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Ketogenic diet for mitochondrial disease: a systematic review on efficacy and safety

BACKGROUND: No curative therapy for mitochondrial disease (MD) exists, prioritizing supportive treatment for symptom relief. In animal and cell models ketones decrease oxidative stress, increase antioxidants and scavenge free radicals, putting ketogenic diets (KDs) on the list of management options...

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Autores principales: Zweers, Heidi, van Wegberg, Annemiek M. J., Janssen, Mirian C. H., Wortmann, Saskia B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8254320/
https://www.ncbi.nlm.nih.gov/pubmed/34217336
http://dx.doi.org/10.1186/s13023-021-01927-w
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author Zweers, Heidi
van Wegberg, Annemiek M. J.
Janssen, Mirian C. H.
Wortmann, Saskia B.
author_facet Zweers, Heidi
van Wegberg, Annemiek M. J.
Janssen, Mirian C. H.
Wortmann, Saskia B.
author_sort Zweers, Heidi
collection PubMed
description BACKGROUND: No curative therapy for mitochondrial disease (MD) exists, prioritizing supportive treatment for symptom relief. In animal and cell models ketones decrease oxidative stress, increase antioxidants and scavenge free radicals, putting ketogenic diets (KDs) on the list of management options for MD. Furthermore, KDs are well-known, safe and effective treatments for epilepsy, a frequent symptom of MD. This systematic review evaluates efficacy and safety of KD for MD. METHODS: We searched Pubmed, Cochrane, Embase and Cinahl (November 2020) with search terms linked to MD and KD. From the identified records, we excluded studies on Pyruvate Dehydrogenase Complex deficiency. From these eligible reports, cases without a genetically confirmed diagnosis and cases without sufficient data on KD and clinical course were excluded. The remaining studies were included in the qualitative analysis. RESULTS: Only 20 cases (14 pediatric) from the 694 papers identified met the inclusion criteria (one controlled trial (n = 5), 15 case reports). KD led to seizure control in 7 out of 8 cases and improved muscular symptoms in 3 of 10 individuals. In 4 of 20 cases KD reversed the clinical phenotype (e.g. cardiomyopathy, movement disorder). In 5 adults with mitochondrial DNA deletion(s) related myopathy rhabdomyolysis led to cessation of KD. Three individuals with POLG mutations died while being on KD, however, their survival was not different compared to individuals with POLG mutations without KD. CONCLUSION: Data on efficacy and safety of KD for MD is too scarce for general recommendations. KD should be considered in individuals with MD and therapy refractory epilepsy, while KD is contraindicated in mitochondrial DNA deletion(s) related myopathy. When considering KD for MD the high rate of adverse effects should be taken into account, but also spectacular improvements in individual cases. KD is a highly individual management option in this fragile patient group and requires an experienced team. To increase knowledge on this—individually—promising management option more (prospective) studies using adequate outcome measures are crucial. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13023-021-01927-w.
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spelling pubmed-82543202021-07-06 Ketogenic diet for mitochondrial disease: a systematic review on efficacy and safety Zweers, Heidi van Wegberg, Annemiek M. J. Janssen, Mirian C. H. Wortmann, Saskia B. Orphanet J Rare Dis Review BACKGROUND: No curative therapy for mitochondrial disease (MD) exists, prioritizing supportive treatment for symptom relief. In animal and cell models ketones decrease oxidative stress, increase antioxidants and scavenge free radicals, putting ketogenic diets (KDs) on the list of management options for MD. Furthermore, KDs are well-known, safe and effective treatments for epilepsy, a frequent symptom of MD. This systematic review evaluates efficacy and safety of KD for MD. METHODS: We searched Pubmed, Cochrane, Embase and Cinahl (November 2020) with search terms linked to MD and KD. From the identified records, we excluded studies on Pyruvate Dehydrogenase Complex deficiency. From these eligible reports, cases without a genetically confirmed diagnosis and cases without sufficient data on KD and clinical course were excluded. The remaining studies were included in the qualitative analysis. RESULTS: Only 20 cases (14 pediatric) from the 694 papers identified met the inclusion criteria (one controlled trial (n = 5), 15 case reports). KD led to seizure control in 7 out of 8 cases and improved muscular symptoms in 3 of 10 individuals. In 4 of 20 cases KD reversed the clinical phenotype (e.g. cardiomyopathy, movement disorder). In 5 adults with mitochondrial DNA deletion(s) related myopathy rhabdomyolysis led to cessation of KD. Three individuals with POLG mutations died while being on KD, however, their survival was not different compared to individuals with POLG mutations without KD. CONCLUSION: Data on efficacy and safety of KD for MD is too scarce for general recommendations. KD should be considered in individuals with MD and therapy refractory epilepsy, while KD is contraindicated in mitochondrial DNA deletion(s) related myopathy. When considering KD for MD the high rate of adverse effects should be taken into account, but also spectacular improvements in individual cases. KD is a highly individual management option in this fragile patient group and requires an experienced team. To increase knowledge on this—individually—promising management option more (prospective) studies using adequate outcome measures are crucial. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13023-021-01927-w. BioMed Central 2021-07-03 /pmc/articles/PMC8254320/ /pubmed/34217336 http://dx.doi.org/10.1186/s13023-021-01927-w Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Review
Zweers, Heidi
van Wegberg, Annemiek M. J.
Janssen, Mirian C. H.
Wortmann, Saskia B.
Ketogenic diet for mitochondrial disease: a systematic review on efficacy and safety
title Ketogenic diet for mitochondrial disease: a systematic review on efficacy and safety
title_full Ketogenic diet for mitochondrial disease: a systematic review on efficacy and safety
title_fullStr Ketogenic diet for mitochondrial disease: a systematic review on efficacy and safety
title_full_unstemmed Ketogenic diet for mitochondrial disease: a systematic review on efficacy and safety
title_short Ketogenic diet for mitochondrial disease: a systematic review on efficacy and safety
title_sort ketogenic diet for mitochondrial disease: a systematic review on efficacy and safety
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8254320/
https://www.ncbi.nlm.nih.gov/pubmed/34217336
http://dx.doi.org/10.1186/s13023-021-01927-w
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