Evidence map›Paper›PMID 37623894›Full record

ArticleMetabolites2023

The Effects of Hospitalisation on the Serum Metabolome in COVID-19 Patients.

Tim Hensen, Daniel Fässler, Liam O'Mahony, Werner C Albrich, Beatrice Barda, Christian Garzoni, Gian-Reto Kleger, Urs Pietsch, Noémie Suh, Johannes Hertel and 1 more

Abstract read
In one paragraph

Article in Metabolites, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed, 1 pooled it
–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 synthesis or guideline pooled it.

  1. Pooled it
  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

11 authors.

Tim HensenSchool of Medicine, University of Galway, H91 TK33 Galway, Ireland.ORCID 0000-0003-2459-3755
Daniel FässlerDepartment of Psychiatry and Psychotherapy, University Medicine Greifswald, 17475 Greifswald, Germany.ORCID 0000-0002-8295-5390
Liam O'MahonyAPC Microbiome Ireland, T12 K8AF Cork, Ireland.
Werner C AlbrichAPC Microbiome Ireland, T12 K8AF Cork, Ireland.ORCID 0000-0003-0607-7159
Beatrice BardaFondazione Epatocentro Ticino, Via Soldino 5, 6900 Lugano, Switzerland.
Christian GarzoniFondazione Epatocentro Ticino, Via Soldino 5, 6900 Lugano, Switzerland.
Gian-Reto KlegerDivision of Intensive Care, Cantonal Hospital St. Gallen, Rorschacherstrasse 95, 9007 St. Gallen, Switzerland.
Urs PietschDepartment of Anesthesia, Intensive Care, Emergency and Pain Medicine, Cantonal Hospital St. Gallen, Rorschacherstrasse 95, 9007 St. Gallen, Switzerland.ORCID 0000-0001-6957-2638
Noémie SuhDivision of Intensive Care, Geneva University Hospitals, The Faculty of Medicine, University of Geneva, 1211 Geneva, Switzerland.
Johannes HertelDepartment of Psychiatry and Psychotherapy, University Medicine Greifswald, 17475 Greifswald, Germany.ORCID 0000-0002-7641-0132
Ines ThieleSchool of Medicine, University of Galway, H91 TK33 Galway, Ireland.ORCID 0000-0002-8071-7110

Funding

European Research Council 757922
6 · The paper itself

Abstract

COVID-19, a systemic multi-organ disease resulting from infection with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), is known to result in a wide array of disease outcomes, ranging from asymptomatic to fatal. Despite persistent progress, there is a continued need for more accurate determinants of disease outcomes, including post-acute symptoms after COVID-19. In this study, we characterised the serum metabolomic changes due to hospitalisation and COVID-19 disease progression by mapping the serum metabolomic trajectories of 71 newly hospitalised moderate and severe patients in their first week after hospitalisation. These 71 patients were spread out over three hospitals in Switzerland, enabling us to meta-analyse the metabolomic trajectories and filter consistently changing metabolites. Additionally, we investigated differential metabolite-metabolite trajectories between fatal, severe, and moderate disease outcomes to find prognostic markers of disease severity. We found drastic changes in serum metabolite concentrations for 448 out of the 901 metabolites. These results included markers of hospitalisation, such as environmental exposures, dietary changes, and altered drug administration, but also possible markers of physiological functioning, including carboxyethyl-GABA and fibrinopeptides, which might be prognostic for worsening lung injury. Possible markers of disease progression included altered urea cycle metabolites and metabolites of the tricarboxylic acid (TCA) cycle, indicating a SARS-CoV-2-induced reprogramming of the host metabolism. Glycerophosphorylcholine was identified as a potential marker of disease severity. Taken together, this study describes the metabolome-wide changes due to hospitalisation and COVID-19 disease progression. Moreover, we propose a wide range of novel potential biomarkers for monitoring COVID-19 disease course, both dependent and independent of the severity.

Indexed as

COVID-19disease progressionhospitalisationmetabolomicsmulti-centreserum

Identifiers

PMID37623894
PMCPMC10456321

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.