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Application value of blood metagenomic next-generation sequencing in patients with connective tissue diseases

OBJECTIVE: This study aimed to analyze the application value of blood metagenomic next-generation sequencing (mNGS) in patients with connective tissue diseases (CTDs) to provide a reference for infection diagnosis and guidance for treatment. METHODS: A total of 126 CTD patients with suspected infect...

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Autores principales: Su, Rui, Yan, Huanhuan, Li, Na, Ding, Tingting, Li, Baochen, Xie, Yuhuan, Gao, Chong, Li, Xiaofeng, Wang, Caihong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9376218/
https://www.ncbi.nlm.nih.gov/pubmed/35979346
http://dx.doi.org/10.3389/fimmu.2022.939057
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author Su, Rui
Yan, Huanhuan
Li, Na
Ding, Tingting
Li, Baochen
Xie, Yuhuan
Gao, Chong
Li, Xiaofeng
Wang, Caihong
author_facet Su, Rui
Yan, Huanhuan
Li, Na
Ding, Tingting
Li, Baochen
Xie, Yuhuan
Gao, Chong
Li, Xiaofeng
Wang, Caihong
author_sort Su, Rui
collection PubMed
description OBJECTIVE: This study aimed to analyze the application value of blood metagenomic next-generation sequencing (mNGS) in patients with connective tissue diseases (CTDs) to provide a reference for infection diagnosis and guidance for treatment. METHODS: A total of 126 CTD patients with suspected infections who were hospitalized in the Department of Rheumatology, the Second Hospital of Shanxi Medical University from January 2020 to December 2021 were enrolled in this study. We retrospectively reviewed the results of mNGS and conventional diagnostic tests (CDTs). RESULTS: Systemic lupus erythematosus (SLE) and polymyositis/dermatomyositis (DM/PM) had the highest incidence of infections. The positive pathogen detection rates of mNGS were higher than those of CDT. The virus infections are the most common type in CTD patients with single or mixed infection, especially Human gammaherpesvirus 4 (EBV), Human betaherpesvirus 5 (CMV), and Human alphaherpesvirus 1. The incidence of prokaryote and eukaryote infections is secondary to viruses. Bloodstream infections of rare pathogens such as Pneumocystis jirovecii should be of concern. Meanwhile, the most common mixed infection was bacterial–virus coinfection. CONCLUSION: mNGS has incremental application value in patients with CTD suspected of co-infection. It has a high sensitivity, and a wide detection range for microorganisms in CTD patients. Furthermore, the high incidence of opportunistic virus infections in CTD patients should be of sufficient concern.
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spelling pubmed-93762182022-08-16 Application value of blood metagenomic next-generation sequencing in patients with connective tissue diseases Su, Rui Yan, Huanhuan Li, Na Ding, Tingting Li, Baochen Xie, Yuhuan Gao, Chong Li, Xiaofeng Wang, Caihong Front Immunol Immunology OBJECTIVE: This study aimed to analyze the application value of blood metagenomic next-generation sequencing (mNGS) in patients with connective tissue diseases (CTDs) to provide a reference for infection diagnosis and guidance for treatment. METHODS: A total of 126 CTD patients with suspected infections who were hospitalized in the Department of Rheumatology, the Second Hospital of Shanxi Medical University from January 2020 to December 2021 were enrolled in this study. We retrospectively reviewed the results of mNGS and conventional diagnostic tests (CDTs). RESULTS: Systemic lupus erythematosus (SLE) and polymyositis/dermatomyositis (DM/PM) had the highest incidence of infections. The positive pathogen detection rates of mNGS were higher than those of CDT. The virus infections are the most common type in CTD patients with single or mixed infection, especially Human gammaherpesvirus 4 (EBV), Human betaherpesvirus 5 (CMV), and Human alphaherpesvirus 1. The incidence of prokaryote and eukaryote infections is secondary to viruses. Bloodstream infections of rare pathogens such as Pneumocystis jirovecii should be of concern. Meanwhile, the most common mixed infection was bacterial–virus coinfection. CONCLUSION: mNGS has incremental application value in patients with CTD suspected of co-infection. It has a high sensitivity, and a wide detection range for microorganisms in CTD patients. Furthermore, the high incidence of opportunistic virus infections in CTD patients should be of sufficient concern. Frontiers Media S.A. 2022-08-01 /pmc/articles/PMC9376218/ /pubmed/35979346 http://dx.doi.org/10.3389/fimmu.2022.939057 Text en Copyright © 2022 Su, Yan, Li, Ding, Li, Xie, Gao, Li and Wang https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Immunology
Su, Rui
Yan, Huanhuan
Li, Na
Ding, Tingting
Li, Baochen
Xie, Yuhuan
Gao, Chong
Li, Xiaofeng
Wang, Caihong
Application value of blood metagenomic next-generation sequencing in patients with connective tissue diseases
title Application value of blood metagenomic next-generation sequencing in patients with connective tissue diseases
title_full Application value of blood metagenomic next-generation sequencing in patients with connective tissue diseases
title_fullStr Application value of blood metagenomic next-generation sequencing in patients with connective tissue diseases
title_full_unstemmed Application value of blood metagenomic next-generation sequencing in patients with connective tissue diseases
title_short Application value of blood metagenomic next-generation sequencing in patients with connective tissue diseases
title_sort application value of blood metagenomic next-generation sequencing in patients with connective tissue diseases
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9376218/
https://www.ncbi.nlm.nih.gov/pubmed/35979346
http://dx.doi.org/10.3389/fimmu.2022.939057
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