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Randomised controlled trial of simvastatin treatment for autism in young children with neurofibromatosis type 1 (SANTA)
BACKGROUND: Neurofibromatosis 1 (NF1) is a monogenic model for syndromic autism. Statins rescue the social and cognitive phenotype in animal knockout models, but translational trials with subjects > 8 years using cognition/behaviour outcomes have shown mixed results. This trial breaks new ground...
Autores principales: | , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5824534/ https://www.ncbi.nlm.nih.gov/pubmed/29484149 http://dx.doi.org/10.1186/s13229-018-0190-z |
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author | Stivaros, Stavros Garg, Shruti Tziraki, Maria Cai, Ying Thomas, Owen Mellor, Joseph Morris, Andrew A. Jim, Carly Szumanska-Ryt, Karolina Parkes, Laura M Haroon, Hamied A. Montaldi, Daniela Webb, Nicholas Keane, John Castellanos, Francisco X. Silva, Alcino J. Huson, Sue Williams, Stephen Gareth Evans, D. Emsley, Richard Green, Jonathan |
author_facet | Stivaros, Stavros Garg, Shruti Tziraki, Maria Cai, Ying Thomas, Owen Mellor, Joseph Morris, Andrew A. Jim, Carly Szumanska-Ryt, Karolina Parkes, Laura M Haroon, Hamied A. Montaldi, Daniela Webb, Nicholas Keane, John Castellanos, Francisco X. Silva, Alcino J. Huson, Sue Williams, Stephen Gareth Evans, D. Emsley, Richard Green, Jonathan |
author_sort | Stivaros, Stavros |
collection | PubMed |
description | BACKGROUND: Neurofibromatosis 1 (NF1) is a monogenic model for syndromic autism. Statins rescue the social and cognitive phenotype in animal knockout models, but translational trials with subjects > 8 years using cognition/behaviour outcomes have shown mixed results. This trial breaks new ground by studying statin effects for the first time in younger children with NF1 and co-morbid autism and by using multiparametric imaging outcomes. METHODS: A single-site triple-blind RCT of simvastatin vs. placebo was done. Assessment (baseline and 12-week endpoint) included peripheral MAPK assay, awake magnetic resonance imaging spectroscopy (MRS; GABA and glutamate+glutamine (Glx)), arterial spin labelling (ASL), apparent diffusion coefficient (ADC), resting state functional MRI, and autism behavioural outcomes (Aberrant Behaviour Checklist and Clinical Global Impression). RESULTS: Thirty subjects had a mean age of 8.1 years (SD 1.8). Simvastatin was well tolerated. The amount of imaging data varied by test. Simvastatin treatment was associated with (i) increased frontal white matter MRS GABA (t(12) = − 2.12, p = .055), GABA/Glx ratio (t(12) = − 2.78, p = .016), and reduced grey nuclei Glx (ANCOVA p < 0.05, Mann-Whitney p < 0.01); (ii) increased ASL perfusion in ventral diencephalon (Mann-Whitney p < 0.01); and (iii) decreased ADC in cingulate gyrus (Mann-Whitney p < 0.01). Machine-learning classification of imaging outcomes achieved 79% (p < .05) accuracy differentiating groups at endpoint against chance level (64%, p = 0.25) at baseline. Three of 12 (25%) simvastatin cases compared to none in placebo met ‘clinical responder’ criteria for behavioural outcome. CONCLUSIONS: We show feasibility of peripheral MAPK assay and autism symptom measurement, but the study was not powered to test effectiveness. Multiparametric imaging suggests possible simvastatin effects in brain areas previously associated with NF1 pathophysiology and the social brain network. TRIAL REGISTRATION: EU Clinical Trial Register (EudraCT) 2012-005742-38 (www.clinicaltrialsregister.eu) ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13229-018-0190-z) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5824534 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-58245342018-02-26 Randomised controlled trial of simvastatin treatment for autism in young children with neurofibromatosis type 1 (SANTA) Stivaros, Stavros Garg, Shruti Tziraki, Maria Cai, Ying Thomas, Owen Mellor, Joseph Morris, Andrew A. Jim, Carly Szumanska-Ryt, Karolina Parkes, Laura M Haroon, Hamied A. Montaldi, Daniela Webb, Nicholas Keane, John Castellanos, Francisco X. Silva, Alcino J. Huson, Sue Williams, Stephen Gareth Evans, D. Emsley, Richard Green, Jonathan Mol Autism Research BACKGROUND: Neurofibromatosis 1 (NF1) is a monogenic model for syndromic autism. Statins rescue the social and cognitive phenotype in animal knockout models, but translational trials with subjects > 8 years using cognition/behaviour outcomes have shown mixed results. This trial breaks new ground by studying statin effects for the first time in younger children with NF1 and co-morbid autism and by using multiparametric imaging outcomes. METHODS: A single-site triple-blind RCT of simvastatin vs. placebo was done. Assessment (baseline and 12-week endpoint) included peripheral MAPK assay, awake magnetic resonance imaging spectroscopy (MRS; GABA and glutamate+glutamine (Glx)), arterial spin labelling (ASL), apparent diffusion coefficient (ADC), resting state functional MRI, and autism behavioural outcomes (Aberrant Behaviour Checklist and Clinical Global Impression). RESULTS: Thirty subjects had a mean age of 8.1 years (SD 1.8). Simvastatin was well tolerated. The amount of imaging data varied by test. Simvastatin treatment was associated with (i) increased frontal white matter MRS GABA (t(12) = − 2.12, p = .055), GABA/Glx ratio (t(12) = − 2.78, p = .016), and reduced grey nuclei Glx (ANCOVA p < 0.05, Mann-Whitney p < 0.01); (ii) increased ASL perfusion in ventral diencephalon (Mann-Whitney p < 0.01); and (iii) decreased ADC in cingulate gyrus (Mann-Whitney p < 0.01). Machine-learning classification of imaging outcomes achieved 79% (p < .05) accuracy differentiating groups at endpoint against chance level (64%, p = 0.25) at baseline. Three of 12 (25%) simvastatin cases compared to none in placebo met ‘clinical responder’ criteria for behavioural outcome. CONCLUSIONS: We show feasibility of peripheral MAPK assay and autism symptom measurement, but the study was not powered to test effectiveness. Multiparametric imaging suggests possible simvastatin effects in brain areas previously associated with NF1 pathophysiology and the social brain network. TRIAL REGISTRATION: EU Clinical Trial Register (EudraCT) 2012-005742-38 (www.clinicaltrialsregister.eu) ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13229-018-0190-z) contains supplementary material, which is available to authorized users. BioMed Central 2018-02-22 /pmc/articles/PMC5824534/ /pubmed/29484149 http://dx.doi.org/10.1186/s13229-018-0190-z Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Stivaros, Stavros Garg, Shruti Tziraki, Maria Cai, Ying Thomas, Owen Mellor, Joseph Morris, Andrew A. Jim, Carly Szumanska-Ryt, Karolina Parkes, Laura M Haroon, Hamied A. Montaldi, Daniela Webb, Nicholas Keane, John Castellanos, Francisco X. Silva, Alcino J. Huson, Sue Williams, Stephen Gareth Evans, D. Emsley, Richard Green, Jonathan Randomised controlled trial of simvastatin treatment for autism in young children with neurofibromatosis type 1 (SANTA) |
title | Randomised controlled trial of simvastatin treatment for autism in young children with neurofibromatosis type 1 (SANTA) |
title_full | Randomised controlled trial of simvastatin treatment for autism in young children with neurofibromatosis type 1 (SANTA) |
title_fullStr | Randomised controlled trial of simvastatin treatment for autism in young children with neurofibromatosis type 1 (SANTA) |
title_full_unstemmed | Randomised controlled trial of simvastatin treatment for autism in young children with neurofibromatosis type 1 (SANTA) |
title_short | Randomised controlled trial of simvastatin treatment for autism in young children with neurofibromatosis type 1 (SANTA) |
title_sort | randomised controlled trial of simvastatin treatment for autism in young children with neurofibromatosis type 1 (santa) |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5824534/ https://www.ncbi.nlm.nih.gov/pubmed/29484149 http://dx.doi.org/10.1186/s13229-018-0190-z |
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