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载脂蛋白和补体因子能否成为阿尔茨海默病的生物标志物?

Can apolipoproteins and complement factors be biomarkers of Alzheimer's disease?

机构信息

Department of Biophysics, All India Institute of Medical Sciences, New Delhi, India.

出版信息

Curr Alzheimer Res. 2012 Oct;9(8):935-43. doi: 10.2174/156720512803251110.

Abstract

Alzheimer's disease is the most common cause of dementia in elderly persons. Quick diagnosis of Alzheimer's disease will allow treatments that may help slow its progression. The correlation between cerebrospinal fluid (CSF) parameters and progression of Alzheimer's disease is higher than and independent of other risk factors. We have compared sixteen CSF samples of clinically diagnosed Alzheimer's disease patients with non demented subjects using proteomics approach. Apolipoprotein E, apolipoprotein J, complement C4b, hemopexin and complement factor B were identified as differentially expressed proteins. Pathway analyses show that these proteins have interacting partners in Alzheimer's and apoptotic pathways. The possible roles of these proteins in relation to the disease are discussed.

摘要

阿尔茨海默病是老年人中最常见的痴呆症病因。快速诊断阿尔茨海默病将有助于治疗,可能减缓其进展。脑脊液(CSF)参数与阿尔茨海默病进展的相关性高于其他风险因素且独立于其他风险因素。我们使用蛋白质组学方法比较了十六例临床诊断为阿尔茨海默病患者的脑脊液样本与非痴呆患者的脑脊液样本。鉴定到载脂蛋白 E、载脂蛋白 J、补体 C4b、血红素结合蛋白和补体因子 B 为差异表达蛋白。途径分析显示这些蛋白在阿尔茨海默病和凋亡途径中有相互作用的伙伴。讨论了这些蛋白与疾病的可能关系。

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