Personalized and Circuit-Based Transcranial Magnetic Stimulation: Evidence, Controversies, and Opportunities

被引:37
作者
Cash, Robin F. H. [1 ]
Zalesky, Andrew
机构
[1] Univ Melbourne, Melbourne Neuropsychiat Ctr, Parkville, Vic, Australia
基金
英国医学研究理事会;
关键词
TREATMENT-RESISTANT DEPRESSION; NONINVASIVE BRAIN-STIMULATION; TREATING MAJOR DEPRESSION; THETA-BURST STIMULATION; RIGHT PARIETAL CORTEX; FUNCTIONAL CONNECTIVITY; NETWORK LOCALIZATION; COIL PLACEMENT; DOUBLE-BLIND; HZ RTMS;
D O I
10.1016/j.biopsych.2023.11.013
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The development of neuroimaging methodologies to map brain connectivity has transformed our understanding of psychiatric disorders, the distributed effects of brain stimulation, and how transcranial magnetic stimulation can be best employed to target and ameliorate psychiatric symptoms. In parallel, neuroimaging research has revealed that higher-order brain regions such as the prefrontal cortex, which represent the most common therapeutic brain stimulation targets for psychiatric disorders, show some of the highest levels of interindividual variation in brain connectivity. These findings provide the rationale for personalized target site selection based on person-specific brain network architecture. Recent advances have made it possible to determine reproducible personalized targets with millimeter precision in clinically tractable acquisition times. These advances enable the potential advantages of spatially personalized transcranial magnetic stimulation targeting to be evaluated and translated to basic and clinical applications. In this review, we outline the motivation for target site personalization, preliminary support (mostly in depression), convergent evidence from other brain stimulation modalities, and generalizability beyond depression and the prefrontal cortex. We end by detailing methodological recommendations, controversies, and notable alternatives. Overall, while this research area appears highly promising, the value of personalized targeting remains unclear, and dedicated large prospective randomized clinical trials using validated methodology are critical.
引用
收藏
页码:510 / 522
页数:13
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