Evidence mapPaperPMID 41580828Full record

ReviewRespiratory research2026

Gut microbiota and metabolites in acute lung injury: mechanisms and therapeutic perspectives.

Shuyuan Yi, Xiaoli Zhuang, Lan Luo, Lin Fu, Ziyuan Dong, Kan Wang, Yu Jiang, Xiaofang Yang, Feilong Hei

Abstract readReview
In one paragraph

Review in Respiratory research, 2026. 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

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

3 citing papers in PubMed.

  1. Frontiers in microbiology · 2026
    Article
  2. Review
  3. Review
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

9 authors.

Shuyuan YiDepartment of Extracorporeal Circulation and Mechanical Circulation Assistants, Center for Cardiac Intensive Care, Beijing Anzhen Hospital, Capital Medical University, Beijing, China.
Xiaoli ZhuangDepartment of Extracorporeal Circulation and Mechanical Circulation Assistants, Center for Cardiac Intensive Care, Beijing Anzhen Hospital, Capital Medical University, Beijing, China.
Lan LuoDepartment of Extracorporeal Circulation and Mechanical Circulation Assistants, Center for Cardiac Intensive Care, Beijing Anzhen Hospital, Capital Medical University, Beijing, China.
Lin FuDepartment of Extracorporeal Circulation and Mechanical Circulation Assistants, Center for Cardiac Intensive Care, Beijing Anzhen Hospital, Capital Medical University, Beijing, China.
Ziyuan DongDepartment of Extracorporeal Circulation and Mechanical Circulation Assistants, Center for Cardiac Intensive Care, Beijing Anzhen Hospital, Capital Medical University, Beijing, China.
Kan WangDepartment of Extracorporeal Circulation and Mechanical Circulation Assistants, Center for Cardiac Intensive Care, Beijing Anzhen Hospital, Capital Medical University, Beijing, China.
Yu JiangDepartment of Extracorporeal Circulation and Mechanical Circulation Assistants, Center for Cardiac Intensive Care, Beijing Anzhen Hospital, Capital Medical University, Beijing, China.
Xiaofang YangDepartment of Extracorporeal Circulation and Mechanical Circulation Assistants, Center for Cardiac Intensive Care, Beijing Anzhen Hospital, Capital Medical University, Beijing, China. yangxiaofang_1985@163.com.
Feilong HeiDepartment of Extracorporeal Circulation and Mechanical Circulation Assistants, Center for Cardiac Intensive Care, Beijing Anzhen Hospital, Capital Medical University, Beijing, China. heifeilong@126.com.

Funding

Chinese Institutes for Medical Research Grant CX24PY21
6 · The paper itself

Abstract

Acute lung injury (ALI) and its severe form, acute respiratory distress syndrome (ARDS), represent a clinical syndrome with high mortality, characterized by excessive pulmonary inflammation and oxidative stress. Despite advancements in conventional supportive care, mortality rates for ALI/ARDS remain persistently high (30%-50%). In recent years, increasing attention has focused on the regulatory mechanisms of the gut microbiota and their metabolites in ALI through the bidirectional ‘gut-lung axis’ interaction. This paper systematically reviews the mechanisms by which gut dysbiosis exacerbates lung inflammation and barrier damage via immune cell migration, inflammatory pathway activation, and metabolite imbalance. It also explores the potential of microbiome-based interventions—including probiotics, fecal microbiota transplantation (FMT), and dietary modification—for ALI treatment. This review not only elucidates the complex link between the gut microbiota and lung disease but also provides a theoretical basis for developing novel diagnostic and therapeutic approaches targeting the gut-lung axis. These insights hold significant implications for improving ALI patient prognosis and advancing precision medicine.

Indexed as

Acute Lung InjuryGastrointestinal MicrobiomeAnimalsDysbiosisFecal Microbiota TransplantationHumansProbioticsRespiratory Distress SyndromeAcute lung injury/acute respiratory distress syndromeGut-lung axisGut microbiotaMetabolites

Identifiers

PMID41580828
PMCPMC12914935

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

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 Socratic graph.