• 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

基于宏基因组二代测序的成人斯蒂尔病与脓毒症患者血液微生物组分析。

Analysis of blood microbiota in patients with adult-onset Still's disease and sepsis by metagenomic next-generation sequencing.

机构信息

Department of Rheumatology and Immunology, The Affiliated Hospital of Xuzhou Medical University, Xuzhou, Jiangsu, China.

出版信息

Br J Hosp Med (Lond). 2024 Jul 30;85(7):1-16. doi: 10.12968/hmed.2024.0121.

DOI:10.12968/hmed.2024.0121
PMID:39078906
Abstract

Adult-onset Still's disease (AOSD) shares similar clinical symptoms with sepsis. Thus, differentiating between AOSD and sepsis presents a great challenge while making diagnosis. This study aimed to analyse the changes in blood microbiota related to AOSD and sepsis using metagenomic next-generation sequencing (mNGS), identify potential biomarkers that distinguish AOSD from sepsis, and explore the diagnostic value of mNGS in differentiation between these two pathological conditions. Clinical data of four AOSD patients and four sepsis patients treated in the Department of Rheumatology and Immunology, The Affiliated Hospital of Xuzhou Medical University between October 2021 and February 2022 were collected. The mNGS diagnostic records of these patients were analysed for microbial correlations in terms of species taxonomic structure and beta diversity by comparing blood microbiota between AOSD and sepsis. The biomarkers with the strongest capability in distinguishing the subgroups were screened using a random forest algorithm. There was no statistically significant differences between AOSD patients and sepsis controls in terms of gender and age ( > 0.05). A total of 91 operational taxonomic units (OTUs) were obtained. At the level of phylum, , and were present in high abundances in both groups (79.76%, 14.18% and 3.30% vs 54.03%, 32.77% and 5.81%). At the genus level, the abundances of , and were the top three highest in the AOSD group (73.88%, 10.92% and 5.48%), while , and were ranked as the top three in the sepsis group in term of abundance (48.69%, 27.36% and 5.52%). In beta-diversity analysis, there were advances shown in visual principal coordinates analysis (PCoA) and non-metric multidimensional scaling (NMDS) between the AOSD group and sepsis group ( < 0.05), with little significant differences in the analysis of similarities (Anosim) ( > 0.05). Linear discriminant analysis effect size (LEfSe) showed that , , , , , , , , , , , and were more enriched in sepsis group ( < 0.05). The top five variables with the strongest capability in distinguishing between AOSD and sepsis were , , , and . The blood microorganisms in AOSD were different from sepsis, and mNGS was potential to distinguish between AOSD and sepsis.

摘要

成人斯蒂尔病(AOSD)与脓毒症具有相似的临床症状。因此,在诊断时,区分 AOSD 和脓毒症具有很大的挑战性。本研究旨在通过宏基因组下一代测序(mNGS)分析与 AOSD 和脓毒症相关的血液微生物群的变化,确定区分 AOSD 和脓毒症的潜在生物标志物,并探讨 mNGS 在区分这两种病理状况中的诊断价值。 收集了 2021 年 10 月至 2022 年 2 月在徐州医科大学附属医院风湿免疫科治疗的 4 例 AOSD 患者和 4 例脓毒症患者的临床资料。通过比较 AOSD 和脓毒症患者的血液微生物群,从物种分类结构和β多样性方面分析 mNGS 诊断记录中与微生物相关的信息。使用随机森林算法筛选区分亚组能力最强的生物标志物。 AOSD 患者和脓毒症对照组在性别和年龄方面无统计学差异(>0.05)。共获得 91 个操作分类单元(OTUs)。在门水平上,两组中均存在高丰度的 、 和 (79.76%、14.18%和 3.30%比 54.03%、32.77%和 5.81%)。在属水平上,AOSD 组中丰度最高的前三种菌属为 、 和 (73.88%、10.92%和 5.48%),而脓毒症组中丰度最高的前三种菌属为 、 和 (48.69%、27.36%和 5.52%)。在β多样性分析中,AOSD 组和脓毒症组在可视主坐标分析(PCoA)和非度量多维尺度分析(NMDS)中表现出明显差异(<0.05),相似性分析(Anosim)(>0.05)无显著差异。线性判别分析效应量(LEfSe)显示, 、 、 、 、 、 、 、 、 、 和 在脓毒症组中更为丰富(<0.05)。区分 AOSD 和脓毒症能力最强的前五个变量为 、 、 、 和 。 AOSD 的血液微生物与脓毒症不同,mNGS 有可能区分 AOSD 和脓毒症。

相似文献

1
Analysis of blood microbiota in patients with adult-onset Still's disease and sepsis by metagenomic next-generation sequencing.基于宏基因组二代测序的成人斯蒂尔病与脓毒症患者血液微生物组分析。
Br J Hosp Med (Lond). 2024 Jul 30;85(7):1-16. doi: 10.12968/hmed.2024.0121.
2
Plasma microRNA Profiles as a Potential Biomarker in Differentiating Adult-Onset Still's Disease From Sepsis.血浆 microRNA 谱作为鉴别成人Still 病与脓毒症的潜在生物标志物。
Front Immunol. 2019 Jan 11;9:3099. doi: 10.3389/fimmu.2018.03099. eCollection 2018.
3
Serum Heparin-Binding Protein as a Potential Biomarker to Distinguish Adult-Onset Still's Disease From Sepsis.血清肝素结合蛋白作为鉴别成人Still 病与脓毒症的潜在生物标志物。
Front Immunol. 2021 Mar 31;12:654811. doi: 10.3389/fimmu.2021.654811. eCollection 2021.
4
Biomarker screening and validation for the differentiation of bloodstream infection from adult-onset Still's disease: A prospective cohort study.生物标志物筛选和验证用于区分血流感染与成人Still 病:一项前瞻性队列研究。
Cytokine. 2021 Oct;146:155642. doi: 10.1016/j.cyto.2021.155642. Epub 2021 Jul 26.
5
Red blood cell distribution width is useful in discriminating adult onset Still's disease and sepsis within 24 hours after hospitalization.红细胞分布宽度有助于在住院后 24 小时内鉴别成人Still 病和脓毒症。
Korean J Intern Med. 2018 Nov;33(6):1234-1240. doi: 10.3904/kjim.2016.068. Epub 2017 Aug 25.
6
Interleukin 18: a biomarker for differential diagnosis between adult-onset Still's disease and sepsis.白细胞介素18:成人斯蒂尔病与脓毒症鉴别诊断的生物标志物
J Rheumatol. 2014 Jun;41(6):1118-23. doi: 10.3899/jrheum.130575. Epub 2014 May 1.
7
Interleukin-18 and fibroblast growth factor 2 in combination is a useful diagnostic biomarker to distinguish adult-onset Still's disease from sepsis.白细胞介素-18 和成纤维细胞生长因子 2 的联合应用是一种有用的诊断生物标志物,可用于区分成人Still 病和脓毒症。
Arthritis Res Ther. 2020 May 7;22(1):108. doi: 10.1186/s13075-020-02200-4.
8
Usefulness of Interleukin-18 as a Diagnostic Biomarker to Differentiate Adult-Onset Still's Disease With/Without Macrophage Activation Syndrome From Other Secondary Hemophagocytic Lymphohistiocytosis in Adults.白细胞介素-18 作为一种诊断生物标志物在成人发病Still 病伴/不伴巨噬细胞活化综合征与其他成人继发性噬血细胞性淋巴组织细胞增生症中的鉴别作用。
Front Immunol. 2021 Oct 8;12:750114. doi: 10.3389/fimmu.2021.750114. eCollection 2021.
9
Clinical manifestations but not cytokine profiles differentiate adult-onset Still's disease and sepsis.临床表现而非细胞因子谱可区分成人斯蒂尔病和脓毒症。
J Rheumatol. 2010 Nov;37(11):2369-76. doi: 10.3899/jrheum.100247. Epub 2010 Sep 1.
10
Establishment of a differential diagnosis method and an online prediction platform for AOSD and sepsis based on gradient boosting decision trees algorithm.基于梯度提升决策树算法的 AOSD 和脓毒症鉴别诊断方法的建立和在线预测平台。
Arthritis Res Ther. 2023 Nov 16;25(1):220. doi: 10.1186/s13075-023-03207-3.