Evidence map›Paper›PMID 39583673›Full record

ArticleACS omega2024

Multiplatform Metabolomics: Enhancing the Severity Risk Prognosis of SARS-CoV-2 Infection.

Vinicius S Lima, Sinara T B Morais, Vinicius G Ferreira, Mariana B Almeida, Manuel Pedro Barros Silva, Thais de A Lopes, Juliana M de Oliveira, Joyce R S Raimundo, Danielle Z S Furtado, Fernando L A Fonseca and 4 more

Abstract read
In one paragraph

Article in ACS omega, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
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

2 citing papers in PubMed.

  1. Metabolic signature of COVID-19 progression: potential prognostic markers for severity and outcome.Metabolomics : Official journal of the Metabolomic Society · 2025
    Article
  2. 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

14 authors.

Vinicius S LimaPrograma de Pós-Graduação em Medicina Translacional, Departamento de Medicina, Escola Paulista de Medicina, Universidade Federal de São Paulo, São Paulo 04023-062, Brazil.
Sinara T B MoraisInstituto de Química de São Carlos, Universidade de São Paulo, São Carlos 13566-590, Brazil.
Vinicius G FerreiraInstituto de Química de São Carlos, Universidade de São Paulo, São Carlos 13566-590, Brazil.
Mariana B AlmeidaInstituto de Química de São Carlos, Universidade de São Paulo, São Carlos 13566-590, Brazil.
Manuel Pedro Barros SilvaPrograma de Pós-Graduação em Medicina Translacional, Departamento de Medicina, Escola Paulista de Medicina, Universidade Federal de São Paulo, São Paulo 04023-062, Brazil.
Thais de A LopesDepartamento de Química, Universidade Federal de São Carlos, São Carlos, São Paulo 13565-905, Brazil.
Juliana M de OliveiraDepartamento de Química, Universidade Federal de São Carlos, São Carlos, São Paulo 13565-905, Brazil.
Joyce R S RaimundoFaculdade de Medicina do ABC, Santo André, São Paulo 09060-870, Brazil.ORCID https://orcid.org/0000-0002-5215-0997
Danielle Z S FurtadoPrograma de Pós-Graduação em Medicina Translacional, Departamento de Medicina, Escola Paulista de Medicina, Universidade Federal de São Paulo, São Paulo 04023-062, Brazil.
Fernando L A FonsecaFaculdade de Medicina do ABC, Santo André, São Paulo 09060-870, Brazil.
Regina V OliveiraDepartamento de Química, Universidade Federal de São Carlos, São Carlos, São Paulo 13565-905, Brazil.
Daniel R CardosoInstituto de Química de São Carlos, Universidade de São Paulo, São Carlos 13566-590, Brazil.ORCID https://orcid.org/0000-0002-3492-3327
Emanuel CarrilhoInstituto de Química de São Carlos, Universidade de São Paulo, São Carlos 13566-590, Brazil.ORCID https://orcid.org/0000-0001-7351-8220
Nilson A AssunçãoPrograma de Pós-Graduação em Medicina Translacional, Departamento de Medicina, Escola Paulista de Medicina, Universidade Federal de São Paulo, São Paulo 04023-062, Brazil.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Concerns about the SARS-CoV-2 outbreak (COVID-19) continue to persist even years later, with the emergence of new variants and the risk of disease severity. Common clinical symptoms, like cough, fever, and respiratory symptoms, characterize the noncritical patients, classifying them from mild to moderate. In a more severe and complex scenario, the virus infection can affect vital organs, resulting, for instance, in pneumonia and impaired kidney and heart function. However, it is well-known that subclinical symptoms at a metabolic level can be observed previously but require a proper diagnosis because viral replication on the host leaves a track with a different profile depending on the severity of the illness. Metabolomic profiles of mild, moderate, and severe COVID-19 patients were obtained by multiple platforms (LC-HRMS and MALDI-MS), increasing the chance to elucidate a prognosis for severity risk. A strong link was discovered between phenylalanine metabolism and increased COVID-19 severity symptoms, a pathway linked to cardiac and neurological consequences. Glycerophospholipids and sphingolipid metabolisms were also dysregulated linearly with the increasing symptom severity, which can be related to virus proliferation, immune system avoidance, and apoptosis escaping. Our data, endorsed by other literature, strengthens the notion that these pathways might play a vital role in a patient's prognosis.

Identifiers

PMID39583673
PMCPMC11579725

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.