Effects of Creatine Supplementation in Rett Syndrome
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Purpose
Creatine supplementation in RTT: a randomized controlled trial
Rett Syndrome (RTT) is a neurodevelopmental disorder characterised by apparently normal early development (stage 1 of RTT) followed by loss of purposeful hand use, distinctive hand stereotypes, slow brain growth, loss of language, respiratory irregularities, gastrointestinal disturbances, gait abnormalities, seizures, and mental retardation. These symptoms typically appear between 6 and 18 months of age (stage 2). Subsequently, there is gradual stabilisation of severe mental retardation and motor compromise (stage 3). The majority (70% to 80%) of patients show mutations in the methyl-CpG-binding-protein-2 (MeCP2) gene, located on chromosome Xq28. MeCP2 encodes a transcription repressor protein that is ubiquitously expressed in all tissues.
As RTT primarily affects females, only very few males with mutations in MeCP2 have been identified. Mutations in MeCP2 have also been identified in children with X-linked mental retardation, autism and a clinical phenotype that resembles Angelman Syndrome.
The aim of this study is to investigate the effects of a dietary supplement on the biochemical and clinical parameter of RTT. About 80 % of labile methyl groups generated through the re-methylation cycle are used for the synthesis of creatine within the human organism. Supplementation of creatine will therefore increase the availability of labile methyl groups for different methylation reactions including methylation of DNA.
The study will be double blind and cross-over. The patients will get creatine monophosphate (200 mg/kg/d in three dosages per day) or placebo. After 6 months and a wash-out period of 4 weeks the groups are changed for the next 6 months.
All participants with RTT and mutations in MeCP2 will undergo physical and neurological exam, quantitative EEG, behavioral assessment, laboratory testing, and neuropsychological evaluations. Participants will have a follow-up after 3, 6, 10, 13 and 16 months (3 months after finishing the study), which will include similar assessments.
| Condition | Intervention |
|---|---|
|
Rett Syndrome |
Dietary Supplement: Creatine monohydrate Dietary Supplement: Placebo |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Endpoint Classification: Safety/Efficacy Study Intervention Model: Crossover Assignment Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor) Primary Purpose: Basic Science |
| Official Title: | Effects of Creatine Supplementation in Rett Syndrome: A Randomized, Placebo-controlled Trial |
- Global DNA Methylation in serum [ Time Frame: 6 months ] [ Designated as safety issue: No ]Global DNA methylation as one primary outcome measure is analyzed at time 0 and after 6 months.
- Rett Syndrome Motor and Behavioral Assessment (RSMBA) [ Time Frame: 6 months ] [ Designated as safety issue: Yes ]
- Metabolic markers of methylation cycle [ Time Frame: 6 months ] [ Designated as safety issue: No ]Markers: Methionine (µmol/l), Homocysteine (µmol/l), SAM (µmol/l), SAH (µmol/l)
| Enrollment: | 21 |
| Study Start Date: | January 2005 |
| Study Completion Date: | January 2009 |
| Primary Completion Date: | January 2008 (Final data collection date for primary outcome measure) |
| Arms | Assigned Interventions |
|---|---|
|
Active Comparator: Creatine monohydrate
The patients received orally 200 mg CMH per kg body weight divided in three doses per day. Following period 1 (6 months) of supplementation and a wash-out period of 4 weeks without CMH respectively the groups were switched for another 6 months (period 2).
|
Dietary Supplement: Creatine monohydrate
The patients received orally 200 mg CMH per kg body weight divided in three doses per day. Following period 1 (6 months) of supplementation and a wash-out period of 4 weeks without CMH the groups were switched for another 6 months (period 2).
Other Name: Creatine monohydrate
|
|
Placebo Comparator: Placebo
The patients received orally 200 mg Placebo per kg body weight divided in three doses per day in identically prepared capsules. Following period 1 (6 months) of supplementation and a wash-out period of 4 weeks without Placebo respectively the groups were switched for another 6 months (period 2).
|
Dietary Supplement: Placebo
The patients received orally 200 mg Placebo per kg body weight divided in three doses per day. Following period 1 (6 months) of supplementation and a wash-out period of 4 weeks without placebo the groups were switched for another 6 months (period 2).
|
Eligibility| Ages Eligible for Study: | 3 Years to 24 Years |
| Genders Eligible for Study: | Female |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria:
- RTT Syndrome, diagnosed by current consensus criteria
Exclusion Criteria:
- taking supplements containing either folic acid or vitamin B12 or knowingly consuming any vitamin-fortified food items
Contacts and Locations| Austria | |
| Medical University Vienna, Dep. of Pediatric and Adolescent Medicine | |
| Vienna, Austria, 1090 | |
| Principal Investigator: | Michael Freilinger, MD | Medical University Vienna, Dep. Pediatrics |
More Information
No publications provided by Medical University of Vienna
Additional publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):
| Responsible Party: | M Freilinger, MD, Medical University Vienna, Department of Pediatric and Adolescent Medicine |
| ClinicalTrials.gov Identifier: | NCT01147575 History of Changes |
| Other Study ID Numbers: | OENB11758 |
| Study First Received: | June 17, 2010 |
| Last Updated: | June 18, 2010 |
| Health Authority: | Austria: Ethikkommission |
Keywords provided by Medical University of Vienna:
|
Rett Syndrome, Randomized, Methylation |
Additional relevant MeSH terms:
|
Rett Syndrome Heredodegenerative Disorders, Nervous System Neurodegenerative Diseases Nervous System Diseases Mental Retardation, X-Linked |
Mental Retardation Neurobehavioral Manifestations Neurologic Manifestations Genetic Diseases, X-Linked Genetic Diseases, Inborn |
ClinicalTrials.gov processed this record on May 22, 2013