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寻找代谢组学生物标志物的分析过程。

The analytical process to search for metabolomics biomarkers.

机构信息

Department of Analytical Chemistry, Annex Marie Curie Building, Campus of Rabanales, University of Córdoba, E-14071, Córdoba, Spain; Institute of Biomedical Research Maimónides (IMIBIC), Reina Sofía University Hospital, University of Córdoba, E-14004, Córdoba, Spain; CIBER Fragilidad y Envejecimiento Saludable (CIBERfes), Instituto de Salud Carlos III, Spain.

出版信息

J Pharm Biomed Anal. 2018 Jan 5;147:341-349. doi: 10.1016/j.jpba.2017.06.073. Epub 2017 Jul 6.

Abstract

The scant number of available metabolomics biomarkers does not reflect the extent of the research in this field. Looking for the reasons of failure, the authors, as analytical chemists, critically discuss each of the steps in the analytical process that requires improvements. They find insufficient information about how the experimental part is developed. After revising the steps from sampling to obtainment of the analytical sample (from typical samples such as blood and urine to others less common such as sweat or saliva), the need for data and metadata for either reproduction of a given study or for taking the study as starting point after biomarker discovery is criticized. The separation and analysis steps are also revised as does data treatment. After the sources of errors from the analytical process are overcome, subsequent steps in the implementation of biomarkers to reach the final aim of clinical adoption should be supported as required.

摘要

可用的代谢组学生物标志物数量很少,这并不能反映该领域的研究程度。为了寻找失败的原因,作为分析化学家的作者批判性地讨论了分析过程中需要改进的每一个步骤。他们发现关于实验部分如何开展的信息不足。在修订了从采样到获得分析样本(从典型样本如血液和尿液到其他不太常见的样本如汗液或唾液)的步骤后,作者批评了缺乏重现给定研究或在发现生物标志物后将研究作为起点所需的数据和元数据。分离和分析步骤也进行了修订,数据处理也是如此。在克服了分析过程中的误差源后,应该根据需要支持将生物标志物应用于实现最终临床目标的后续步骤。

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