Randomised controlled trial of simvastatin treatment for autism in young children with neurofibromat...
Randomised controlled trial of simvastatin treatment for autism in young children with neurofibromatosis type 1 (SANTA)
About this item
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Author / Creator
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 and SANTA Consortium
Publisher
England: BioMed Central Ltd
Journal title
Language
English
Formats
Publication information
Publisher
England: BioMed Central Ltd
Subjects
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Scope and Contents
Contents
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.
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).
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 (
(12) = - 2.12,
= .055), GABA/Glx ratio (
(12) = - 2.78,
= .016), and reduced grey nuclei Glx (ANCOVA
< 0.05, Mann-Whitney
< 0.01); (ii) increased ASL perfusion in ventral diencephalon (Mann-Whitney
< 0.01); and (iii) decreased ADC in cingulate gyrus (Mann-Whitney
< 0.01). Machine-learning classification of imaging outcomes achieved 79% (
< .05) accuracy differentiating groups at endpoint against chance level (64%,
= 0.25) at baseline. Three of 12 (25%) simvastatin cases compared to none in placebo met 'clinical responder' criteria for behavioural outcome.
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.
EU Clinical Trial Register (EudraCT) 2012-005742-38 (www.clinicaltrialsregister.eu)....
Alternative Titles
Full title
Randomised controlled trial of simvastatin treatment for autism in young children with neurofibromatosis type 1 (SANTA)
Authors, Artists and Contributors
Author / Creator
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
SANTA Consortium
Identifiers
Primary Identifiers
Record Identifier
TN_cdi_doaj_primary_oai_doaj_org_article_dafd5e775ca6491c9657b16a73c4e0fa
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_dafd5e775ca6491c9657b16a73c4e0fa
Other Identifiers
ISSN
2040-2392
E-ISSN
2040-2392
DOI
10.1186/s13229-018-0190-z