Evidence map›Paper›PMID 33292164›Full record

ArticleClinical proteomics2020

Subclinical effects of remote ischaemic conditioning in human kidney transplants revealed by quantitative proteomics.

Adam M Thorne, Honglei Huang, Darragh P O'Brien, Marco Eijken, Nicoline Valentina Krogstrup, Rikke Norregaard, Bjarne Møller, Rutger J Ploeg, Bente Jespersen, Benedikt M Kessler

Open access · goldAbstract read
In one paragraph

Article in Clinical proteomics, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.0field-weighted citation impact, top 23% 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

9 citing papers in PubMed, 11 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

10 authors at 4 institutions in 2 countries.

Adam M ThorneNuffield Department of Surgical Sciences and Oxford Biomedical Research Centre, University of Oxford, Oxford, UK.
Honglei HuangNuffield Department of Surgical Sciences and Oxford Biomedical Research Centre, University of Oxford, Oxford, UK.
Darragh P O'BrienTarget Discovery Institute, Nuffield Department of Medicine, University of Oxford, Oxford, UK.
Marco EijkenDepartment of Renal Medicine, Aarhus University Hospital, Aarhus, Denmark.
Nicoline Valentina KrogstrupDepartment of Renal Medicine, Aarhus University Hospital, Aarhus, Denmark.ORCID http://orcid.org/0000-0001-7144-730X
Rikke NorregaardDepartment of Clinical Medicine, Aarhus University, Aarhus, Denmark.
Bjarne MøllerDepartment of Clinical Immunology, Aarhus University Hospital, Aarhus, Denmark.
Rutger J PloegNuffield Department of Surgical Sciences and Oxford Biomedical Research Centre, University of Oxford, Oxford, UK. rutger.ploeg@nds.ox.ac.uk.
Bente JespersenDepartment of Renal Medicine, Aarhus University Hospital, Aarhus, Denmark. bente.jespersen@clin.au.dk.
Benedikt M KesslerTarget Discovery Institute, Nuffield Department of Medicine, University of Oxford, Oxford, UK. benedikt.kessler@ndm.ox.ac.uk.ORCID http://orcid.org/0000-0002-8160-2446
University of Oxford · GBAarhus University · DKAarhus University Hospital · DKNuffield Orthopaedic Centre · GB

Funding

Medical Research Council MR/R014132/1
6 · The paper itself

Abstract

backgroundRemote ischaemic conditioning (RIC) is currently being explored as a non-invasive method to attenuate ischaemia/reperfusion injuries in organs. A randomised clinical study (CONTEXT) evaluated the effects of RIC compared to non-RIC controls in human kidney transplants.

methodsRIC was induced prior to kidney reperfusion by episodes of obstruction to arterial flow in the leg opposite the transplant using a tourniquet (4 × 5 min). Although RIC did not lead to clinical improvement of transplant outcomes, we explored whether RIC induced molecular changes through precision analysis of CONTEXT recipient plasma and kidney tissue samples by high-resolution tandem mass spectrometry (MS/MS).

resultsWe observed an accumulation of muscle derived proteins and altered amino acid metabolism in kidney tissue proteomes, likely provoked by RIC, which was not reflected in plasma. In addition, MS/MS analysis demonstrated transient upregulation of several acute phase response proteins (SAA1, SAA2, CRP) in plasma, 1 and 5 days post-transplant in RIC and non-RIC conditions with a variable effect on the magnitude of acute inflammation.

conclusionsTogether, our results indicate sub-clinical systemic and organ-localised effects of RIC.

Indexed as

Acute phase proteinsCONTEXT clinical trialELISAKidney transplantationMass spectrometryProteomicsRemote ischaemic conditioning

Identifiers

PMID33292164
PMCPMC7607690
OpenAlexW3096117876

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Registered trials

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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.