Department of Psychiatry, University of Iowa Hospital and Clinics, Iowa City, IA, USA.
West of Scotland Clinical Genetics Service, Queen Elizabeth University Hospital, Glasgow, UK.
J Neuromuscul Dis. 2019;6(3):321-332. doi: 10.3233/JND-190397.
Few adequately-powered studies have systematically evaluated brain morphology in adult-onset myotonic dystrophy type 1 (DM1).
The goal of the present study was to determine structural brain differences between individuals with and without adult-onset DM1 in a multi-site, case-controlled cohort. We also explored correlations between brain structure and CTG repeat length.
Neuroimaging data was acquired in 58 unaffected individuals (29 women) and 79 individuals with DM1 (50 women). CTG repeat length, expressed as estimated progenitor allele length (ePAL), was determined by small pool PCR. Statistical models were adjusted for age, sex, site, and intracranial volume (ICV).
ICV was reduced in DM1 subjects compared with controls. Accounting for the difference in ICV, the DM1 group exhibited smaller volume in frontal grey and white matter, parietal grey matter as well as smaller volume of the corpus callosum, thalamus, putamen, and accumbens. In contrast, volumes of the hippocampus and amygdala were significantly larger in DM1. Greater ePAL was associated with lower volumes of the putamen, occipital grey matter, and thalamus. A positive ePAL association was observed for amygdala volume and cerebellar white matter.
Smaller ICV may be a marker of aberrant neurodevelopment in adult-onset DM1. Volumetric analysis revealed morphological differences, some associated with CTG repeat length, in structures with plausible links to key DM1 symptoms including cognitive deficits and excessive daytime somnolence. These data offer further insights into the basis of CNS disease in DM1, and highlight avenues for further work to identify therapeutic targets and imaging biomarkers.
很少有充分有力的研究系统地评估成人型肌强直性营养不良 1 型(DM1)的大脑形态。
本研究的目的是在多中心、病例对照队列中确定成年型 DM1 患者与无病个体之间的结构性脑差异。我们还探讨了大脑结构与 CTG 重复长度之间的相关性。
在 58 名无影响个体(29 名女性)和 79 名 DM1 个体(50 名女性)中获得神经影像学数据。CTG 重复长度表示为估计祖细胞等位基因长度(ePAL),通过小池 PCR 确定。统计模型调整了年龄、性别、部位和颅内体积(ICV)。
与对照组相比,DM1 受试者的 ICV 降低。在考虑 ICV 差异的情况下,DM1 组表现出额状和白质、顶叶灰质以及胼胝体、丘脑、壳核和伏隔核体积减小。相反,DM1 组的海马体和杏仁核体积明显增大。更大的 ePAL 与壳核、枕叶灰质和丘脑的体积降低相关。ePAL 与杏仁核体积和小脑白质的正相关。
较小的 ICV 可能是成年型 DM1 神经发育异常的标志物。体积分析显示,与 CTG 重复长度相关的结构存在形态学差异,这些结构与 DM1 的关键症状有关,包括认知缺陷和日间过度嗜睡。这些数据为 DM1 中枢神经系统疾病的基础提供了进一步的见解,并强调了进一步工作的途径,以确定治疗靶点和成像生物标志物。