Dubowitz Neuromuscular Centre, UCL Great Ormond Street Institute of Child Health, London WC1N 1EH, UK.
Queen Square Centre for Neuromuscular Diseases, University College London, London WC1N 3BG, UK.
Brain. 2023 Jan 5;146(1):252-265. doi: 10.1093/brain/awac048.
Duchenne muscular dystrophy (DMD) is characterized by loss of dystrophin in muscle, however patients also have variable degree of intellectual disability and neurobehavioural co-morbidities. In contrast to muscle, in which a single full-length dystrophin isoform (Dp427) is produced, multiple isoforms are produced in the brain, and their deficiency accounts for the variability of CNS manifestations, with increased risk of comorbidities in patients carrying mutations affecting the 3' end of the gene, which disrupt expression of shorter Dp140 and Dp71 isoforms. A mouse model (mdx mouse) lacks Dp427 in muscle and CNS and exhibits exaggerated startle responses to threat, linked to the deficiency of dystrophin in limbic structures such as the amygdala, which normalize with postnatal brain dystrophin-restoration therapies. A pathological startle response is not a recognized feature of DMD, and its characterization has implications for improved clinical management and translational research. To investigate startle responses in DMD, we used a novel fear-conditioning task in an observational study of 56 males aged 7-12 years (31 affected boys, mean age 9.7 ± 1.8 years; 25 controls, mean age 9.6 ± 1.4 years). Trials of two neutral visual stimuli were presented to participants: one 'safe' cue presented alone; one 'threat' cue paired with an aversive noise to enable conditioning of physiological startle responses (skin conductance response and heart rate). Retention of conditioned physiological responses was subsequently tested by presenting both cues without the aversive noise in an 'Extinction' phase. Primary outcomes were the initial unconditioned skin conductance and change in heart rate responses to the aversive 'threat' and acquisition and retention of conditioned responses after conditioning. Secondary and exploratory outcomes were neuropsychological measures and genotype associations. The mean unconditioned skin conductance response was greater in the DMD group than controls [mean difference 3.0 µS (1.0, 5.1); P = 0.004], associated with a significant threat-induced bradycardia only in the patient group [mean difference -8.7 bpm (-16.9, -0.51); P = 0.04]. Participants with DMD found the task more aversive than controls, with increased early termination rates during the Extinction phase (26% of DMD group versus 0% of controls; P = 0.007). This study provides the first evidence that boys with DMD show similar increased unconditioned startle responses to threat to the mdx mouse, which in the mouse respond to brain dystrophin restoration. Our study provides new insights into the neurobiology underlying the complex neuropsychiatric co-morbidities in DMD and defines an objective measure of this CNS phenotype, which will be valuable for future CNS-targeted dystrophin-restoration studies.
杜氏肌营养不良症(DMD)的特征是肌肉中肌营养不良蛋白的缺失,但患者也存在不同程度的智力障碍和神经行为合并症。与肌肉不同,在肌肉中产生单一全长肌营养不良蛋白异构体(Dp427),在大脑中产生多种异构体,其缺乏导致中枢神经系统表现的可变性,携带影响基因 3'端的突变的患者发生合并症的风险增加,从而中断较短的 Dp140 和 Dp71 异构体的表达。一种小鼠模型(mdx 小鼠)缺乏肌肉和中枢神经系统中的 Dp427,并对威胁表现出过度的惊跳反应,这与杏仁核等边缘结构中肌营养不良蛋白的缺乏有关,这种反应在出生后大脑肌营养不良蛋白修复治疗后会恢复正常。惊跳反应异常不是 DMD 的公认特征,其特征对改善临床管理和转化研究具有重要意义。为了研究 DMD 中的惊跳反应,我们在一项对 56 名 7-12 岁男性(31 名受影响的男孩,平均年龄 9.7 ± 1.8 岁;25 名对照者,平均年龄 9.6 ± 1.4 岁)进行的观察性研究中使用了一种新的恐惧条件反射任务。向参与者呈现两种中性视觉刺激的试验:一种是单独呈现的“安全”线索;一种是与令人厌恶的噪音配对的“威胁”线索,以实现生理性惊跳反应(皮肤电导反应和心率)的条件反射。随后通过在“消退”阶段不使用令人厌恶的噪音呈现两种线索来测试条件反射生理反应的保留情况。主要结局是对厌恶的“威胁”的初始非条件性皮肤电导和心率反应的变化,以及条件反射后的获得和保留。次要和探索性结局是神经心理学测量和基因型关联。与对照组相比,DMD 组的未条件性皮肤电导反应平均值更大[平均差异 3.0 µS(1.0,5.1);P = 0.004],仅在患者组中与威胁引起的心动过缓显著相关[平均差异-8.7 bpm(-16.9,-0.51);P = 0.04]。与对照组相比,DMD 组的参与者认为任务更具威胁性,在消退阶段的早期终止率更高(DMD 组为 26%,对照组为 0%;P = 0.007)。这项研究首次提供了证据表明,患有 DMD 的男孩对威胁的非条件性惊跳反应与 mdx 小鼠相似,而 mdx 小鼠对大脑肌营养不良蛋白修复有反应。我们的研究为 DMD 中复杂的神经精神合并症的神经生物学提供了新的见解,并定义了这种中枢神经系统表型的客观测量方法,这将对未来的中枢神经系统靶向肌营养不良蛋白修复研究具有重要价值。