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Long-term follow-up of nutritional status in children with GLUT1 Deficiency Syndrome treated with classic ketogenic diet: a 5-year prospective study

INTRODUCTION: The classic ketogenic diet (cKD) is an isocaloric, high fat, low-carbohydrate diet that induces the production of ketone bodies. High consumption of dietary fatty acids, particularly long-chain saturated fatty acids, could impair nutritional status and increase cardiovascular risk. The...

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Autores principales: De Amicis, Ramona, Leone, Alessandro, Pellizzari, Marta, Foppiani, Andrea, Battezzati, Alberto, Lessa, Chiara, Tagliabue, Anna, Ferraris, Cinzia, De Giorgis, Valentina, Olivotto, Sara, Previtali, Roberto, Veggiotti, Pierangelo, Bertoli, Simona
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10244766/
https://www.ncbi.nlm.nih.gov/pubmed/37293674
http://dx.doi.org/10.3389/fnut.2023.1148960
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author De Amicis, Ramona
Leone, Alessandro
Pellizzari, Marta
Foppiani, Andrea
Battezzati, Alberto
Lessa, Chiara
Tagliabue, Anna
Ferraris, Cinzia
De Giorgis, Valentina
Olivotto, Sara
Previtali, Roberto
Veggiotti, Pierangelo
Bertoli, Simona
author_facet De Amicis, Ramona
Leone, Alessandro
Pellizzari, Marta
Foppiani, Andrea
Battezzati, Alberto
Lessa, Chiara
Tagliabue, Anna
Ferraris, Cinzia
De Giorgis, Valentina
Olivotto, Sara
Previtali, Roberto
Veggiotti, Pierangelo
Bertoli, Simona
author_sort De Amicis, Ramona
collection PubMed
description INTRODUCTION: The classic ketogenic diet (cKD) is an isocaloric, high fat, low-carbohydrate diet that induces the production of ketone bodies. High consumption of dietary fatty acids, particularly long-chain saturated fatty acids, could impair nutritional status and increase cardiovascular risk. The purpose of this study was to evaluate the long-term effects of a 5-year cKD on body composition, resting energy expenditure, and biochemical parameters in children affected by Glucose Transporter 1 Deficiency Syndrome (GLUT1DS). METHODS: This was a prospective, multicenter, 5-year longitudinal study of children with GLUT1DS treated with a cKD. The primary outcome was to assess the change in nutritional status compared with pre-intervention, considering anthropometric measurements, body composition, resting energy expenditure, and biochemical parameters such as glucose and lipid profiles, liver enzymes, uric acid, creatinine, and ketonemia. Assessments were conducted at pre-intervention and every 12 months of cKD interventions. RESULTS: Ketone bodies increased significantly in children and adolescents, and remained stable at 5 years, depending on the diet. No significant differences were reported in anthropometric and body composition standards, as well as in resting energy expenditure and biochemical parameters. Bone mineral density increased significantly over time according to increasing age. Body fat percentage significantly and gradually decreased in line with the increase in body weight and the consequent growth in lean mass. As expected, we observed a negative trend in respiratory quotient, while fasting insulin and insulin resistance were found to decrease significantly after cKD initiation. CONCLUSION: Long-term adherence to cKD showed a good safety profile on anthropometric measurements, body composition, resting energy expenditure, and biochemical parameters, and we found no evidence of potential adverse effects on the nutritional status of children and adolescents.
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spelling pubmed-102447662023-06-08 Long-term follow-up of nutritional status in children with GLUT1 Deficiency Syndrome treated with classic ketogenic diet: a 5-year prospective study De Amicis, Ramona Leone, Alessandro Pellizzari, Marta Foppiani, Andrea Battezzati, Alberto Lessa, Chiara Tagliabue, Anna Ferraris, Cinzia De Giorgis, Valentina Olivotto, Sara Previtali, Roberto Veggiotti, Pierangelo Bertoli, Simona Front Nutr Nutrition INTRODUCTION: The classic ketogenic diet (cKD) is an isocaloric, high fat, low-carbohydrate diet that induces the production of ketone bodies. High consumption of dietary fatty acids, particularly long-chain saturated fatty acids, could impair nutritional status and increase cardiovascular risk. The purpose of this study was to evaluate the long-term effects of a 5-year cKD on body composition, resting energy expenditure, and biochemical parameters in children affected by Glucose Transporter 1 Deficiency Syndrome (GLUT1DS). METHODS: This was a prospective, multicenter, 5-year longitudinal study of children with GLUT1DS treated with a cKD. The primary outcome was to assess the change in nutritional status compared with pre-intervention, considering anthropometric measurements, body composition, resting energy expenditure, and biochemical parameters such as glucose and lipid profiles, liver enzymes, uric acid, creatinine, and ketonemia. Assessments were conducted at pre-intervention and every 12 months of cKD interventions. RESULTS: Ketone bodies increased significantly in children and adolescents, and remained stable at 5 years, depending on the diet. No significant differences were reported in anthropometric and body composition standards, as well as in resting energy expenditure and biochemical parameters. Bone mineral density increased significantly over time according to increasing age. Body fat percentage significantly and gradually decreased in line with the increase in body weight and the consequent growth in lean mass. As expected, we observed a negative trend in respiratory quotient, while fasting insulin and insulin resistance were found to decrease significantly after cKD initiation. CONCLUSION: Long-term adherence to cKD showed a good safety profile on anthropometric measurements, body composition, resting energy expenditure, and biochemical parameters, and we found no evidence of potential adverse effects on the nutritional status of children and adolescents. Frontiers Media S.A. 2023-05-24 /pmc/articles/PMC10244766/ /pubmed/37293674 http://dx.doi.org/10.3389/fnut.2023.1148960 Text en Copyright © 2023 De Amicis, Leone, Pellizzari, Foppiani, Battezzati, Lessa, Tagliabue, Ferraris, De Giorgis, Olivotto, Previtali, Veggiotti and Bertoli. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Nutrition
De Amicis, Ramona
Leone, Alessandro
Pellizzari, Marta
Foppiani, Andrea
Battezzati, Alberto
Lessa, Chiara
Tagliabue, Anna
Ferraris, Cinzia
De Giorgis, Valentina
Olivotto, Sara
Previtali, Roberto
Veggiotti, Pierangelo
Bertoli, Simona
Long-term follow-up of nutritional status in children with GLUT1 Deficiency Syndrome treated with classic ketogenic diet: a 5-year prospective study
title Long-term follow-up of nutritional status in children with GLUT1 Deficiency Syndrome treated with classic ketogenic diet: a 5-year prospective study
title_full Long-term follow-up of nutritional status in children with GLUT1 Deficiency Syndrome treated with classic ketogenic diet: a 5-year prospective study
title_fullStr Long-term follow-up of nutritional status in children with GLUT1 Deficiency Syndrome treated with classic ketogenic diet: a 5-year prospective study
title_full_unstemmed Long-term follow-up of nutritional status in children with GLUT1 Deficiency Syndrome treated with classic ketogenic diet: a 5-year prospective study
title_short Long-term follow-up of nutritional status in children with GLUT1 Deficiency Syndrome treated with classic ketogenic diet: a 5-year prospective study
title_sort long-term follow-up of nutritional status in children with glut1 deficiency syndrome treated with classic ketogenic diet: a 5-year prospective study
topic Nutrition
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10244766/
https://www.ncbi.nlm.nih.gov/pubmed/37293674
http://dx.doi.org/10.3389/fnut.2023.1148960
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