。

A polymorphism in the complement component C1r is not associated with sporadic Alzheimer's disease.

作者信息

Rosenmann Hanna, Meiner Zeev, Kahana Esther, Aladjem Zoja, Friedman Gideon, Ben-Yehuda Arie, Grenader Tal, Wertman Eli, Abramsky Oded

机构信息

The Agnes Ginges Center for Human Neurogenetics, Department of Neurology, Hadassah University Hospital, Ein Karem, Jerusalem 91120, Israel.

出版信息

Neurosci Lett. 2003 Jan 16;336(2):101-4. doi: 10.1016/s0304-3940(02)01218-1.

Abstract

A growing body of evidence suggests that Alzheimer's disease (AD) is associated with local inflammation processes. Complement activation is one of the cardinal pathological features of the inflammation. Intensive AD association studies investigating polymorphisms in inflammatory-related genes have been recently performed, mainly in cytokines, but much less has been focused on AD association with polymorphisms in complement components. We performed a case-control association study between the codon 135 polymorphism in the complement component C1r gene and sporadic AD. No association was detected with AD: neither as a risk factor, and nor as a modifier gene affecting the age at disease onset and disease progression. No interactive effect was found with apolipoprotein E e4. These findings show no evidence for association between C1r codon 135 polymorphism and AD in our population.

摘要

越来越多的证据表明,阿尔茨海默病(AD)与局部炎症过程有关。补体激活是炎症的主要病理特征之一。最近开展了大量针对炎症相关基因多态性的AD关联研究,主要集中在细胞因子方面,但较少关注AD与补体成分多态性的关联。我们进行了一项病例对照关联研究,以探讨补体成分C1r基因密码子135多态性与散发性AD之间的关系。未检测到该基因多态性与AD存在关联:既不是危险因素,也不是影响发病年龄和疾病进展的修饰基因。未发现与载脂蛋白E e4存在交互作用。这些结果表明,在我们的人群中,C1r密码子135多态性与AD之间无关联证据。

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