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A randomized placebo controlled clinical trial to evaluate the efficacy and safety of minocycline in patients with Angelman syndrome (A-MANECE study)

dc.contributor.authorRuiz-Antoran, Belén
dc.contributor.authorSancho-López, Aranzazu
dc.contributor.authorCazorla-Calleja, Rosario
dc.contributor.authorLópez-Pájaro, Luis Fernando
dc.contributor.authorLeiva, Ágata
dc.contributor.authorIglesias-Escalera, Gema
dc.contributor.authorMarín-Serrano, María Esperanza
dc.contributor.authorRincón-Ortega, Marta
dc.contributor.authorLara-Herguedas, Julián
dc.contributor.authorRossignoli-Palomeque, Teresa
dc.contributor.authorValiente-Rodríguez, Sara
dc.contributor.authorGonzález Marqués, Javier
dc.contributor.authorRomán-Riechmann, Enriqueta
dc.contributor.authorAvendaño-Solá, Cristina
dc.date.accessioned2024-02-06T10:07:09Z
dc.date.available2024-02-06T10:07:09Z
dc.date.issued2018-08-20
dc.description.abstractBackground: Minocycline is an old tetracycline antibiotic that has shown antiinflammatory and antiapoptotic properties in different neurological disease mouse models. Previous single arm study in humans demonstrated benefits in individuals with Angelman Syndrome (AS); however, its efficacy in patients with Angelman Syndrome has not been assessed in a controlled trial. This was a randomized, double-blind, placebo-controlled, crossover trial in individuals with AS, aged 6 years to 30 years (n = 32, mean age 12 [SD 6·29] years). Participants were randomized to minocycline or placebo for 8 weeks and then switched to the other treatment (a subset of 22 patients) or to receive minocycline for up to 16 weeks (10 patients). After week 16, all patients entered a wash-out 8-week follow-up period. Results: Thirty-six subjects were screened and 34 were randomized. Thirty two subjects (94·1%) completed at least the first period and all of them completed the full trial. Intention-to-treat analysis demonstrated the lack of significantly greater improvements in the primary outcome, mean changes in age equivalent of the development index of the Merrill-Palmer Revised Scale after minocycline compared with placebo (1·90 ± 3·16 and 2·00 ± 3·28, respectively, p = 0·937). Longer treatment duration up to 16 weeks did not result in better treatment outcomes (1·86 ± 3·35 for 8 weeks treatment vs 1·20 ± 5·53 for 16 weeks treatment, p = 0·667). Side effects were not significantly different during minocycline and placebo treatments. No serious adverse events occurred on minocycline. Conclusions: Minocycline treatment for up to 16 weeks in children and young adults with AS resulted in lack of significant improvements in development indexes compared to placebo treatment. Treatment with minocycline appears safe and well tolerated; even if it cannot be completely ruled out that longer trials might be required for a potential minocycline effect to be expressed, available results and lack of knowledge on the actual mechanism of action do not support this hypothesis. Trial registration: European Clinical Trial database (EudraCT 2013-002154-67), registered 16th September 2013; US Clinical trials database (NCT02056665), registered 6th February 2014.
dc.description.departmentDepto. de Psicología Experimental, Procesos Cognitivos y Logopedia
dc.description.facultyFac. de Psicología
dc.description.refereedTRUE
dc.description.statuspub
dc.identifier.citationRuiz-Antoran, B., Sancho-López, A., Cazorla-Calleja, R., López-Pájaro, L.F., Leiva, A., Iglesias-Escalera, G., Marín-Serrano, M.E., Rincón-Ortega, M., Lara-Herguedas, J., Rossignoli-Palomeque, T., Valiente-Rodríguez, S., González-Marqués, J., Román-Riechmann, E., Avendaño-Solá, C. A randomized placebo controlled clinical trial to evaluate the efficacy and safety of minocycline in patients with Angelman syndrome (A-MANECE study). Orphanet Journal of Rare Diseases. 2018 13:144. https://doi.org/10.1186/s13023-018-0891-6
dc.identifier.doi10.1186/s13023-018-0891-6
dc.identifier.issn1750-1172
dc.identifier.officialurlhttps://ojrd.biomedcentral.com/articles/10.1186/s13023-018-0891-6
dc.identifier.urihttps://hdl.handle.net/20.500.14352/99340
dc.issue.number1
dc.journal.titleOrphanet Journal of Rare Diseases
dc.language.isoeng
dc.page.initial144
dc.publisherBMC
dc.rightsAttribution 4.0 Internationalen
dc.rights.accessRightsopen access
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.subject.keywordAngelman syndrome
dc.subject.keywordTreatment
dc.subject.keywordMinocycline
dc.subject.keywordDevelopmental changes
dc.subject.keywordPharmacological intervention
dc.subject.ucmCiencias Biomédicas
dc.subject.ucmMedicina
dc.subject.ucmMedicina interna
dc.subject.ucmPsicología (Psicología)
dc.subject.ucmNeuropsicología
dc.subject.unesco32 Ciencias Médicas
dc.subject.unesco3205 Medicina Interna
dc.subject.unesco3205.07 Neurología
dc.subject.unesco61 Psicología
dc.subject.unesco6101 Patología
dc.subject.unesco6101.03 Deficiencia Mental
dc.subject.unesco6102 Psicología del Niño y del Adolescente
dc.titleA randomized placebo controlled clinical trial to evaluate the efficacy and safety of minocycline in patients with Angelman syndrome (A-MANECE study)
dc.typejournal article
dc.type.hasVersionVoR
dc.volume.number13
dspace.entity.typePublication
relation.isAuthorOfPublication23f8c731-89eb-4429-9112-0c915d3d1a84
relation.isAuthorOfPublication.latestForDiscovery23f8c731-89eb-4429-9112-0c915d3d1a84

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