Doucet Gaelle E, Kruse Jordanna A, Mertens Attakias, Goldsmith Callum, Eden Nichole M, Oleson Jacob, McGregor Karla K
Institute for Human Neuroscience, Boys Town National Research Hospital, Omaha, NE; Center for Pediatric Brain Health, Boys Town National Research Hospital, Omaha, NE; Department of Pharmacology and Neuroscience, Creighton University School of Medicine, Omaha, NE.
Institute for Human Neuroscience, Boys Town National Research Hospital, Omaha, NE.
Brain Lang. 2025 Feb;261:105531. doi: 10.1016/j.bandl.2024.105531. Epub 2025 Jan 4.
Developmental Language Disorder (DLD) is a common neurodevelopmental condition characterized by significant difficulty with language learning, comprehension, and expression. The neurocognitive bases of DLD are underspecified but are thought to be related, in part, to altered basal ganglia (BG). The BG are known to have a high level of brain iron, which contributes to myelination and dopaminergic pathways among other physiological mechanisms. In this study, we investigated whether a brain iron imbalance might contribute to the altered BG function that characterizes individuals with DLD. Using a T2*-weighted signal, we compared BG brain iron levels in 7-to-13-year olds with DLD and typical language development (TD). We found a significant age-by-group interaction in the caudate with children with DLD showing a positive association between brain iron and age, which was not the case in TD children. A sex-by-age-by-group interaction was also reported in the right putamen and right nucleus accumbens. Higher brain iron in the caudate was associated with poorer story recall; there was no relation between brain iron levels and recall of word lists. This first-ever investigation of brain iron levels in individuals with DLD provides preliminary evidence of an abnormal developmental trajectory of brain iron balance and offers a potential explanation for the altered BG function and verbal impairments that characterize DLD.
发育性语言障碍(DLD)是一种常见的神经发育疾病,其特征是在语言学习、理解和表达方面存在显著困难。DLD的神经认知基础尚不清楚,但部分被认为与基底神经节(BG)的改变有关。已知BG含有高水平的脑铁,这有助于髓鞘形成和多巴胺能通路以及其他生理机制。在本研究中,我们调查了脑铁失衡是否可能导致DLD患者特征性的BG功能改变。使用T2 *加权信号,我们比较了7至13岁患有DLD和典型语言发育(TD)的儿童的BG脑铁水平。我们发现尾状核存在显著的年龄×组间交互作用,患有DLD的儿童脑铁与年龄呈正相关,而TD儿童则不然。右侧壳核和右侧伏隔核也报告了性别×年龄×组间交互作用。尾状核中较高的脑铁与较差的故事回忆相关;脑铁水平与单词列表回忆之间没有关系。这项对DLD患者脑铁水平的首次调查提供了脑铁平衡异常发育轨迹的初步证据,并为DLD患者特征性的BG功能改变和语言障碍提供了潜在解释。