Discrimination sensitivity of visual shapes sharpens in autistic adults but only after explicit category learning.

IF 6.3 1区 医学 Q1 GENETICS & HEREDITY Molecular Autism Pub Date : 2024-06-03 DOI:10.1186/s13229-024-00604-6
Jaana Van Overwalle, Birte Geusens, Stephanie Van der Donck, Bart Boets, Johan Wagemans
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引用次数: 0

Abstract

Background: Categorization and its influence on perceptual discrimination are essential processes to organize information efficiently. Individuals with Autism Spectrum Condition (ASC) are suggested to display enhanced discrimination on the one hand, but also to experience difficulties with generalization and ignoring irrelevant differences on the other, which underlie categorization. Studies on categorization and discrimination in ASC have mainly focused on one process at a time, however, and typically only used either behavioral or neural measures in isolation. Here, we aim to investigate the interrelationships between these perceptual processes using novel stimuli sampled from a well-controlled artificial stimulus space. In addition, we complement standard behavioral psychophysical tasks with frequency-tagging EEG (FT-EEG) to obtain a direct, non-task related neural index of discrimination and categorization.

Methods: The study was completed by 38 adults with ASC and 38 matched neurotypical (NT) individuals. First, we assessed baseline discrimination sensitivity by administering FT-EEG measures and a complementary behavioral task. Second, participants were trained to categorize the stimuli into two groups. Finally, participants again completed the neural and behavioral discrimination sensitivity measures.

Results: Before training, NT participants immediately revealed a categorical tuning of discrimination, unlike ASC participants who showed largely similar discrimination sensitivity across the stimuli. During training, both autistic and non-autistic participants were able to categorize the stimuli into two groups. However, in the initial training phase, ASC participants were less accurate and showed more variability, as compared to their non-autistic peers. After training, ASC participants showed significantly enhanced neural and behavioral discrimination sensitivity across the category boundary. Behavioral indices of a reduced categorical processing and perception were related to the presence of more severe autistic traits. Bayesian analyses confirmed overall results.

Limitations: Data-collection occurred during the COVID-19 pandemic.

Conclusions: Our behavioral and neural findings indicate that adults with and without ASC are able to categorize highly similar stimuli. However, while categorical tuning of discrimination sensitivity was spontaneously present in the NT group, it only emerged in the autistic group after explicit categorization training. Additionally, during training, adults with autism were slower at category learning. Finally, this multi-level approach sheds light on the mechanisms underlying sensory and information processing issues in ASC.

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自闭症成人对视觉形状的辨别灵敏度会提高,但只有在明确的类别学习之后才会提高。
背景介绍分类及其对知觉辨别的影响是有效组织信息的重要过程。自闭症谱系障碍(ASC)患者一方面会表现出更强的辨别能力,但另一方面也会在泛化和忽略无关差异方面遇到困难,而这正是分类的基础。然而,有关 ASC 分类和辨别能力的研究主要集中在一个过程上,而且通常只单独使用行为或神经测量方法。在这里,我们旨在利用从控制良好的人工刺激空间中采样的新刺激,研究这些知觉过程之间的相互关系。此外,我们还利用频率标记脑电图(FT-EEG)对标准的行为心理物理任务进行补充,以获得直接的、与任务无关的辨别和分类神经指标:这项研究由 38 名患有 ASC 的成年人和 38 名匹配的神经典型(NT)个体共同完成。首先,我们通过实施 FT-EEG 测量和辅助行为任务来评估基线辨别敏感度。其次,训练参与者将刺激物分为两组。最后,参与者再次完成神经和行为辨别灵敏度测量:结果:在训练前,NT 受试者立即显示出分类辨别的调整,而 ASC 受试者则不同,他们对各种刺激的辨别敏感度基本相似。在训练过程中,自闭症和非自闭症参与者都能将刺激分为两组。然而,与非自闭症参与者相比,在最初的训练阶段,自闭症参与者的准确性较低,而且表现出更大的变异性。经过训练后,ASC 参与者在类别边界上的神经和行为辨别灵敏度明显提高。分类处理和感知能力下降的行为指数与存在更严重的自闭症特征有关。贝叶斯分析证实了总体结果:数据收集发生在 COVID-19 大流行期间:我们的行为和神经研究结果表明,有自闭症和没有自闭症的成年人都能对高度相似的刺激进行分类。然而,虽然辨别灵敏度的分类调谐在 NT 组中自发存在,但只有在明确的分类训练后才会在自闭症组中出现。此外,在训练过程中,成年自闭症患者的分类学习速度较慢。最后,这种多层次方法揭示了自闭症成人感官和信息处理问题的内在机制。
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来源期刊
Molecular Autism
Molecular Autism GENETICS & HEREDITY-NEUROSCIENCES
CiteScore
12.10
自引率
1.60%
发文量
44
审稿时长
17 weeks
期刊介绍: Molecular Autism is a peer-reviewed, open access journal that publishes high-quality basic, translational and clinical research that has relevance to the etiology, pathobiology, or treatment of autism and related neurodevelopmental conditions. Research that includes integration across levels is encouraged. Molecular Autism publishes empirical studies, reviews, and brief communications.
期刊最新文献
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