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阿尔茨海默病脑脊液生物标志物的蛋白质组学研究进展。

Proteomic studies of cerebrospinal fluid biomarkers of Alzheimer's disease: an update.

机构信息

a Institute of Neuroscience and Physiology, Department of Psychiatry and Neurochemistry , The Sahlgrenska Academy at the University of Gothenburg , Mölndal , Sweden.

b Clinical Neurochemistry Laboratory , Sahlgrenska University Hospital , Mölndal , Sweden.

出版信息

Expert Rev Proteomics. 2017 Nov;14(11):1007-1020. doi: 10.1080/14789450.2017.1384697. Epub 2017 Oct 3.

Abstract

Alzheimer's disease (AD) is a neurodegenerative disease affecting the brain. Today there are three cerebrospinal fluid (CSF) biomarkers, amyloid-β consisting of 42 amino acids (Aβ42), total-tau (t-tau) and phosphorylated-tau (p-tau), which combined have sensitivity and specificity figures around 80%. However, pathological studies have shown that comorbidity is a common feature in AD and that the three currently used CSF biomarkers do not optimally reflect the activity of the disease process. Thus, additional markers are needed. Areas covered: In the present review, we screened PubMed for articles published the last five years (2012-2017) for proteomic studies in CSF with the criteria that AD had to be included as one of the diagnostic groups. Based on inclusion criteria, 28 papers were included reporting in total 224 biomarker-data that were altered in AD compared to control. Both mass spectrometry and multi-panel immunoassays were considered as proteomic studies. Expert commentary: A large number of pilot studies have been reported but so far there is a lack of replicated findings and to date no CSF biomarker discovered in proteomic studies has reached the clinic to aid in the diagnostic work-up of patients with cognitive impairment.

摘要

阿尔茨海默病(AD)是一种影响大脑的神经退行性疾病。目前有三种脑脊液(CSF)生物标志物,由 42 个氨基酸组成的淀粉样蛋白-β(Aβ42)、总tau(t-tau)和磷酸化 tau(p-tau),它们结合在一起的敏感性和特异性约为 80%。然而,病理学研究表明,共病是 AD 的一个常见特征,目前使用的三种 CSF 生物标志物不能最佳地反映疾病过程的活性。因此,需要额外的标志物。涵盖领域:在本综述中,我们在 PubMed 上筛选了过去五年(2012-2017 年)发表的关于 CSF 蛋白质组学研究的文章,其标准是 AD 必须作为诊断组之一。根据纳入标准,共有 28 篇论文纳入了总计 224 个生物标志物数据,这些数据与对照相比在 AD 中发生了改变。质谱和多面板免疫测定都被认为是蛋白质组学研究。专家评论:已经报告了大量的初步研究,但迄今为止,缺乏可复制的发现,迄今为止,蛋白质组学研究中没有发现任何 CSF 生物标志物能够进入临床,以帮助对认知障碍患者进行诊断性检查。

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