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A Systems Perspective on the Effective Connectivity of Overt Speech Production

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Abstract

The aim of this study was to provide a computational system model of effective connectivity in the human brain underlying overt speech production. Meta-analysis of neuroimaging studies and functional magnetic resonance imaging data acquired during a verbal fluency task revealed a core network consisting of Brodmann's area (BA) 44 in Broca's region, anterior insula, basal ganglia, cerebellum, premotor cortex (PMC, BA 6) and primary motor cortex (M1, areas 4a/4p). Dynamic causal modelling (DCM) indicated the highest evidence for a system architecture featuring the insula in a serial position between BA 44 and two parallel nodes (cerebellum/basal ganglia), from which information converges onto the PMC and finally M1. Parameter inference revealed that effective connectivity from the insular relay into the cerebellum/basal ganglia is primarily task driven (preparation) while the output into the cortical motor system strongly depends on the actual word production rate (execution). DCM hence allowed not only a quantitative characterization of the human speech production network, but also the distinction of a preparatory and an executive subsystem within it. The proposed model of physiological integration during speech production may now serve as a reference for investigations into the neurobiology of pathological states such as dysarthria and apraxia of speech.

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References
1.
Vigneau M, Beaucousin V, Herve P, Duffau H, Crivello F, Houde O . Meta-analyzing left hemisphere language areas: phonology, semantics, and sentence processing. Neuroimage. 2006; 30(4):1414-32. DOI: 10.1016/j.neuroimage.2005.11.002. View

2.
Stephan K . On the role of general system theory for functional neuroimaging. J Anat. 2004; 205(6):443-70. PMC: 1571423. DOI: 10.1111/j.0021-8782.2004.00359.x. View

3.
Guenther F . Cortical interactions underlying the production of speech sounds. J Commun Disord. 2006; 39(5):350-65. DOI: 10.1016/j.jcomdis.2006.06.013. View

4.
Kleber B, Birbaumer N, Veit R, Trevorrow T, Lotze M . Overt and imagined singing of an Italian aria. Neuroimage. 2007; 36(3):889-900. DOI: 10.1016/j.neuroimage.2007.02.053. View

5.
Mesulam M, Mufson E . Insula of the old world monkey. III: Efferent cortical output and comments on function. J Comp Neurol. 1982; 212(1):38-52. DOI: 10.1002/cne.902120104. View