Evidence map›Paper›PMID 39266570›Full record

ArticleNPJ biofilms and microbiomes2024

Integrating respiratory microbiome and host immune response through machine learning for respiratory tract infection diagnosis.

Hongbin Chen, Tianqi Qi, Siyu Guo, Xiaoyang Zhang, Minghua Zhan, Si Liu, Yuyao Yin, Yifan Guo, Yawei Zhang, Chunjiang Zhao and 2 more

Erratum issuedAbstract read
In one paragraph

Article in NPJ biofilms and microbiomes, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

7 citing papers in PubMed.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

12 authors.

Hongbin Chen *Department of Clinical Laboratory, Peking University People's Hospital, Beijing, P. R. China. chenhongbin_pkuph@163.com.ORCID http://orcid.org/0000-0001-5071-2768
Tianqi Qi *Department of Clinical Laboratory, Aerospace Center Hospital, Beijing, P. R. China.
Siyu GuoDepartment of Clinical Laboratory, Peking University People's Hospital, Beijing, P. R. China.
Xiaoyang ZhangDepartment of Clinical Laboratory, Peking University People's Hospital, Beijing, P. R. China.
Minghua ZhanDepartment of Clinical Laboratory, Peking University People's Hospital, Beijing, P. R. China.
Si LiuDepartment of Clinical Laboratory, Peking University People's Hospital, Beijing, P. R. China.
Yuyao YinDepartment of Clinical Laboratory, Peking University People's Hospital, Beijing, P. R. China.
Yifan GuoDepartment of Clinical Laboratory, Peking University People's Hospital, Beijing, P. R. China.
Yawei ZhangDepartment of Clinical Laboratory, Peking University People's Hospital, Beijing, P. R. China.
Chunjiang ZhaoDepartment of Clinical Laboratory, Peking University People's Hospital, Beijing, P. R. China.
Xiaojuan WangDepartment of Clinical Laboratory, Peking University People's Hospital, Beijing, P. R. China.
Hui WangDepartment of Clinical Laboratory, Peking University People's Hospital, Beijing, P. R. China. whuibj@163.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

At present, the diagnosis of lower respiratory tract infections (LRTIs) is difficult, and there is an urgent need for better diagnostic methods. This study enrolled 136 patients from 2020 to 2021 and collected bronchoalveolar lavage fluid (BALF) specimens. We used metatranscriptome to analyze the lower respiratory tract microbiome (LRTM) and host immune response. The diversity of the LRTM in LRTIs significantly decreased, manifested by a decrease in the abundance of normal microbiota and an increase in the abundance of opportunistic pathogens. The upregulated differentially expressed genes (DEGs) in the LRTIs group were mainly enriched in infection immune response-related pathways. Klebsiella pneumoniae had the most significant increase in abundance in LRTIs, which was strongly correlated with host infection or inflammation genes TNFRSF1B, CSF3R, and IL6R. We combined LRTM and host transcriptome data to construct a machine-learning model with 12 screened features to discriminate LRTIs and non-LRTIs. The results showed that the model trained by Random Forest in the validate set had the best performance (ROC AUC: 0.937, 95% CI: 0.832-1). The independent external dataset showed an accuracy of 76.5% for this model. This study suggests that the model integrating LRTM and host transcriptome data can be an effective tool for LRTIs diagnosis.

Indexed as

Bronchoalveolar Lavage FluidMachine LearningMicrobiotaRespiratory Tract InfectionsAdultAgedFemaleHumansKlebsiella pneumoniaeMaleMiddle AgedTranscriptome

Identifiers

PMID39266570
PMCPMC11393347

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.