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Billet publié sur Bluesky le 22/10/2023 20:30

Bluesky Publication avec DOI crossref Extrait cité dans le billet Question posée par Dawson dans le billet Lien intégré au billet Termes sur l’autisme

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Jente Meijer, Bruno Hebling Vieira, Camille Elleaume, Zofia Baranczuk-Turska, Nicolas Langer, Dorothea L. Floris (2023). Towards Understanding Autism Heterogeneity: Identifying Clinical Subgroups and Neuroanatomical Deviations. openRxiv.

Date de publication
22/10/2023
Identifiant
10.1101/2023.10.21.23297299
Auteurs
Jente Meijer, Bruno Hebling Vieira, Camille Elleaume, Zofia Baranczuk-Turska, Nicolas Langer, Dorothea L. Floris
Type de référence
preprint
Éditeur
openRxiv
Source de métadonnées
crossref

Résumé

Abstract Autism Spectrum Disorder (‘autism’) is a neurodevelopmental condition characterized by substantial behavioural and neuroanatomical heterogeneity. This poses significant challenges to understanding its neurobiological mechanisms and developing effective interventions. Identifying phenotypically more homogeneous subgroups and shifting the focus from average group differences to individuals is a promising approach to addressing heterogeneity. In the present study, we aimed to parse clinical and neuroanatomical heterogeneity in autism by combining clustering of clinical features with normative modeling based on neuroanatomical measures (cortical thickness [CT] and subcortical volume) within the ABIDE datasets (N autism=861, N neurotypical=886, age-range 5-64). First, model-based clustering was applied to autistic symptoms as measured by the Autism Diagnostic Observation Schedule to identify clinical subgroups of autism. Next, we examined whether clinical subgrouping resulted in increased neurobiological homogeneity within the subgroups compared to the entire autism group by comparing their spatial overlap of neuroanatomical deviations. We further investigated whether the identified subgroups improved the accuracy of autism classification based on the neuroanatomical deviations using supervised machine learning with cross-validation. Results yielded two clinical subgroups primarily differing in restrictive and repetitive behaviours (RRB). Both subgroups showed increased homogeneity in localized deviations with the high-RRB subgroup showing increased volume deviations in cerebellum and the low-RRB subgroup showing decreased CT deviations predominantly in the postcentral gyrus and fusiform cortex. Nevertheless, substantial within-group heterogeneity remained highlighted by the failure of the classifier to distinguish between the subgroups. Identifying subgroups of autism has substantial clinical implications opening the potential for more tailored behavioural interventions and improving clinical outcomes. General Scientific Summary Autism is characterized by pronounced behavioural and neurobiological heterogeneity. This study suggests that reducing this heterogeneity at the clinical level by employing subgrouping also results in more similar neuroanatomical profiles in the identified clinical subgroups. Although we could demonstrate that clinical subgrouping reduces neuroanatomical heterogeneity, simultaneously, there remained substantial heterogeneity potentially pointing towards multiple pathways resulting in high RRBs and neurobiological subgroups with similar clinical phenotypes.

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