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支气管肺泡灌洗液体宏基因组学下一代测序对疑似肺部感染患者诊断和管理的影响

The impact of bronchoalveolar lavage fluid metagenomics next-generation sequencing on the diagnosis and management of patients with suspected pulmonary infection.

作者信息

Zhou Mei, Sun Shengwen, Chen Long, Xu Huan, Liu Lanlan, Lv Jiaxi, Zhang Jianchu, Xiong Xianzhi

机构信息

Department of Respiratory and Critical Care Medicine, NHC Key Laboratory of Pulmonary Diseases, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, Hubei, China.

Department of Critical Care Medicine, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, Hubei, China.

出版信息

Front Cell Infect Microbiol. 2025 Jun 23;15:1521641. doi: 10.3389/fcimb.2025.1521641. eCollection 2025.


DOI:10.3389/fcimb.2025.1521641
PMID:40625833
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12230576/
Abstract

OBJECTIVES: This study aimed to enhance the comprehension of the practical utility of bronchoalveolar lavage fluid (BALF) metagenomic next-generation sequencing (mNGS) in the clinical management of patients with suspected pneumonia. METHODS: We retrospectively analyzed 296 individuals who underwent BALF mNGS and conventional microbial tests (CMTs) for suspected pneumonia. We compared the clinical characteristics between patients with pulmonary infection (PI) and those without pulmonary infection (NPI). The detection rate of mNGS and CMTs in different groups of patients were compared. The Sankey diagram was used to present the results of the influence of mNGS on diagnosis and treatment. RESULTS: Comparison between PI and NPI showed that individuals with fever, concurrent malignant tumors, consolidation or ground-glass opacity on chest CT(Computed tomography) images, and elevated inflammatory markers on blood tests were more likely to develop lung infections. Analysis of the rate of positive detection between CMTs and mNGS in various subgroups revealed that mNGS had a significantly higher positive detection rate in patients with pulmonary infections (87.95% vs. 71.06%, p<0.001), in immunocompetent patients (86.91% vs. 68.08%, p<0.001), and in patients with malignant tumors (92.31% vs. 69.23%, p=0.035). Furthermore, mNGS helped initiate appropriate antibiotic treatment and confirmed the effectiveness of empirical treatment. Compared to immunocompetent patients, BALF mNGS in immunocompromised individuals with suspected lung infections yielded higher rates of accurate diagnosis (62.86% vs. 42.79%, p = 0.027) and more effective treatment (71.43% vs. 58.56%, p = 0.148). CONCLUSIONS: BALF mNGS identified a greater variety of pathogens than CMTs. Immunocompromised patients with suspected pneumonia may benefit more from BALF mNGS.

摘要

目的:本研究旨在提高对支气管肺泡灌洗术(BALF)宏基因组下一代测序(mNGS)在疑似肺炎患者临床管理中的实际应用的理解。 方法:我们回顾性分析了296例因疑似肺炎接受BALF mNGS和传统微生物检测(CMTs)的个体。我们比较了肺部感染(PI)患者和无肺部感染(NPI)患者的临床特征。比较了不同组患者中mNGS和CMTs的检测率。使用桑基图展示mNGS对诊断和治疗影响的结果。 结果:PI组和NPI组的比较表明,发热、并发恶性肿瘤、胸部CT(计算机断层扫描)图像上有实变或磨玻璃影以及血液检查中炎症标志物升高的个体更易发生肺部感染。对各亚组中CMTs和mNGS的阳性检出率分析显示,mNGS在肺部感染患者(87.95%对71.06%,p<0.001)、免疫功能正常患者(86.91%对68.08%,p<0.001)和恶性肿瘤患者(92.31%对69.23%,p = 0.035)中的阳性检出率显著更高。此外,mNGS有助于启动适当的抗生素治疗并证实经验性治疗的有效性。与免疫功能正常患者相比,疑似肺部感染的免疫功能低下个体的BALF mNGS诊断准确率更高(62.86%对42.79%,p = 0.027),治疗效果更好(71.43%对58.56%,p = 0.148)。 结论:BALF mNGS比CMTs能鉴定出更多种类的病原体。疑似肺炎的免疫功能低下患者可能从BALF mNGS中获益更多。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6527/12230576/9fada940db48/fcimb-15-1521641-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6527/12230576/3e0a09c2a569/fcimb-15-1521641-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6527/12230576/5d60d79f4183/fcimb-15-1521641-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6527/12230576/8a53906e0399/fcimb-15-1521641-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6527/12230576/9fada940db48/fcimb-15-1521641-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6527/12230576/3e0a09c2a569/fcimb-15-1521641-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6527/12230576/5d60d79f4183/fcimb-15-1521641-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6527/12230576/8a53906e0399/fcimb-15-1521641-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6527/12230576/9fada940db48/fcimb-15-1521641-g004.jpg

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本文引用的文献

[1]
Metagenomic versus targeted next-generation sequencing for detection of microorganisms in bronchoalveolar lavage fluid among renal transplantation recipients.

Front Immunol. 2024

[2]
Clinical applications of metagenomics next-generation sequencing in infectious diseases.

J Zhejiang Univ Sci B. 2024-5-17

[3]
Epidemiological and clinical characteristics of psittacosis among cases with complicated or atypical pulmonary infection using metagenomic next-generation sequencing: a multi-center observational study in China.

Ann Clin Microbiol Antimicrob. 2023-9-7

[4]
Metagenomic Next-Generation Sequencing for Pathogens in Bronchoalveolar Lavage Fluid Improves the Survival of Patients with Pulmonary Complications After Allogeneic Hematopoietic Stem Cell Transplantation.

Infect Dis Ther. 2023-8

[5]
Metagenomic next-generation sequencing for rapid detection of pulmonary infection in patients with acquired immunodeficiency syndrome.

Ann Clin Microbiol Antimicrob. 2023-7-10

[6]
Metagenomic next-generation sequencing confirms the diagnosis of pneumonia with rhabdomyolysis and acute kidney injury in a limited resource area: a case report and review.

Front Public Health. 2023

[7]
Microbiological diagnostic performance of metagenomic next-generation sequencing compared with conventional culture for patients with community-acquired pneumonia.

Front Cell Infect Microbiol. 2023

[8]
The Real-World Clinical Impact of Plasma mNGS Testing: an Observational Study.

Microbiol Spectr. 2023-3-22

[9]
Rapid diagnosis of non-tuberculous mycobacterial pulmonary diseases by metagenomic next-generation sequencing in non-referral hospitals.

Front Cell Infect Microbiol. 2022

[10]
Metagenomic next-generation sequencing for the diagnosis of Pneumocystis jirovecii Pneumonia in critically pediatric patients.

Ann Clin Microbiol Antimicrob. 2023-1-16

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