A therapeutic trial of pro-methylation dietary supplements in Angelman syndrome
- PMID: 22002941
- PMCID: PMC3222728
- DOI: 10.1002/ajmg.a.34297
A therapeutic trial of pro-methylation dietary supplements in Angelman syndrome
Abstract
Angelman syndrome (AS) is due to deficient ubiquitin protein ligase 3a, the gene for which (UBE3A) maps to chromosome 15q11-q13 and is imprinted such that only the maternally inherited gene is expressed. The paternally inherited UBE3A gene is silenced, a process mediated by an antisense transcript. We conducted a trial using methylation-promoting dietary supplements (betaine, metafolin, creatine, and vitamin B(12) ) in an attempt to reduce antisense transcript production, increase UBE3A expression, and ameliorate the symptoms of AS. Neuropsychological evaluations, biochemical testing, and assessment of DNA methylation were performed at the beginning and at the end of 1 year of supplementation. The primary outcome measures were changes in the level of developmental function (cognitive, motor, and language) as measured using standardized instruments. The secondary outcomes measures were changes in biochemical parameters and global DNA methylation. These data were compared to those of a control group from a previous randomized double-blind trial using folic acid and betaine. There were no statistically significant changes in the developmental performance of children treated with supplements. There were no unexpected changes in biochemical parameters and no change in site-specific DNA methylation when comparing samples from before and after treatment. There were 10 adverse events that resulted in study withdrawal of 7 participants (worsening of seizures, onset, or worsening of sleep problems, constipation, and anorexia). Supplementation with betaine, metafolin, creatine, and vitamin B(12) appears safe but ineffective in decreasing the severity of AS.
Trial registration: ClinicalTrials.gov NCT00348933.
Copyright © 2011 Wiley Periodicals, Inc.
Figures

Similar articles
-
A placebo-controlled trial of folic acid and betaine in identical twins with Angelman syndrome.Orphanet J Rare Dis. 2019 Oct 22;14(1):232. doi: 10.1186/s13023-019-1216-0. Orphanet J Rare Dis. 2019. PMID: 31640736 Free PMC article. Clinical Trial.
-
Double-blind therapeutic trial in Angelman syndrome using betaine and folic acid.Am J Med Genet A. 2010 Aug;152A(8):1994-2001. doi: 10.1002/ajmg.a.33509. Am J Med Genet A. 2010. PMID: 20635355 Free PMC article. Clinical Trial.
-
Folic acid supplementation and malaria susceptibility and severity among people taking antifolate antimalarial drugs in endemic areas.Cochrane Database Syst Rev. 2022 Feb 1;2(2022):CD014217. doi: 10.1002/14651858.CD014217. Cochrane Database Syst Rev. 2022. PMID: 36321557 Free PMC article.
-
Intergenerational impact of paternal lifetime exposures to both folic acid deficiency and supplementation on reproductive outcomes and imprinted gene methylation.Mol Hum Reprod. 2017 Jul 1;23(7):461-477. doi: 10.1093/molehr/gax029. Mol Hum Reprod. 2017. PMID: 28535307 Free PMC article.
-
Pharmacological therapies for Angelman syndrome.Wien Med Wochenschr. 2017 Jun;167(9-10):205-218. doi: 10.1007/s10354-015-0408-z. Epub 2016 Jan 12. Wien Med Wochenschr. 2017. PMID: 26758979 Review. English.
Cited by
-
A placebo-controlled trial of folic acid and betaine in identical twins with Angelman syndrome.Orphanet J Rare Dis. 2019 Oct 22;14(1):232. doi: 10.1186/s13023-019-1216-0. Orphanet J Rare Dis. 2019. PMID: 31640736 Free PMC article. Clinical Trial.
-
Qualitative Insights into Key Angelman Syndrome Motor Related Concepts Reported by Caregivers-A Thematic Analysis of Semi-Structured Interviews.Children (Basel). 2023 Aug 28;10(9):1462. doi: 10.3390/children10091462. Children (Basel). 2023. PMID: 37761423 Free PMC article.
-
Angelman syndrome - insights into a rare neurogenetic disorder.Nat Rev Neurol. 2016 Oct;12(10):584-93. doi: 10.1038/nrneurol.2016.133. Epub 2016 Sep 12. Nat Rev Neurol. 2016. PMID: 27615419 Review.
-
Translational outcomes in a full gene deletion of ubiquitin protein ligase E3A rat model of Angelman syndrome.Transl Psychiatry. 2020 Jan 27;10(1):39. doi: 10.1038/s41398-020-0720-2. Transl Psychiatry. 2020. PMID: 32066685 Free PMC article.
-
UBE3A: The Role in Autism Spectrum Disorders (ASDs) and a Potential Candidate for Biomarker Studies and Designing Therapeutic Strategies.Diseases. 2023 Dec 27;12(1):7. doi: 10.3390/diseases12010007. Diseases. 2023. PMID: 38248358 Free PMC article. Review.
References
-
- Bayley N. Bayley Scales of Infant and Toddler Development. 3. San Antonio, TX: Harcourt Assessment, Inc; 2005. (Bayley-III)
-
- Dindot SV, Antalffy BA, Bhattacharjee MB, Beaudet AL. The Angelman syndrome ubiquitin ligase localizes to the synapse and nucleus, and maternal deficiency results in abnormal dendritic spine morphology. Hum Mol Genet. 2008;17(1):111–118. - PubMed
-
- Dykens EM, Hodapp RM, Evans DW. Profiles and development of adaptive behavior in children with Down syndrome. Am J Ment Retard. 1994;98:580–587. - PubMed
Publication types
MeSH terms
Associated data
Grants and funding
LinkOut - more resources
Full Text Sources
Medical
Molecular Biology Databases
Research Materials