Evidence map›Paper›PMID 31858521›Full record

ArticleThrombosis and haemostasis2020

Hypoxia Modulates Platelet Purinergic Signalling Pathways.

Gordon G Paterson, Jason M Young, Joseph A Willson, Christopher J Graham, Rebecca C Dru, Eleanor W Lee, Greig S Torpey, Sarah R Walmsley, Melissa V Chan, Timothy D Warner and 2 more

Open access · hybridAbstract read
In one paragraph

Article in Thrombosis and haemostasis, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.7field-weighted citation impact, top 13% 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

13 citing papers in PubMed, 18 citations in OpenAlex.

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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 at 4 institutions in 1 country.

Gordon G PatersonAPEX (Altitude Physiology Expeditions), Edinburgh, United Kingdom.
Jason M YoungAPEX (Altitude Physiology Expeditions), Edinburgh, United Kingdom.
Joseph A WillsonUniversity of Edinburgh Centre for Inflammation Research, The Queen's Medical Research Institute, University of Edinburgh, Edinburgh, United Kingdom.
Christopher J GrahamAPEX (Altitude Physiology Expeditions), Edinburgh, United Kingdom.ORCID 0000-0002-1144-7970
Rebecca C DruAPEX (Altitude Physiology Expeditions), Edinburgh, United Kingdom.
Eleanor W LeeAPEX (Altitude Physiology Expeditions), Edinburgh, United Kingdom.
Greig S TorpeyAPEX (Altitude Physiology Expeditions), Edinburgh, United Kingdom.
Sarah R WalmsleyUniversity of Edinburgh Centre for Inflammation Research, The Queen's Medical Research Institute, University of Edinburgh, Edinburgh, United Kingdom.
Melissa V ChanCentre for Immunobiology, Blizard Institute, Barts and The London School of Medicine and Dentistry, Queen Mary University of London, London, United Kingdom.
Timothy D WarnerCentre for Immunobiology, Blizard Institute, Barts and The London School of Medicine and Dentistry, Queen Mary University of London, London, United Kingdom.ORCID 0000-0003-3988-4408
John Kenneth BaillieAPEX (Altitude Physiology Expeditions), Edinburgh, United Kingdom.
Alfred Arthur Roger ThompsonAPEX (Altitude Physiology Expeditions), Edinburgh, United Kingdom.ORCID 0000-0002-0717-4551
Expedition (United Kingdom) · GBCentre for Inflammation Research · GBQueen Mary University of London · GBNHS Lothian · GB

Funding

103258/Z/13/Z,A Wellcome TrustBritish Heart Foundation FS/18/13/33281British Heart Foundation PG/15/47/31591Charles S. Houston grant Wilderness Medicine SocietyFS/18/13/3328; PG/15/47/31591 British Heart FoundationWellcome Trust 209220/Z/17/Z
6 · The paper itself

Abstract

backgroundHypoxia resulting from ascent to high-altitude or pathological states at sea level is known to increase platelet reactivity. Previous work from our group has suggested that this may be adenosine diphosphate (ADP)-specific. Given the clinical importance of drugs targeting ADP pathways, research into the impact of hypoxia on platelet ADP pathways is highly important.

methodsOptimul aggregometry was performed on plasma from 29 lowland residents ascending to 4,700 m, allowing systematic assessment of platelet reactivity in response to several platelet agonists. Aggregometry was also performed in response to ADP in the presence of inhibitors of the two main ADP receptors, P2Y

resultsHypobaric hypoxia significantly reduced the ability of a fixed concentration of cangrelor to inhibit ADP-induced aggregation and increased basal VASP phosphorylation. However, in the absence of P2Y receptor inhibitors, we did not find evidence of increased platelet sensitivity to any of the agonists tested and found reduced sensitivity to thrombin receptor-activating peptide-6 amide.

conclusionOur results provide evidence of increased P2Y

Indexed as

HypoxiaPlatelet AggregationSignal TransductionAdenosine DiphosphateAdenosine MonophosphateAdolescentAdultAltitudeBlood PlateletsCell Adhesion MoleculesCohort StudiesFemaleHumansMaleMicrofilament ProteinsOxygenAdenosine DiphosphateAdenosine MonophosphatecangrelorCell Adhesion MoleculesMicrofilament ProteinsOxygenPhosphoproteinsPlatelet Aggregation InhibitorsReceptors, PurinergicReceptors, ThrombinVasodilator-Stimulated Phosphoprotein

Identifiers

PMID31858521
PMCPMC7286126
OpenAlexW2996255601

What Socratic holds

Textmetadata
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.