Evidence map›Paper›PMID 35931319›Full record

ArticleMolecular & cellular proteomics : MCP2022

Early Prediction of COVID-19 Patient Survival by Targeted Plasma Multi-Omics and Machine Learning.

Vincent R Richard, Claudia Gaither, Robert Popp, Daria Chaplygina, Alexander Brzhozovskiy, Alexey Kononikhin, Yassene Mohammed, René P Zahedi, Evgeny N Nikolaev, Christoph H Borchers

Open access · goldAbstract read
In one paragraph

Article in Molecular & cellular proteomics : MCP, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed, 2 pooled it
3.5field-weighted citation impact, top 6% 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

27 citing papers in PubMed, 2 syntheses or guidelines pooled it, 45 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 3 countries.

Vincent R RichardSegal Cancer Proteomics Centre, Lady Davis Institute for Medical Research, McGill University, Montreal, Quebec, Canada.
Claudia GaitherMRM Proteomics, Montreal, Canada.
Robert PoppMRM Proteomics, Montreal, Canada.
Daria ChaplyginaCenter for Molecular and Cellular Biology, Skolkovo Institute of Science and Technology, Moscow, Russia.
Alexander BrzhozovskiyCenter for Molecular and Cellular Biology, Skolkovo Institute of Science and Technology, Moscow, Russia.
Alexey KononikhinCenter for Molecular and Cellular Biology, Skolkovo Institute of Science and Technology, Moscow, Russia.
Yassene MohammedCenter for Proteomics and Metabolomics, Leiden University Medical Center, Leiden, the Netherlands; Genome BC Proteomics Centre, University of Victoria, Victoria, Canada.
René P ZahediSegal Cancer Proteomics Centre, Lady Davis Institute for Medical Research, McGill University, Montreal, Quebec, Canada; Manitoba Centre for Proteomics & Systems Biology, John Buhler Research Centre, University of Manitoba, Winnipeg, Canada; Department of Internal Medicine, University of Manitoba, Winnipeg, Canada.
Evgeny N NikolaevCenter for Molecular and Cellular Biology, Skolkovo Institute of Science and Technology, Moscow, Russia.
Christoph H BorchersSegal Cancer Proteomics Centre, Lady Davis Institute for Medical Research, McGill University, Montreal, Quebec, Canada; Gerald Bronfman Department of Oncology, Division of Experimental Medicine, Lady Davis Institute for Medical Research, McGill University, Montreal, Canada; Department of Pathology, McGill University, Montreal, Canada. Electronic address: Christoph.Borchers@mcgill.ca.
Skolkovo Institute of Science and Technology · RUMcGill University · CAUniversity of Manitoba · CAUniversity of Victoria · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The recent surge of coronavirus disease 2019 (COVID-19) hospitalizations severely challenges healthcare systems around the globe and has increased the demand for reliable tests predictive of disease severity and mortality. Using multiplexed targeted mass spectrometry assays on a robust triple quadrupole MS setup which is available in many clinical laboratories, we determined the precise concentrations of hundreds of proteins and metabolites in plasma from hospitalized COVID-19 patients. We observed a clear distinction between COVID-19 patients and controls and, strikingly, a significant difference between survivors and nonsurvivors. With increasing length of hospitalization, the survivors' samples showed a trend toward normal concentrations, indicating a potential sensitive readout of treatment success. Building a machine learning multi-omic model that considers the concentrations of 10 proteins and five metabolites, we could predict patient survival with 92% accuracy (area under the receiver operating characteristic curve: 0.97) on the day of hospitalization. Hence, our standardized assays represent a unique opportunity for the early stratification of hospitalized COVID-19 patients.

Indexed as

COVID-19HospitalizationHumansMachine LearningRetrospective StudiesROC CurveSARS-CoV-2

Identifiers

PMID35931319
PMCPMC9345792
OpenAlexW4289526446

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.