• 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

血液基因表达可预测 COVID-19 住院患者入住重症监护病房。

Blood gene expression predicts intensive care unit admission in hospitalised patients with COVID-19.

机构信息

Institute of Infection, Veterinary and Ecological Sciences, University of Liverpool, Liverpool, United Kingdom.

TopMD Precision Medicine Ltd, Southampton, United Kingdom.

出版信息

Front Immunol. 2022 Sep 20;13:988685. doi: 10.3389/fimmu.2022.988685. eCollection 2022.

DOI:10.3389/fimmu.2022.988685
PMID:36203591
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9530807/
Abstract

BACKGROUND

The COVID-19 pandemic has created pressure on healthcare systems worldwide. Tools that can stratify individuals according to prognosis could allow for more efficient allocation of healthcare resources and thus improved patient outcomes. It is currently unclear if blood gene expression signatures derived from patients at the point of admission to hospital could provide useful prognostic information.

METHODS

Gene expression of whole blood obtained at the point of admission from a cohort of 78 patients hospitalised with COVID-19 during the first wave was measured by high resolution RNA sequencing. Gene signatures predictive of admission to Intensive Care Unit were identified and tested using machine learning and topological data analysis, TopMD.

RESULTS

The best gene expression signature predictive of ICU admission was defined using topological data analysis with an accuracy: 0.72 and ROC AUC: 0.76. The gene signature was primarily based on differentially activated pathways controlling epidermal growth factor receptor (EGFR) presentation, Peroxisome proliferator-activated receptor alpha (PPAR-α) signalling and Transforming growth factor beta (TGF-β) signalling.

CONCLUSIONS

Gene expression signatures from blood taken at the point of admission to hospital predicted ICU admission of treatment naïve patients with COVID-19.

摘要

背景

COVID-19 大流行给全球医疗体系带来了压力。能够根据预后对个体进行分层的工具可以更有效地分配医疗资源,从而改善患者的预后。目前尚不清楚患者入院时的血液基因表达特征是否能提供有用的预后信息。

方法

通过高分辨率 RNA 测序测量了在 COVID-19 第一波期间住院的 78 名患者入院时采集的全血的基因表达。使用机器学习和拓扑数据分析(TopMD)识别并测试了预测入住重症监护病房(ICU)的基因特征。

结果

使用拓扑数据分析定义了预测 ICU 入院的最佳基因表达特征,其准确性为 0.72,ROC AUC 为 0.76。该基因特征主要基于控制表皮生长因子受体(EGFR)呈现、过氧化物酶体增殖物激活受体α(PPAR-α)信号和转化生长因子β(TGF-β)信号的差异激活途径。

结论

从入院时采集的血液中的基因表达特征预测了 COVID-19 治疗初治患者的 ICU 入院。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/01d2/9530807/e0619a7f5744/fimmu-13-988685-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/01d2/9530807/75e229f44a7d/fimmu-13-988685-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/01d2/9530807/eab648d6e859/fimmu-13-988685-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/01d2/9530807/e0619a7f5744/fimmu-13-988685-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/01d2/9530807/75e229f44a7d/fimmu-13-988685-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/01d2/9530807/eab648d6e859/fimmu-13-988685-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/01d2/9530807/e0619a7f5744/fimmu-13-988685-g003.jpg

相似文献

1
Blood gene expression predicts intensive care unit admission in hospitalised patients with COVID-19.血液基因表达可预测 COVID-19 住院患者入住重症监护病房。
Front Immunol. 2022 Sep 20;13:988685. doi: 10.3389/fimmu.2022.988685. eCollection 2022.
2
Clinical Characteristics and Prognostic Factors for Intensive Care Unit Admission of Patients With COVID-19: Retrospective Study Using Machine Learning and Natural Language Processing.新型冠状病毒肺炎患者入住重症监护病房的临床特征及预后因素:运用机器学习和自然语言处理的回顾性研究
J Med Internet Res. 2020 Oct 28;22(10):e21801. doi: 10.2196/21801.
3
Risk factors for severe outcomes for COVID-19 patients hospitalised in Switzerland during the first pandemic wave, February to August 2020: prospective observational cohort study.2020年2月至8月第一波疫情期间瑞士住院的COVID-19患者出现严重后果的风险因素:前瞻性观察队列研究。
Swiss Med Wkly. 2021 Jul 28;151:w20547. doi: 10.4414/smw.2021.20547. eCollection 2021 Jul 19.
4
The Development and Validation of Simplified Machine Learning Algorithms to Predict Prognosis of Hospitalized Patients With COVID-19: Multicenter, Retrospective Study.中文译文:简化机器学习算法预测 COVID-19 住院患者预后的开发和验证:多中心回顾性研究。
J Med Internet Res. 2022 Jan 21;24(1):e31549. doi: 10.2196/31549.
5
A retrospective cohort study of outcomes in hospitalised COVID-19 patients during the first pandemic wave in Ireland.爱尔兰第一波大流行期间住院 COVID-19 患者结局的回顾性队列研究。
Ir J Med Sci. 2022 Oct;191(5):1973-1983. doi: 10.1007/s11845-021-02753-6. Epub 2021 Nov 19.
6
Angiopoietin-2 as a marker of endothelial activation is a good predictor factor for intensive care unit admission of COVID-19 patients.血管生成素-2 作为内皮细胞激活的标志物,是预测 COVID-19 患者入住重症监护病房的良好预测因子。
Angiogenesis. 2020 Nov;23(4):611-620. doi: 10.1007/s10456-020-09730-0. Epub 2020 May 27.
7
Predictors of Intensive Care Unit admission in patients with coronavirus disease 2019 (COVID-19).2019冠状病毒病(COVID-19)患者入住重症监护病房的预测因素
Monaldi Arch Chest Dis. 2020 Jul 15;90(3). doi: 10.4081/monaldi.2020.1410.
8
Prognostic accuracy of inflammatory markers in predicting risk of ICU admission for COVID-19: application of time-dependent receiver operating characteristic curves.炎症标志物预测 COVID-19 患者 ICU 收治风险的预后准确性:时间依赖性受试者工作特征曲线的应用。
J Int Med Res. 2022 Jun;50(6):3000605221102217. doi: 10.1177/03000605221102217.
9
Predictive Machine Learning Models and Survival Analysis for COVID-19 Prognosis Based on Hematochemical Parameters.基于血液化学参数的 COVID-19 预后预测机器学习模型和生存分析。
Sensors (Basel). 2021 Dec 20;21(24):8503. doi: 10.3390/s21248503.
10
Comparison of prognostic scores for inpatients with COVID-19: a retrospective monocentric cohort study.比较 COVID-19 住院患者预后评分:一项回顾性单中心队列研究。
BMJ Open Respir Res. 2022 Aug;9(1). doi: 10.1136/bmjresp-2022-001340.

引用本文的文献

1
APNet, an explainable sparse deep learning model to discover differentially active drivers of severe COVID-19.APNet,一种可解释的稀疏深度学习模型,用于发现重症新冠肺炎的差异活跃驱动因素。
Bioinformatics. 2025 Mar 4;41(3). doi: 10.1093/bioinformatics/btaf063.
2
Unlocking the Potential of RNA Sequencing in COVID-19: Toward Accurate Diagnosis and Personalized Medicine.解锁RNA测序在新冠病毒肺炎中的潜力:迈向精准诊断与个性化医疗
Diagnostics (Basel). 2025 Jan 20;15(2):229. doi: 10.3390/diagnostics15020229.
3
Alterations of the IKZF1-IKZF2 tandem in immune cells of schizophrenia patients regulate associated phenotypes.

本文引用的文献

1
Evaluating the Immune Response in Treatment-Naive Hospitalised Patients With Influenza and COVID-19.评估治疗初治的住院流感和 COVID-19 患者的免疫反应。
Front Immunol. 2022 May 19;13:853265. doi: 10.3389/fimmu.2022.853265. eCollection 2022.
2
Palmitoylethanolamide (PEA) Inhibits SARS-CoV-2 Entry by Interacting with S Protein and ACE-2 Receptor.棕榈酰乙醇酰胺(PEA)通过与 S 蛋白和 ACE-2 受体相互作用抑制 SARS-CoV-2 进入。
Viruses. 2022 May 17;14(5):1080. doi: 10.3390/v14051080.
3
Blocking EGFR with nimotuzumab: a novel strategy for COVID-19 treatment.
精神分裂症患者免疫细胞中IKZF1 - IKZF2串联体的改变调节相关表型。
J Neuroinflammation. 2024 Dec 18;21(1):326. doi: 10.1186/s12974-024-03320-3.
4
Non-human primate model of long-COVID identifies immune associates of hyperglycemia.长新冠非人类灵长类动物模型鉴定出与高血糖相关的免疫标志物。
Nat Commun. 2024 Aug 20;15(1):6664. doi: 10.1038/s41467-024-50339-4.
5
Donor white blood cell differential is the single largest determinant of whole blood gene expression patterns.供者白细胞分类计数是全血基因表达模式的唯一最大决定因素。
Genomics. 2023 Nov;115(6):110708. doi: 10.1016/j.ygeno.2023.110708. Epub 2023 Sep 18.
6
Systems Biology in Asthma.哮喘中的系统生物学。
Adv Exp Med Biol. 2023;1426:215-235. doi: 10.1007/978-3-031-32259-4_10.
7
Classification of COVID-19 Patients into Clinically Relevant Subsets by a Novel Machine Learning Pipeline Using Transcriptomic Features.基于转录组特征的新型机器学习管道对 COVID-19 患者进行临床相关亚组分类。
Int J Mol Sci. 2023 Mar 3;24(5):4905. doi: 10.3390/ijms24054905.
用尼妥珠单抗阻断表皮生长因子受体:一种治疗新冠肺炎的新策略。
Immunotherapy. 2022 May;14(7):521-530. doi: 10.2217/imt-2022-0027. Epub 2022 Mar 21.
4
Possible therapeutic effects of boron citrate and oleoylethanolamide supplementation in patients with COVID-19: A pilot randomized, double-blind, clinical trial.补充柠檬酸硼和油酰乙醇胺对新冠肺炎患者可能的治疗效果:一项前瞻性随机双盲临床试验
J Trace Elem Med Biol. 2022 May;71:126945. doi: 10.1016/j.jtemb.2022.126945. Epub 2022 Feb 12.
5
Nimotuzumab for COVID-19: case series.尼妥珠单抗治疗新型冠状病毒肺炎:病例系列
Immunotherapy. 2021 Nov 22;14(3):185-193. doi: 10.2217/imt-2021-0269.
6
Nrf2/Keap1/ARE signaling: Towards specific regulation.Nrf2/Keap1/ARE 信号通路:走向特异性调控。
Life Sci. 2022 Feb 15;291:120111. doi: 10.1016/j.lfs.2021.120111. Epub 2021 Oct 31.
7
Tissue Proteomic Analysis Identifies Mechanisms and Stages of Immunopathology in Fatal COVID-19.组织蛋白质组学分析鉴定了致命性 COVID-19 中的免疫病理学机制和阶段。
Am J Respir Cell Mol Biol. 2022 Feb;66(2):196-205. doi: 10.1165/rcmb.2021-0358OC.
8
Ultramicronized Palmitoylethanolamide Inhibits NLRP3 Inflammasome Expression and Pro-Inflammatory Response Activated by SARS-CoV-2 Spike Protein in Cultured Murine Alveolar Macrophages.超微化棕榈酰乙醇胺抑制培养的小鼠肺泡巨噬细胞中NLRP3炎性小体的表达以及由SARS-CoV-2刺突蛋白激活的促炎反应。
Metabolites. 2021 Sep 2;11(9):592. doi: 10.3390/metabo11090592.
9
Management of COVID-19-induced cytokine storm by Keap1-Nrf2 system: a review.KEAP1-Nrf2 系统对 COVID-19 诱导的细胞因子风暴的管理:综述。
Inflammopharmacology. 2021 Oct;29(5):1347-1355. doi: 10.1007/s10787-021-00860-5. Epub 2021 Aug 9.
10
Immune Signature Linked to COVID-19 Severity: A SARS-Score for Personalized Medicine.与 COVID-19 严重程度相关的免疫特征:个性化医学的 SARS 评分。
Front Immunol. 2021 Jul 12;12:701273. doi: 10.3389/fimmu.2021.701273. eCollection 2021.