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| Sponsor: | Office of Rare Diseases (ORD) |
|---|---|
| Collaborator: |
Rare Diseases Clinical Research Network |
| Information provided by: | Office of Rare Diseases (ORD) |
| ClinicalTrials.gov Identifier: | NCT00348933 |
Purpose
Angelman syndrome (AS) is a complex genetic disorder that affects the nervous system. The purpose of this study is to determine the effectiveness of certain dietary supplements in treating the symptoms of AS.
| Condition | Intervention |
|---|---|
|
Angelman Syndrome Nervous System Diseases |
Drug: Betaine Drug: Creatine Drug: Metafolin Drug: Vitamin B12 |
| Study Type: | Interventional |
| Study Design: | Treatment, Non-Randomized, Open Label, Uncontrolled, Single Group Assignment, Efficacy Study |
| Official Title: | Efficacy of a Therapeutic Treatment Trial in Angelman Syndrome |
| Estimated Enrollment: | 80 |
| Study Start Date: | July 2006 |
| Estimated Study Completion Date: | February 2009 |
| Estimated Primary Completion Date: | February 2009 (Final data collection date for primary outcome measure) |
| Arms | Assigned Interventions |
|---|---|
|
1: Experimental
Participants will receive two daily doses of Metafolin, betaine, and creatine, and one daily dose of vitamin B12 for 12 months.
|
Drug: Betaine
100-200 mg per kg per day by mouth with a maximum of 6 grams divided in two daily doses
Drug: Creatine
200 mg per kg per day with a daily maximum of 5 grams divided in two daily doses
Drug: Metafolin
0.5 mg per kg per day by mouth with a maximum of 8 milligrams divided in two daily doses
Drug: Vitamin B12
1 mg by mouth per day for all weights and ages
|
AS is a neurologic disorder that may cause developmental delay, mental retardation, severe speech impairment, seizures, small head size, and problems with movement and balance in young children. AS is caused by a missing or incomplete chromosome 15 that is inherited from the mother. Diagnosis of AS is usually made between three and seven years of age, when the characteristic behaviors and features of the disease become most evident. Prior to AS diagnosis, the symptoms may be mistaken for cerebral palsy or autism. Physical, occupational, and speech therapy, communication skills development, and behavior modification help to improve the quality of life of these children, but other treatments are needed.
In a previous study, decreased DNA methylation, which is a type of chemical change in DNA, was observed in an individual with AS; this condition may be a primary cause of AS. It is hypothesized that promoting increased DNA methylation might reduce the severity of AS symptoms. Betaine, creatine, Metafolin, and vitamin B12 are compounds normally found in the body that are involved in the DNA methylation pathway. Increasing the concentrations of these compounds in the body may enhance DNA methylation. This study will evaluate the efficacy of four dietary supplements in treating the symptoms of AS.
This study will last 12 months. Study visits will occur at study entry and Month 12. A selected group of participants, those who meet the diagnostic criteria for autism, will also be evaluated at Month 6. At study visits, participants will undergo an electroencephalogram (EEG). Medical history, physical exam, neurological exams, and developmental assessments will also be performed. Urine and blood collection, including tests to determine the blood levels of the dietary supplements, will occur at study entry and Months 6 and 12. Participants will receive two daily doses of Metafolin, betaine, and creatine, and one daily dose of vitamin B12 for the duration of the study. Parents will be asked to complete a questionnaire at each visit to report their child's behavior while taking the dietary supplements. Parents will also be contacted by phone periodically to assess changes and/or progress in their children.
Eligibility| Ages Eligible for Study: | up to 5 Years |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria:
Exclusion Criteria:
Contacts and Locations| United States, California | |
| Children's Hospital San Diego | |
| San Diego, California, United States | |
| United States, Massachusetts | |
| Children's Hospital Boston | |
| Boston, Massachusetts, United States | |
| United States, South Carolina | |
| Greenwood Genetics Center | |
| Greenwood, South Carolina, United States | |
| United States, Texas | |
| Baylor College of Medicine | |
| Houston, Texas, United States | |
| Principal Investigator: | Arthur L. Beaudet, MD | Department of Molecular and Human Genetics, Baylor College of Medicine |
| Principal Investigator: | Carlos A. Bacino, MD | Department of Molecular and Human Genetics, Baylor College of Medicine |
| Principal Investigator: | Wen-Hann Tan, BMBS | Harvard Medical School, Children's Hospital Boston |
| Principal Investigator: | Lynne M. Bird, MD | Division of Dysmorphology/Genetics, Children's Hospital San Diego, Department of Pediatrics, University of California, San Diego |
| Principal Investigator: | Steven A. Skinner, MD | Greenwood Genetic Center |
More Information
| Responsible Party: | Baylor College of Medicine ( Carlos A. Bacino ) |
| Study ID Numbers: | RDCRN 5204 |
| Study First Received: | July 3, 2006 |
| Last Updated: | June 1, 2009 |
| ClinicalTrials.gov Identifier: | NCT00348933 History of Changes |
| Health Authority: | United States: Federal Government |
|
Developmental Delay Mental Retardation Ataxia Microcephaly Seizures |
|
Disease Vitamin B Complex Growth Substances Physiological Effects of Drugs Nervous System Diseases Chromosome Disorders Central Nervous System Diseases Vitamin B 12 Pharmacologic Actions |
Pathologic Processes Genetic Diseases, Inborn Movement Disorders Vitamins Syndrome Abnormalities, Multiple Micronutrients Angelman Syndrome Congenital Abnormalities |