Background and aims: Children infected with SARS-CoV-2 may develop multisystem inflammatory syndrome (MIS-C) 4–6 weeks after exposure. MIS-C is characterized by elevated markers of inflammation and low blood values of linoleic acid (LA), arachidonic acid (AA) and docosahexaenoic acid (DHA) during acute phase. The aim of this pilot exploratory study was to assess the short-term beneficial impact on the blood fatty acid profile following DHA supplementation in children who have suffered from MIS-C. Methods: Fifty-two children aged 2–18 years with diagnosed MIS-C, were enrolled between December ‘20 and March ‘22. Blood samples were collected at hospital discharge (T0), and at 3 (T1) and 6 months (T2) post-discharge using dried blood spots for fatty acid analysis by gas chromatography. Inflammatory and metabolic blood markers were assessed at T0 and T2. All participants received healthy dietary advice throughout the study. In Group 1 23 consecutive patients received DHA supplementation (250 mg/day of DHA) from T0 to T1, followed by dietary advice alone until T2. In Group 2 29 children with MIS-C received only dietary advice throughout the observation period. Results: An altered inflammatory status, independent of treatment, was shown in all children compared to pediatric reference values. After intervention, Group 1 experienced a significant enrichment in both total n-6 and n-3 blood FAs when compared to baseline (p < 0.0001). Specifically, there was a significant increase of DHA (1.19 ± 0.25 at T0 vs. 2.67 ± 0.78 at T1) and EPA (0.32 ± 0.09 at T0 vs. 0.46 ± 0.10 at T1) levels, that remained consistent at T2 (p = 0.0002 and p < 0.0001, respectively). Within Group 2 only n-3 alpha linolenic acid (ALA) significantly increased at T1 compared to baseline (p < 0.05). The total increase in n-3 after intervention (ΔT1-T0) was significantly higher in Group 1 compared to Group 2 [1.90(0.9) vs. 0.49(0.8), p < 0.0001 and padj = 0.005]. Erythrocyte sedimentation rate (ESR) and IL-6 showed a better tendency toward normalization in Group 1, although without statistical significance. Conclusion: This pilot study is the first to explore the potential effects of DHA supplementation in children with MIS-C. DHA was associated with improvements in the blood fatty acid profile, which persisted beyond the supplementation period, and showed a trend toward normalization of selected biochemical parameters. Further adequately powered, controlled studies are needed to confirm these observations and to evaluate the potential role of early n-3 PUFA supplementation during the stable and recovery phases in critically ill pediatric patients.

Exploratory study of the effect of DHA supplementation on blood fatty acids and inflammatory markers in children with MIS-C / E. Verduci, P. Risè, G. Fiore, S. Vizzuso, A. Bonomi, D. Dilillo, L. Fiori, E. Di Profio, V. Calcaterra, S. Mannarino, E. Zoia, E. D'Auria, A. Sala, G. Zuccotti. - In: FRONTIERS IN NUTRITION. - ISSN 2296-861X. - 12:(2025 Jul 16), pp. 1597868.1-1597868.14. [10.3389/fnut.2025.1597868]

Exploratory study of the effect of DHA supplementation on blood fatty acids and inflammatory markers in children with MIS-C

E. Verduci
Primo
;
G. Fiore
;
S. Vizzuso;L. Fiori;E. Di Profio;E. D'Auria;A. Sala
Penultimo
;
G. Zuccotti
Ultimo
2025

Abstract

Background and aims: Children infected with SARS-CoV-2 may develop multisystem inflammatory syndrome (MIS-C) 4–6 weeks after exposure. MIS-C is characterized by elevated markers of inflammation and low blood values of linoleic acid (LA), arachidonic acid (AA) and docosahexaenoic acid (DHA) during acute phase. The aim of this pilot exploratory study was to assess the short-term beneficial impact on the blood fatty acid profile following DHA supplementation in children who have suffered from MIS-C. Methods: Fifty-two children aged 2–18 years with diagnosed MIS-C, were enrolled between December ‘20 and March ‘22. Blood samples were collected at hospital discharge (T0), and at 3 (T1) and 6 months (T2) post-discharge using dried blood spots for fatty acid analysis by gas chromatography. Inflammatory and metabolic blood markers were assessed at T0 and T2. All participants received healthy dietary advice throughout the study. In Group 1 23 consecutive patients received DHA supplementation (250 mg/day of DHA) from T0 to T1, followed by dietary advice alone until T2. In Group 2 29 children with MIS-C received only dietary advice throughout the observation period. Results: An altered inflammatory status, independent of treatment, was shown in all children compared to pediatric reference values. After intervention, Group 1 experienced a significant enrichment in both total n-6 and n-3 blood FAs when compared to baseline (p < 0.0001). Specifically, there was a significant increase of DHA (1.19 ± 0.25 at T0 vs. 2.67 ± 0.78 at T1) and EPA (0.32 ± 0.09 at T0 vs. 0.46 ± 0.10 at T1) levels, that remained consistent at T2 (p = 0.0002 and p < 0.0001, respectively). Within Group 2 only n-3 alpha linolenic acid (ALA) significantly increased at T1 compared to baseline (p < 0.05). The total increase in n-3 after intervention (ΔT1-T0) was significantly higher in Group 1 compared to Group 2 [1.90(0.9) vs. 0.49(0.8), p < 0.0001 and padj = 0.005]. Erythrocyte sedimentation rate (ESR) and IL-6 showed a better tendency toward normalization in Group 1, although without statistical significance. Conclusion: This pilot study is the first to explore the potential effects of DHA supplementation in children with MIS-C. DHA was associated with improvements in the blood fatty acid profile, which persisted beyond the supplementation period, and showed a trend toward normalization of selected biochemical parameters. Further adequately powered, controlled studies are needed to confirm these observations and to evaluate the potential role of early n-3 PUFA supplementation during the stable and recovery phases in critically ill pediatric patients.
SARS-CoV-2; long COVID; hospitalized children; polyunsaturated fatty acids; docosahexaenoic acid; inflammation
Settore MEDS-20/A - Pediatria generale e specialistica
Settore MEDS-08/C - Scienza dell'alimentazione e delle tecniche dietetiche applicate
Settore BIOS-11/A - Farmacologia
16-lug-2025
Article (author)
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/1175895
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