Children with Post COVID-19 Multisystem Inflammatory Syndrome Display Unique Pathophysiological Metabolic Phenotypes

SARS-CoV-2 infections in children lead to symptoms from mild respiratory illness to severe postacute sequelae of COVID-19, including multisystem inflammatory syndrome in Children (MIS-C). We conducted a metabolic profiling of 147 children's serum samples, including acute COVID-19 patients, MIS-C patients, and healthy controls. Using nuclear magnetic resonance spectroscopy and liquid chromatography-mass spectrometry, we measured 1101 metabolites. The results revealed distinct metabolic profiles in acute COVID-19 and MIS-C patients, with significant alterations in lipid classes. Both conditions exhibited an elevated Apo-B100/Apo-A1 ratio and increased serum inflammatory markers. MIS-C patients showed unique disruptions, including increased triglycerides and altered lipoprotein composition. Despite milder clinical respiratory symptoms, children's metabolic disturbances mirrored those seen in severe adult COVID-19 patients, indicating a shared inflammatory response to SARS-CoV-2. This suggests potential long-term health impacts, underscoring the need for continued research into the metabolic consequences of COVID-19 in children.

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Publication Details

Journal
Journal of Proteome Research
Published
2025-06-09
DOI
https://doi.org/10.1021/acs.jproteome.5c00062
Citations
5
Primary Topic
COVID-19 Clinical Research Studies
Type
article
Field-Weighted Citation Impact
6.98

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article

Children with Post COVID-19 Multisystem Inflammatory Syndrome Display Unique Pathophysiological Metabolic Phenotypes

Jeremy K. Nicholson, Lael M. Yonker, Luke Whiley, Philipp Nitschke et al.
5 citations
Journal of Proteome Research
COVID-19 Clinical Research Studies
6.98
article

Children with Post COVID-19 Multisystem Inflammatory Syndrome Display Unique Pathophysiological Metabolic Phenotypes

Jeremy K. Nicholson, Lael M. Yonker, Luke Whiley, Philipp Nitschke, Julien Wist, Elaine Holmes, Nicola Gray, Maureen M. Leonard, Reika Masuda, Nathan G. Lawler, Samantha Lodge, Alessio Fasano
article en
5 citations

Abstract

SARS-CoV-2 infections in children lead to symptoms from mild respiratory illness to severe postacute sequelae of COVID-19, including multisystem inflammatory syndrome in Children (MIS-C). We conducted a metabolic profiling of 147 children's serum samples, including acute COVID-19 patients, MIS-C patients, and healthy controls. Using nuclear magnetic resonance spectroscopy and liquid chromatography-mass spectrometry, we measured 1101 metabolites. The results revealed distinct metabolic profiles in acute COVID-19 and MIS-C patients, with significant alterations in lipid classes. Both conditions exhibited an elevated Apo-B100/Apo-A1 ratio and increased serum inflammatory markers. MIS-C patients showed unique disruptions, including increased triglycerides and altered lipoprotein composition. Despite milder clinical respiratory symptoms, children's metabolic disturbances mirrored those seen in severe adult COVID-19 patients, indicating a shared inflammatory response to SARS-CoV-2. This suggests potential long-term health impacts, underscoring the need for continued research into the metabolic consequences of COVID-19 in children.

Journal of Proteome ResearchVol. 24(7)
Harvard University (US), Murdoch University (AU), Massachusetts General Hospital (US), Division of Chemistry (US), Imperial College London (GB), Universidad del Valle (CO)
Australian Research Council, Department of Jobs, Tourism, Science and Innovation, Government of Western Australia, National Heart, Lung, and Blood Institute, National Institute of Allergy and Infectious Diseases, National Institute of Diabetes and Digestive and Kidney Diseases
Zero hunger
Openalex Percentile: Top 3%
COVID-19 Clinical Research Studies
6.98
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