Metabolites and metabolic pathways associated with rheumatoid arthritis and systemic lupus erythematosus

IF 4.7 Q2 IMMUNOLOGY
Nancy P. Duarte-Delgado , Mónica P. Cala , Alfonso Barreto , Luz-Stella Rodríguez C
{"title":"Metabolites and metabolic pathways associated with rheumatoid arthritis and systemic lupus erythematosus","authors":"Nancy P. Duarte-Delgado ,&nbsp;Mónica P. Cala ,&nbsp;Alfonso Barreto ,&nbsp;Luz-Stella Rodríguez C","doi":"10.1016/j.jtauto.2022.100150","DOIUrl":null,"url":null,"abstract":"<div><p>Rheumatoid arthritis (RA) and systemic lupus erythematosus (SLE) are chronic autoimmune diseases that result from the combined influence of genetic and environmental factors that promotes the loss of tolerance to cellular components. The complexity of these diseases converts them into a major challenge at the diagnostic and treatment level. Therefore, it is convenient to implement the use of tools for a better understanding of the physiopathology of these diseases to propose reliable biomarkers. The “omics” disciplines like metabolomics and lipidomics allow to study RA and SLE in a higher degree of detail since they evaluate the metabolites and metabolic pathways involved in disease pathogenesis. This review has compiled the information of metabolomics and lipidomics studies where samples obtained from RA and SLE patients were evaluated to find the metabolites and pathways differences between patients and healthy controls. In both diseases, there is a decrease in several amino acids and oxidative stress-related metabolites like glutathione. These findings may be useful for functional metabolomics studies aiming to reprogram the metabolism in a disease setting to recover normal immune cell homeostasis and function.</p></div>","PeriodicalId":36425,"journal":{"name":"Journal of Translational Autoimmunity","volume":null,"pages":null},"PeriodicalIF":4.7000,"publicationDate":"2022-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2589909022000119/pdfft?md5=2abddc594b51821c7b9a93f98789b40b&pid=1-s2.0-S2589909022000119-main.pdf","citationCount":"7","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Translational Autoimmunity","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2589909022000119","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"IMMUNOLOGY","Score":null,"Total":0}
引用次数: 7

Abstract

Rheumatoid arthritis (RA) and systemic lupus erythematosus (SLE) are chronic autoimmune diseases that result from the combined influence of genetic and environmental factors that promotes the loss of tolerance to cellular components. The complexity of these diseases converts them into a major challenge at the diagnostic and treatment level. Therefore, it is convenient to implement the use of tools for a better understanding of the physiopathology of these diseases to propose reliable biomarkers. The “omics” disciplines like metabolomics and lipidomics allow to study RA and SLE in a higher degree of detail since they evaluate the metabolites and metabolic pathways involved in disease pathogenesis. This review has compiled the information of metabolomics and lipidomics studies where samples obtained from RA and SLE patients were evaluated to find the metabolites and pathways differences between patients and healthy controls. In both diseases, there is a decrease in several amino acids and oxidative stress-related metabolites like glutathione. These findings may be useful for functional metabolomics studies aiming to reprogram the metabolism in a disease setting to recover normal immune cell homeostasis and function.

类风湿性关节炎和系统性红斑狼疮的代谢产物和代谢途径
类风湿性关节炎(RA)和系统性红斑狼疮(SLE)是由遗传和环境因素共同影响导致的慢性自身免疫性疾病,可促进对细胞成分的耐受性丧失。这些疾病的复杂性使它们成为诊断和治疗水平上的重大挑战。因此,可以方便地使用工具来更好地了解这些疾病的生理病理,从而提出可靠的生物标志物。代谢组学和脂质组学等“组学”学科可以更详细地研究RA和SLE,因为它们评估了疾病发病机制中涉及的代谢物和代谢途径。本综述汇编了代谢组学和脂质组学研究的信息,对RA和SLE患者的样本进行了评估,以发现患者与健康对照组之间代谢物和途径的差异。在这两种疾病中,几种氨基酸和与氧化应激相关的代谢物(如谷胱甘肽)都会减少。这些发现可能有助于功能代谢组学研究,旨在重新编程疾病环境中的代谢,以恢复正常的免疫细胞稳态和功能。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Journal of Translational Autoimmunity
Journal of Translational Autoimmunity Medicine-Immunology and Allergy
CiteScore
7.80
自引率
2.60%
发文量
33
审稿时长
55 days
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信