用脑电与近红外数据融合提升戒毒评估可靠性
NeuroCLIP: A Multimodal Contrastive Learning Method for rTMS-treated Methamphetamine Addiction Analysis
- 融合同步采集的EEG与fNIRS数据,通过渐进学习构建多模态模型
- 对戒毒者与健康人区分准确率显著优于单一模态模型
- 结果与渴求量表高度相关,适合临床戒毒疗效评估
甲基苯丙胺成瘾是全球重大健康挑战,其评估和重复经颅磁刺激(rTMS)疗效评价常依赖主观自述,存在不确定性。尽管脑电图(EEG)和功能性近红外光谱(fNIRS)等神经影像技术可提供客观替代方案,但各自存在局限性,且传统手工特征提取方法影响生物标志物可靠性。为此,我们提出NeuroCLIP,一种整合同步记录的EEG与fNIRS数据的深度学习框架,采用渐进学习策略。验证实验表明,相较于仅使用EEG或仅使用fNIRS的模型,NeuroCLIP在区分甲基苯丙胺依赖个体与健康对照方面显著提升判别能力。此外,该框架实现了对rTMS治疗效果的客观、基于大脑的评估,显示治疗后神经模式向健康对照组显著趋近。关键的是,该多模态数据驱动的生物标志物与心理测量学验证的渴求评分呈强相关性。结果表明,通过NeuroCLIP从EEG-fNIRS数据中提取的生物标志物,相比单模态方法具有更强鲁棒性和可靠性,为成瘾神经科学研究提供有力工具,并有望改善临床评估。
原文摘要 · Abstract (English)
Methamphetamine dependence poses a significant global health challenge, yet its assessment and the evaluation of treatments like repetitive transcranial magnetic stimulation (rTMS) frequently depend on subjective self-reports, which may introduce uncertainties. While objective neuroimaging modalities such as electroencephalography (EEG) and functional near-infrared spectroscopy (fNIRS) offer alternatives, their individual limitations and the reliance on conventional, often hand-crafted, feature extraction can compromise the reliability of derived biomarkers. To overcome these limitations, we propose NeuroCLIP, a novel deep learning framework integrating simultaneously recorded EEG and fNIRS data through a progressive learning strategy. This approach offers a robust and trustworthy biomarker for methamphetamine addiction. Validation experiments show that NeuroCLIP significantly improves discriminative capabilities among the methamphetamine-dependent individuals and healthy controls compared to models using either EEG or only fNIRS alone. Furthermore, the proposed framework facilitates objective, brain-based evaluation of rTMS treatment efficacy, demonstrating measurable shifts in neural patterns towards healthy control profiles after treatment. Critically, we establish the trustworthiness of the multimodal data-driven biomarker by showing its strong correlation with psychometrically validated craving scores. These findings suggest that biomarker derived from EEG-fNIRS data via NeuroCLIP offers enhanced robustness and reliability over single-modality approaches, providing a valuable tool for addiction neuroscience research and potentially improving clinical assessments.
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