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Blood-based diagnosis of Alzheimer's disease using fingerprinting metabolomics based on hydrophilic interaction liquid chromatography with mass spectrometry and multivariate statistical analysis

机译:基于指纹图谱的代谢组学基于亲水相互作用液相色谱-质谱和多元统计分析的血液学诊断阿尔茨海默氏病

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Early and definitive diagnosis of Alzheimer's disease (AD) can lead to a better and more-targeted treatment and/or prevention for patients. In the diagnostic biomarkers of AD, the blood sample represents a more non-invasive, inexpensive and acceptable sources for repeated measurements than the cerebrospinal fluid. In this study, the fingerprinting metabolomics was proposed for the challenge of the blood-based diagnosis of defined AD by hydrophilic interaction liquid chromatography mass spectrometry (HILIC/MS). These plasma samples were selected from postmortem specimens based on these pathological examinations. Firstly, we compared these HILIC columns for the non-targeted metabolic assay using pooled plasma. The principal component analysis plot of these seven columns was performed using the repeatability of these chromatograms, and can be used to visualize trends in data sets by three-dimensional dispersion, contributory standard deviation and the number of detections. Based on these results, TSK-Amide 80 and TSKgel-NH2 columns are used as a reliable HILIC/MS assay of blood-based AD metabolomics that showed metabolic profiling of the AD pathology in MS chromatograms that ranged from 1182 to 2284 compounds. A total of 54 peaks were evaluated in order to identify useful ion signal candidates using an orthogonal partial least-squares-discriminant analysis. These peaks were then specifically analyzed using the HILIC-tandem MS assay by a receiver operating characteristic curve and linear discriminant analysis for the diagnosis of the defined AD. The fingerprinting metabolomics can overcome the limitations of previous challenging blood-based diagnosis of AD, and directly evaluates the specific comparative statistical values from the raw data. (C) 2014 Elsevier B.V. All rights reserved.
机译:阿尔茨海默氏病(AD)的早期和明确诊断可以为患者带来更好,更有针对性的治疗和/或预防。在AD的诊断生物标志物中,与脑脊髓液相比,血样代表了一种非侵入性,廉价且可接受的重复测量来源。在这项研究中,提出了指纹代谢组学,以通过亲水相互作用液相色谱质谱法(HILIC / MS)挑战基于血液的明确AD诊断。这些血浆样品是基于这些病理检查从验尸标本中选择的。首先,我们将这些HILIC色谱柱用于使用合并血浆进行的非靶向代谢分析。这七个色谱柱的主成分分析图是使用这些色谱图的可重复性进行的,可用于通过三维分散,辅助标准偏差和检测次数来可视化数据集中的趋势。基于这些结果,TSK-Amide 80和TSKgel-NH2色谱柱被用作基于血液的AD代谢组学的可靠HILIC / MS分析,该方法在MS色谱图中显示了AD病理学的代谢谱,其质谱图范围为1182至2284种化合物。为了评估有用的离子信号候选者,使用正交偏最小二乘判别分析对总共54个峰进行了评估。然后使用HILIC串联MS分析通过接收器工作特征曲线和线性判别分析对这些峰进行特异性分析,以诊断定义的AD。指纹代谢组学可以克服以前具有挑战性的基于血液的AD诊断的局限性,并可以直接从原始数据评估特定的比较统计值。 (C)2014 Elsevier B.V.保留所有权利。

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