Evidence map›Paper›PMID 41735888›Full record

ArticleBMC infectious diseases2026

Integration of single-cell and bulk transcriptomics with machine learning identifies LDHA as a lactate-related diagnostic and prognostic biomarker in sepsis.

Zhiying Lin, Hanping Shi, Xiaohong Chen, Chunli Yang

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Article in BMC infectious diseases, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

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4 authors.

Zhiying LinJiangxi Provincial People's Hospital, The First Affiliated Hospital of Nanchang Medical College, No.92 Aiguo Road, Nanchang, Jiangxi Province, 330006, China.
Hanping ShiJiangxi Provincial Key Laboratory of Preventive Medicine, School of Public Health, Nanchang University, Nanchang, Jiangxi, 330006, China.
Xiaohong ChenJiangxi Provincial People's Hospital, The First Affiliated Hospital of Nanchang Medical College, No.92 Aiguo Road, Nanchang, Jiangxi Province, 330006, China.
Chunli YangJiangxi Provincial People's Hospital, The First Affiliated Hospital of Nanchang Medical College, No.92 Aiguo Road, Nanchang, Jiangxi Province, 330006, China. syzzyxk@126.com.

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6 · The paper itself

Abstract

backgroundSepsis-induced metabolic dysregulation, particularly abnormal lactate metabolism, is closely associated with disease severity and mortality. This study aimed to systematically identify lactate-related genes involved in sepsis and evaluate their diagnostic and prognostic value using integrated transcriptomic analyses.

methodsSingle-cell RNA sequencing data were analyzed using AUCell, singscore, and ssGSEA algorithms combined with correlation analysis to identify lactate-related genes. A comprehensive machine learning framework incorporating 131 algorithms was applied for feature selection and construction of a diagnostic model. Survival analyses were performed to assess the prognostic significance of candidate genes. The expression of key genes was further validated by qPCR and western blotting in clinical samples and a sepsis animal model.

resultsSepsis patients were stratified into distinct molecular subgroups exhibiting significant differences in prognosis, clinical characteristics, pathway enrichment, immune infiltration, and immune checkpoint gene expression. Single-cell analysis revealed that MARCO⁺ macrophages exhibited relatively high lactate-related activity compared with most immune populations, while plasma cells showed comparable levels. Sixteen genes were identified at the intersection of macrophage differentially expressed genes and lactate-related genes. Machine learning analysis further identified six core diagnostic genes. Survival analysis demonstrated that high LDHA expression was significantly associated with poor prognosis in sepsis patients. Consistently, elevated LDHA expression was observed in septic animals compared with controls.

conclusionBy integrating single-cell and bulk RNA-seq data, we developed and validated a novel diagnostic model for sepsis, termed the Lacty Model, and identified LDHA as a key biomarker associated with poor prognosis. These findings highlight the potential clinical relevance of lactate metabolism–related genes in sepsis and provide a foundation for future mechanistic and therapeutic studies.

Indexed as

Lactic AcidL-Lactate DehydrogenaseMachine LearningSepsisAnimalsBiomarkersFemaleGene Expression ProfilingHumansMacrophagesMalePrognosisSingle-Cell AnalysisSingle-Cell Gene Expression AnalysisTranscriptomeBiomarkersLactic AcidLDHA protein, humanL-Lactate DehydrogenaseLDHAMachine learning algorithmsRNA-seq dataSepsisSingle-cell sequencing data

Identifiers

PMID41735888
PMCPMC13037293

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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.