Department of Psychiatry and Behavioral Sciences, Stanford University School of Medicine, Stanford, CA 94305.
Wu Tsai Neurosciences Institute, Stanford University School of Medicine, Stanford, CA 94305.
Proc Natl Acad Sci U S A. 2024 May 28;121(22):e2316149121. doi: 10.1073/pnas.2316149121. Epub 2024 May 20.
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.
言语障碍是帕金森病(PD)的一个突出但研究不足的症状。虽然丘脑底核(STN)是治疗运动症状的既定临床靶点,但这些干预措施可能导致言语进一步恶化。多巴胺能药物、STN 回路及其对 PD 患者言语和认知功能的下游影响之间的相互作用尚未完全理解。在这里,我们研究了多巴胺能药物对 STN 回路的影响,并探讨了其与 PD 患者言语和认知功能的关系。我们发现,STN 内在功能连接的变化与 PD 患者言语功能的改变有关。有趣的是,这种关系的特征是 STN 的背外侧和腹侧部分与语言网络之间的功能连接发生改变。至关重要的是,STN 背外侧部分与语言网络中的关键区域之间的功能连接的药物诱导变化,包括左额下回和左颞上回,与需要口头反应的标准化神经心理学测试的变化相关。在同一测试的书面版本中未观察到这种关系。此外,STN 与语言区域之间功能连接的变化预测了药物对与言语相关的认知表现的下游影响。这些发现揭示了一个以前未被识别的大脑机制,通过该机制,多巴胺能药物影响 PD 中的言语功能。我们的研究揭示了 PD 中言语控制受损的皮质下-皮质回路机制。这里获得的见解可以为旨在减轻 PD 中的言语缺陷和提高受影响个体的生活质量的治疗策略提供信息。