Potential locations for non-invasive brain stimulation in treating ADHD: Results from a cross-dataset validation of functional connectivity analysis.

IF 5.8 1区 医学 Q1 PSYCHIATRY
Yue Yang, Sitong Yuan, Huize Lin, Yi Han, Binlong Zhang, Jinna Yu
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引用次数: 0

Abstract

Noninvasive brain stimulation (NIBS) has emerged as a promising therapeutic approach for attention-deficit/hyperactivity disorder (ADHD), yet the inaccurate selection of stimulation sites may constrain its efficacy. This study aimed to identify novel NIBS targets for ADHD by integrating meta-analytic findings with cross-dataset validation of functional connectivity patterns. A meta-analysis including 124 functional magnetic resonance imaging (fMRI) studies was first conducted to delineate critical brain regions associated with ADHD, which were defined as regions of interest (ROIs). Subsequently, functional connectivity (FC) analysis was performed using resting-state fMRI data from two independent databases comprising 116 patients with ADHD. Surface brain regions exhibiting consistent FC patterns with the ADHD-related ROIs across both datasets were identified as candidate NIBS targets. These targets were then translated to scalp-level stimulation sites using the 10-20 system and continuous proportional coordinates (CPC). Key regions mapped to the scalp included the bilateral dorsolateral prefrontal cortex, right inferior frontal gyrus, bilateral inferior parietal lobule, supplementary motor area (SMA), and pre-SMA. These findings propose a set of precise stimulation location for NIBS interventions in ADHD, potentially broadening the scope of neuromodulation strategies for this disorder. The study emphasized the utility of cross-dataset functional connectivity analysis in refining NIBS target selection and highlights novel brain targets that warrant further investigation in clinical trials.

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来源期刊
CiteScore
11.50
自引率
2.90%
发文量
484
审稿时长
23 weeks
期刊介绍: Psychiatry has suffered tremendously by the limited translational pipeline. Nobel laureate Julius Axelrod''s discovery in 1961 of monoamine reuptake by pre-synaptic neurons still forms the basis of contemporary antidepressant treatment. There is a grievous gap between the explosion of knowledge in neuroscience and conceptually novel treatments for our patients. Translational Psychiatry bridges this gap by fostering and highlighting the pathway from discovery to clinical applications, healthcare and global health. We view translation broadly as the full spectrum of work that marks the pathway from discovery to global health, inclusive. The steps of translation that are within the scope of Translational Psychiatry include (i) fundamental discovery, (ii) bench to bedside, (iii) bedside to clinical applications (clinical trials), (iv) translation to policy and health care guidelines, (v) assessment of health policy and usage, and (vi) global health. All areas of medical research, including — but not restricted to — molecular biology, genetics, pharmacology, imaging and epidemiology are welcome as they contribute to enhance the field of translational psychiatry.
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