Improvement on BAF53B Mutation Caused Developmental and Epileptic Encephalopathy with a Ketogenic Diet
Danli Wanga*, Linlin Fanb, Haoying Yangb, Mingming Panb, Junping Shic, Ang Lib, Nini Wangd, Xue Xiab*, Yang Liub*
aZhoushan People’s Hospital, Zhoushan, Zhejiang, China
bHenan Key Laboratory of Brain Targeted Bio-Nanomedicine, School of Life Sciences & School of Pharmacy, Henan University, Kaifeng, Henan, China
cKaifeng Central Hospital, Kaifeng, Henan, China
dNeurology Department of Zhengzhou Central Hospital, Zhengzhou, Henan, China
*Corresponding Authors: Danli Wang, Zhoushan People’s Hospital, Zhoushan, Zhejiang, China
Xue Xia and Yang Liu, Henan Key Laboratory of Brain Targeted Bio-Nanomedicine, School of Life Sciences & School of Pharmacy, Henan University, Kaifeng, Henan, China.
Received: 17 September 2022; Accepted: 22 September 2022; Published: 09 November 2022
Citation: Danli Wang, Linlin Fan, Haoying Yang, Mingming Pan, Junping Shi, Ang Li, Nini Wang, Xue Xia, Yang Liu. Improvement on BAF53B mutation caused developmental and epileptic encephalopathy with a ketogenic diet. Journal of Food Science and Nutrition Research 5 (2022): 712-715.View / Download Pdf Share at Facebook
Purpose: Genetic mutation is the leading cause of Developmental and Epileptic Encephalopathy (DEE, OMIM 308350), a spectrum of disorders characterized by severe epilepsy and usually begins in infancy, accompanied with psychomotor development arrest and hypsarrhythmiaon electroencephalogram (EEG).Up till now, mutations of 101 genes were confirmed as the cause of DEE, and were categorized accordingly into 101 different sub-types (DEE1-101). Here, we report a case of DEE76 with a tortuous path to genetic diagnosis and an illuminating treatment of ketogenic diet (KD).
Methods: Through high throughput sequencing, we identified a DEE76 case caused by biallelic BAF53B mutation inherited in an autosomal recessive manner, and report the pathogenic variants NM_016188.4:c.892C>T (p.Arg298*) and NM_016188.4:c.991_996delinsAA (p.Gly331Asnfs*44) for the first time.
Results: The proband commenced seizures on day five after birth and rapidly deteriorated during development. After a series of therapeutic exploration, ketogenic diet turned out to be the most hopeful treatment available.
Conclusion: To ultra-rare conditions including DEE76, gene therapy seems to be a logical way to cure, which inevitably faces the challenge of very limited survival time that patients bear with. With application of KD, seizures could be alleviated, which not only expanded the usage of KD but also provided with a new inspiration to those with similar symptoms.
Developmental and Epileptic Encephalopathy, BAF53B, Gene mutation, Ketogenic diet, Case report
Genetic mutation is the leading cause of Developmental and Epileptic Encephalopathy (DEE, OMIM 308350), a spectrum of disorders characterized by severe epilepsy and usually begins in infancy, accompanied with psychomotor development arrest and hypsarrhythmia on electroencephalogram (EEG). Up till now, mutations of 101 genes were confirmed as the causes of DEE, and were categorized accordingly categorized DEE into 101 different sub-types (DEE1-101). These genes encode membrane receptors, ion channels, ATP transports and involved in neurotransmitter synthesis etc . Here we report a DEE76 case caused by biallelic BAF53B mutation inherited in an autosomal recessive manner. Seizures commenced on day five and rapidly deteriorated. Patient’s brain magnetic resonance imaging (MRI) revealed rare structural abnormalities, and the EEG confirmed severe epileptiform abnormalities. After a series of therapeutic exploration, the patient has currently following a ketogenic diet (KD) combined with medication treatment and got his DEE associated epileptic symptom under control. By far most types of DEE still lack of sufficient investigation of their underlying mechanisms and treatment approaches are urgently to be explored, while this case of DEE76 induced by compound heterozygous mutations in BAF53B gene highlighted the therapeutic potential of KD.
The proband is the only child of healthy, nonconsanguineous parents. No history of neurological problems has been reported within the family. He was born by caesarean section at 39 weeks in the year of 2016. At birth his weight and length and head circumference (HC) were within the normal range. At day 5 he presented with frequently nodding-like myoclonic jerks accompanied with difficulties in feeding and dystonia. At 3 months of age, he was hospitalized for emergency laparoscopy surgery because of "umbilical hernia and inguinal hernia incarceration". After surgery, his symptoms of tonic and colonic seizures was noted by the doctor, EEG and brain MRI were arranged, revealed epileptiform activity in both occipital areas and brain structure abnormalities by imaging (Figure 1A). He showed no sustained response to oral valproate (Depakine) combined with topiramate (Topamax) and levetiracetam (Kaplan). Consequently a trio whole exome sequencing (Trio-WES) was performed but no specific pathogenic mutations or copy number variation (CNVs) were identified (not shown). As his symptoms deteriorated, his psychomotor developmental arrestment and intellectual disability were also been noticed. In the meantime, epileptiform activity have progressed to his right temporal region as detected by EEG (also not shown) and he showed signs of focal epilepsy. At 9-month-old, after supplemented with clonazepam and failed to response, he was treated with KD. After 3 months, a greater than 50% reduction in seizure frequency was reported by his guardians.
At 1.5 years old, EEG reassessment displayed severe multifocal epileptic activity over all his brain (Figure 1B), although his seizure attacks appeared to be less deteriorated reported by his guardians. He was then treated with high-dose intravenous corticosteroid therapy but without response, soon the proband resumed the V.T.L.C.K treatment (Valproate, Topiramate, Levetiracetam, Clonazepam and Ketogenic diet). At 2 years old, he had been briefly treated with vigabatrin (Sabril) at a dosage of 125 mg after each generalized seizure attack, which characterized by lost consciousness briefly and shouting and crying afterwards. About the same time, persist in finding the genetic causes, his family attended a clinical trial (NCT03424772) which aimed to identify rare and undiagnosed diseases among Chinese children by whole genome sequencing (WGS). The Trio-WGS revealed that he inherited a different pathogenic variants in BAF53B from each parent (NM_016188.4:c.892C>T, NM_016188.4:c.991_996delinsAA) and the suggestive diagnosis could be DEE76 (OMIM 618468). When he was 3-year and 2-month old, the proband was carried to our hospital to verify the previous genome sequencing results. He had normal HC, and his weight and height was -4SD and -3SD, respectively. He suffered from seizure attacks about 20 times per day, and displayed severely impaired global development, non-verbal and non-ambulatory, unable to hold his head up or sit unassisted, displayed no purposeful movements, and unresponsive to any visual stimuli. After obtained written informed consent for genetic testing, Trio-WES was scheduled. The heterozygous variant c.892C > T (p.Arg298*) was identified in both the proband and his father in exon 9 in BAF53B, and the heterozygous variant c.991_996delinsAA (p.Gly331 Asnfs*44) was identified in both the proband and his mother in exon 10 in BAF53B (Figure 2). Both variants were considered pathogenic in accordance with the PM1, PM2, PP3, and PP5 criteria. Sanger sequencing was also applied for variants validation. Together confirmed the genetic diagnosis of the proband is DEE76 induced by compound heterozygous mutants in BAF53B.
Human BAF53B, also known as ACTL6B (Actin Like 6B), which includes 1-14 exons, is located on chromosome 7q22.1, which includes 1-14 exons (Figure 2C). BAF53B plays a very important role in chromatin remodeling and histone acetylation and also regulates gene expression during neurodevelopment. A collection of BAF53B mutation related symptoms was reported in 2019 , summarized 11 children with various BAF53B variants presented with 2 major clinical phenotypes. One is DEE76 (OMIM 618468), an autosomal recessive neurodevelopmental disorder with severe, early-onset, refractory seizures and global developmental delay, caused by either homozygous or compound heterozygous mutation in BAF53B. Another is the autosomal dominant intellectual developmental disorder (OMIM 618470) with less severe symptoms caused by heterozygous mutation in the gene. Thus firstly illustrated the diagnostic clues for BAF53B mutants. Later study discovered the linkage between mutated BAF53B and heritable autism spectrum disorder . As other rare genetic diseases, the diagnosis for BAF53B mutants carriers also highly dependent on high-throughput sequencing. KD is a high-fat, low-carbohydrate, adequate protein diet, promotes production of ketone bodies and physiological ketosis, and had been recommended as particularly useful for treatment of certain epilepsy and genetic syndromes . Though seizures of DEE patients tend to be refractory to most treatment, but some may respond to KD . In this case of DEE76 induced by rare variants in BAF53B, KD turned out to be the most applicable treatment that available, suggesting KD as a potentially therapeutic measure which could be advisable for epilepsy of DEE76.
Supported by Zhejiang Medicine & Health Science Technology Project, Health Committee of Zhejiang Province, 2021KY382.
The authors declare no conflict of interest.
Ethical publication statement
The study was approved by the Ethic Committee of The Kaifeng Central Hospital of Henan University and written informed consent was obtained from the patient's guardian. We confirmed that this report is consistent with the journal’s ethical guidelines.
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