• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

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

基于 UPLC-MS/MS 的广泛靶向代谢组学揭示 COVID-19 的代谢特征。

Metabolite profile of COVID-19 revealed by UPLC-MS/MS-based widely targeted metabolomics.

机构信息

Medical Research Center, Yue Bei People's Hospital, Shantou University Medical College, Shaoguan, China.

The Central Laboratory, Yangjiang People's Hospital, Yangjiang, China.

出版信息

Front Immunol. 2022 Jul 18;13:894170. doi: 10.3389/fimmu.2022.894170. eCollection 2022.

DOI:10.3389/fimmu.2022.894170
PMID:35924246
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9339702/
Abstract

The metabolic characteristics of COVID-19 disease are still largely unknown. Here, 44 patients with COVID-19 (31 mild COVID-19 patients and 13 severe COVID-19 patients), 42 healthy controls (HC), and 42 patients with community-acquired pneumonia (CAP), were involved in the study to assess their serum metabolomic profiles. We used widely targeted metabolomics based on an ultra-performance liquid chromatography-tandem mass spectrometry (UPLC-MS/MS). The differentially expressed metabolites in the plasma of mild and severe COVID-19 patients, CAP patients, and HC subjects were screened, and the main metabolic pathways involved were analyzed. Multiple mature machine learning algorithms confirmed that the metabolites performed excellently in discriminating COVID-19 groups from CAP and HC subjects, with an area under the curve (AUC) of 1. The specific dysregulation of AMP, dGMP, -glycero-3-phosphocholine, and carnitine was observed in the severe COVID-19 group. Moreover, random forest analysis suggested that these metabolites could discriminate between severe COVID-19 patients and mild COVID-19 patients, with an AUC of 0.921. This study may broaden our understanding of pathophysiological mechanisms of COVID-19 and may offer an experimental basis for developing novel treatment strategies against it.

摘要

新型冠状病毒肺炎(COVID-19)的代谢特征仍知之甚少。本研究纳入 44 例 COVID-19 患者(31 例轻症 COVID-19 患者和 13 例重症 COVID-19 患者)、42 例健康对照者(HC)和 42 例社区获得性肺炎(CAP)患者,评估其血清代谢组学特征。我们采用基于超高效液相色谱-串联质谱(UPLC-MS/MS)的广泛靶向代谢组学方法。筛选轻症和重症 COVID-19 患者、CAP 患者和 HC 受试者血浆中差异表达的代谢物,并分析其涉及的主要代谢途径。多种成熟的机器学习算法证实,这些代谢物在区分 COVID-19 组与 CAP 和 HC 组方面表现出色,曲线下面积(AUC)为 1。在重症 COVID-19 组中观察到 AMP、dGMP、-甘油磷酸胆碱和肉碱的特异性失调。此外,随机森林分析表明,这些代谢物可区分重症 COVID-19 患者和轻症 COVID-19 患者,AUC 为 0.921。本研究可能拓宽我们对 COVID-19 病理生理机制的理解,并为开发针对 COVID-19 的新型治疗策略提供实验基础。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc6f/9339702/d269727d459e/fimmu-13-894170-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc6f/9339702/9c161a4e5dae/fimmu-13-894170-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc6f/9339702/89289d5281f1/fimmu-13-894170-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc6f/9339702/4dff41b707b4/fimmu-13-894170-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc6f/9339702/1c32fec377dd/fimmu-13-894170-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc6f/9339702/b55f35847f15/fimmu-13-894170-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc6f/9339702/d58c2b7dd194/fimmu-13-894170-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc6f/9339702/bbc1faa25aad/fimmu-13-894170-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc6f/9339702/d269727d459e/fimmu-13-894170-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc6f/9339702/9c161a4e5dae/fimmu-13-894170-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc6f/9339702/89289d5281f1/fimmu-13-894170-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc6f/9339702/4dff41b707b4/fimmu-13-894170-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc6f/9339702/1c32fec377dd/fimmu-13-894170-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc6f/9339702/b55f35847f15/fimmu-13-894170-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc6f/9339702/d58c2b7dd194/fimmu-13-894170-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc6f/9339702/bbc1faa25aad/fimmu-13-894170-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc6f/9339702/d269727d459e/fimmu-13-894170-g008.jpg

相似文献

1
Metabolite profile of COVID-19 revealed by UPLC-MS/MS-based widely targeted metabolomics.基于 UPLC-MS/MS 的广泛靶向代谢组学揭示 COVID-19 的代谢特征。
Front Immunol. 2022 Jul 18;13:894170. doi: 10.3389/fimmu.2022.894170. eCollection 2022.
2
Metabolic profiles in community-acquired pneumonia: developing assessment tools for disease severity.社区获得性肺炎的代谢特征:疾病严重程度评估工具的开发。
Crit Care. 2018 May 14;22(1):130. doi: 10.1186/s13054-018-2049-2.
3
Serum metabolomics profile identifies patients with community-acquired pneumonia infected by bacteria, fungi, and viruses.血清代谢组学图谱可识别由细菌、真菌和病毒感染引起的社区获得性肺炎患者。
Ann Med. 2024 Dec;56(1):2399320. doi: 10.1080/07853890.2024.2399320. Epub 2024 Sep 16.
4
Plasma characteristic metabolites of pediatric community-acquired pneumonia in traditional Chinese medicine syndrome differentiation.小儿社区获得性肺炎中医辨证的血浆特征性代谢产物
Anat Rec (Hoboken). 2021 Nov;304(11):2579-2591. doi: 10.1002/ar.24767. Epub 2021 Sep 22.
5
A metabolomics approach to studying the effects of Jinxin oral liquid on RSV-infected mice using UPLC/LTQ-Orbitrap mass spectrometry.一种基于超高效液相色谱/线性离子阱-静电场轨道阱质谱联用技术研究金欣口服液对呼吸道合胞病毒感染小鼠影响的代谢组学方法。
J Ethnopharmacol. 2015 Nov 4;174:25-36. doi: 10.1016/j.jep.2015.07.040. Epub 2015 Jul 30.
6
Metabolic Disturbances in Adult-Onset Still's Disease Evaluated Using Liquid Chromatography/Mass Spectrometry-Based Metabolomic Analysis.基于液相色谱/质谱代谢组学分析评估成人斯蒂尔病中的代谢紊乱
PLoS One. 2016 Dec 22;11(12):e0168147. doi: 10.1371/journal.pone.0168147. eCollection 2016.
7
Integrated metabolomic profiling of hepatocellular carcinoma in hepatitis C cirrhosis through GC/MS and UPLC/MS-MS.通过气相色谱/质谱联用仪(GC/MS)和超高效液相色谱/串联质谱仪(UPLC/MS-MS)对丙型肝炎肝硬化中的肝细胞癌进行综合代谢组学分析。
Liver Int. 2014 Oct;34(9):1428-44. doi: 10.1111/liv.12541. Epub 2014 Apr 28.
8
Metabolomic profiling of dengue infection: unraveling molecular signatures by LC-MS/MS and machine learning models.基于 LC-MS/MS 和机器学习模型的登革热感染代谢组学分析:揭示分子特征。
Metabolomics. 2024 Sep 21;20(5):104. doi: 10.1007/s11306-024-02169-0.
9
Urinary metabolomics for discovering metabolic biomarkers of bladder cancer by UPLC-MS.采用 UPLC-MS 技术进行尿液代谢组学研究,以发现膀胱癌的代谢生物标志物。
BMC Cancer. 2022 Feb 28;22(1):214. doi: 10.1186/s12885-022-09318-5.
10
Widely targeted metabolomics of Alzheimer's disease postmortem cerebrospinal fluid based on 9-fluorenylmethyl chloroformate derivatized ultra-high performance liquid chromatography tandem mass spectrometry.基于 9-芴甲氧羰酰氯衍生的超高效液相色谱串联质谱法对阿尔茨海默病死后脑脊液进行广泛靶向代谢组学分析。
J Chromatogr B Analyt Technol Biomed Life Sci. 2018 Aug 1;1091:53-66. doi: 10.1016/j.jchromb.2018.05.031. Epub 2018 May 23.

引用本文的文献

1
Severe acute respiratory syndrome coronavirus 2 infection unevenly impacts metabolism in the coronal periphery of the lungs.严重急性呼吸综合征冠状病毒2感染对肺冠状周边区域的新陈代谢产生不均衡影响。
iScience. 2025 Jan 2;28(2):111727. doi: 10.1016/j.isci.2024.111727. eCollection 2025 Feb 21.
2
Metabolomic Insights into COVID-19 Severity: A Scoping Review.对新冠病毒疾病严重程度的代谢组学见解:一项范围综述
Metabolites. 2024 Nov 12;14(11):617. doi: 10.3390/metabo14110617.
3
Metabolic profiling during COVID-19 infection in humans: Identification of potential biomarkers for occurrence, severity and outcomes using machine learning.

本文引用的文献

1
Is Ferroptosis a Key Component of the Process Leading to Multiorgan Damage in COVID-19?铁死亡是否是导致COVID-19多器官损伤过程的关键组成部分?
Antioxidants (Basel). 2021 Oct 25;10(11):1677. doi: 10.3390/antiox10111677.
2
The serum amino acid profile in COVID-19.血清氨基酸谱与 COVID-19。
Amino Acids. 2021 Oct;53(10):1569-1588. doi: 10.1007/s00726-021-03081-w. Epub 2021 Oct 4.
3
Targeted metabolomics identifies high performing diagnostic and prognostic biomarkers for COVID-19.靶向代谢组学鉴定出 COVID-19 的高表现诊断和预后生物标志物。
在人类 COVID-19 感染期间的代谢组学分析:利用机器学习识别发生、严重程度和结局的潜在生物标志物。
PLoS One. 2024 May 30;19(5):e0302977. doi: 10.1371/journal.pone.0302977. eCollection 2024.
4
Nucleotide, Phospholipid, and Kynurenine Metabolites Are Robustly Associated with COVID-19 Severity and Time of Plasma Sample Collection in a Prospective Cohort Study.核苷酸、磷脂和犬尿氨酸代谢物与前瞻性队列研究中 COVID-19 严重程度和血浆样本采集时间具有强相关性。
Int J Mol Sci. 2023 Dec 26;25(1):346. doi: 10.3390/ijms25010346.
5
Systematic Mendelian randomization study of the effect of gut microbiome and plasma metabolome on severe COVID-19.基于孟德尔随机化的肠道微生物组和血浆代谢组对严重 COVID-19 影响的系统研究。
Front Immunol. 2023 Aug 16;14:1211612. doi: 10.3389/fimmu.2023.1211612. eCollection 2023.
6
Lipid Metabolism Disorder in Cerebrospinal Fluid Related to Parkinson's Disease.脑脊液中与帕金森病相关的脂质代谢紊乱
Brain Sci. 2023 Aug 4;13(8):1166. doi: 10.3390/brainsci13081166.
7
Gastrointestinal symptoms of long COVID-19 related to the ectopic colonization of specific bacteria that move between the upper and lower alimentary tract and alterations in serum metabolites.长新冠相关的胃肠道症状与特定细菌的异位定植有关,这些细菌在上消化道和下消化道之间移动,并改变血清代谢物。
BMC Med. 2023 Jul 19;21(1):264. doi: 10.1186/s12916-023-02972-x.
8
Common molecular signatures between coronavirus infection and Alzheimer's disease reveal targets for drug development.冠状病毒感染与阿尔茨海默病之间的共同分子特征揭示了药物开发的靶点。
bioRxiv. 2023 Jun 15:2023.06.14.544970. doi: 10.1101/2023.06.14.544970.
9
Metabolomics as a powerful tool for diagnostic, pronostic and drug intervention analysis in COVID-19.代谢组学作为COVID-19诊断、预后和药物干预分析的有力工具。
Front Mol Biosci. 2023 Feb 15;10:1111482. doi: 10.3389/fmolb.2023.1111482. eCollection 2023.
10
Integrated Metabolic and Inflammatory Signatures Associated with Severity of, Fatality of, and Recovery from COVID-19.与新冠病毒疾病(COVID-19)的严重程度、死亡率及康复相关的综合代谢和炎症特征
Microbiol Spectr. 2023 Feb 28;11(2):e0219422. doi: 10.1128/spectrum.02194-22.
Sci Rep. 2021 Jul 19;11(1):14732. doi: 10.1038/s41598-021-94171-y.
4
COVID-19 infection, progression, and vaccination: Focus on obesity and related metabolic disturbances.COVID-19 感染、进展和疫苗接种:关注肥胖及相关代谢紊乱。
Obes Rev. 2021 Oct;22(10):e13313. doi: 10.1111/obr.13313. Epub 2021 Jul 16.
5
Altered amino acid profile in patients with SARS-CoV-2 infection.感染 SARS-CoV-2 患者的氨基酸谱改变。
Proc Natl Acad Sci U S A. 2021 Jun 22;118(25). doi: 10.1073/pnas.2101708118.
6
SARS-CoV-2 suppresses mRNA expression of selenoproteins associated with ferroptosis, endoplasmic reticulum stress and DNA synthesis.SARS-CoV-2 抑制与铁死亡、内质网应激和 DNA 合成相关的硒蛋白的 mRNA 表达。
Food Chem Toxicol. 2021 Jul;153:112286. doi: 10.1016/j.fct.2021.112286. Epub 2021 May 21.
7
Metabolomics analysis reveals a modified amino acid metabolism that correlates with altered oxygen homeostasis in COVID-19 patients.代谢组学分析揭示了 COVID-19 患者中与氧平衡改变相关的氨基酸代谢改变。
Sci Rep. 2021 Mar 18;11(1):6350. doi: 10.1038/s41598-021-85788-0.
8
Lessons learned 1 year after SARS-CoV-2 emergence leading to COVID-19 pandemic.SARS-CoV-2 引发 COVID-19 大流行一年后的经验教训。
Emerg Microbes Infect. 2021 Dec;10(1):507-535. doi: 10.1080/22221751.2021.1898291.
9
Metabolism pathways of arachidonic acids: mechanisms and potential therapeutic targets.花生四烯酸的代谢途径:机制与潜在治疗靶点。
Signal Transduct Target Ther. 2021 Feb 26;6(1):94. doi: 10.1038/s41392-020-00443-w.
10
The coronavirus is here to stay - here's what that means.新冠病毒将长期存在——以下是这意味着什么。
Nature. 2021 Feb;590(7846):382-384. doi: 10.1038/d41586-021-00396-2.