Metagenomic next-generation sequencing of plasma cell-free DNA improves the early diagnosis of suspected infections

Abstract Background Metagenomic next-generation sequencing (mNGS) could improve the diagnosed efficiency of pathogens in bloodstream infections or sepsis. Little is known about the clinical impact of mNGS test when used for the early diagnosis of suspected infections. Herein, our main objective was...

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Main Authors: Hui Zhang, Ruobing Liang, Yunzhu Zhu, Lifen Hu, Han Xia, Jiabin Li, Ying Ye
Format: Article
Language:English
Published: BMC 2024-02-01
Series:BMC Infectious Diseases
Subjects:
Online Access:https://doi.org/10.1186/s12879-024-09043-3
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author Hui Zhang
Ruobing Liang
Yunzhu Zhu
Lifen Hu
Han Xia
Jiabin Li
Ying Ye
author_facet Hui Zhang
Ruobing Liang
Yunzhu Zhu
Lifen Hu
Han Xia
Jiabin Li
Ying Ye
author_sort Hui Zhang
collection DOAJ
description Abstract Background Metagenomic next-generation sequencing (mNGS) could improve the diagnosed efficiency of pathogens in bloodstream infections or sepsis. Little is known about the clinical impact of mNGS test when used for the early diagnosis of suspected infections. Herein, our main objective was to assess the clinical efficacy of utilizing blood samples to perform mNGS for early diagnosis of suspected infections, as well as to evaluate its potential in guiding antimicrobial therapy decisions. Methods In this study, 212 adult hospitalized patients who underwent blood mNGS test in the early stage of suspected infections were enrolled. Diagnostic efficacy of mNGS test and blood culture was compared, and the clinical impact of mNGS on clinical care was analyzed. Results In our study, the total detection rate of blood mNGS was significantly higher than that of culture method (74.4% vs. 12.1%, P < 0.001) in the paired mNGS test and blood culture. Blood stream infection (107, 67.3%) comprised the largest component of all the diseases in our patients, and the detection rate of single blood sample subgroup was similar with that of multiple type of samples subgroup. Among the 187 patients complained with fever, there was no difference in the diagnostic efficacy of mNGS when blood specimens or additional other specimens were used in cases presenting only with fever. While, when patients had other symptoms except fever, the performance of mNGS was superior in cases with specimens of suspected infected sites and blood collected at the same time. Guided by mNGS results, therapeutic regimens for 70.3% cases (149/212) were changed, and the average hospitalized days were significantly shortened in cases with the earlier sampling time of admission. Conclusion In this study, we emphasized the importance of blood mNGS in early infectious patients with mild and non-specific symptoms. Blood mNGS can be used as a supplement to conventional laboratory examination, and should be performed as soon as possible to guide clinicians to perform appropriate anti-infection treatment timely and effectively. Additionally, combining the contemporaneous samples from suspected infection sites could improve disease diagnosis and prognoses. Further research needs to be better validated in large-scale clinical trials to optimize diagnostic protocol, and the cost-utility analysis should be performed.
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spelling doaj.art-45496a3a1b504510b16c0ff4050a936e2024-03-05T17:48:38ZengBMCBMC Infectious Diseases1471-23342024-02-0124111110.1186/s12879-024-09043-3Metagenomic next-generation sequencing of plasma cell-free DNA improves the early diagnosis of suspected infectionsHui Zhang0Ruobing Liang1Yunzhu Zhu2Lifen Hu3Han Xia4Jiabin Li5Ying Ye6Department of Infectious Diseases, The First Affiliated Hospital of Anhui Medical UniversityDepartment of Scientific Affaires, Hugobiotech Co., LtdDepartment of Infectious Diseases, The First Affiliated Hospital of Anhui Medical UniversityDepartment of Infectious Diseases, The First Affiliated Hospital of Anhui Medical UniversityDepartment of Scientific Affaires, Hugobiotech Co., LtdDepartment of Infectious Diseases, The First Affiliated Hospital of Anhui Medical UniversityDepartment of Infectious Diseases, The First Affiliated Hospital of Anhui Medical UniversityAbstract Background Metagenomic next-generation sequencing (mNGS) could improve the diagnosed efficiency of pathogens in bloodstream infections or sepsis. Little is known about the clinical impact of mNGS test when used for the early diagnosis of suspected infections. Herein, our main objective was to assess the clinical efficacy of utilizing blood samples to perform mNGS for early diagnosis of suspected infections, as well as to evaluate its potential in guiding antimicrobial therapy decisions. Methods In this study, 212 adult hospitalized patients who underwent blood mNGS test in the early stage of suspected infections were enrolled. Diagnostic efficacy of mNGS test and blood culture was compared, and the clinical impact of mNGS on clinical care was analyzed. Results In our study, the total detection rate of blood mNGS was significantly higher than that of culture method (74.4% vs. 12.1%, P < 0.001) in the paired mNGS test and blood culture. Blood stream infection (107, 67.3%) comprised the largest component of all the diseases in our patients, and the detection rate of single blood sample subgroup was similar with that of multiple type of samples subgroup. Among the 187 patients complained with fever, there was no difference in the diagnostic efficacy of mNGS when blood specimens or additional other specimens were used in cases presenting only with fever. While, when patients had other symptoms except fever, the performance of mNGS was superior in cases with specimens of suspected infected sites and blood collected at the same time. Guided by mNGS results, therapeutic regimens for 70.3% cases (149/212) were changed, and the average hospitalized days were significantly shortened in cases with the earlier sampling time of admission. Conclusion In this study, we emphasized the importance of blood mNGS in early infectious patients with mild and non-specific symptoms. Blood mNGS can be used as a supplement to conventional laboratory examination, and should be performed as soon as possible to guide clinicians to perform appropriate anti-infection treatment timely and effectively. Additionally, combining the contemporaneous samples from suspected infection sites could improve disease diagnosis and prognoses. Further research needs to be better validated in large-scale clinical trials to optimize diagnostic protocol, and the cost-utility analysis should be performed.https://doi.org/10.1186/s12879-024-09043-3Plasma cell-free DNAMetagenomic next-generation sequencingEarly diagnosisSuspected infectionsFebrile illness
spellingShingle Hui Zhang
Ruobing Liang
Yunzhu Zhu
Lifen Hu
Han Xia
Jiabin Li
Ying Ye
Metagenomic next-generation sequencing of plasma cell-free DNA improves the early diagnosis of suspected infections
BMC Infectious Diseases
Plasma cell-free DNA
Metagenomic next-generation sequencing
Early diagnosis
Suspected infections
Febrile illness
title Metagenomic next-generation sequencing of plasma cell-free DNA improves the early diagnosis of suspected infections
title_full Metagenomic next-generation sequencing of plasma cell-free DNA improves the early diagnosis of suspected infections
title_fullStr Metagenomic next-generation sequencing of plasma cell-free DNA improves the early diagnosis of suspected infections
title_full_unstemmed Metagenomic next-generation sequencing of plasma cell-free DNA improves the early diagnosis of suspected infections
title_short Metagenomic next-generation sequencing of plasma cell-free DNA improves the early diagnosis of suspected infections
title_sort metagenomic next generation sequencing of plasma cell free dna improves the early diagnosis of suspected infections
topic Plasma cell-free DNA
Metagenomic next-generation sequencing
Early diagnosis
Suspected infections
Febrile illness
url https://doi.org/10.1186/s12879-024-09043-3
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