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基于光谱和代谢组学的阿尔茨海默病血液分子特征。

Blood-based molecular signature of Alzheimer's disease via spectroscopy and metabolomics.

机构信息

Department of Analytical Chemistry, University of Chemistry and Technology Prague, Technická 5, 166 28 Prague 6, Czech Republic.

Department of Analytical Chemistry, University of Chemistry and Technology Prague, Technická 5, 166 28 Prague 6, Czech Republic.

出版信息

Clin Biochem. 2019 Oct;72:58-63. doi: 10.1016/j.clinbiochem.2019.04.004. Epub 2019 Apr 4.

Abstract

OBJECTIVES

With over 35 million cases worldwide, Alzheimer's disease (AD) represents the main cause of dementia. The differentiation of AD from other types of dementia is challenging and its early diagnosis is complicated. The established biomarkers are not only based on the invasive collection of cerebrospinal fluid, but also lack sufficient sensitivity and specificity. Therefore, much current effort is aimed at the identification of new biomarkers of AD in peripheral blood.

DESIGN AND METHODS

We focused on blood-based analyses using chiroptical spectroscopy (Raman optical activity, electronic circular dichroism) supplemented with conventional vibrational spectroscopy (infrared, Raman) and metabolomics (high-performance liquid chromatography with a high-resolution mass detection).

RESULTS

This unique approach enabled us to identify the spectral pattern of AD and variations in metabolite levels. Subsequent linear discriminant analysis of the spectral data resulted in differentiation between the AD patients and control subjects.

CONCLUSIONS

It may be stated that this less invasive approach has strong potential for the identification of disease-related changes within essential plasmatic biomolecules and metabolites.

摘要

目的

全球有超过 3500 万例病例,阿尔茨海默病(AD)是痴呆症的主要病因。AD 与其他类型痴呆症的区分具有挑战性,早期诊断也很复杂。现有的既定生物标志物不仅基于对脑脊液的有创采集,而且缺乏足够的灵敏度和特异性。因此,目前的研究主要集中在识别外周血中的 AD 新型生物标志物上。

设计和方法

我们专注于使用手性光学光谱(拉曼光学活性、电子圆二色性)结合常规振动光谱(红外、拉曼)和代谢组学(带有高分辨率质量检测的高效液相色谱)进行基于血液的分析。

结果

这种独特的方法使我们能够识别 AD 的光谱模式和代谢物水平的变化。随后对光谱数据进行线性判别分析,可区分 AD 患者和对照组。

结论

可以说,这种微创方法具有识别重要血浆生物分子和代谢物中与疾病相关变化的强大潜力。

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