F46 Relationship between distinct motor symptoms and apathy in huntington’s disease: clues to mechanism

A. Nair, N. Aziz, R. Rutledge, G. Rees, S. Tabrizi
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引用次数: 1

Abstract

Introduction Disrupted gating of motor control through striatal pathways is thought to drive the development of motor symptoms in Huntington’s disease (HD). The range of motor symptoms, from chorea to bradykinesia, is thought to be driven by disruption in different striatal pathways. Aside from motor control, striatal pathways are also thought to play a key role in the expression of motivated behaviour. On this basis we asked whether the association between apathy and specific motor symptoms is in keeping with the hypothesis that apathy in HD is another manifestation of dysfunctional striatal gating. Methods Clinical data on 2608 patients with manifest HD disease was retrieved from the ENROLL-HD database. A linear mixed model was built to assess the relationship between motor symptoms and apathy (measured using the PBA and square root transformed) controlling for cognitive impairment, depression, medication use, disease duration, CAG repeat size and age. In a separate analysis the bradykinesia item was replaced by voluntary finger tapping performance. Results Although both bradykinesia and chorea were significantly associated with apathy, their effects were in opposite directions. Bradykinesia was associated with greater apathy (β=0.14, p<0.001) whereas chorea was associated with lower apathy (β=−0.12, p<0.001). By comparison rigidity had no significant effect in this large cohort (β=−0.04, p=0.08). In a similar model, slower finger tapping performance was also associated with greater apathy (β=0.07, p=0.001). Depression, medication use and cognitive slowing were also associated with apathy. Conclusion This analysis suggests that the processes driving distinct motor symptoms in HD may also underlie hard-to-treat psychiatric symptoms such as apathy. A common substrate and likely target for this shared mechanism is the disruption of specific striatal pathways that gate actions, decisions and motivated behaviour.
F46亨廷顿病不同运动症状与冷漠的关系:机制线索
通过纹状体通路的运动控制门控被认为是亨廷顿病(HD)运动症状发展的驱动因素。运动症状的范围,从舞蹈病到运动迟缓,被认为是由不同纹状体通路的破坏所驱动的。除了运动控制外,纹状体通路也被认为在动机行为的表达中起着关键作用。在此基础上,我们询问冷漠与特定运动症状之间的联系是否符合HD患者冷漠是纹状体门控功能失调的另一种表现的假设。方法从ENROLL-HD数据库中检索2608例显性HD患者的临床资料。建立一个线性混合模型来评估运动症状与冷漠之间的关系(使用PBA和平方根变换测量),控制认知障碍、抑郁、药物使用、疾病持续时间、CAG重复大小和年龄。在另一项单独的分析中,运动迟缓项目被自愿的手指敲击行为所取代。结果虽然运动迟缓和舞蹈病都与冷漠有显著的相关性,但它们的作用是相反的。运动迟缓与较严重的冷漠相关(β=0.14, p<0.001),而舞蹈病与较低的冷漠相关(β= - 0.12, p<0.001)。相比之下,刚性在这个大队列中没有显著影响(β= - 0.04, p=0.08)。在一个类似的模型中,较慢的手指敲击动作也与更大的冷漠相关(β=0.07, p=0.001)。抑郁、药物使用和认知减缓也与冷漠有关。结论:这一分析表明,HD患者驱动明显运动症状的过程也可能是难以治疗的精神症状(如冷漠)的基础。这种共同机制的共同基础和可能的目标是特定纹状体通路的破坏,这些通道控制着行为、决策和动机行为。
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