Underconnectivity Between Visual and Salience Networks and Links With Sensory Abnormalities in Autism Spectrum Disorders - 26/01/21
, Ellyn B. Pueschel, BA a, Yangfeifei Gao, MS a, b, Afrooz Jahedi, MS a, c, Kalekirstos Alemu, BS a, Ruth Carper, PhD a, b, Inna Fishman, PhD a, b, Ralph-Axel Müller, PhD a, bAbstract |
Objective |
The anterior insular cortex (AI), which is a part of the salience network, is critically involved in visual awareness, multisensory perception, and social and emotional processing, among other functions. In children and adolescents with autism spectrum disorders (ASDs), evidence has suggested aberrant functional connectivity (FC) of AI compared with typically developing peers. While recent studies have primarily focused on the functional connections between salience and social networks, much less is known about connectivity between AI and primary sensory regions, including visual areas, and how these patterns may be linked to autism symptomatology.
Method |
The current investigation implemented functional magnetic resonance imaging to examine resting-state FC patterns of salience and visual networks in children and adolescents with ASDs compared with typically developing controls, and to relate them to behavioral measures.
Results |
Functional underconnectivity was found in the ASD group between left AI and bilateral visual cortices. Moreover, in an ASD subgroup with more atypical visual sensory profiles, FC was positively correlated with abnormal social motivational responsivity.
Conclusion |
Findings of reduced FC between salience and visual networks in ASDs potentially indicate deficient selection of salient information. Moreover, in children and adolescents with ASDs who show strongly atypical visual sensory profiles, connectivity at seemingly more neurotypical levels may be paradoxically associated with greater impairment of social motivation.
Le texte complet de cet article est disponible en PDF.Key words : anterior insula, autism, functional connectivity MRI, salience network, vision
Plan
| This research was supported by the National Institutes of Health (grant K01-MH113819 to R.J.J.K.; grants R01-MH081023 and R01-MH101173 to R.-A.M.; grant K01-MH097972 to I.F.). The funding sources had no role in the study design, writing of the report, or decision to submit the article for publication. |
|
| This study was presented as an abstract at the Society of Biological Psychiatry 72nd Annual Meeting; San Diego, CA; May 18–20, 2017. |
|
| Author Contributions |
|
| Conceptualization: Jao Keehn, Müller |
|
| Data curation: Pueschel, Gao, Jahedi, Alemu |
|
| Formal analysis: Jao Keehn |
|
| Funding acquisition: Jao Keehn, Fishman, Müller |
|
| Investigation: Jao Keehn, Gao, Fishman |
|
| Methodology: Jao Keehn |
|
| Resources: Müller |
|
| Supervision: Jao Keehn, Carper, Fishman, Müller |
|
| Validation: Jao Keehn, Jahedi |
|
| Visualization: Jao Keehn |
|
| Writing – original draft: Jao Keehn, Carper, Müller |
|
| Writing – review and editing: Jao Keehn, Gao, Carper, Fishman, Müller |
|
| ORCID |
|
| R. Joanne Jao Keehn, PhD: 0000-0001-9417-608X |
|
| Ellyn B. Pueschel, BA: 0000-0001-6972-8364 |
|
| Yangfeifei Gao, MS: 0000-0003-0052-6275 |
|
| Afrooz Jahedi, MS: 0000-0002-3891-8808 |
|
| Kalekirstos Alemu, BS: 0000-0001-8349-5675 |
|
| Ruth Carper, PhD: 0000-0002-1195-5473 |
|
| Inna Fishman, PhD: 0000-0002-5873-2365 |
|
| Ralph-Axel Müller, PhD: 0000-0001-7299-6757 |
|
| Disclosure: Drs. Jao Keehn, Carper, Fishman, and Müller, Mss. Pueschel, Gao, and Jahedi, and Mr. Alemu have reported no biomedical financial interests or potential conflicts of interest. |
Vol 60 - N° 2
P. 274-285 - février 2021 Retour au numéroBienvenue sur EM-consulte, la référence des professionnels de santé.
L’accès au texte intégral de cet article nécessite un abonnement.
Déjà abonné à cette revue ?
