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Aline Lefebvre, Julian Tillmann, Freddy Cliquet, Frederique Amsellem, Anna Maruani, Claire Leblond, Anita Beggiato, David Germanaud, et al. (2023). Tackling hypo and hyper sensory processing heterogeneity in autism: From clinical stratification to genetic pathways. Autism Research, 16(2), 364-378. Wiley.

Publication date
4 Dec 2022
Identifier
10.1002/aur.2861
Authors
Aline Lefebvre, Julian Tillmann, Freddy Cliquet, Frederique Amsellem, Anna Maruani, Claire Leblond, Anita Beggiato, David Germanaud, Anouck Amestoy, Myriam Ly‐Le Moal, Daniel Umbricht, Christopher Chatham, Lorraine Murtagh, Manuel Bouvard, Marion Leboyer, Tony Charman, Thomas Bourgeron, Richard Delorme, Guillaume Dumas, and the EU‐AIMS LEAP group
Source
Autism Research
Details
16(2), 364-378
Reference type
article
Publisher
Wiley
Metadata source
crossref

Abstract

Abstract As an integral part of autism spectrum symptoms, sensory processing issues including both hypo and hyper sensory sensitivities. These sensory specificities may result from an excitation/inhibition imbalance with a poorly understood of their level of convergence with genetic alterations in GABA‐ergic and glutamatergic pathways. In our study, we aimed to characterize the hypo/hyper‐sensory profile among autistic individuals. We then explored its link with the burden of deleterious mutations in a subset of individuals with available whole‐genome sequencing data. To characterize the hypo/hyper‐sensory profile, the differential Short Sensory Profile (dSSP) was defined as a normalized and centralized hypo/hypersensitivity ratio from the Short Sensory Profile (SSP). Including 1136 participants (533 autistic individuals, 210 first‐degree relatives, and 267 controls) from two independent study samples (PARIS and LEAP), we observed a statistically significant dSSP mean difference between autistic individuals and controls, driven mostly by a high dSSP variability, with an intermediated profile represented by relatives. Our genetic analysis tended to associate the dSSP and the hyposensitivity with mutations of the GABAergic pathway. The major limitation was the dSSP difficulty to discriminate subjects with a similar quantum of hypo‐ and hyper‐sensory symptoms to those with no such symptoms, resulting both in a similar ratio score of 0. However, the dSSP could be a relevant clinical score, and combined with additional sensory descriptions, genetics and endophenotypic substrates, will improve the exploration of the underlying neurobiological mechanisms of sensory processing differences in autism spectrum.

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