Evidence map›Paper›PMID 33704068›Full record

ArticleeLife2021

Longitudinal proteomic profiling of dialysis patients with COVID-19 reveals markers of severity and predictors of death.

Jack Gisby, Candice L Clarke, Nicholas Medjeral-Thomas, Talat H Malik, Artemis Papadaki, Paige M Mortimer, Norzawani B Buang, Shanice Lewis, Marie Pereira, Frederic Toulza and 15 more

Open access · goldAbstract read
In one paragraph

Article in eLife, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 53 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
53citing papers in PubMed, 1 pooled it
4.6field-weighted citation impact, top 4% 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

53 citing papers in PubMed, 1 synthesis or guideline pooled it, 78 citations in OpenAlex.

  1. Pooled it
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  4. Review
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  8. Article
  9. ADAM-17 Activity and Its Relation to ACE2: Implications for Severe COVID-19.International journal of molecular sciences · 2024
    Article
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  11. Observational
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  19. The role of immune activation and antigen persistence in acute and long COVID.Journal of investigative medicine : the official publication of the American Federation for Clinical Research · 2023
    Review
  20. 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

25 authors at 4 institutions in 1 country.

Jack Gisby *Centre for Inflammatory Disease, Department of Immunology and Inflammation, Imperial College London, London, United Kingdom.ORCID https://orcid.org/0000-0003-0511-8123
Candice L Clarke *Centre for Inflammatory Disease, Department of Immunology and Inflammation, Imperial College London, London, United Kingdom.
Nicholas Medjeral-Thomas *Centre for Inflammatory Disease, Department of Immunology and Inflammation, Imperial College London, London, United Kingdom.
Talat H MalikCentre for Inflammatory Disease, Department of Immunology and Inflammation, Imperial College London, London, United Kingdom.
Artemis PapadakiCentre for Inflammatory Disease, Department of Immunology and Inflammation, Imperial College London, London, United Kingdom.
Paige M MortimerCentre for Inflammatory Disease, Department of Immunology and Inflammation, Imperial College London, London, United Kingdom.
Norzawani B BuangCentre for Inflammatory Disease, Department of Immunology and Inflammation, Imperial College London, London, United Kingdom.
Shanice LewisCentre for Inflammatory Disease, Department of Immunology and Inflammation, Imperial College London, London, United Kingdom.
Marie PereiraCentre for Inflammatory Disease, Department of Immunology and Inflammation, Imperial College London, London, United Kingdom.ORCID http://orcid.org/0000-0003-0711-3385
Frederic ToulzaCentre for Inflammatory Disease, Department of Immunology and Inflammation, Imperial College London, London, United Kingdom.
Ester FagnanoCentre for Inflammatory Disease, Department of Immunology and Inflammation, Imperial College London, London, United Kingdom.
Marie-Anne MawhinCentre for Inflammatory Disease, Department of Immunology and Inflammation, Imperial College London, London, United Kingdom.
Emma E DuttonCentre for Inflammatory Disease, Department of Immunology and Inflammation, Imperial College London, London, United Kingdom.
Lunnathaya TapengCentre for Inflammatory Disease, Department of Immunology and Inflammation, Imperial College London, London, United Kingdom.
Arianne C RichardCambridge Institute for Medical Research, University of Cambridge, Cambridge, United Kingdom.ORCID https://orcid.org/0000-0002-8708-9997
Paul Dw KirkMRC Biostatistics Unit, Forvie Way, University of Cambridge, Cambridge, United Kingdom.
Jacques BehmoarasCentre for Inflammatory Disease, Department of Immunology and Inflammation, Imperial College London, London, United Kingdom.
Eleanor SandhuCentre for Inflammatory Disease, Department of Immunology and Inflammation, Imperial College London, London, United Kingdom.
Stephen P McAdooCentre for Inflammatory Disease, Department of Immunology and Inflammation, Imperial College London, London, United Kingdom.
Maria F PrendeckiCentre for Inflammatory Disease, Department of Immunology and Inflammation, Imperial College London, London, United Kingdom.ORCID https://orcid.org/0000-0001-7048-7457
Matthew C PickeringCentre for Inflammatory Disease, Department of Immunology and Inflammation, Imperial College London, London, United Kingdom.
Marina BottoCentre for Inflammatory Disease, Department of Immunology and Inflammation, Imperial College London, London, United Kingdom.ORCID https://orcid.org/0000-0002-1458-3791
Michelle Willicombe *Centre for Inflammatory Disease, Department of Immunology and Inflammation, Imperial College London, London, United Kingdom.
David C Thomas *Centre for Inflammatory Disease, Department of Immunology and Inflammation, Imperial College London, London, United Kingdom.
James E Peters *Centre for Inflammatory Disease, Department of Immunology and Inflammation, Imperial College London, London, United Kingdom.ORCID https://orcid.org/0000-0002-9415-3440
Imperial College London · GBImperial College Healthcare NHS Trust · GBUniversity of Cambridge · GBHealth Data Research UK · GB

Funding

Medical Research Council MC_UU_00002/13Medical Research Council MR/N01121X/1Medical Research Council MR/S004068/2Medical Research Council MR/V027638/1Wellcome TrustWellcome Trust Wellcome-Beit Prize Clinical Research Career Development Fellowship (206617/A/17/A)Wellcome Trust Wellcome Trust and Imperial College London Research FellowshipWellcome Trust Wellcome Trust Senior Fellow in Clinical Science (212252/Z/18/Z)
6 · The paper itself

Abstract

End-stage kidney disease (ESKD) patients are at high risk of severe COVID-19. We measured 436 circulating proteins in serial blood samples from hospitalised and non-hospitalised ESKD patients with COVID-19 (n = 256 samples from 55 patients). Comparison to 51 non-infected patients revealed 221 differentially expressed proteins, with consistent results in a separate subcohort of 46 COVID-19 patients. Two hundred and three proteins were associated with clinical severity, including IL6, markers of monocyte recruitment (e.g. CCL2, CCL7), neutrophil activation (e.g. proteinase-3), and epithelial injury (e.g. KRT19). Machine-learning identified predictors of severity including IL18BP, CTSD, GDF15, and KRT19. Survival analysis with joint models revealed 69 predictors of death. Longitudinal modelling with linear mixed models uncovered 32 proteins displaying different temporal profiles in severe versus non-severe disease, including integrins and adhesion molecules. These data implicate epithelial damage, innate immune activation, and leucocyte-endothelial interactions in the pathology of severe COVID-19 and provide a resource for identifying drug targets.

Indexed as

AgedBiomarkersCOVID-19FemaleForecastingHospitalizationHumansKidney Failure, ChronicLongitudinal StudiesMaleMiddle AgedPrognosisProteomicsRenal DialysisSARS-CoV-2Severity of Illness IndexBiomarkersbiomarkersCOVID-19cytokinesend-stage kidney diseasehumanimmunologyinflammationlongitudinalmedicineproteomics

Identifiers

PMID33704068
PMCPMC8064756
OpenAlexW3133512685

What OpenQuestion 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 OpenQuestion graph.