探究雷特综合征听觉感官处理非典型性的神经不可靠原因。

IF 4.1 2区 医学 Q1 CLINICAL NEUROLOGY Journal of Neurodevelopmental Disorders Pub Date : 2024-06-03 DOI:10.1186/s11689-024-09544-x
Tufikameni Brima, Shlomit Beker, Kevin D Prinsloo, John S Butler, Aleksandra Djukic, Edward G Freedman, Sophie Molholm, John J Foxe
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引用次数: 0

摘要

背景:在寻找量化雷特综合征(Rett Syndrome,RTT)神经功能的客观工具的过程中,使用事件相关电位(ERP)方法记录感觉-知觉功能已成为潜在的有力工具。大量研究表明,RTT 患者的听觉诱发电位(AEP)高度异常。然而,用于得出这些测量结果的典型信号平均法的一个假设是基本反应的 "静止性",即对每个输入的神经反应都是高度定型的。另一种可能性是,对重复刺激的反应在 RTT 中变化很大。如果是这样,这将极大地影响对潜在神经功能障碍假设的有效性,并可能导致对潜在神经病理的高估。为了评估这种可能性,有必要在单次试验水平上进行分析,评估信噪比(SNR)、试验间变异性(ITV)和试验间相位一致性(ITPC):对 18 名 RTT 和 27 名年龄匹配的对照组患者(年龄:6-22 岁)简单的 100 赫兹音调记录 AEP。我们采用了标准的 AEP 平均法,以及单次试验水平的神经元可靠性测量方法(即 SNR、ITV、ITPC)。为了从非神经噪声源中分离出信号携带成分,我们还采用了去噪源分离(DSS)算法,然后重复了可靠性测量:结果:在 RTT 参与者的听觉反应中观察到 ITV 大幅增加、信噪比降低和 ITPC 降低,这支持了 "神经不可靠 "的说法。DSS 技术的应用清楚地表明,非神经噪音源会导致高估 RTT 处理缺陷的程度。DSS 后,ITV 测量值大幅降低,以至于不再能检测到 RTT 和 TD 患者之间 DSS 前的 ITV 差异。在 SNR 和 ITPC 方面,DSS 大幅改善了 RTT 患者的估计值,但 RTT 和 TD 之间的显著差异仍然十分明显:结论:要利用 ERP 技术准确反映 RTT 神经功能障碍的程度,建议考虑单次试验水平的反应可靠性。非神经噪音源会导致高估 RTT 的病理处理程度,而信号处理过程中的去噪源分离技术可大大改善这一问题。
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Probing a neural unreliability account of auditory sensory processing atypicalities in Rett Syndrome.

Background: In the search for objective tools to quantify neural function in Rett Syndrome (RTT), which are crucial in the evaluation of therapeutic efficacy in clinical trials, recordings of sensory-perceptual functioning using event-related potential (ERP) approaches have emerged as potentially powerful tools. Considerable work points to highly anomalous auditory evoked potentials (AEPs) in RTT. However, an assumption of the typical signal-averaging method used to derive these measures is "stationarity" of the underlying responses - i.e. neural responses to each input are highly stereotyped. An alternate possibility is that responses to repeated stimuli are highly variable in RTT. If so, this will significantly impact the validity of assumptions about underlying neural dysfunction, and likely lead to overestimation of underlying neuropathology. To assess this possibility, analyses at the single-trial level assessing signal-to-noise ratios (SNR), inter-trial variability (ITV) and inter-trial phase coherence (ITPC) are necessary.

Methods: AEPs were recorded to simple 100 Hz tones from 18 RTT and 27 age-matched controls (Ages: 6-22 years). We applied standard AEP averaging, as well as measures of neuronal reliability at the single-trial level (i.e. SNR, ITV, ITPC). To separate signal-carrying components from non-neural noise sources, we also applied a denoising source separation (DSS) algorithm and then repeated the reliability measures.

Results: Substantially increased ITV, lower SNRs, and reduced ITPC were observed in auditory responses of RTT participants, supporting a "neural unreliability" account. Application of the DSS technique made it clear that non-neural noise sources contribute to overestimation of the extent of processing deficits in RTT. Post-DSS, ITV measures were substantially reduced, so much so that pre-DSS ITV differences between RTT and TD populations were no longer detected. In the case of SNR and ITPC, DSS substantially improved these estimates in the RTT population, but robust differences between RTT and TD were still fully evident.

Conclusions: To accurately represent the degree of neural dysfunction in RTT using the ERP technique, a consideration of response reliability at the single-trial level is highly advised. Non-neural sources of noise lead to overestimation of the degree of pathological processing in RTT, and denoising source separation techniques during signal processing substantially ameliorate this issue.

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来源期刊
CiteScore
7.60
自引率
4.10%
发文量
58
审稿时长
>12 weeks
期刊介绍: Journal of Neurodevelopmental Disorders is an open access journal that integrates current, cutting-edge research across a number of disciplines, including neurobiology, genetics, cognitive neuroscience, psychiatry and psychology. The journal’s primary focus is on the pathogenesis of neurodevelopmental disorders including autism, fragile X syndrome, tuberous sclerosis, Turner Syndrome, 22q Deletion Syndrome, Prader-Willi and Angelman Syndrome, Williams syndrome, lysosomal storage diseases, dyslexia, specific language impairment and fetal alcohol syndrome. With the discovery of specific genes underlying neurodevelopmental syndromes, the emergence of powerful tools for studying neural circuitry, and the development of new approaches for exploring molecular mechanisms, interdisciplinary research on the pathogenesis of neurodevelopmental disorders is now increasingly common. Journal of Neurodevelopmental Disorders provides a unique venue for researchers interested in comparing and contrasting mechanisms and characteristics related to the pathogenesis of the full range of neurodevelopmental disorders, sharpening our understanding of the etiology and relevant phenotypes of each condition.
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