ReviewRedox biology2026
Biomarkers and potential subtypes of acute mountain sickness: A state-of-the-science review.
Review in Redox biology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.
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.
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.
Who cites it
2 citing papers in PubMed.
- Article
- Low hypoxia tolerance as a determinant of the proinflammatory phenotype: a trained immunity perspective.Frontiers in immunology · 2026Review
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
7 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Exposure to high altitude can cause acute mountain sickness (AMS) characterized by headache, gastrointestinal symptoms, dizziness and fatigue, which may progress to life-threatening conditions like high-altitude cerebral edema (HACE). Although the pathophysiology and development of AMS have been intensely investigated, the risk factors and underlying mechanisms remain incompletely understood. In addition, objective criteria for the diagnosis of AMS and reliable biomarkers are missing. Here we provide an overview of the molecular and pathophysiological foundations of AMS and review which potential biomarkers have been suggested and in combination with which physiological and psychological correlates of AMS they could improve diagnosis. Moreover, we point out current knowledge gaps and discuss which future research is required to enable AMS diagnosis based on more objective biomedical and psychophysical criteria. Emphasizing the apparent heterogeneity in AMS pathogenesis, we support the classification of different AMS subtypes according to etiological parameters. We propose the hypothesis that both insufficient and excessive hypoxia responses can cause AMS and that the differentiation according to these divergent mechanisms might allow the identification of AMS subtypes that can be characterized better using biomarkers and correlates of AMS.
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Registered trials
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.