Suppr超能文献

代谢组学用于鉴定未分类的尿毒症毒素:一项全面的文献综述。

Metabolomics to Identify Unclassified Uremic Toxins: A Comprehensive Literature Review.

作者信息

Vanholder Raymond, Glorieux Griet, Argiles Angel, Burtey Stéphane, Cohen Gerald, Duranton Flore, Koppe Laetitia, Massy Ziad A, Ortiz Alberto, Masereeuw Rosalinde, Stamatialis Dimitrios, Jankowski Joachim

机构信息

Nephrology Section, Department of Internal Medicine and Pediatrics, Ghent University Hospital, Ghent, Belgium.

RD Néphrologie, Montpellier, France.

出版信息

Kidney Med. 2024 Dec 26;7(3):100955. doi: 10.1016/j.xkme.2024.100955. eCollection 2025 Mar.

Abstract

A comprehensive review of known uremic retention molecules goes back to more than 10 years ago and did not consider metabolomic analyses. The present analysis searches for as of yet unclassified solutes retained in chronic kidney disease (CKD) by analyzing metabolites associated with relevant outcomes of CKD. This untargeted metabolomics-based approach is compared with a conventional targeted literature search. For the selected molecules, the literature was screened for arguments regarding toxic (harmful), beneficial, or neutral effects in experimental or clinical studies. Findings were independently crosschecked. In total, 103 molecules were selected. No literature on any effect was found for 55 substances, 3 molecules had no significant effect, and 13 others showed beneficial effects. For the remaining 32 compounds, we found at least one report of a toxic effect. Whereas 62.5% of the compounds with at least one study on a toxic effect was retrieved via the bottom-up approach, 69.2% of the substances originating from metabolomics-based approaches showed a beneficial effect. Our results suggest that untargeted metabolomics offer a more balanced view of uremic retention than the targeted approaches, with higher chances of revealing the beneficial potential of some of the metabolites.

摘要

对已知尿毒症潴留分子的全面综述可追溯到10多年前,且未考虑代谢组学分析。本分析通过分析与慢性肾脏病(CKD)相关结局相关的代谢物,寻找尚未分类的CKD潴留溶质。将这种基于非靶向代谢组学的方法与传统的靶向文献检索进行比较。对于选定的分子,在文献中筛选关于其在实验或临床研究中的毒性(有害)、有益或中性作用的论据。研究结果进行了独立核对。总共选择了103种分子。55种物质未找到关于任何作用的文献,3种分子无显著作用,另有13种显示出有益作用。对于其余32种化合物,我们发现至少有一份关于其毒性作用的报告。通过自下而上的方法检索到了至少有一项关于毒性作用研究的化合物中的62.5%,而基于代谢组学方法的物质中有69.2%显示出有益作用。我们的结果表明,与靶向方法相比,非靶向代谢组学对尿毒症潴留的看法更为平衡,揭示某些代谢物有益潜力的机会更高。

相似文献

5

本文引用的文献

4
Risk of malignancy in patients with chronic kidney disease.慢性肾脏病患者的恶性肿瘤风险。
PLoS One. 2022 Aug 17;17(8):e0272910. doi: 10.1371/journal.pone.0272910. eCollection 2022.
7
Classification of Uremic Toxins and Their Role in Kidney Failure.尿毒症毒素的分类及其在肾衰竭中的作用。
Clin J Am Soc Nephrol. 2021 Dec;16(12):1918-1928. doi: 10.2215/CJN.02660221. Epub 2021 Jul 7.

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验