Meta-analytic Connectivity Modelling of Functional Magnetic Resonance Imaging Studies in Autism Spectrum Disorders
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Psychology
Radiology
Social Sciences
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Social and non-social deficits in autism spectrum disorders (ASD) persist into adulthood and may share common regions of aberrant neural activations. The current meta-analysis investigated activation differences between ASD and neurotypical controls irrespective of task type. Activation likelihood estimation meta-analyses were performed to examine consistent hypo-activated and/or hyper-activated regions for all tasks combined, and for social and non-social tasks separately; meta-analytic connectivity modelling and behavioral/paradigm analyses were performed to examine co-activated regions and associated behaviors. One hundred studies (mean age range = 18-41 years) were included. For all tasks combined, the ASD group showed significant (p < .05) hypo-activation in one cluster around the left amygdala (peak - 26, -2, -20, volume = 1336 mm, maximum ALE = 0.0327), and this cluster co-activated with two other clusters around the right cerebellum (peak 42, -56, -22, volume = 2560mm, maximum ALE = 0.049) Lobule VI/Crus I and the left fusiform gyrus (BA47) (peak - 42, -46, -18, volume = 1616 mm, maximum ALE = 0.046) and left cerebellum (peak - 42, -58, -20, volume = 1616mm, maximum ALE = 0.033) Lobule VI/Crus I. While the left amygdala was associated with negative emotion (fear) (z = 3.047), the left fusiform gyrus/cerebellum Lobule VI/Crus I cluster was associated with language semantics (z = 3.724) and action observation (z = 3.077). These findings highlight the left amygdala as a region consistently hypo-activated in ASD and suggest the potential involvement of fusiform gyrus and cerebellum in social cognition in ASD. Future research should further elucidate if and how amygdala-fusiform/cerebellar connectivity relates to social and non-social cognition in adults with ASD.
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van der Plas E, Nelson E, Becknell B, Dawson A, Wilson C, Dawson J JAMA Netw Open. 2025; 8(2):e2457601.
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Attanasio M, Mazza M, Le Donne I, Nigri A, Valenti M Eur Arch Psychiatry Clin Neurosci. 2024; .
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Yeung A Heliyon. 2024; 10(18):e38084.
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Nagai Y, Kirino E, Tanaka S, Usui C, Inami R, Inoue R Cereb Cortex. 2023; 34(13):129-145.
PMID: 38012112 PMC: 11065111. DOI: 10.1093/cercor/bhad451.