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Updated: Jun 1, 2025

Cell-free Biochemical Fluorometric Enzymatic Assay for High-throughput Measurement of Lipid Peroxidation in High Density Lipoprotein
Published on: October 12, 2017
Serum HDL and their subfractions are impaired in multisystem inflammatory syndrome in children (MIS-C)
Antonietta Giannattasio1, Alice Castaldo2,3, Michela Grieco1
1Dipartimento di Pediatria Generale e d'Urgenza, AORN Santobono-Pausilipon, Naples, Italy.
Insights
Multisystem inflammatory syndrome in children (MIS-C) involves altered high-density lipoproteins (HDL). Lower HDL and specific HDL subfractions (HDL-SUB) may serve as biomarkers for MIS-C diagnosis.
Area of Science:
- Immunology
- Cardiovascular Research
- Pediatric Infectious Diseases
Background:
- Multisystem inflammatory syndrome in children (MIS-C) is a severe post-COVID-19 condition characterized by a hyperimmune response.
- High-density lipoproteins (HDL) play a crucial role in modulating inflammation and immune responses through their subfractions.
Purpose of the Study:
- To investigate the role of serum cholesterol, HDL, and HDL subfractions (HDL-SUB) in the pathogenesis of MIS-C.
- To determine the potential of HDL and HDL-SUB as diagnostic biomarkers for MIS-C.
Main Methods:
- Serum levels of cholesterol, HDL, and HDL-SUB were analyzed using capillary electrophoresis.
- These lipid parameters were correlated with biomarkers of inflammation and endothelial damage measured by microfluidic immunoassays.
- The study included 48 MIS-C patients at hospital admission and 48 age- and sex-matched healthy controls.
Main Results:
- MIS-C patients exhibited significantly lower serum cholesterol and HDL levels compared to controls.
- Serum cholesterol inversely correlated with inflammation biomarkers, indicating cytokine impact on reverse cholesterol transport.
- HDL levels inversely correlated with endothelial damage biomarkers, suggesting HDL's role in MIS-C endothelial dysfunction. A remodeling of HDL-SUB was observed, with a decrease in anti-inflammatory small HDL particles.
Conclusions:
- The study confirms a severe impairment of reverse cholesterol transport in MIS-C.
- Serum HDL and HDL-SUB show promise as valuable diagnostic biomarkers for MIS-C.
Background:
Multisystem inflammatory syndrome in children (MIS-C) is a severe post-COVID condition due to a delayed hyperimmune response to SARS-CoV-2. High-density lipoproteins (HDL) are pivotal players in inflammatory and immune modulation through the remodeling of their subfractions.
Methods:
This study aimed to evaluate serum levels of cholesterol, HDL, and HDL subfractions (HDL-SUB) to define their role in the pathogenesis of MIS-C and their potential use as biomarkers of this condition. We analyzed serum cholesterol, HDL and HDL-SUB (by capillary electrophoresis) in relation to serum values of biomarkers of inflammation and endothelial damage (by microfluidic immunoassays) in 48 patients with MIS-C at hospital admission and in 48 age- and sex-matched healthy controls.
Results:
Serum cholesterol, as well as HDL, were significantly lower in MIS-C patients than controls. Serum cholesterol was inversely correlated with all biomarkers of inflammation, confirming the impact of cytokines on reverse cholesterol transport, whereas HDL values were inversely correlated with serum biomarkers of endothelial damage, suggesting a role of HDL in endothelial damage in MIS-C patients. Furthermore, we found a remodeling of HDL-SUB with a more pronounced decrease in small HDL that have anti-inflammatory activity.
Conclusions:
These data confirm the severe impairment of reverse cholesterol transport in MIS-C and indicate serum HDL and HDL-SUB as potential useful diagnostic biomarkers of MIS-C.
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