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首页> 外文期刊>Lancet Neurology >Regional brain volume abnormalities in Lesch-Nyhan disease and its variants: A cross-sectional study
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Regional brain volume abnormalities in Lesch-Nyhan disease and its variants: A cross-sectional study

机译:Lesch-Nyhan疾病及其变体的局部脑容量异常:一项横断面研究

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摘要

Background: Lesch-Nyhan disease is a rare, X-linked, neurodevelopmental metabolic disorder that is caused by abnormalities in the levels of hypoxanthine-guanine phosphoribosyltransferase enzyme activity. The neural substrates associated with Lesch-Nyhan disease remain poorly understood. We aimed to use voxel-based morphometry to identify affected brain regions in classic Lesch-Nyhan disease and Lesch-Nyhan variant disease, and to identify regions that differ between the two disease types. Methods: In this cross-sectional study, we recruited patients with classic Lesch-Nyhan disease or Lesch-Nyhan variant disease from clinics, referrals, the Lesch-Nyhan Syndrome Registry, and the Matheny School and Hospital (Peapack, NJ, USA), and healthy controls from the Baltimore metropolitan area (MD, USA). We used voxel-based morphometry to analyse grey matter volume between groups using a three-group ANCOVA, followed by six pairwise post-hoc group comparisons. Findings: Between Oct 3, 1993, and April 29, 2013, we recruited 21 patients with classic Lesch-Nyhan disease, 17 patients with variant disease, and 33 healthy controls. Patients with classic Lesch-Nyhan disease had a 20% reduction in intracranial volume (17% reduction in grey matter volume; 26% reduction in white matter volume) compared with healthy adults. The largest differences were in basal ganglia, and frontotemporal and limbic regions, with sparing of parieto-occipital regions. Grey matter volumes of patients with Lesch-Nyhan variant disease were invariably between those of patients with classic Lesch-Nyhan disease and healthy controls. Compared with healthy controls, patients with classic disease showed additional grey matter volume reductions in the temporal lobe and left lateralised structures, and patients with variant disease showed additional reductions in lingual and precuneus regions with sparing of right frontal and temporal regions. Patients with classic disease had reductions of volume in the ventral striatum and prefrontal areas compared with those with the variant form. Interpretation: We noted regional abnormalities associated with known neurological and behavioural deficits in patients with classic Lesch-Nyhan disease. Patients with Lesch-Nyhan variant disease show milder grey matter abnormalities in many of the same brain regions and preservation of grey matter volume in other regions, which could provide important clues to the neural substrates of differences between the phenotypes. Funding: National Institute of Child Health and Human Development, Therapeutic Cognitive Neuroscience Fund, and Benjamin and Adith Miller Family Endowment on Aging, Alzheimer's and Autism Research.
机译:背景:Lesch-Nyhan病是一种罕见的X连锁神经发育代谢性疾病,由次黄嘌呤-鸟嘌呤磷酸核糖基转移酶活性水平异常引起。与Lesch-Nyhan病相关的神经基质仍然知之甚少。我们旨在使用基于体素的形态计量学来识别经典的Lesch-Nyhan病和Lesch-Nyhan变异病中的受影响大脑区域,并确定两种疾病类型之间存在差异的区域。方法:在这项横断面研究中,我们从临床,转诊,Lesch-Nyhan综合征登记处和Matheny学校和医院(美国新泽西州Pepack)招募了患有典型Lesch-Nyhan病或Lesch-Nyhan变异病的患者,和来自巴尔的摩都会区(美国马里兰州)的健康对照。我们使用基于体素的形态计量学,使用三组ANCOVA分析组之间的灰质体积,然后进行六对成对的事后组比较。研究结果:在1993年10月3日至2013年4月29日期间,我们招募了21例经典的Lesch-Nyhan病患者,17例变异病患者和33例健康对照者。与健康成年人相比,患有经典Lesch-Nyhan病的患者的颅内体积减少了20%(灰质减少17%;白质减少26%)。差异最大的是基底神经节,额颞和边缘区,顶枕区不多。患有Lesch-Nyhan变异病的患者的灰质量始终介于经典Lesch-Nyhan病患者和健康对照的患者之间。与健康对照组相比,经典疾病患者的颞叶和左侧外侧结构灰质体积减少更多,而变异性疾病患者的舌侧和前突神经区域减少更多,右侧额叶和颞侧区域减少。与变异型患者相比,经典疾病患者的腹侧纹状体和额叶前额区体积减少。解释:我们注意到与典型的Lesch-Nyhan病患者已知的神经和行为缺陷相关的区域异常。患有Lesch-Nyhan变异病的患者在许多相同的大脑区域显示出较轻的灰质异常,而在其他区域则保留了灰质体积,这可能为表型之间差异的神经底物提供重要线索。资金:美国国家儿童健康与人类发展研究所,认知认知神经科学治疗基金以及本杰明和阿迪思·米勒的家庭养老基金,老年痴呆症和自闭症研究。

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