Stratifying the autistic phenotype using electrophysiological indices of social perception

Author:

Mason Luke1ORCID,Moessnang Carolin2,Chatham Christopher3ORCID,Ham Lindsay3ORCID,Tillmann Julian4ORCID,Dumas Guillaume56ORCID,Ellis Claire4ORCID,Leblond Claire S.5ORCID,Cliquet Freddy5ORCID,Bourgeron Thomas5,Beckmann Christian7ORCID,Charman Tony4ORCID,Oakley Beth4,Banaschewski Tobias2ORCID,Meyer-Lindenberg Andreas2ORCID,Baron-Cohen Simon8,Bölte Sven9ORCID,Buitelaar Jan K.7ORCID,Durston Sarah10,Loth Eva4ORCID,Oranje Bob10,Persico Antonio11ORCID,Dell’Acqua Flavio4ORCID,Ecker Christine12,Johnson Mark H.18,Murphy Declan4ORCID,Jones Emily J. H.1ORCID

Affiliation:

1. Centre for Brain and Cognitive Development, Birkbeck, University of London, WC1E 7HX, London, UK.

2. Department of Child and Adolescent Psychiatry, Central Institute of Mental Health, Medical Faculty Mannheim, University of Heidelberg, 68159 Mannheim, Germany.

3. F. Hoffmann-La Roche Ltd., Grenzacherstrasse 124, 4070 Basel, Switzerland.

4. Institute of Psychiatry, Psychology and Neuroscience, King’s College, London, London, UK.

5. Human Genetics and Cognitive Functions, Institut Pasteur, UMR3571 CNRS, Université de Paris, 75015 Paris, France.

6. Precision Psychiatry and Social Physiology laboratory, CHU Sainte-Justine Research Center, Department of Psychiatry, University of Montreal, H3T 1C5 Quebec, Canada.

7. Department of Cognitive Neuroscience, Donders Institute for Brain, Cognition and Behavior, Radboudumc, 6525 EN Nijmegen, Netherlands.

8. Department of Psychology, University of Cambridge, CB2 3EB Cambridge, UK.

9. Center of Neurodevelopmental Disorders (KIND), Centre for Psychiatry Research Child and Adolescent Psychiatry, Stockholm Health Care Services, Region Stockholm, Stockholm 171 77, Sweden.

10. NICHE-lab, Department of Psychiatry, Brain Center of University Medical Center Utrecht, 3584 CX Utrecht, Netherlands.

11. Universita Campus Bio-Medico, 00128 Rome, Italy.

12. Curtin Autism Research Group, School of Occupational Therapy, Social Work and Speech Pathology, Curtin University, Perth, Western Australia 6102, Australia.

Abstract

Autism spectrum disorder (ASD) is a neurodevelopmental condition characterized by difficulties in social communication, but also great heterogeneity. To offer individualized medicine approaches, we need to better target interventions by stratifying autistic people into subgroups with different biological profiles and/or prognoses. We sought to validate neural responses to faces as a potential stratification factor in ASD by measuring neural (electroencephalography) responses to faces (critical in social interaction) in N = 436 children and adults with and without ASD. The speed of early-stage face processing (N170 latency) was on average slower in ASD than in age-matched controls. In addition, N170 latency was associated with responses to faces in the fusiform gyrus, measured with functional magnetic resonance imaging, and polygenic scores for ASD. Within the ASD group, N170 latency predicted change in adaptive socialization skills over an 18-month follow-up period; data-driven clustering identified a subgroup with slower brain responses and poor social prognosis. Use of a distributional data-driven cutoff was associated with predicted improvements of power in simulated clinical trials targeting social functioning. Together, the data provide converging evidence for the utility of the N170 as a stratification factor to identify biologically and prognostically defined subgroups in ASD.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

General Medicine

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