|Year : 2021 | Volume
| Issue : 4 | Page : 470-480
Emerging role of the ketogenic dietary therapies beyond epilepsy in child neurology
Dipti Kapoor1, Divyani Garg2, Suvasini Sharma1
1 Department of Pediatrics (Neurology Division), Lady Hardinge Medical College and Kalawati Saran Children's Hospital, New Delhi, India
2 Department of Neurology, Lady Hardinge Medical College and Smt. Sucheta Kriplani Hospital, New Delhi, India
|Date of Submission||08-Jan-2021|
|Date of Acceptance||23-Jan-2021|
|Date of Web Publication||11-May-2021|
Dr. Suvasini Sharma
Department of Pediatrics (Neurology Division), Lady Hardinge Medical College and Kalawati Saran Children's Hospital, New Delhi
Source of Support: None, Conflict of Interest: None
| Abstract|| |
Ketogenic dietary therapies (KDTs) have been in use for refractory paediatric epilepsy for a century now. Over time, KDTs themselves have undergone various modifications to improve tolerability and clinical feasibility, including the Modified Atkins diet (MAD), medium chain triglyceride (MCT) diet and the low glycaemic index treatment (LGIT). Animal and observational studies indicate numerous benefits of KDTs in paediatric neurological conditions apart from their evident benefits in childhood intractable epilepsy, including neurodevelopmental disorders such as autism spectrum disorder, rarer neurogenetic conditions such as Rett syndrome, Fragile X syndrome and Kabuki syndrome, neurodegenerative conditions such as Pelizaeus-Merzbacher disease, and other conditions such as stroke and migraine. A large proportion of the evidence is derived from individual case reports, case series and some small clinical trials, emphasising the vast scope for research in this avenue. The term 'neuroketotherapeutics' has been coined recently to encompass the rapid strides in this field. In the 100th year of its use for paediatric epilepsy, this review covers the role of the KDTs in non-epilepsy neurological conditions among children.
Keywords: Bioenergetics, ketogenic dietary therapy, modified atkins diet, neuroketotherapeutics
|How to cite this article:|
Kapoor D, Garg D, Sharma S. Emerging role of the ketogenic dietary therapies beyond epilepsy in child neurology. Ann Indian Acad Neurol 2021;24:470-80
| Introduction|| |
Ketogenic Dietary Therapies (KDTs) have traditionally been used in the treatment of paediatric refractory epilepsy., Over nearly 100 years (since 1921) of use for paediatric epilepsy, and better understanding about the mechanisms of action, the spectrum of therapeutic indications of KDTs seems to be evolving, with parallel substantial increment in publications on KD in the last decade.
There are four forms of KDT available, which include the classic KD, the modified Atkins diet (MAD), the medium-chain triglyceride diet (MCT) and the low glycaemic index treatment (LGIT). The classic KD used a 3:1 to 4:1 ratio of fat to carbohydrates (in grams). In the MAD, carbohydrates are restricted to 20 g per day and fats are increased. The major advantage of the MAD is that it can be initiated on an outpatient basis, unlike the classic KD. The MCT diet involves the use of medium-chain triglycerides as a rich ketogenic source thereby permitting relative liberalisation of carbohydrates in the diet. In the LGIT diet, complex carbohydrates with high glycaemic index are employed.
Even among epilepsy patients, additional effects of the KDTs were noted apart from seizure control, namely improvement in alertness, behaviour, sleep and cognition. These effects were not totally explained by either seizure control or reduction in antiseizure medication dosages. However, apart from these effects in epilepsy, the ketogenic diet was shown to confer a host of benefits including improved energy, decreased negative affect, improved social functioning, working memory and quality of life. The broad range of non-epilepsy conditions in which the KDTs have been studied with varying degrees of therapeutic efficacy includes autism spectrum disorders, Angelman syndrome, mitochondrial diseases, headache, traumatic brain injury, Alzheimer's disease, Parkinson's disease, sleep disorders, amyotrophic lateral sclerosis, brain tumours, etc.
Bioenergetic dysregulation, including energy failure as seen in mitochondrial conditions, is increasingly considered to be a key mechanism underlying neuronal death in neurodegenerative conditions, leading to considerable interest in the repurposed role of the ketogenic diet in these diseases. The various mechanisms underlying the efficacy of the KDT in both epilepsy and non-epilepsy conditions are summarised in [Figure 1]. The term 'neuroketotherapeutics' was recently coined to refer to the use of ketosis for the improvement of diseased conditions of the nervous system. The target interval of ketone blood concentrations is from >0.2 up to 5-8 mM, which is in the range of moderate ketosis and has been reported to be safe and helpful.,,
|Figure 1: Mechanisms of action of ketogenic dietary therapy. ATP= adenosine triphosphate; BHB= betahydroxybutyrate; GABA= gamma aminobutyric acid; PUFA= polyunsaturated fatty acids; ROS=reactive oxygen species|
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In the 100th year anniversary of its use for epilepsy, this paper aims to explore the utility of the ketogenic use in non-epileptic conditions in children.
| Search Methodology|| |
We have conducted a narrative review using PubMed database which was searched and all published data available on uses of the ketogenic diet in child neurology other than epilepsy up to December 2020 was reviewed, using the search terms 'ketogenic diet' or 'ketogenic dietary therapy' or 'Modified Atkins diet' and 'paediatric neurology' or 'child neurology.' Additional cross-search was conducted for specific conditions such as 'stroke', 'migraine', 'autism spectrum disorder', 'Rett syndrome', 'global developmental delay', 'Fragile X syndrome', 'Kabuki syndrome', 'Pelizaeus Merzbacher disease' and 'Subacute sclerosing panencephalitis.' All types of studies including reviews, clinical studies, case series, case reports were included in the review. The abstracts were screened for relevance to the review topic.
| KD in Neurodevelopmental Disorders|| |
Autism spectrum disorder (ASD)
ASD is characterised by impairments in social communication and social interaction, and the presence of repetitive, restricted, patterns of behaviour and interests. No specific therapy is currently available for social deficits and repetitive behaviours.
KDT has been shown to reduce cortical excitability, restore bioenergetics dysfunction, improve myelin formation and white matter development and improve gut microbiota [Figure 1]. At the molecular level, the role of chronic neuroinflammation and altered ATP synthesis have been suggested to underlie some aspects of ASD., Recently, insight into possible genetic-environmental interactions as a cause of ASD have provided a clue to the possible role of physiological abnormalities in the functioning of mitochondria.
Several animal studies have demonstrated that ketogenic diet might be effective in treating an ASD-like behavioural phenotype by improving sociability and decreasing repetitive behaviour.,,
In human trials also [Table 1], ketogenic diet was observed to be effective in mitigating deficits in social behaviour, communication and repetitive behavioural patterns. The KD has been studied for ASD in two uncontrolled and one controlled open-label clinical trials and the MAD has been studied in one controlled open-label trial. Most commonly, majority of the children tolerated the diet and demonstrated moderate improvement in ASD symptoms, as monitored by Childhood Autism Rating Scale (CARS) or Autism Diagnostic Observation Schedule (ADOS) scores.,,,
|Table 1: Some neurological conditions for which KDTs has been used in human studies among children|
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Global developmental delay is defined as significant delay in two or more developmental domains. There is very limited data on the role of KDTs in this entity.
To explore the role of KDTs in children with global developmental delay, Zhu et al. conducted a prospective case-control study for hospitalised children with global developmental delay who were divided into a KD treatment group or a conventional treatment group [Table 1]. The authors concluded that the KD can improve neurobehavioral development and emotional behaviours in children with global developmental delay, with few adverse effects. However, this study did not mention effects on comorbid epilepsy or seizures.
Attention deficit hyperactivity disorder (ADHD)
ADHD in children is characterised by impulsivity, motor hyperactivity, inappropriate behaviour and inattention. These symptoms are attributed to altered neurotransmission and reduced prefrontal cortex metabolism.
Several animal studies have shown that administration of KD caused reduction in hyperactivity and decreased exploratory behaviour compared to controls [Table 1].
Although there is no human study so far aiming to study the effect of KD in ADHD, a case study investigated behaviour and development in children with severe seizures before commencing a ketogenic diet. KD was found to significantly reduce seizure frequency within one year along with significant improvement in motor functioning, self-help skills, attention and social skills with ketogenic diet in children with abnormal emotional and behavioural responses. Although the primary outcome in this study was seizure control, it suggested possible beneficial implications of ketogenic diet on ADHD-like symptoms in children.
Balance of evidence
Further studies are required, specifically focusing on the effects of ketogenic diet in ADHD to directly assess its efficacy.
| KD in Neurogenetic Conditions|| |
Rett syndrome (RTT)
RTT, an X-linked neurodevelopmental disorder caused by mutations in the MECP2 gene, is one of the leading causes of intellectual disability in female children. The GABAergic signalling system has been implicated as a key pathway commonly disturbed in neurodevelopmental diseases including RTT. The GABA-A receptor is a therapeutic target for neurodevelopmental disorders. One of the proposed mechanisms of action of the KD is increase in the synthesis of GABA and decrease in synthesis of excitatory neurotransmitters, such as glutamate [Figure 1].
It has been shown that mice with Mecp2-deficiency exclusively in GABAergic neurons rapidly develop forepaw stereotyped movements, compulsive grooming, learning and memory deficits, abnormal social behaviour, electroencephalography hyperexcitability, lack of motor coordination, severe respiratory dysrhythmias and premature lethality [Table 1].
KDTs have been shown promising results in controlling refractory epilepsy associated with RTT. Though reports on application of this diet to RTT cases and in RTT-mice models are scarce, Mantis et al. in their study on Mecp2 null mice models, observed that the KD ameliorated anxiety and motor measurements. However, further studies are required to explore the role of KDTs in non-epileptic symptomatology spectrum in RTT.
Fragile X syndrome (FXS)
FXS is a neurodevelopmental disorder clinically characterised by intellectual disability (overall IQ < 70), autistic-like behaviours and seizures. FXS results from a triplet repeat expansion mutation in FMR1 gene on the X chromosome.
Westmark et al. tested the effects of chronic ketogenic diet treatment on seizures, body weight, ketone and glucose levels, diurnal activity levels, learning and memory, and anxiety behaviours in affected mice models [Table 1]. They observed that KD selectively attenuates seizures in male mice but not female mice and differentially affects weight gain and diurnal activity levels dependent on genotype, sex and age. Since there is growing evidence that KDTs might be beneficial in ASD, future research is warranted to delineate their potential utility in this syndrome.
Kabuki syndrome is a monogenic disorder, the manifestations of which include intellectual disability, postnatal growth retardation, immunological dysfunction, and characteristic facial features. The underlying pathophysiology involves defects in opening of chromatin, a process essential for transcription of genes. Hence, agents that promote open chromatin states, such as histone deacetylase inhibitors (HDACis), could have a role in ameliorating disease progression. Recently, beta-hydroxybutyrate (BHB), a ketone body, has been shown to have HDACi activity.
Benjamin et al. demonstrated rescue of hippocampal memory defects and deficiency of adult neurogenesis in a mouse model of Kabuki syndrome by imposing a ketogenic diet [Table 1]. This strategy might have worked by raising the level of the ketone beta-hydroxybutyrate, an endogenous HDACi. This work suggests that KDTs might be considered a feasible treatment option for Kabuki syndrome.
Prader-Willi Syndrome (PWS)
PWS is the most common genetic cause of obesity caused by mutations in the paternal genes on chromosome 15q11-q13. During childhood, patients develop insatiable appetite, hyperphagia and obesity. Various dietary strategies have been used for weight management in PWS.
Felix et al. conducted a study to test the use of the MAD (low carbohydrate and high fat) for children with PWS ages 6–12 years who were overweight/obese [Table 1]. They observed positive effects on hyperphagia and behaviour in patients, with minimal adverse effects.
Though the sample size was small, this study could act as pilot study for larger clinical trials investigating the role of KDTs in children with PWS.
| KD and Brain Tumours|| |
There is preferential dependence of malignant cells on glucose and aerobic glycolysis as a source of energy (Warburg effect) which renders them susceptible to strategies that reduce glucose availability. As rapidly proliferating cancer cells are dependent on abundant levels of glucose, a ketogenic diet may put the cancer cells under metabolic stress and inhibit or delay the cancer's growth. Other possible mechanisms of action could be potential anti-angiogenic and anti-proliferative effects, decreased substrates for macromolecular synthesis, as well as possible effects on oxidative stress, the NLRP3 inflammasome, and regulation of gene expression.,
There are limited studies demonstrating the benefit to this diet for patients with central nervous system (CNS) malignancies, more so in paediatric population. There have been few studies in adults exploring the role of KDTs in CNS tumours. They have observed beneficial effect, but all had limitations of very small sample size, concurrent treatment, and lack of uniformity regarding diagnosis and stage of disease.,
Nebeling et al. reported positive responses in two children with astrocytoma. A systematic review evaluating the role of KDTs in therapeutic management of adult and paediatric gliomas revealed that though the diet is well tolerated, there is insufficient evidence to suggest any therapeutic effect of KDTs in the management of gliomas. They recommended further high-quality research to determine effectiveness of KDTs in management of gliomas. KD has also been tried in recurrent diffuse intrinsic pontine glioma and subependymal giant cell tumour (SEGCT) among children with tuberous sclerosis (TSC) with no success., There are various ongoing prospective clinical trials evaluating the effectiveness of KDTs in management of CNS malignancies. (NCT03451799, NCT03328858, NCT03160599, NCT02694094)
| KDT in Inborn Errors of Metabolism (IEM)|| |
The KD diet has been effective in improving cognition and behaviour in glucose transporter protein 1 deficiency syndrome, pyruvate dehydrogenase complex deficiency and glycogen storage disease type V.
Glucose transporter protein 1 (GLUT-1) deficiency
GLUT-1 deficiency syndrome, associated usually with SLC2A mutations, presents phenotypically with developmental delay, epilepsy, microcephaly and movement disorders.
Ramm-Pettersen et al. demonstrated improvements in general alertness, expressive language, articulation and cognitive index after starting the KD in patients diagnosed with glucose transporter protein 1 deficiency complex. In another study, MAD was tried in 10 patients with improvement in epilepsy as well as movement disorders observed.
Pyruvate dehydrogenase complex (PDC) deficiency
KD use has been reported for PDH deficiency since 1976. In PDC deficiency, the end product of glycolysis, pyruvate, cannot be optimally routed through the tricarboxylic acid pathway, leading to lactate accumulation and impaired ATP production. The ketone bodies produced during ketogenesis provide alternate fuel sources to the brain.
Sofou et al. implemented the KD on 19 children diagnosed with pyruvate dehydrogenase complex deficiency and observed improvements in speech and language, ataxia, sleep disturbances, behaviour and social functioning.
Glycogen storage disease type V
Glycogen storage disease type V (GSDV), also known as McArdle disease, is a rare inborn error of carbohydrate metabolism in skeletal muscle caused by mutations in the muscle glycogen phosphorylase gene. Absence of myophosphorylase results in inability to mobilise muscle glycogen stores. Accordingly, exercise tolerance is limited and varies as a function of the availability of alternative fuels. Currently, there is no satisfactory treatment for GSDV. Since ketone bodies can act as an alternative fuel to muscle glycogenolysis during exercise, the role of KD in this disorder needs to be explored.
There is one case report in literature, where administration of KD to a 55-year-old patient for one year led to improvement in exercise tolerance. Lokken et al. conducted their study in 10 patients and observed that there was improvement in exercise tolerance assessed by heart rate changes during constant load cycling along with reduction in perceived exertion by the patients [Table 1].
Larger, adequately powered trials are needed to investigate the role of KD in this disorder.
| KDT in Neurodegenerative Disorders|| |
Glucose hypometabolism, mitochondrial dysfunction and increased reactive oxygen species (ROS) production are common features in several neurodegenerative diseases, including ALS, AD, Parkinson's (PD) and Huntington's (HD) diseases, linking deficient energy metabolism to neurodegeneration. Hence, the use of energy fuels such as ketones has been suggested as a strategy for the treatment of neurodegenerative diseases.
Apart from this altered energy metabolism, the other proposed mechanisms of action of KD in neurodegenerative conditions are reduction of oxidative stress and neuroinflammation as observed in the nervous system of animal models.
Subacute sclerosing panencephalitis (SSPE)
SSPE is a chronic, progressive, inflammatory, and degenerative affliction of the brain caused by a persistent infection by, or, mutation of the measles virus (MV). The pathogenesis of SSPE is related to direct infection of the central nervous system (CNS) by measles virus, causing progressive inflammation and sclerosis (neurodegeneration) of the brain due to an impaired immune response.
Since the KD was found effective in refractory epilepsy, with anti-inflammatory and neuroprotective properties in neurodegenerative conditions, Nathan et al. explored its role in SSPE. They observed that treatment of an 8-year-old boy diagnosed with SSPE, led to a significant improvement in the physical parameters and cognition and resulted in the cessation of the myoclonic jerks within a month of starting the therapy. Bautista et al. also reported a 9-year old patient with SSPE whose myoclonus improved significantly, albeit temporarily, after being placed on the ketogenic diet. However, a multicentre, randomised controlled trial would be helpful in determining the potential of the KD therapy in SSPE.
Other neurodegenerative disorders
KDTs have been studied in a limited manner in very small studies in other neurodegenerative conditions, such as Lafora body disease (LBD). In a preliminary observation among five patients with LBD, KD was found to not impact disease progression.
In patients with neuronal ceroid lipofuscinosis (NCL), the KD was shown to be complementary for seizure control to drug therapy among patients with CLN2 disease.
In a prospective open-label study, four patients (7-20 years) with North Sea Progressive Myoclonic Epilepsy underwent the modified Atkins diet. The primary outcome, which was health-related quality of life, improved in one patient but remained unchanged in the remaining three patients.
Pelizaeus–Merzbacher disease (PMD)
PMD is a potentially fatal leukodystrophy characterised by pathological hypomyelination resulting in nystagmus, hypotonia, spasticity, ataxia and retarded cognitive development. Currently, PMD lacks any definitive therapeutic option. It has been observed in vitro and in vivo that lipid supplementation can enhance myelination in hypomyelinating pathologies and thereby promote repair. However, under physiological conditions, plasma cholesterol cannot cross the intact blood–brain barrier (BBB).
Stumpf et al. in their experiment on PMD mouse model with preserved BBB demonstrated that a high-fat/low-carbohydrate ketogenic diet restored oligodendrocyte integrity and increased CNS myelination [Table 1]. This dietary intervention also ameliorated axonal degeneration and normalized motor functions. They suggested that KDTs could have a potential therapeutic role in this disorder.
Alternating hemiplegia of childhood (AHC)
AHC is a severe neurological disorder with infantile-onset recurrent episodes of hemiplegia in either side of the body. Pathogenic variants of ATP1A3 primarily cause AHC with altered function of the Na+-K+- ATPase pump, which maintains the resting state of the cell and functions as a signal transducer.
Isolated case reports and case series described the potential beneficial effect of the ketogenic diet.,, They observed reduced frequency and severity of attacks, prolonged attack-free periods (12-15 months), reduced seizure frequency and anti-epileptic drugs burden and improved neurocognition and motor skills [Table 1]. The mechanism of action of KD could be improvement in brain glucose hypometabolism and activation of widely distributed Na+-K+- ATPase channels, which are present in an inhibited state in AHC.
| KDT in Acute Neurological Emergencies|| |
Traumatic brain injury
Animal studies have suggested that the brain's ability to use glucose as a fuel is impaired after brain injury. In addition, there is evidence that in state of acquired brain injury, ketone uptake and metabolism is favoured.
Many studies have shown that a ketogenic diet is an effective treatment therapy for traumatic brain injuries in rat models.,, Therefore, ketogenic diet therapy may be a potential therapeutic option in patients with acquired brain injury in paediatric ICUs. The various mechanisms implicated are reduced ability of brain to utilise glucose in times of oxidative stress and ketones being more energy efficient, tend to improve the cellular metabolism, reduce apoptosis and free radical generation and lead to improvement in cerebral blood flow.
A more recent animal study was conducted to assess the neuropathological changes in the ipsilateral cortex homogenates and mitochondria for markers of oxidative and antioxidant expression and mitochondrial function in an animal-based injury model fed with KD. They observed that the markers of oxidative stress were significantly attenuated and mitochondrial dysfunction was prevented with the KD. It could be concluded that ketogenic diet may improve cerebral metabolism in TBI.
Apart from animal models, two studies have reported adults with traumatic brain injuries treated with a ketogenic diet., They observed that ketogenic diets avoided states of hyperglycemia in post-traumatic brain injury, despite providing sufficient calories. Such biochemical changes were shown to be neuro-protective, without any serious adverse safety events.
Balance of evidence
Based on all the above-mentioned studies, it is evident that ketone bodies might play a vital role in the neurological recovery. Though most evidence stems mainly from animal studies and small clinical studies, there is evident need for randomised clinical studies to understand a stronger correlation between introduction of KD and its effect on recovery post-TBI. A pilot study about the safety and feasibility of Ketogenic Diet in Traumatic Brain Injury (KETI) is currently underway. (https://clinicaltrials.gov/ct2/show/NCT03982602)
Ischemic strokes cause brain damage by excitotoxicity and apoptosis within hours of insult. Few animal studies have demonstrated that ketones are associated with a decrease in biomarkers of apoptosis thereby implying relative neuron sparing effect after stroke. Ketone bodies protect neurons and prolong their survival from mechanisms that precipitate excitotoxicity and eventually death thereby exerting neuroprotective effects.
The KD has been demonstrated to ameliorate free radical injury to neurons post-stroke by improving the neuron's ability to eliminate free radicals and protecting mitochondria from oxidative stress-induced damage by an improvement of mitochondrial antioxidant capacity.
Julio-Ampilas et al. in their study on animal models also concluded that the KD leads to decreased cerebral oedema formation, infarct volume and reactive oxygen production after an ischemic insult. Shaafi et al. in their study to evaluate the effects of KD preconditioning on early behaviour-motor outcome of rats with induced cerebral ischemic stroke observed that rats in the KD group were able to adjust their steps quickly and efficiently and were also able to have more symmetrical hand movements compared to other groups. This suggested the putative role of KD in preconditioning with improvement of early motor and behavioural outcomes after ischemic stroke. In another study by Yang et al., KD-fed mice were compared to mice fed low fat, high carbohydrate (HC group) diet and standard chow (control group) after diet administration for 3 weeks followed by reversible middle cerebral artery occlusion. KD-fed mice showed low volume of infarct development and better regional cerebral blood flow, increased extracellular adenosine, increased expression of hypoxia inducible factor (HIF)- related genes, and erythropoietin and VEGF protein levels compared to the other two groups [Table 1].
Balance of evidence
These observations support the therapeutic potential of KD in ischemic insults, which are associated with energy impairment and oxidative stress and which require treatments that can be effective when administered after the insult.
| KDT in Other Neurological Conditions|| |
Migraine is a common, often underdiagnosed problem in children. The pathophysiology of the disorder presumably involves recurrent attacks of neurovascular pain triggered by a hyperexcitable and hypometabolic brain. Even in absence of robust scientific evidence, there has been a long debate regarding certain foods triggering the migraine attacks and role of dietary restrictions in prevention.
This led to the thought of exploring the possible role of KDTs in preventive treatment of migraine. Experimental evidence indicates that KD may favourably act at different stages of migraine pathophysiology. It might help in restoring brain metabolism and excitability by inhibiting propagation of cortical spreading depression, improving the unbalance between excitatory and inhibitory neurotransmission, counteracting neuroinflammation and oxidative stress.
Animal studies have revealed KD significantly enhances brain metabolism by upregulation of genes encoding energy metabolism enzymes/mitochondrial proteins and increases the number of mitochondrial profiles and the phosphocreatine/creatine ratio.
Several human trials have also observed beneficial role of KDTs in migraine prophylaxis, causing significant reduction in attack frequency and intensity.,,
Balance of evidence
Although KDTs seem a promising therapeutic tool for migraine prevention in adults; however, well-designed therapeutic trials evaluating benefits of KDTs in paediatric migraine are warranted.
The indications for KDT in neurological conditions in children are summarised in [Table 2], based on efficacy.
|Table 2: Summary of conditions other than epilepsy with probable/ possible benefit from KDT [Adapted from Kossoff et al.]|
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| Future Avenues for Research|| |
The above review presents the evidence for KDTs in a host of conditions, apart from epilepsy.
More clarity is required in the mechanism of action of KDT, and how these mechanisms vary in different indications. It is clear that the evidence is in continual evolution, and data from high-quality clinical trials is the need of the hour. Future research must focus on finetuning selection of patients who would benefit from the diet. Additionally, in resource constrained settings, the efficacy and tolerability of KD variants such as the MAD must also be assessed in randomised trials, as these are better accessible and affordable.
Further longitudinal data is also necessary on long-term implications and possible adverse effects of KDTs, especially among patients with progressive neurological conditions who will require the KDT for prolonged durations.
| Conclusions|| |
The use of KDTs demonstrates numerous metabolic ramifications in the brain. As a consequence, these dietary therapies may be of benefit in several neurological conditions, apart from established benefit in epilepsy. However, this field is continuing to evolve, and much of the present evidence emanates from animal studies, case reports, case series and small studies. However, this may be worth trying in desperate situations, neurodegenerative conditions, several intellectual disability and malignant brain tumours. Apart from research settings, KDTs may be offered in selected patients after weighing risks and benefits with caretakers and family members. The understanding that the ketogenic diet needs regular medical supervision must be imparted. These dietary therapies must always be offered in concert with standard treatment and supportive care.
Financial support and sponsorship
Conflicts of interest
There are no conflicts of interest.
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[Table 1], [Table 2]