超越同质性:绘制神经发育和精神脑电图异质性的图景。

IF 5.8 1区 医学 Q1 PSYCHIATRY
Aida Ebadi, Sahar Allouch, Ahmad Mheich, Judie Tabbal, Aya Kabbara, Gabriel Robert, Aline Lefebvre, Anton Iftimovici, Borja Rodríguez-Herreros, Nadia Chabane, Mahmoud Hassan
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引用次数: 0

摘要

脑电图(EEG)在神经发育和精神病学研究中已经深入研究了几十年。然而,将其作为诊断/预后工具纳入临床实践仍未实现。我们假设一个关键原因是潜在的患者异质性,在依赖病例对照方法的脑电图研究中被忽视了。我们将高密度脑电图与规范建模相结合,利用两种完善且广泛研究的脑电图特征——频谱功率和功能连通性,对1674名患有注意缺陷/多动障碍、自闭症谱系障碍、学习障碍或焦虑症的患者和560名匹配对照进行量化。规范模型显示,患者与人群规范的偏差是高度异质性和频率依赖性的。在频谱和连通性上,患者间的偏差空间重叠分别不超过40%和24%。考虑到患者的个体偏差显著增强了比较分析,并且患者特异性标记物的识别已证明与临床评估相关,这是通过脑电图获得精确精神病学的关键一步。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Beyond homogeneity: charting the landscape of heterogeneity in neurodevelopmental and psychiatric electroencephalography.

Electroencephalography (EEG) has been thoroughly studied for decades in neurodevelopmental and psychiatric research. Yet its integration into clinical practice as a diagnostic/prognostic tool remains unachieved. We hypothesize that a key reason is the underlying patient's heterogeneity, overlooked in EEG research relying on a case-control approach. We combine high-density EEG with normative modeling to quantify this heterogeneity using two well-established and extensively investigated EEG characteristics -spectral power and functional connectivity- across a cohort of 1674 patients with attention-deficit/hyperactivity disorder, autism spectrum disorder, learning disorder, or anxiety, and 560 matched controls. Normative models showed that deviations from population norms among patients were highly heterogeneous and frequency-dependent. Deviation spatial overlap across patients did not exceed 40% and 24% for spectral and connectivity, respectively. Considering individual deviations in patients has significantly enhanced comparative analysis, and the identification of patient-specific markers has demonstrated a correlation with clinical assessments, representing a crucial step towards attaining precision psychiatry through EEG.

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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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