# Multi-modal data to identify key factors influencing lung injury in ARDS patients undergoing invasive mechanical ventilation: A prospective multi-center observational study protocol

**Authors:** Zhimei Duan, Di Lian, Kaifei Wang, Ye Hu, Han Fu, Ruoxuan Wen, Ying Zhao, Xingshuo Hu, Pan Pan, Jianqiao Xu, Jin Chen, Li Xiao, Lin Wang, Xiao Yu, Xiaobo Han, Wuxiang Xie, Fei Xie, Lixin Xie, Zhihai Han

PMC · DOI: 10.1371/journal.pone.0332985 · PLOS One · 2026-01-23

## TL;DR

This study aims to uncover key factors influencing lung injury in ARDS patients through multi-modal data analysis to improve precision medicine.

## Contribution

The study introduces a novel approach combining multi-omics data and clinical monitoring to identify ARDS subtypes and biomarkers.

## Key findings

- Multi-omics data will be analyzed to identify specific markers and risk factors for ARDS clinical trajectories.
- The study will reveal critical immune cell subtypes influencing ARDS onset and prognosis.
- Predictive models will be developed to identify core prognostic markers for ARDS patients.

## Abstract

Patients with moderate to severe acute respiratory distress syndrome (ARDS) exhibit extremely poor prognoses following mechanical ventilation, with mortality rates as high as 40% to 55%. Despite extensive research into ARDS classification and prognostic assessment, the disease’s pathogenesis remains incompletely understood, and there remains a critical lack of specific biomarkers and effective therapeutic targets for its prevention and management. The core challenges lie in two key areas. First, ARDS demonstrates marked heterogeneity in etiology, pathophysiology, and pathogenesis. Existing research, predominantly reliant on population-level average data, fails to capture inter-individual variability, hindering the precise identification of patient subgroups responsive to specific therapeutic regimens. Second, current definitions of ARDS phenotypes are often confined to clinical symptoms and routine diagnostic indices, lacking integrated analysis of deeper mechanistic indicators, such as key biomarkers and respiratory mechanics parameters, thereby limiting the stability and clinical utility of existing classification systems.

We designed a prospective multicenter cohort study incorporating multi-omics analyses. This research aims to investigate the mechanisms underlying the development and progression of ARDS during mechanical ventilation, providing a theoretical foundation and practical guidance for future ARDS therapies. The study plans to enroll over 165 patients with moderate to severe ARDS receiving mechanical ventilation across 10 medical centers. Peripheral blood and bronchoalveolar lavage fluid (BALF) samples will be collected on the first 24 hours after enrollment and at extubation for metagenomic/meta-transcriptomic sequencing, bulk RNA sequencing, single-cell RNA sequencing, proteomics detection, and metabolomics analyses. Concurrently, comprehensive monitoring of physiological indices, electrical impedance tomography, transpulmonary pressure, pulmonary ultrasound findings, and other relevant parameters will be conducted during the enrollment. Study participants will be stratified by survival and mortality outcomes to analyze the dynamic trends of all measured indices and their underlying molecular mechanisms. Biomarkers derived from multi-omics data and clinical baseline characteristics will be evaluated and integrated, followed by multidimensional dimensionality reduction. Predictive models will be subsequently constructed via early or late fusion to identify core prognostic markers, with performance validated using standardized metrics.

Through comparative analysis of multi-omics data, we aim to identify specific markers and risk factors associated with distinct clinical trajectories of ARDS, further clarifying the key determinants of lung injury. Ultimately, this research will reveal critical immune cell subtypes that govern ARDS onset and prognosis, offering novel insights and therapeutic targets to advance precision medicine for ARDS.

ClinicalTrials.gov NCT05922826.

## Linked entities

- **Diseases:** acute respiratory distress syndrome (MONDO:0006502), ARDS (MONDO:0006502)

## Full-text entities

- **Genes:** GSK3B (glycogen synthase kinase 3 beta) [NCBI Gene 2932], TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}, METTL16 (methyltransferase 16, RNA N6-adenosine) [NCBI Gene 79066] {aka METT10D}, EP300 (EP300 lysine acetyltransferase) [NCBI Gene 2033] {aka KAT3B, MKHK2, RSTS2, p300}, ELAVL1 (ELAV like RNA binding protein 1) [NCBI Gene 1994] {aka ELAV1, HUR, Hua, MelG}, CREBBP (CREB binding lysine acetyltransferase) [NCBI Gene 1387] {aka CBP, KAT3A, MKHK1, RSTS, RSTS1}, IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}, CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}, MYD88 (MYD88 innate immune signal transduction adaptor) [NCBI Gene 4615] {aka IMD68, MYD88D, WM1}, FTO (FTO alpha-ketoglutarate dependent dioxygenase) [NCBI Gene 79068] {aka ALKBH9, BMIQ14, GDFD, IFEX9}
- **Diseases:** ARDS (MESH:D012128), burns (MESH:D002056), pleural fistula (MESH:D010995), kidney disease (MESH:D007674), shock (MESH:D012769), lung opacity (MESH:D008171), pleural effusion (MESH:D010996), inflammation (MESH:D007249), atelectasis (MESH:D001261), pneumonia (MESH:D011014), diabetes (MESH:D003920), severe acute respiratory distress syndrome (MESH:D045169), COVID-19 (MESH:D000086382), trauma (MESH:D014947), heart failure (MESH:D006333), pneumothorax (MESH:D011030), death (MESH:D003643), coronary heart disease (MESH:D003327), aspiration (MESH:D011015), hypoxia (MESH:D000860), respiratory failure (MESH:D012131), infectious disease (MESH:D003141), SOFA (MESH:D009102), coagulation (MESH:D001778), cancer (MESH:D009369), intracranial hypertension (MESH:D019586), hepatopathy (MESH:D020754), autoimmunity disease (MESH:D001327), pulmonary edema (MESH:D011654), acute coronary syndrome (MESH:D054058), cardiogenic (MESH:D013575), infection (MESH:D007239), subcutaneous emphysema (MESH:D013352), cerebrovascular disease (MESH:D002561), Failure (MESH:D051437), pulmonary infiltrates (MESH:D017254), lung injury (MESH:D055370), hypertension (MESH:D006973)
- **Chemicals:** lipopolysaccharide (MESH:D008070), noradrenaline (MESH:D009638), proline (MESH:D011392), isoleucine (MESH:D007532), oxygen (MESH:D010100), EP (-), Trizol (MESH:C411644), glucose (MESH:D005947), leucine (MESH:D007930)
- **Species:** Homo sapiens (human, species) [taxon 9606]
- **Mutations:** rs1800796, rs1800629, rs7744

## Full text

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## References

32 references — full list in the complete paper: https://tomesphere.com/paper/PMC12829816/full.md

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Source: https://tomesphere.com/paper/PMC12829816