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亨廷顿舞蹈病中舞蹈样动作不自知是否总是病理性的?

Is non-recognition of choreic movements in Huntington disease always pathological?

机构信息

UPMC Univ Paris 06, UMR_S975, F-75013, Paris, France.

出版信息

Neuropsychologia. 2013 Mar;51(4):748-59. doi: 10.1016/j.neuropsychologia.2012.12.005. Epub 2012 Dec 21.

Abstract

Clinical experience and prior studies suggest that Huntington disease (HD) patients have low insight into their motor disturbances and poor real-time awareness (concurrent awareness) of chorea. This has been attributed to sensory deficits but, until now, concurrent awareness of choreic movements has not been compared to the degree of insight that presymptomatic carriers of the HD gene and healthy control subjects have into non-pathological involuntary movements. To further investigate loss of insight into motor dysfunction in HD patients, we administered a video-recorded interview and 4 experimental tasks to 68 subjects from the TRACK-HD cohort, including 28 high-functioning patients in early stages of HD, 28 premanifest mutation carriers and 12 controls. All underwent full neurological and neuropsychological evaluations and 3T MRI examinations. Subjects were asked to assess the presence, body location, frequency, practical consequences and probable causes of motor impairments, as well as the presence and body location of involuntary movements during 4 experimental tasks. The accuracy of their judgments, assessed by comparison with objective criteria, was used as a measure of their insight into motor disturbances and of their concurrent awareness of involuntary movements. Insight was poor in early HD patients: motor symptoms were nearly always underestimated. In contrast, concurrent awareness of involuntary movements, although also poor, was essentially indistinguishable across the 3 groups of subjects: non-pathological involuntary movements were as difficult to perceive by controls and premanifest carriers as was chorea for early HD patients. GLM analysis suggested that both concurrent awareness and perception of practical consequences of movement disorder had a positive effect on intellectual insight, and that mental flexibility is involved in concurrent awareness. Our results suggest that low insight into motor dysfunction in early HD, although marginally modulated by cognitive factors, is mainly non-pathological, and parallels a general tendency, shared by healthy subjects, to neglect self-generated involuntary movements in real time. This tendency, combined with the paucity of functional consequences of incipient chorea, could explain the difficulty of its discovery by the patients.

摘要

临床经验和先前的研究表明,亨廷顿病(HD)患者对自身运动障碍的洞察力较低,对舞蹈症的实时意识(并发意识)较差。这归因于感觉缺失,但直到现在,对舞蹈运动的并发意识还没有与 HD 基因的前症状携带者和健康对照者对非病理性不自主运动的洞察力进行比较。为了进一步研究 HD 患者对运动功能障碍的洞察力丧失,我们对 TRACK-HD 队列中的 68 名受试者进行了视频记录访谈和 4 项实验任务,其中包括 28 名处于 HD 早期阶段的高功能患者、28 名前显性突变携带者和 12 名对照者。所有受试者均接受了全面的神经学和神经心理学评估以及 3T MRI 检查。要求受试者评估运动障碍的存在、身体位置、频率、实际后果和可能原因,以及在 4 项实验任务期间不自主运动的存在和身体位置。通过与客观标准进行比较来评估他们判断的准确性,作为衡量他们对运动障碍的洞察力和对不自主运动的实时意识的指标。早期 HD 患者的洞察力很差:运动症状几乎总是被低估。相比之下,不自主运动的并发意识虽然也很差,但在 3 组受试者中基本无法区分:非病理性不自主运动与对照者和前显性携带者一样难以察觉,就像早期 HD 患者的舞蹈症一样。GLM 分析表明,并发意识和对运动障碍实际后果的感知对智力洞察力都有积极影响,并且心理灵活性与并发意识有关。我们的结果表明,早期 HD 患者对运动功能障碍的洞察力较低,尽管受到认知因素的轻微调节,但主要是非病理性的,并且与健康受试者实时忽略自身产生的不自主运动的普遍趋势相平行。这种趋势,加上初期舞蹈症的功能后果很少,可能解释了患者难以发现它。

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