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      Repetitive transcranial magnetic stimulation (rTMS) in autism spectrum disorder: protocol for a multicentre randomised controlled clinical trial

      other
      1 , 2 , , 3 , 4 , 5 , 6 , 7 , 8 , 9 , 10 , 3 , 4 , 8 , 11 , 12 , 5 , 13 , 6 , 7 , 8 , 6 , 7 , 12 , 3 , 4 , 14 , 1 , 8 , 1 , 15 , 1 , 1 , 16 , 1 , 1 , 1 , 2 , 17
      BMJ Open
      BMJ Publishing Group
      child & adolescent psychiatry, developmental neurology & neurodisability, paediatric neurology, neurophysiology

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          Abstract

          Introduction

          There are no well-established biomedical treatments for the core symptoms of autism spectrum disorder (ASD). A small number of studies suggest that repetitive transcranial magnetic stimulation (rTMS), a non-invasive brain stimulation technique, may improve clinical and cognitive outcomes in ASD. We describe here the protocol for a funded multicentre randomised controlled clinical trial to investigate whether a course of rTMS to the right temporoparietal junction (rTPJ), which has demonstrated abnormal brain activation in ASD, can improve social communication in adolescents and young adults with ASD.

          Methods and analysis

          This study will evaluate the safety and efficacy of a 4-week course of intermittent theta burst stimulation (iTBS, a variant of rTMS) in ASD. Participants meeting criteria for Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition ASD (n=150, aged 14–40 years) will receive 20 sessions of either active iTBS (600 pulses) or sham iTBS (in which a sham coil mimics the sensation of iTBS, but no active stimulation is delivered) to the rTPJ. Participants will undergo a range of clinical, cognitive, epi/genetic, and neurophysiological assessments before and at multiple time points up to 6 months after iTBS. Safety will be assessed via a structured questionnaire and adverse event reporting. The study will be conducted from November 2020 to October 2024.

          Ethics and dissemination

          The study was approved by the Human Research Ethics Committee of Monash Health (Melbourne, Australia) under Australia’s National Mutual Acceptance scheme. The trial will be conducted according to Good Clinical Practice, and findings will be written up for scholarly publication.

          Trial registration number

          Australian New Zealand Clinical Trials Registry (ACTRN12620000890932).

          Related collections

          Most cited references42

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          The REDCap consortium: Building an international community of software platform partners

          The Research Electronic Data Capture (REDCap) data management platform was developed in 2004 to address an institutional need at Vanderbilt University, then shared with a limited number of adopting sites beginning in 2006. Given bi-directional benefit in early sharing experiments, we created a broader consortium sharing and support model for any academic, non-profit, or government partner wishing to adopt the software. Our sharing framework and consortium-based support model have evolved over time along with the size of the consortium (currently more than 3200 REDCap partners across 128 countries). While the "REDCap Consortium" model represents only one example of how to build and disseminate a software platform, lessons learned from our approach may assist other research institutions seeking to build and disseminate innovative technologies.
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            • Record: found
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            Identification of common genetic risk variants for autism spectrum disorder

            Autism spectrum disorder (ASD) is a highly heritable and heterogeneous group of neurodevelopmental phenotypes diagnosed in more than 1% of children. Common genetic variants contribute substantially to ASD susceptibility, but to date no individual variants have been robustly associated with ASD. With a marked sample-size increase from a unique Danish population resource, we report a genome-wide association meta-analysis of 18,381 individuals with ASD and 27,969 controls that identified five genome-wide-significant loci. Leveraging GWAS results from three phenotypes with significantly overlapping genetic architectures (schizophrenia, major depression, and educational attainment), we identified seven additional loci shared with other traits at equally strict significance levels. Dissecting the polygenic architecture, we found both quantitative and qualitative polygenic heterogeneity across ASD subtypes. These results highlight biological insights, particularly relating to neuronal function and corticogenesis, and establish that GWAS performed at scale will be much more productive in the near term in ASD.
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              Safety, ethical considerations, and application guidelines for the use of transcranial magnetic stimulation in clinical practice and research.

              This article is based on a consensus conference, which took place in Certosa di Pontignano, Siena (Italy) on March 7-9, 2008, intended to update the previous safety guidelines for the application of transcranial magnetic stimulation (TMS) in research and clinical settings. Over the past decade the scientific and medical community has had the opportunity to evaluate the safety record of research studies and clinical applications of TMS and repetitive TMS (rTMS). In these years the number of applications of conventional TMS has grown impressively, new paradigms of stimulation have been developed (e.g., patterned repetitive TMS) and technical advances have led to new device designs and to the real-time integration of TMS with electroencephalography (EEG), positron emission tomography (PET) and functional magnetic resonance imaging (fMRI). Thousands of healthy subjects and patients with various neurological and psychiatric diseases have undergone TMS allowing a better assessment of relative risks. The occurrence of seizures (i.e., the most serious TMS-related acute adverse effect) has been extremely rare, with most of the few new cases receiving rTMS exceeding previous guidelines, often in patients under treatment with drugs which potentially lower the seizure threshold. The present updated guidelines review issues of risk and safety of conventional TMS protocols, address the undesired effects and risks of emerging TMS interventions, the applications of TMS in patients with implanted electrodes in the central nervous system, and safety aspects of TMS in neuroimaging environments. We cover recommended limits of stimulation parameters and other important precautions, monitoring of subjects, expertise of the rTMS team, and ethical issues. While all the recommendations here are expert based, they utilize published data to the extent possible.
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                Author and article information

                Journal
                BMJ Open
                BMJ Open
                bmjopen
                bmjopen
                BMJ Open
                BMJ Publishing Group (BMA House, Tavistock Square, London, WC1H 9JR )
                2044-6055
                2021
                7 July 2021
                : 11
                : 7
                : e046830
                Affiliations
                [1 ]departmentSchool of Psychology , Deakin University , Geelong, Victoria, Australia
                [2 ]departmentCentral Clinical School , Monash University , Melbourne, Victoria, Australia
                [3 ]departmentChild Health Research Centre , The University of Queensland , South Brisbane, Queensland, Australia
                [4 ]Children's Health Queensland Hospital and Health Service , South Brisbane, Queensland, Australia
                [5 ]departmentAutism Clinic for Translational Research, Brain and Mind Centre, Children’s Hospital Westmead Clinical School, Faculty of Medicine and Health , The University of Sydney , Camperdown, New South Wales, Australia
                [6 ]Telethon Kids Institute , Perth, Western Australia, Australia
                [7 ]University of Western Australia , Crawley, Western Australia, Australia
                [8 ]departmentDiscipline of Psychiatry , The University of Adelaide , Adelaide, South Australia, Australia
                [9 ]departmentHopwood Centre for Neurobiology, Lifelong Health Theme , South Australian Health and Medical Research Institute , Adelaide, South Australia, Australia
                [10 ]departmentTurner Institute for Brain and Mental Health, School of Psychological Sciences and Monash Biomedical Imaging , Monash University , Melbourne, Victoria, Australia
                [11 ]departmentCentre for Molecular Medicine and Innovative Therapeutics , Murdoch University , Murdoch, Western Australia, Australia
                [12 ]departmentDiscipline of Psychology , Murdoch University , Murdoch, Western Australia, Australia
                [13 ]departmentBrain and Mind Centre, Central Clinical School, Faculty of Medicine and Health , The University of Sydney , Camperdown, New South Wales, Australia
                [14 ]departmentIMPACT – the Institute for Mental and Physical Health and Clinical Translation, School of Medicine , Deakin University , Geelong, Victoria, Australia
                [15 ]departmentKrongold Clinic, Monash Education , Monash University , Clayton, Victoria, Australia
                [16 ]departmentCentre for Human Psychopharmacology, Faculty of Heath, Arts and Design , Swinburne University of Technology , Melbourne, Victoria, Australia
                [17 ]departmentEpworth Centre for Innovation in Mental Health , Epworth HealthCare , Camperwell, Victoria, Australia
                Author notes
                [Correspondence to ] Professor Peter G Enticott; peter.enticott@ 123456deakin.edu.au
                Author information
                http://orcid.org/0000-0002-6638-951X
                http://orcid.org/0000-0003-2612-8507
                http://orcid.org/0000-0001-8178-4625
                http://orcid.org/0000-0003-3705-5323
                http://orcid.org/0000-0002-4484-1069
                http://orcid.org/0000-0002-6218-0428
                http://orcid.org/0000-0001-9190-6366
                http://orcid.org/0000-0002-9408-7367
                http://orcid.org/0000-0001-8832-9895
                http://orcid.org/0000-0001-6185-9677
                http://orcid.org/0000-0003-3351-5919
                http://orcid.org/0000-0002-7546-6636
                http://orcid.org/0000-0003-0666-7810
                http://orcid.org/0000-0003-3979-7849
                http://orcid.org/0000-0003-3395-8525
                http://orcid.org/0000-0003-3255-5118
                http://orcid.org/0000-0001-6109-3958
                http://orcid.org/0000-0001-7715-8891
                http://orcid.org/0000-0001-5400-2659
                http://orcid.org/0000-0001-7009-6843
                http://orcid.org/0000-0001-7841-018X
                http://orcid.org/0000-0002-8055-0365
                http://orcid.org/0000-0003-4217-8096
                Article
                bmjopen-2020-046830
                10.1136/bmjopen-2020-046830
                8264904
                34233985
                a417d318-1a54-453a-8fcf-a09d47eea197
                © Author(s) (or their employer(s)) 2021. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ.

                This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See:  http://creativecommons.org/licenses/by-nc/4.0/.

                History
                : 11 November 2020
                : 23 June 2021
                Funding
                Funded by: FundRef http://dx.doi.org/10.13039/501100000925, National Health and Medical Research Council;
                Award ID: APP1199298
                Categories
                Neurology
                1506
                1713
                Protocol
                Custom metadata
                unlocked

                Medicine
                child & adolescent psychiatry,developmental neurology & neurodisability,paediatric neurology,neurophysiology

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