One size fits null: attentional brain responses differ depending on insomnia subtype.

IF 5.6 2区 医学 Q1 Medicine
Sleep Pub Date : 2025-05-22 DOI:10.1093/sleep/zsaf056
Wenrui Zhao, Eus J W Van Someren, Glenn J M van der Lande, Sjors van de Ven, Frank J van Schalkwijk, Tessa F Blanken, Jennifer R Ramautar, Roy Cox
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引用次数: 0

Abstract

Study objectives: Event-related potential (ERP) studies on attentional brain processes in insomnia disorder (ID) have yielded inconsistent findings. Such inconsistencies may relate to small sample sizes, limited corrections for multiple comparisons, and the possibility of heterogeneity within the clinical population. We aimed to overcome these limitations by studying ERP responses both across and within subtypes in a larger sample of ID.

Methods: ERPs were recorded in 201 participants with ID and 70 normal sleeper controls (NS) with an auditory oddball task. Participants with ID were subtyped using a validated multivariate trait profile. Analyses evaluated subtype-specific and nonspecific deviations using both conventional ERP components as well as cluster-based permutation tests.

Results: All five subtypes were well-represented in the ID sample (subtypes 1-5 respectively N = 31, 83, 28, 29 and 19). ERP component analyses with false discovery rate corrections revealed no evidence for differences between the heterogeneous ID group and NS. However, subtype-specific analyses revealed that ERPs were significantly altered, but in different ways for different subtypes. Specifically, ERP component analyses revealed stronger N100 amplitudes for standards and deviants both in subtypes 2 and 3, and a lower P300 amplitude and longer P300 latency for deviants in subtype 3. Cluster-based permutation tests on ERPs corroborated the P300 amplitude effect for deviants in subtype 3, with subtype 3 and 4 additionally showing a smaller difference between deviant and standard P300 amplitudes.

Conclusion: Our findings indicate that ID is a heterogeneous disorder. Ignoring subtype identity dilutes ERP alterations occurring only in specific insomnia subtypes.

一种解释不成立:大脑的注意力反应因失眠亚型而异。
研究目的:事件相关电位(ERP)对失眠障碍(ID)的注意脑过程的研究得出了不一致的结果。这种不一致可能与样本量小、多次比较的修正有限以及临床人群中存在异质性的可能性有关。我们的目标是通过在更大的ID样本中研究跨亚型和亚型内的ERP反应来克服这些局限性。方法:对201名睡眠障碍被试和70名正常睡眠者(NS)进行erp记录。使用有效的多变量特征档案对ID参与者进行亚型分类。分析评估了亚型特异性和非特异性偏差,使用传统的ERP组件以及基于簇的排列测试。结果:所有5种亚型在ID样本中均有很好的代表性(亚型1-5分别为N = 31、83、28、29和19)。错误发现率校正后的ERP成分分析显示异质ID组和NS组之间没有差异的证据。然而,亚型特异性分析显示,erp显著改变,但不同亚型以不同的方式改变。具体来说,ERP成分分析显示亚型2和亚型3中标准者和偏差者的N100振幅更强,亚型3中偏差者的P300振幅更低,P300潜伏期更长。基于聚类的erp排列测试证实了亚型3偏差者的P300振幅效应,亚型3和亚型4偏差者与标准P300振幅之间的差异较小。结论:我们的研究结果表明,ID是一种异质性障碍。忽略亚型身份会稀释仅在特定失眠亚型中发生的ERP改变。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Sleep
Sleep Medicine-Neurology (clinical)
CiteScore
8.70
自引率
10.70%
发文量
0
期刊介绍: SLEEP® publishes findings from studies conducted at any level of analysis, including: Genes Molecules Cells Physiology Neural systems and circuits Behavior and cognition Self-report SLEEP® publishes articles that use a wide variety of scientific approaches and address a broad range of topics. These may include, but are not limited to: Basic and neuroscience studies of sleep and circadian mechanisms In vitro and animal models of sleep, circadian rhythms, and human disorders Pre-clinical human investigations, including the measurement and manipulation of sleep and circadian rhythms Studies in clinical or population samples. These may address factors influencing sleep and circadian rhythms (e.g., development and aging, and social and environmental influences) and relationships between sleep, circadian rhythms, health, and disease Clinical trials, epidemiology studies, implementation, and dissemination research.
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