Evidence map›Paper›PMID 24265281›Full record

ArticleJournal of applied physiology (Bethesda, Md. : 1985)2014

Exploratory proteomic analysis of hypobaric hypoxia and acute mountain sickness in humans.

Colleen G Julian, Andrew W Subudhi, Ryan C Hill, Megan J Wilson, Andrew C Dimmen, Kirk C Hansen, Robert C Roach

Abstract read
In one paragraph

Article in Journal of applied physiology (Bethesda, Md. : 1985), 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed, 1 pooled it
3.5field-weighted citation impact, top 8% of its field
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

23 citing papers in PubMed, 1 synthesis or guideline pooled it, 48 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. SAA4: An Underdog Within the Serum Amyloid a Superfamily?International journal of molecular sciences · 2026
    Review
  4. Article
  5. Article
  6. Article
  7. [Status of Research on Molecular Mechanisms and Management of Acute Mountain Sickness].Sichuan da xue xue bao. Yi xue ban = Journal of Sichuan University. Medical science edition · 2024
    Review
  8. Article
  9. Article
  10. Review
  11. Article
  12. Review
  13. Review
  14. Article
  15. Review
  16. The phospholipase AJournal of lipid research · 2018
    Review
  17. Article
  18. Article
  19. Article
  20. Hypertension at high altitude: the interplay between genetic and biochemical factors in the setting of oxidative stress.Hypertension research : official journal of the Japanese Society of Hypertension · 2016
    Article
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

7 authors at 1 institution in 1 country.

Colleen G JulianAltitude Research Center, Department of Emergency Medicine, University of Colorado Denver, Aurora, Colorado;
Andrew W Subudhi
Ryan C Hill
Megan J Wilson
Andrew C Dimmen
Kirk C Hansen
Robert C Roach
University of Colorado Denver · US

Funding

Excercise induced rise in Severity of Altitude IllnessR01HL070362 · NHLBI · UNIVERSITY OF COLORADO DENVER · PI ROACH, ROBERT C · 2001 to 2004
$2.0M
NHLBI NIH HHS HL-070362
6 · The paper itself

Abstract

Our objective in this exploratory study was to identify novel biomarkers of importance for acute mountain sickness (AMS) using discovery-based proteomic methods. Peripheral blood samples were collected and AMS symptoms were assessed in 20 healthy volunteers prior to [-15 h (baseline) and 0 h; 1,609 m; barometric pressure = 625 mmHg] and after a 9-h exposure to hypobaric hypoxia (9 h; 4,875 m; barometric pressure = 425 mmHg). AMS status was assessed using the Lake Louise Questionnaire. Plasma samples were pooled according to AMS status at each time point. Protein composition of the samples was determined by a GeLC-MS/MS approach using two analytical platforms (LTQ-XL linear ion trap mass spectrometer and a LTQ-FT ultra hybrid mass spectrometer) for technical replication. Spectral counting was used to make semiquantitative comparisons of protein abundance between AMS-susceptible (AMS) and AMS-resistant (AMS·R) subjects with exposure to hypobaric hypoxia. After 9 h of hypoxia, the abundance of proteins with antioxidant properties (i.e., peroxiredoxin 6, glutathione peroxidase, and sulfhydryl oxidase 1) rose in AMS but not AMS·R. Our exploratory analyses suggest that exposure to hypobaric hypoxia enhances enzymatic antioxidant systems in AMS vs. AMS·R, which, we propose, may be an overcompensation for hypoxia-induced oxidant production. On the basis of our findings we 1) speculate that quenching oxidant activity may have adverse downstream effects that are of pathophysiological importance for AMS such as interrupting oxidant-sensitive cell signaling and gene transcription and 2) question the existing assumption that increased oxidant production in AMS is pathological.

Indexed as

ProteomicsAcclimatizationAcute DiseaseAdultAltitudeAltitude SicknessAntioxidantsBiomarkersBlood ProteinsCase-Control StudiesChromatography, High Pressure LiquidEnzymesFemaleHumansHypoxiaMaleAntioxidantsBiomarkersBlood ProteinsEnzymesacute mountain sicknesshypoxiaproteomics

Identifiers

PMID24265281
PMCPMC3972748
OpenAlexW1993213544

What OpenQuestion holds

Textmetadata
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 OpenQuestion graph.