Evidence map›Paper›PMID 35751188›Full record

ArticleComputers in biology and medicine2022

Diagnosis and prognosis of COVID-19 employing analysis of patients' plasma and serum via LC-MS and machine learning.

Alexandre de Fátima Cobre, Monica Surek, Dile Pontarolo Stremel, Mariana Millan Fachi, Helena Hiemisch Lobo Borba, Fernanda Stumpf Tonin, Roberto Pontarolo

Open access · greenAbstract read
In one paragraph

Article in Computers in biology and medicine, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
3.7field-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

15 citing papers in PubMed, 26 citations in OpenAlex.

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  11. ANPELA: Significantly Enhanced Quantification Tool for Cytometry-Based Single-Cell Proteomics.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2023
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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

7 authors at 3 institutions in 2 countries.

Alexandre de Fátima CobrePharmaceutical Sciences Postgraduate Program, Universidade Federal Do Paraná, Curitiba, Brazil. Electronic address: alexandrecobre@gmail.com.
Monica SurekPharmaceutical Sciences Postgraduate Program, Universidade Federal Do Paraná, Curitiba, Brazil. Electronic address: monicasurek13@gmail.com.
Dile Pontarolo StremelDepartment of Forest Engineering and Technology, Universidade Federal Do Paraná, Curitiba, Brazil. Electronic address: dile.stremel@gmail.com.
Mariana Millan FachiPharmaceutical Sciences Postgraduate Program, Universidade Federal Do Paraná, Curitiba, Brazil. Electronic address: marianamfachi@gmail.com.
Helena Hiemisch Lobo BorbaDepartment of Pharmacy, Universidade Federal Do Paraná, Curitiba, Brazil. Electronic address: helena.hlb@gmail.com.
Fernanda Stumpf ToninPharmaceutical Sciences Postgraduate Program, Universidade Federal Do Paraná, Curitiba, Brazil; H&TRC- Health & Technology Research Center, ESTeSL, Escola Superior de Tecnologia da Saúde, Instituto Politécnico de Lisboa, Lisbon, Portugal. Electronic address: stumpf.tonin@ufpr.br.
Roberto PontaroloDepartment of Pharmacy, Universidade Federal Do Paraná, Curitiba, Brazil. Electronic address: pontarolo@ufpr.br.
Universidade Federal do Paraná · BRInstituto Politécnico de Lisboa · PTUniversidade Tecnológica Federal do Paraná · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveTo implement and evaluate machine learning (ML) algorithms for the prediction of COVID-19 diagnosis, severity, and fatality and to assess biomarkers potentially associated with these outcomes. MATERIAL AND

methodsSerum (n = 96) and plasma (n = 96) samples from patients with COVID-19 (acute, severe and fatal illness) from two independent hospitals in China were analyzed by LC-MS. Samples from healthy volunteers and from patients with pneumonia caused by other viruses (i.e. negative RT-PCR for COVID-19) were used as controls. Seven different ML-based models were built: PLS-DA, ANNDA, XGBoostDA, SIMCA, SVM, LREG and KNN.

resultsThe PLS-DA model presented the best performance for both datasets, with accuracy rates to predict the diagnosis, severity and fatality of COVID-19 of 93%, 94% and 97%, respectively. Low levels of the metabolites ribothymidine, 4-hydroxyphenylacetoylcarnitine and uridine were associated with COVID-19 positivity, whereas high levels of N-acetyl-glucosamine-1-phosphate, cysteinylglycine, methyl isobutyrate, l-ornithine and 5,6-dihydro-5-methyluracil were significantly related to greater severity and fatality from COVID-19.

conclusionThe PLS-DA model can help to predict SARS-CoV-2 diagnosis, severity and fatality in daily practice. Some biomarkers typically increased in COVID-19 patients' serum or plasma (i.e. ribothymidine, N-acetyl-glucosamine-1-phosphate, l-ornithine, 5,6-dihydro-5-methyluracil) should be further evaluated as prognostic indicators of the disease.

Indexed as

COVID-19BiomarkersChromatography, LiquidCOVID-19 TestingGlucosamineHumansMachine LearningOrnithinePhosphatesSARS-CoV-2Tandem Mass SpectrometryThymineBiomarkersGlucosamineOrnithinePhosphatesThymineBiomarkerCOVID 19DiagnosisFatalityMachine learningSeverity

Identifiers

PMID35751188
PMCPMC9123826
OpenAlexW4281253976

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.