Phenotypic Exploration of Autism Spectrum Disorders Retrospective and Prospective Data

Autism Spectrum Disorders (ASD) are a heterogeneous and severe developmental abnormalities of the nervous system characterized by deficits affecting social interactions and verbal and nonverbal communication (DSM-5, 2013), affecting approximately 1% of the general population (Brugha, 2012). In 5-40% of cases, genetic factors are identified as the cause of these disorders, prevalence depending on the technique used (Exome and/or SNPs Array) and the associated intellectual deficit. In the majority of cases, the etiology remains unknown. The familial aggregation of ASDs and the significant excess of concordant monozygotic twins over dizygotic twins demonstrate the strong involvement of genetic factors in autism. Studies of microdeletions/microduplications (copy number variants) or by Whole Exome Sequencing and Whole Genome Sequencing (Single Nucleotide Variants) show the involvement of many genes in the predisposition to autism. However, ASD remains a clinically and genetically heterogeneous disorder, since several hundred genes have been identified to date.

The main objective of our project is to allow the retrospective and prospective collection of data on the phenotypic and genetic characterization of ASD patients in a structured way in order to allow the development of a new dynamic in terms of research. The identification of genetic factors (Delorme et al, Nature Medicine, 2013) and biological pathways involved in the emergence of autistic symptoms (Bourgeron, Nature Neuroscience 2015) is fundamental. The identification of biological pathways is an indispensable step for the development of new therapeutic strategies. In addition, a major challenge of this study is to better understand the phenotype/genotype relationships in ASD. This requires the constitution of a large cohort of patients taking into account their multimodal, extensive and precise exploration of clinical, neuroanatomical (MRI, EEG) and biological phenotypes and to correlate them with genetic data.

The work carried out by our teams and collaborators has led to the identification of numerous genes associated with ASD and involved in synaptic formation and regulation: NLGN3-4 (Jamain et al, Nature Genetics 2003), SHANK1-3 (Durand el al Nature Genetics 2007, Sato et al Am J Hum Genet 2013, Leblond et al Plos Genetics 2013, 2014), CNTN-6 (Mercati et al Mol Psychiatry 2016) and CNTNAP4 (Karayannis, Nature, 2014) (for review Toro et al, TIGS 2012; Delorme et al, Nature Medicine ,2013; Bourgeron, Nature Neuroscience 2015). This work was combined with extensive phenotypic explorations of patients and their relatives. It has allowed us to specify the neuroanatomical characteristics of the patients (Lefebvre et al. Biol Psychiatry 2014) and their genetic substrate (Toro et al, Mol Psychiatry 2015), but also the underlying cognitive processes (Dumas et al, PNAS, 2014; Zalla et al. Cortex 2014, 2015; Grezes et al Hum Brain Mapp, 2014). More recently, we have shown the existence of abnormalities in the regulation of the melatonin synthesis pathway (Pagan et al, TransPsychiatry 2014; Pagan et al, J pineal Res 2015) or immunological abnormalities (in particular HLA anomalies (Bennabi et al, 2018)

Description of the population to be studied and rationale for its choice

We wish to explore the heterogeneity of autism spectrum disorders in a population received in routine care in our evaluation units. These are patients followed in the Child and Adolescent Psychiatry Department at the Robert Debré Hospital in Paris, who meet the diagnostic criteria of ASD according to DSM-5, aged 0 to 17 years.