Electrophysiological Markers for Interventions in Phelan-McDermid Syndrome and Idiopathic Autism
Project Description:
Recent work suggests that up to 2% of individuals with autism spectrum disorder (ASD) and intellectual disability (ID) have deletions or point mutations in the SHANK3 gene, resulting in Phelan-McDermid syndrome (PMS), and approximately 85% of people with PMS meet criteria for ASD. SHANK3 codes for a master scaffolding protein that forms a key framework in the postsynaptic density of glutamatergic (excitatory) synapses and plays a critical role in synaptic function. SHANK3 and glutamate pathways are implicated in multiple forms of ASD and this convergence implies shared biochemical pathways with potentially overlapping therapeutic targets. Thus, targeting SHANK3 deficiency in PMS as a specific genetic cause of ASD allows us to inform treatment in broader idiopathic ASD (iASD). Our ongoing studies provide in-depth phenotyping of PMS, pointing toward a specific clinical and electrophysiological (EEG) profile. However, the efficacy of potential EEG biomarkers as a measure of treatment response remains to be determined. Preliminary data using visual evoked potentials (VEPs) to examine cortical excitatory postsynaptic potentials demonstrate promising links to disease mechanisms in PMS and iASD. Biomarkers and novel clinical measures for evaluating response to intervention have also been piloted successfully at our site in cohorts of patients with PMS and iASD. We have identified a unique VEP profile of excitatory deficits in PMS (markedly reduced P60-N75 amplitude) that is also present in a subset of children with iASD. Here, we propose to extend this work to a larger sample in PMS and to parallel excitatory processes in the auditory domain, in order to stratify individuals with iASD and select those we predict will show response to IGF-1. We will enroll 150 children (60 PMS; 90 iASD; age 5-12 years), specifically recruiting intellectually disabled and minimally verbal children given the prominence of this profile in PMS and the critical need to address this group in broader ASD research. Our short-term goal is to show that select electrophysiological markers in PMS are relevant to iASD and predictive of treatment response. Our long-term goal is to optimize treatment selection in iASD by establishing biological signature(s) derived from PMS that are: a) useful for predicting treatment responders, and b) responsive to intervention. The expected outcome of this study is to establish the feasibility of electrophysiological biomarkers for use in clinical trials in PMS and iASD and to define a biological profile that will mark a subset of patients with iASD likely to show neural and clinical response to IGF-1. PI: KOLEVZON, ALEXANDER
Keyword(s):
Mental/Behavioral Health – Autism, Developmental Disabilities, Early Childhood – Developmental Health (including developmental screening), Health Equity, Heritable Disorders (excluding sickle cell), Mental/Behavioral Health – General , Children, Adolescents, and Young Adults with Special Health Care Needs
Core Function(s):
Performing Direct and/or Demonstration Services, Performing Research or Evaluation, Other Direct/Model Services
Area of Emphasis
Education & Early Intervention, Health-Related Activities, Quality of Life
Target Audience:
Professionals and Para-Professionals, Family Members/Caregivers, Adults with Disabilities, Children/Adolescents with Disabilities/SHCN
Unserved or Under-served Populations:
Specific Groups
Primary Target Audience Geographic Descriptor:
Not Applicable
COVID-19 Related Data:
N/A
