Abstract
Singing-based treatments of aphasia can improve language outcomes, but the neural benefits of group-based singing in aphasia are unknown. Here, we set out to determine the structural neuroplasticity changes underpinning group-based singing-induced treatment effects in chronic aphasia. Twenty-eight patients with at least mild nonfluent poststroke aphasia were randomized into two groups that received a 4-month multicomponent singing intervention (singing group) or standard care (control group). High-resolution T1 images and multishell diffusion-weighted MRI data were collected in two time points (baseline/5 months). Structural gray matter (GM) and white matter (WM) neuroplasticity changes were assessed using language network region of interest-based voxel-based morphometry (VBM) and quantitative anisotropy-based connectometry, and their associations to improved language outcomes (Western Aphasia Battery Naming and Repetition) were evaluated. Connectometry analyses showed that the singing group enhanced structural WM connectivity in the left arcuate fasciculus (AF) and corpus callosum as well as in the frontal aslant tract (FAT), superior longitudinal fasciculus, and corticostriatal tract bilaterally compared with the control group. Moreover, in VBM, the singing group showed GM volume increase in the left inferior frontal cortex (Brodmann area 44) compared with the control group. The neuroplasticity effects in the left BA44, AF, and FAT correlated with improved naming abilities after the intervention. These findings suggest that in the poststroke aphasia group, singing can bring about structural neuroplasticity changes in left frontal language areas and in bilateral language pathways, which underpin treatment-induced improvement in speech production.
Footnotes
The authors declare no competing financial interests.
We thank Andrea Norton and Jeanette Tamplin as well as all the PSA participants and their family members for their invaluable input in this project. This study was supported by the Academy of Finland (Grants 299044, 306625, 327996, and 346211), Fundació La Marató de TV3 (Grant 201729.32), and European Research Council (Grant 803466). A.J.S received funding from the Finnish Cultural Foundation (Grant 191230), the Orion Research Foundation, and the Signe and Ane Gyllenberg Foundation, and V.S. was supported by Instrumentarium Science Foundation sr and Orion Research Foundation sr.
↵*A.J.S. and A.P. contributed equally to this work.
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