Evidence map›Paper›PMID 37943960›Full record

ArticlePLoS pathogens2023

COVID-19: A complex disease with a unique metabolic signature.

Veronica Ghini, Walter Vieri, Tommaso Celli, Valentina Pecchioli, Nunzia Boccia, Tania Alonso-Vásquez, Lorenzo Pelagatti, Marco Fondi, Claudio Luchinat, Laura Bertini and 3 more

Abstract read
In one paragraph

Article in PLoS pathogens, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing 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

11 citing papers in PubMed.

  1. Recent Trends in Metabolomics by NMR Spectroscopy.Angewandte Chemie (International ed. in English) · 2026
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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

13 authors.

Veronica GhiniDepartment of Chemistry "Ugo Schiff", University of Florence, Sesto Fiorentino Florence, Italy.
Walter VieriDepartment of Chemistry "Ugo Schiff", University of Florence, Sesto Fiorentino Florence, Italy.
Tommaso CelliInternal Medicine, Santa Maria Nuova Hospital, Florence, Florence, Italy.
Valentina PecchioliDepartment of Chemistry "Ugo Schiff", University of Florence, Sesto Fiorentino Florence, Italy.
Nunzia BocciaInternal Medicine, Santa Maria Nuova Hospital, Florence, Florence, Italy.
Tania Alonso-VásquezDepartment of Biology, University of Florence, Sesto Fiorentino, Florence, Italy.
Lorenzo PelagattiInternal Medicine, Santa Maria Nuova Hospital, Florence, Florence, Italy.
Marco FondiDepartment of Biology, University of Florence, Sesto Fiorentino, Florence, Italy.
Claudio LuchinatDepartment of Chemistry "Ugo Schiff", University of Florence, Sesto Fiorentino Florence, Italy.
Laura BertiniInternal Medicine, Santa Maria Nuova Hospital, Florence, Florence, Italy.
Vieri VannucchiInternal Medicine, Santa Maria Nuova Hospital, Florence, Florence, Italy.
Giancarlo LandiniInternal Medicine, Santa Maria Nuova Hospital, Florence, Florence, Italy.
Paola TuranoDepartment of Chemistry "Ugo Schiff", University of Florence, Sesto Fiorentino Florence, Italy.ORCID 0000-0002-7683-8614

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Plasma of COVID-19 patients contains a strong metabolomic/lipoproteomic signature, revealed by the NMR analysis of a cohort of >500 patients sampled during various waves of COVID-19 infection, corresponding to the spread of different variants, and having different vaccination status. This composite signature highlights common traits of the SARS-CoV-2 infection. The most dysregulated molecules display concentration trends that scale with disease severity and might serve as prognostic markers for fatal events. Metabolomics evidence is then used as input data for a sex-specific multi-organ metabolic model. This reconstruction provides a comprehensive view of the impact of COVID-19 on the entire human metabolism. The human (male and female) metabolic network is strongly impacted by the disease to an extent dictated by its severity. A marked metabolic reprogramming at the level of many organs indicates an increase in the generic energetic demand of the organism following infection. Sex-specific modulation of immune response is also suggested.

Indexed as

COVID-19FemaleHumansMaleMetabolomicsPatient AcuityPhenotypeSARS-CoV-2

Identifiers

PMID37943960
PMCPMC10662774

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.