Collie Blake, Troisi Jacopo, Lombardi Martina, Symes Steven, Richards Sean
Department of Biology, University of Tennessee at Chattanooga, Chattanooga, TN 37403, USA .
Department of Medicine, Surgery and Dentistry, "Scuola Medica Salernitana", University of Salerno, 84081 Baronissi, Italy.
Metabolites. 2025 Jan 14;15(1):50. doi: 10.3390/metabo15010050.
Endometriosis is a common gynecological disease that affects approximately 10-15% of reproductive-aged women worldwide. This debilitating disease has a negative impact on the quality of life of those affected. Despite this condition being very common, the pathogenesis is not well understood. Metabolomics is the study of the array of low-weight metabolites in a given sample. This emerging field of omics-based science has proved to be effective at furthering the understanding of endometriosis. In this systematic review, we seek to provide an overview of the application of metabolomics in endometriosis. We highlight the use of metabolomics in locating biomarkers for identification, understanding treatment mechanisms and symptoms, and relating external factors to endometriosis. The literature search took place in the Web of Science, Pubmed, and Google Scholar based on the keywords "metabolomics" AND "endometriosis" or "metabolome" AND "endometriosis". We found 58 articles from 2012 to 2024 that met our search criteria. Significant alterations of lipids, amino acids, as well as other compounds were present in human and animal models. Discrepancies among studies of significantly altered metabolites make it difficult to make general conclusions on the metabolic signature of endometriosis. However, several individual metabolites were elevated in multiple studies of women with endometriosis; these include 3-hydroxybutyrate, lactate, phosphatidic acids, succinate, pyruvate, tetradecenoylcarnitine, hypoxanthine, and xanthine. Accordingly, L-isoleucine and citrate were reduced in multiple studies of women with endometriosis. Including larger cohorts, standardizing testing methods, and studying the individual phenotypes of endometriosis may lead to more separable results.
子宫内膜异位症是一种常见的妇科疾病,全球约10-15%的育龄妇女受其影响。这种使人衰弱的疾病对患者的生活质量有负面影响。尽管这种疾病非常常见,但其发病机制尚未完全明确。代谢组学是对给定样本中一系列低分子量代谢物的研究。这一基于组学的新兴科学领域已被证明有助于进一步了解子宫内膜异位症。在本系统评价中,我们旨在概述代谢组学在子宫内膜异位症中的应用。我们强调代谢组学在寻找生物标志物以进行识别、理解治疗机制和症状以及将外部因素与子宫内膜异位症相关联方面的应用。基于关键词“代谢组学”和“子宫内膜异位症”或“代谢组”和“子宫内膜异位症”在科学网、PubMed和谷歌学术上进行了文献检索。我们发现了2012年至2024年期间符合我们检索标准的58篇文章。在人和动物模型中都存在脂质、氨基酸以及其他化合物的显著变化。关于显著改变的代谢物的研究之间存在差异,这使得难以就子宫内膜异位症的代谢特征得出一般性结论。然而,在多项针对子宫内膜异位症女性的研究中,有几种个体代谢物水平升高;这些包括3-羟基丁酸、乳酸、磷脂酸、琥珀酸、丙酮酸、十四碳烯酰肉碱、次黄嘌呤和黄嘌呤。相应地,在多项针对子宫内膜异位症女性的研究中,L-异亮氨酸和柠檬酸水平降低。纳入更大的队列、标准化检测方法以及研究子宫内膜异位症的个体表型可能会得出更具区分性的结果。