Evidence map›Paper›PMID 40487315›Full record

ArticleFrontiers in cellular and infection microbiology2025

Development of a four autophagy-related gene signature for active tuberculosis diagnosis.

Baoyan Ren, Feng Jia, Qixun Fang, Jingping Xu, Kangfeng Lin, Renhui Huang, Zhenqiong Liu, Xingan Xing

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Article in Frontiers in cellular and infection microbiology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

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3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Baoyan RenYaneng Bioscience Co. Ltd., Shenzhen, Guangdong, China.
Feng JiaDepartment of Clinical Laboratory, Jiangxi Provincial Chest Hospital, Nanchang, Jiangxi, China.
Qixun FangYaneng Bioscience Co. Ltd., Shenzhen, Guangdong, China.
Jingping XuYaneng Bioscience Co. Ltd., Shenzhen, Guangdong, China.
Kangfeng LinYaneng Bioscience Co. Ltd., Shenzhen, Guangdong, China.
Renhui HuangYaneng Bioscience Co. Ltd., Shenzhen, Guangdong, China.
Zhenqiong LiuDepartment of Clinical Laboratory, Jiangxi Provincial Chest Hospital, Nanchang, Jiangxi, China.
Xingan XingYaneng Bioscience Co. Ltd., Shenzhen, Guangdong, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Tuberculosis (TB) diagnostics urgently require non-sputum biomarkers to address the limitations of conventional methods in distinguishing active TB (ATB) from latent infection (LTBI), healthy controls (HCs), and TB-mimicking diseases (ODs, other diseases). Methods: Transcriptomic data from GSE83456 and GSE152532 were combined to form the selection dataset. Marker genes were identified from differentially expressed autophagy-related genes using a Random Forest classifier. The optimal gene signature was selected based on optimal performance through a linear Support Vector Machine (SVM) classifier with cross-validation. The signature was subsequently evaluated in six independent evaluation datasets and validated using whole blood samples collected from 70 participants. Results: We identified a novel four-gene autophagy-related signature ( Conclusions: Our findings yielded a four-gene signature in whole blood that is robustly diagnostic for ATB, validated across multiple evaluation datasets and clinical samples. The autophagy-driven specificity and PCR-compatible design of this signature offer a blood-based, cost-effective strategy to enhance TB detection, addressing WHO-aligned diagnostic needs.

Indexed as

AutophagyTuberculosisAdultBiomarkersFemaleGene Expression ProfilingHumansLatent TuberculosisMaleMycobacterium tuberculosisROC CurveSensitivity and SpecificitySupport Vector MachineTranscriptomeBiomarkersautophagydiagnosissignaturetuberculosiswhole blood

Identifiers

PMID40487315
PMCPMC12141863

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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.