Suppr超能文献

莱施-尼汉病的脑白质微观结构异常。

Microstructural white matter abnormalities in Lesch-Nyhan disease.

机构信息

Department of Psychiatry and Behavioral Sciences, The Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.

Department of Neurology, University of Alabama at Birmingham, Birmingham, Alabama, USA.

出版信息

Eur J Neurosci. 2022 Jan;55(1):264-276. doi: 10.1111/ejn.15512. Epub 2021 Dec 6.

Abstract

Lesch-Nyhan disease is a rare, sex-linked, genetic neurodevelopmental disorder that is characterized by hyperuricemia, dystonia, cognitive impairment and recurrent self-injury. We previously found reduced brain white matter volume in patients with Lesch-Nyhan disease compared with healthy adults using voxel-based morphometry. Here, we address the structural integrity of white matter via diffusion tensor imaging. We hypothesized that white matter integrity would be decreased in men with Lesch-Nyhan disease and to a lesser extent in men with a milder variant of the disease (Lesch-Nyhan variant) relative to healthy men. After acquiring diffusion-weighted brain images from Lesch-Nyhan disease (n = 5), Lesch-Nyhan variant (n = 6) and healthy participants (n = 10), we used both tract-based spatial statistics and a regions of interest approach to analyse between-group fractional anisotropy differences. We first replicated earlier findings of reduced intracranial, grey matter and white matter volumes in patients. We then discovered marked reductions of fractional anisotropy relative to the healthy control group. The Lesch-Nyhan disease group showed more pronounced reductions in white matter integrity than the Lesch-Nyhan variant group. In addition to whole brain fractional anisotropy group differences, reductions in white matter integrity were observed in the corpus callosum, corona radiata, cingulum, internal capsule and superior longitudinal fasciculus. Moreover, the variant group had attenuated dystonia severity symptoms and cognitive deficits. These findings highlight the need to better understand the role of white matter in Lesch-Nyhan disease.

摘要

莱施-尼汉病是一种罕见的性连锁遗传神经发育障碍,其特征是高尿酸血症、肌张力障碍、认知障碍和反复自残。我们之前通过体素形态计量学发现,莱施-尼汉病患者的大脑白质体积较健康成年人减少。在此,我们通过弥散张量成像来研究白质的结构完整性。我们假设莱施-尼汉病男性患者和疾病较轻变体(莱施-尼汉变体)男性患者的白质完整性较健康男性降低。在从莱施-尼汉病患者(n = 5)、莱施-尼汉变体患者(n = 6)和健康参与者(n = 10)获得弥散加权脑图像后,我们使用基于束的空间统计学和感兴趣区方法来分析组间各向异性分数差异。我们首先复制了先前在患者中发现的颅内、灰质和白质体积减少的发现。然后我们发现各向异性分数相对于健康对照组显著降低。莱施-尼汉病组的白质完整性比莱施-尼汉变体组的降低更为明显。除了全脑各向异性分数组差异外,在胼胝体、辐射冠、扣带回、内囊和上纵束也观察到白质完整性的降低。此外,变体组的肌张力障碍严重程度症状和认知缺陷减弱。这些发现强调了需要更好地了解白质在莱施-尼汉病中的作用。

相似文献

1
Microstructural white matter abnormalities in Lesch-Nyhan disease.莱施-尼汉病的脑白质微观结构异常。
Eur J Neurosci. 2022 Jan;55(1):264-276. doi: 10.1111/ejn.15512. Epub 2021 Dec 6.

引用本文的文献

3
Inborn Errors of Purine Salvage and Catabolism.嘌呤补救和分解代谢的先天性缺陷。
Metabolites. 2023 Jun 24;13(7):787. doi: 10.3390/metabo13070787.
4
Abnormalities of neural stem cells in Lesch-Nyhan disease.莱施-尼汉病中神经干细胞的异常。
J Neurogenet. 2022 Mar-Jun;36(2-3):81-87. doi: 10.1080/01677063.2022.2129632. Epub 2022 Oct 13.

本文引用的文献

4
Novel mutation in the human HPRT1 gene and the Lesch-Nyhan disease.人类次黄嘌呤磷酸核糖基转移酶1(HPRT1)基因的新突变与莱施-奈恩综合征
Nucleosides Nucleotides Nucleic Acids. 2017 Nov 2;36(11):704-711. doi: 10.1080/15257770.2017.1395037. Epub 2017 Nov 29.
10
Permutation inference for the general linear model.一般线性模型的排列推断
Neuroimage. 2014 May 15;92(100):381-97. doi: 10.1016/j.neuroimage.2014.01.060. Epub 2014 Feb 11.

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验