No registrations found.
ID
Source
Brief title
Health condition
Sanfilippo syndrome (MPS III)
Sponsors and support
Intervention
Outcome measures
Primary outcome
Does genestein significantly decrease urinary GAGs (in particular heparan sulphate) excretion in Sanfilippo patients?
Secondary outcome
1. Does genestein decrease serum heparan sulphate concentration?
2. Does genestein decrease accumulation of heparan sulphate in skin biopsies?
3. Does hair morphology improve in MPS III patients using genestein?
4. What is the effect of genestein on behaviour?
5. Does genestein improve neurocognitive outcome?
Background summary
Sanfilippo syndrome (MPS III) is an inborn errors of lysosomal degradation of the glycosaminoglycan heparan sulphate (GAGs). Accumulation of heparan sulfate, results in progressive and severe mental deterioration, which is the clinical hallmark of MPS III. Genestein (an isoflavone) is a natural component of the soy-bean. Genistein inhibits GAGs synthesis in vitro and a recent small and open-label study suggested clinical relevant effects of genestein in MPS III patients. In June 2009 a double blind placebo controlled study on the effect of genestein was initiated in the Netherlands. Thirty patients with MPS III type A, B or C are included in this study and receiving either placebo or genestein (10 mg/kg) during two 6 month periods in a cross-over design The outcome of genestein on urinary GAG excretion, plasma heparan sulphate, tissue (skin biopsy) concentration of heparan sulphate, hair structure, cognitive state and behavioural abnormalities will be studied. Currently the trial is still ongoing and first results are expected the end of 2010. Our study will be the extension study of the previous mentioned study.
Study objective
Genestein inhibits the synthesis of heparan sulphate and can possibly slow down disease progression in Sanfilippo Syndrome patients.
Study design
Baseline, 6 months and 12 months.
Intervention
During a 12 month period all particpating patients will receive genestein as food supplement. Genestein dose will be calculated according to the weight of the patients (10 mg/kg/day). The start assessment of this study equals the last assessment of the double blind controlled trial.
Academical Medical Center,
Meiburgdreef 9
Amsterdam 1105 AZ
The Netherlands
+31 (0)20 5668890
f.a.wijburg@amc.uva.nl
Academical Medical Center,
Meiburgdreef 9
Amsterdam 1105 AZ
The Netherlands
+31 (0)20 5668890
f.a.wijburg@amc.uva.nl
Inclusion criteria
Patients participated in the initial double blind placebo controlled study on the effect of genestein in a cross-over design.
Exclusion criteria
The parent or legal representative is unwilling to participate.
Design
Recruitment
Followed up by the following (possibly more current) registration
No registrations found.
Other (possibly less up-to-date) registrations in this register
No registrations found.
In other registers
Register | ID |
---|---|
NTR-new | NL2276 |
NTR-old | NTR2402 |
Other | MEC AMC : 10/080 |
ISRCTN | ISRCTN wordt niet meer aangevraagd. |