Evidence map›Paper›PMID 34938772›Full record

ArticleFrontiers in molecular biosciences2021

Metabolic and Lipidomic Markers Differentiate COVID-19 From Non-Hospitalized and Other Intensive Care Patients.

Franziska Schmelter, Bandik Föh, Alvaro Mallagaray, Johann Rahmöller, Marc Ehlers, Selina Lehrian, Vera von Kopylow, Inga Künsting, Anne Sophie Lixenfeld, Emily Martin and 10 more

Abstract read
In one paragraph

Article in Frontiers in molecular biosciences, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing 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

30 citing papers in PubMed.

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  13. Serum Metabolomic Profiling of Patients with Lipedema.International journal of molecular sciences · 2023
    Article
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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

20 authors.

Franziska SchmelterInstitute of Nutritional Medicine, University of Lübeck, Lübeck, Germany.
Bandik FöhInstitute of Nutritional Medicine, University of Lübeck, Lübeck, Germany.
Alvaro MallagarayInstitute of Chemistry and Metabolomics, University of Lübeck, Lübeck, Germany.
Johann RahmöllerInstitute of Nutritional Medicine, University of Lübeck, Lübeck, Germany.
Marc EhlersInstitute of Nutritional Medicine, University of Lübeck, Lübeck, Germany.
Selina LehrianInstitute of Nutritional Medicine, University of Lübeck, Lübeck, Germany.
Vera von KopylowInstitute of Nutritional Medicine, University of Lübeck, Lübeck, Germany.
Inga KünstingInstitute of Nutritional Medicine, University of Lübeck, Lübeck, Germany.
Anne Sophie LixenfeldInstitute of Nutritional Medicine, University of Lübeck, Lübeck, Germany.
Emily MartinInstitute of Nutritional Medicine, University of Lübeck, Lübeck, Germany.
Mohab RagabInstitute of Nutritional Medicine, University of Lübeck, Lübeck, Germany.
Roza Meyer-SaraeiDepartment of Cardiology, Angiology and Intensive Care Medicine, University Heart Center Lübeck, Lübeck, Germany.
Fabian KreutzmannDepartment of Cardiology, Angiology and Intensive Care Medicine, University Heart Center Lübeck, Lübeck, Germany.
Ingo EitelDepartment of Cardiology, Angiology and Intensive Care Medicine, University Heart Center Lübeck, Lübeck, Germany.
Stefan TaubeInstitute of Virology and Cell Biology, University of Lübeck, Lübeck, Germany.
Nadja KädingDepartment of Infectious Diseases and Microbiology, University of Lübeck, Lübeck, Germany.
Eckard JantzenResearch and Development Department, GALAB Laboratories GmbH, Hamburg, Germany.
Tobias GrafDepartment of Cardiology, Angiology and Intensive Care Medicine, University Heart Center Lübeck, Lübeck, Germany.
Christian SinaInstitute of Nutritional Medicine, University of Lübeck, Lübeck, Germany.
Ulrich L GüntherInstitute of Chemistry and Metabolomics, University of Lübeck, Lübeck, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Coronavirus disease 2019 (COVID-19) is a viral infection affecting multiple organ systems of great significance for metabolic processes. Thus, there is increasing interest in metabolic and lipoprotein signatures of the disease, and early analyses have demonstrated a metabolic pattern typical for atherosclerotic and hepatic damage in COVID-19 patients. However, it remains unclear whether this is specific for COVID-19 and whether the observed signature is caused by the disease or rather represents an underlying risk factor. To answer this question, we have analyzed 482 serum samples using nuclear magnetic resonance metabolomics, including longitudinally collected samples from 12 COVID-19 and 20 cardiogenic shock intensive care patients, samples from 18 severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) antibody-positive individuals, and single time point samples from 58 healthy controls. COVID-19 patients showed a distinct metabolic serum profile, including changes typical for severe dyslipidemia and a deeply altered metabolic status compared with healthy controls. Specifically, very-low-density lipoprotein and intermediate-density lipoprotein particles and associated apolipoprotein B and intermediate-density lipoprotein cholesterol were significantly increased, whereas cholesterol and apolipoprotein A2 were decreased. Moreover, a similarly perturbed profile was apparent when compared with other patients with cardiogenic shock who are in the intensive care unit when looking at a 1-week time course, highlighting close links between COVID-19 and lipid metabolism. The metabolic profile of COVID-19 patients distinguishes those from healthy controls and also from patients with cardiogenic shock. In contrast, anti-SARS-CoV-2 antibody-positive individuals without acute COVID-19 did not show a significantly perturbed metabolic profile compared with age- and sex-matched healthy controls, but SARS-CoV-2 antibody-titers correlated significantly with metabolic parameters, including levels of glycine, ApoA2, and small-sized low- and high-density lipoprotein subfractions. Our data suggest that COVID-19 is associated with dyslipidemia, which is not observed in anti-SARS-CoV-2 antibody-positive individuals who have not developed severe courses of the disease. This suggests that lipoprotein profiles may represent a confounding risk factor for COVID-19 with potential for patient stratification.

Indexed as

COVID-19lipoproteinsmetabolomicsNMRSARS-CoV-2

Identifiers

PMID34938772
PMCPMC8686182

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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.