Evidence map›Paper›PMID 42278620›Full record

ReviewInternational journal of molecular sciences2026

Effects of High-Altitude Environments on Gut Microbiota and Their Mechanisms in Immune Regulation and High-Altitude Adaptation.

Zhipeng Lu, Guojing Chen, Mingyang Chang, Ningning Wang, Tiantian Xia, Yunan Zhang, Gaoyuan Xu, Qianqian Zhao, Pan Shen, Wei Zhou and 2 more

Abstract readReview
In one paragraph

Review in International journal of molecular sciences, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

12 authors.

Zhipeng LuAcademy of Military Medical Sciences, Beijing 100850, China.
Guojing ChenAcademy of Military Medical Sciences, Beijing 100850, China.
Mingyang ChangAcademy of Military Medical Sciences, Beijing 100850, China.
Ningning WangAcademy of Military Medical Sciences, Beijing 100850, China.
Tiantian XiaAcademy of Military Medical Sciences, Beijing 100850, China.
Yunan ZhangAcademy of Military Medical Sciences, Beijing 100850, China.
Gaoyuan XuAcademy of Military Medical Sciences, Beijing 100850, China.
Qianqian ZhaoAcademy of Military Medical Sciences, Beijing 100850, China.
Pan ShenAcademy of Military Medical Sciences, Beijing 100850, China.
Wei ZhouAcademy of Military Medical Sciences, Beijing 100850, China.ORCID 0000-0003-0435-7261
Zhexin NiAcademy of Military Medical Sciences, Beijing 100850, China.
Yue GaoAcademy of Military Medical Sciences, Beijing 100850, China.

Funding

National Natural Science Foundation of China 2025YFC3507500National Natural Science Foundation of China 2025YFC3507502State Administration of Traditional Chinese Medicine of the People's Republic of China zyyzdxk-2023311
6 · The paper itself

Abstract

High-altitude environments, characterized by hypoxia, low temperature, and intense ultraviolet radiation, profoundly disrupt host intestinal homeostasis and reshape the gut microbiota, thereby influencing immune regulation and acclimatization. This review systematically summarizes the dynamic compositional and functional changes in the gut microbiota in high-altitude natives, immigrant populations, short-term visitors, and relevant animal models. Current evidence indicates that long-term high-altitude adaptation is associated with directional microbial remodeling, including the enrichment of anaerobic and short-chain fatty acid (SCFA)-associated taxa, which may support energy metabolism and immune homeostasis. In contrast, acute high-altitude exposure more readily induces dysbiosis, impairs intestinal barrier integrity, and promotes the translocation of endotoxins and bioactive metabolites. Mechanistically, the gut microbiota and its metabolites participate in high-altitude adaptation and high-altitude-related disease pathogenesis by modulating barrier function, inflammatory responses, oxidative stress, and immune signaling, and by mediating interorgan communication-characterized by metabolite-driven systemic inflammation or tolerance-through the gut-lung, gut-heart, gut-brain, gut-kidney, and gut-testis axes. SCFAs, bile acids, amino acid-derived metabolites, and succinic acid may control immune homeostasis and inflammatory responses through pathways including TLR4/NF-κB and NLRP3. Although the causal relationships, core microbial effectors, and population-specific heterogeneity remain incompletely defined, microbiota-targeted interventions, including probiotics, prebiotics, and fecal microbiota transplantation, have shown promise for promoting acclimatization and preventing high-altitude-related disorders. Overall, this review provides an integrated framework linking environmental stress, gut microbial ecology, and host immune-metabolic adaptation at high altitude, and highlights future directions for mechanistic and translational research in high-altitude medicine.

Indexed as

AcclimatizationAdaptation, PhysiologicalAltitudeGastrointestinal MicrobiomeAnimalsDysbiosisHomeostasisHumansIntestinal Barrier Functiondisease mechanismsgut microbiotahigh-altitude adaptationhigh-altitude environmentimmune regulation

Identifiers

PMID42278620
PMCPMC13258058

What Socratic holds

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LicenceCC BY
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.