The Effect of the Ketogenic Diet on Adiponectin, Omentin and Vaspin in Children with Drug-Resistant Epilepsy

Changes in adipokine secretion may be involved in the anti-epileptic effect of a ketogenic diet (KD) in drug-resistant epilepsy (DRE). The assessment of the influence of KD on serum adiponectin, omentin-1, and vaspin in children with DRE. Anthropometric measurements (weight, height, BMI, and waist-t...

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Published in:Nutrients Vol. 14; no. 3; p. 479
Main Authors: Chyra, Marcin, Roczniak, Wojciech, Świętochowska, Elżbieta, Dudzińska, Magdalena, Oświęcimska, Joanna
Format: Journal Article
Language:English
Published: Switzerland MDPI AG 22-01-2022
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Summary:Changes in adipokine secretion may be involved in the anti-epileptic effect of a ketogenic diet (KD) in drug-resistant epilepsy (DRE). The assessment of the influence of KD on serum adiponectin, omentin-1, and vaspin in children with DRE. Anthropometric measurements (weight, height, BMI, and waist-to-hip circumference ratio) were performed in 72 children aged 3-9 years, divided into 3 groups: 24 children with DRE treated with KD, 26-treated with valproic acid (VPA), and a control group of 22 children. Biochemical tests included fasting glucose, insulin, beta-hydroxybutyric acid, lipid profile, aminotransferases activities, and blood gasometry. Serum levels of adiponectin, omentin-1 and vaspin were assayed using commercially available ELISA tests. Serum levels of adiponectin and omentin-1 in the KD group were significantly higher and vaspin-lower in comparison to patients receiving VPA and the control group. In all examined children, serum adiponectin and omentin-1 correlated negatively with WHR and serum triglycerides, insulin, fasting glucose, and HOMA-IR. Vaspin levels correlated negatively with serum triglycerides and positively with body weight, BMI, fasting glucose, insulin, and HOMA-IR. One of the potential mechanisms of KD in children with drug-resistant epilepsy may be a modulation of metabolically beneficial and anti-inflammatory adipokine levels.
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ISSN:2072-6643
2072-6643
DOI:10.3390/nu14030479