G. I. Kuzovleva, Ekaterina Yu. Vlasenko, L. Maltseva, Olga L. Morozova
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引用次数: 0
摘要
代谢组学是一门研究小分子(50-5,000 Da)的科学,这些小分子是在细胞内实施新陈代谢途径并维持其重要功能时形成的。尿液代谢组的研究是小儿泌尿外科诊断泌尿系统各种细胞损伤早期阶段的一个有前途的方向,可以研究生物标志物或其谱系,从而提高对现有疾病的识别能力,多变量分析将为诊断提供更高的准确性。本研究旨在总结泌尿系统先天畸形伴肾发育不良导致急性肾损伤或慢性肾病病例中尿液代谢组及其变化的现有信息。我们使用 PubMed、Embase 和 Google Scholar 进行了文献检索和综述。该综述介绍了代谢组学分析的可能性,它为诊断和监测泌尿系统器官和组织结构的损伤、确定病理进展的预测因素以及制定医疗决策的个性化技术提供了新的质量水平。然而,这种方法受到设备成本高、需要培训高素质人才以及结果解读困难等因素的限制。尿液代谢组研究对于泌尿系统畸形患儿的诊断和选择及时、合理的治疗策略大有可为。
Urine metabolome investigation in pediatric urology. Review
Metabolomics is the science of studying small molecules (50–5,000 Da) formed because of the implementation of metabolic pathways in cells and the maintenance of their vital functions. The study of urine metabolome is a promising direction for diagnosing early stages of damage to various cells of the urinary system in pediatric urology, allowing the study of biomarkers or their spectrum, which can improve the identification of existing disorders, and multivariate analysis will provide greater accuracy in making a diagnosis. This study aimed to summarize existing information on urine metabolome and its changes in cases of congenital malformations of the urinary system, accompanied by renal dysplasia, leading to acute kidney injury or chronic kidney disease. A literature search and review was conducted using PubMed, Embase, and Google Scholar. The review presents the possibilities of metabolomic analysis to provide a qualitatively new level of diagnosis and monitoring of damage to the structures of organs and tissues of the urinary system, identifying predictors of pathology progression, and personalized techniques for making medical decisions. However, this method is limited by the high cost of the equipment, need for training of highly qualified personnel, and difficulty in interpreting the results. The study of urine metabolome is very promising for the diagnosis and selection of a timely, rational treatment strategy for children with malformations of the urinary system.