首页> 外文OA文献 >Serum Metabolomics Analysis of Asthma in Different Inflammatory Phenotypes: A Cross-Sectional Study in Northeast China
【2h】

Serum Metabolomics Analysis of Asthma in Different Inflammatory Phenotypes: A Cross-Sectional Study in Northeast China

机译:不同炎症表型哮喘血清代谢组织分析:东北东北横截面研究

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

Background and Objective. Asthma as a chronic heterogeneous disease seriously affects the quality of life. Incorrect identification for its clinical phenotypes lead to a huge waste of medical resources. Metabolomic technique as a novel approach to explore the pathogenesis of diseases have not been used to study asthma based on their clear defined inflammatory phenotypes. This study is aimed to distinguish the divergent metabolic profile in different asthma phenotypes and clarify the pathogenesis of them. Methods. Participants including eosinophilic asthmatics (EA, n=13), noneosinophilic asthmatics (NEA, n=16), and healthy controls (HC, n=15) were enrolled. A global profile of untargeted serum metabolomics was identified with Ultra Performance Liquid Chromatography–Mass Spectrometry technique. Results. Multivariate analysis was performed and showed a clear distinction between EA, NEA, and HC. A total of 18 different metabolites were recognized between the three groups based on OPLS-DA model and involved in 10 perturbed metabolic pathways. Glycerophospholipid metabolism, retinol metabolism, and sphingolipid metabolism were identified as the most significant changed three pathways (impact > 0.1 and -log(P) > 4) between the phenotypes. Conclusions. We showed that the different inflammatory phenotypes of asthma involve the immune regulation, energy, and nutrients metabolism. The clarified metabolic profile contributes to understanding the pathophysiology of asthma phenotypes and optimizing the therapeutic strategy against asthma heterogeneity.
机译:背景和目标。作为慢性异质疾病的哮喘严重影响了生活质量。其临床表型的识别不正确导致医疗资源的巨大浪费。代谢物技术作为一种探讨疾病发病机制的新方法,尚未用于基于其澄清定义的炎症表型研究哮喘。本研究旨在区分不同哮喘表型的不同代谢型材,并阐明它们的发病机制。方法。参与者包括嗜酸性嗜嗜酸性哮喘(EA,N = 13),非聚氨酯哮喘患者(NEA,N = 16)和健康对照(HC,N = 15)。用超高效液相色谱 - 质谱技术鉴定了未特定血清代谢组科的全局简介。结果。进行多变量分析,并在EA,NEA和HC之间进行了明显的区别。在基于OPLS-DA模型的三组之间,共识别了总共18种不同的代谢物,并参与了10个扰动的代谢途径。甘油磷脂代谢,视黄醇代谢和鞘脂代谢被鉴定为最显着的改变的三种途径(摄影> 0.1和-Log(P)> 4)在表型之间。结论。我们表明,哮喘的不同炎症表型涉及免疫调节,能量和营养物质代谢。澄清的代谢型材有助于了解哮喘表型的病理生理学,并优化哮喘异质性的治疗策略。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号