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自闭症谱系障碍个体及其家庭成员的整体运动连贯缺陷与视网膜功能相关。

Global motion coherent deficits in individuals with autism spectrum disorder and their family members are associated with retinal function.

作者信息

Lee Irene O, Fritsch Dennis M, Kerz Maximilian, Sowden Jane C, Constable Paul A, Skuse David H, Thompson Dorothy A

机构信息

Behavioural and Brain Sciences Unit, Population Policy and Practice Programme, Great Ormond Street Institute of Child Health, University College London, London, UK.

Oceano Azul Foundation and Katapult Ocean, Baden Württemberg, Germany.

出版信息

Sci Rep. 2025 Aug 2;15(1):28249. doi: 10.1038/s41598-025-11789-y.

Abstract

This study aims to evaluate if the reduced sensitivity to global motion observed in some individuals with autism spectrum disorder (ASD) is associated with altered retinal processing. Motion coherence thresholds were measured from individuals with ASD and their family members and compared to the test reference limits derived from control participants. The light adapted electroretinogram (ERG) a- and b-wave amplitudes and peak-times, and photopic negative response (PhNR) parameters were measured from the ASD individuals and their families and compared to those of controls. Abnormally high motion coherence thresholds were found in ASD probands and their family members compared to that in controls, particularly mothers. Altered retinal functions were found in ASD probands and their parents. The PhNR, a- and b-wave time-to-peak were significantly correlated with motion coherence thresholds. The altered retinal function was associated with the age, intelligence and autism severity of the ASD family members. There were associations between the motion coherence and ERG parameters, including smaller amplitudes of the PhNR, and longer time-to-peak of the a- and b-waves and time to the PhNR, compared to those with abnormal motion coherence thresholds. The results showed that global motion coherence deficits were associated with altered retinal function in ASD and their family members. The findings suggest that motion perception deficits follow a familial pattern and that affected mothers may have an increased risk of a child with ASD.

摘要

本研究旨在评估一些自闭症谱系障碍(ASD)个体中观察到的对整体运动敏感性降低是否与视网膜处理改变有关。测量了ASD个体及其家庭成员的运动连贯性阈值,并与从对照参与者得出的测试参考限值进行比较。测量了ASD个体及其家庭成员的明适应视网膜电图(ERG)a波和b波振幅、峰时以及明视负反应(PhNR)参数,并与对照组进行比较。与对照组相比,尤其是母亲,在ASD先证者及其家庭成员中发现了异常高的运动连贯性阈值。在ASD先证者及其父母中发现了视网膜功能改变。PhNR、a波和b波的峰时与运动连贯性阈值显著相关。视网膜功能改变与ASD家庭成员的年龄、智力和自闭症严重程度有关。与运动连贯性阈值异常者相比,运动连贯性与ERG参数之间存在关联,包括PhNR振幅较小,a波和b波的峰时以及PhNR的时间较长。结果表明,整体运动连贯性缺陷与ASD及其家庭成员的视网膜功能改变有关。研究结果表明,运动感知缺陷遵循家族模式,受影响的母亲生育ASD患儿的风险可能增加。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/38b9/12318104/2b7f3075565a/41598_2025_11789_Fig1_HTML.jpg

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