Subthalamic nucleus–language network connectivity predicts dopaminergic modulation of speech function in Parkinson’s disease

Author:

Cai Weidong12ORCID,Young Christina B.3,Yuan Rui1,Lee Byeongwook1,Ryman Sephira3,Kim Jeehyun3,Yang Laurice3,Levine Taylor F.3,Henderson Victor W.234ORCID,Poston Kathleen L.235ORCID,Menon Vinod123

Affiliation:

1. Department of Psychiatry and Behavioral Sciences, Stanford University School of Medicine, Stanford, CA 94305

2. Wu Tsai Neurosciences Institute, Stanford University School of Medicine, Stanford, CA 94305

3. Department of Neurology and Neurological Sciences, Stanford University School of Medicine, Stanford, CA 94305

4. Department of Epidemiology and Population Health, Stanford University School of Medicine, Stanford, CA 94305

5. Department of Neurosurgery, Stanford University School of Medicine, Stanford, CA 94305

Abstract

Speech impediments are a prominent yet understudied symptom of Parkinson’s disease (PD). While the subthalamic nucleus (STN) is an established clinical target for treating motor symptoms, these interventions can lead to further worsening of speech. The interplay between dopaminergic medication, STN circuitry, and their downstream effects on speech in PD is not yet fully understood. Here, we investigate the effect of dopaminergic medication on STN circuitry and probe its association with speech and cognitive functions in PD patients. We found that changes in intrinsic functional connectivity of the STN were associated with alterations in speech functions in PD. Interestingly, this relationship was characterized by altered functional connectivity of the dorsolateral and ventromedial subdivisions of the STN with the language network. Crucially, medication-induced changes in functional connectivity between the STN’s dorsolateral subdivision and key regions in the language network, including the left inferior frontal cortex and the left superior temporal gyrus, correlated with alterations on a standardized neuropsychological test requiring oral responses. This relation was not observed in the written version of the same test. Furthermore, changes in functional connectivity between STN and language regions predicted the medication’s downstream effects on speech-related cognitive performance. These findings reveal a previously unidentified brain mechanism through which dopaminergic medication influences speech function in PD. Our study sheds light into the subcortical-cortical circuit mechanisms underlying impaired speech control in PD. The insights gained here could inform treatment strategies aimed at mitigating speech deficits in PD and enhancing the quality of life for affected individuals.

Funder

HHS | NIH | National Institute on Aging

HHS | NIH | National Institute of Neurological Disorders and Stroke

HHS | NIH | National Institute of Mental Health

Alzheimer's Association

HHS | NIH | National Institute on Deafness and Other Communication Disorders

Publisher

Proceedings of the National Academy of Sciences

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