Morphometry and functional connectivity of auditory cortex in school-age children with profound language disabilities: five comparative case studies

Linke, Annika Carola; Slušná, Dominika; Kohli, Jiwandeep Singh; Álvarez-Linera Prado, Juan; Müller, Ralph-Axel; Hinzen, Wolfram

doi:http://dx.doi.org/10.1016/j.bandc.2021.105822

Morphometry and functional connectivity of auditory cortex in school-age children with profound language disabilities: five comparative case studies

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Linke A, Slušná D, Kohli JS, Álvarez-Linera Prado J, Müller RA, Hinzen W. Morphometry and functional connectivity of auditory cortex in school-age children with profound language disabilities: five comparative case studies. Brain Cogn. 2021;155:105822. DOI: 10.1016/j.bandc.2021.105822

Abstract

Many neurodevelopmental conditions imply absent or severely reduced language capacities at school age. Evidence from functional magnetic resonance imaging is highly limited. We selected a series of five cases scanned with the same fMRI paradigm and the aim of relating individual language profiles onto underlying patterns of functional connectivity (FC) across auditory language cortex: three with neurogenetic syndromes (Coffin-Siris, Landau-Kleffner, and Fragile-X), one with idiopathic intellectual disability, one with autism spectrum disorder (ASD). Compared to both a group with typical development (TD) and a verbal ASD group (total N = 110), they all showed interhemispheric FC below two standard deviations of the TD mean. Children with higher language scores showed higher intrahemispheric FC between Heschl’s gyrus and other auditory language regions, as well as an increase of FC during language stimulation compared to rest. An increase of FC in forward vs. reversed speech in the posterior and middle temporal gyri was seen across all cases. The Coffin-Siris case, the most severe, also had the most anomalous FC patterns and showed reduced myelin content, while the Landau-Kleffner case showed reduced cortical thickness. These results suggest potential for neural markers and mechanisms of severe language processing deficits under highly heterogeneous etiological conditions.