Neurologische Klinik und Poliklinik, Ludwig Maximilians Universität München, Munich, Germany.
Department of Neurology, University of Ulm, Ulm, Germany.
J Neurol. 2019 Feb;266(2):330-338. doi: 10.1007/s00415-018-9134-y. Epub 2018 Dec 1.
The applause sign, i.e., the inability to execute the same amount of claps as performed by the examiner, was originally reported as a sign specific for progressive supranuclear palsy (PSP). Recent research, however, has provided evidence for the occurrence of the applause sign in various conditions. The aim of this study was to determine the prevalence of the applause sign and correlate its presence with neuropsychological and MRI volumetry findings in frontotemporal lobar degeneration and related conditions. The applause sign was elicited with the three clap test (TCT), with a higher score indicating poorer performance. Data were recorded from 272 patients from the cohort of the German consortium for frontotemporal lobar degeneration (FTLDc): 111 with behavioral variant frontotemporal dementia (bvFTD), 98 with primary progressive aphasia (PPA), 30 with progressive supranuclear palsy Richardson's syndrome, 17 with corticobasal syndrome (CBS) and 16 with amyotrophic lateral sclerosis with frontotemporal dementia (ALS/FTD). For comparison, 29 healthy elderly control subjects (HC) were enrolled in the study. All subjects underwent detailed language and neuropsychological assessment. In a subset of 156 subjects, atlas-based volumetry was performed. The applause sign occurred in all patient groups (40% in PSP, 29.5% in CBS, 25% in ALS/FTD, 13.3% in PPA and 9.0% in bvFTD) but not in healthy controls. The prevalence was highest in PSP patients. It was significantly more common in PSP as compared to bvFTD, PPA and HC. The comparison between the other groups failed to show a significant difference regarding the occurrence of the applause sign. The applause sign was highly correlated to a number of neuropsychological findings, especially to measures of executive, visuospatial, and language function as well as measures of disease severity. TCT scores showed an inverse correlation with the volume of the ventral diencephalon and the pallidum. Furthermore the volume of the ventral diencephalon and pallidum were significantly smaller in patients displaying the applause sign. Our study confirms the occurrence of the applause sign in bvFTD, PSP and CBS and adds PPA and ALS/FTD to these conditions. Although still suggestive of PSP, clinically it must be interpreted with caution. From the correlation with various cognitive measures we suggest the applause sign to be indicative of disease severity. Furthermore we suggest that the applause sign represents dysfunction of the pallidum and the subthalamic nucleus, structures which are known to play important roles in response inhibition.
鼓掌征,即无法与检查者做出相同数量的鼓掌动作,最初被报道为一种特异性的进行性核上性麻痹(PSP)的体征。然而,最近的研究表明,鼓掌征也可见于多种疾病。本研究旨在确定鼓掌征在额颞叶变性及相关疾病中的发生率,并将其与神经心理学和磁共振成像(MRI)体积测量结果相关联。鼓掌征通过三拍手测试(TCT)引出,得分越高提示表现越差。数据来自德国额颞叶变性联盟(FTLDc)队列中的 272 名患者:111 名行为变异型额颞叶痴呆(bvFTD)患者,98 名原发性进行性失语(PPA)患者,30 名进行性核上性麻痹 Richardson 综合征患者,17 名皮质基底节综合征(CBS)患者和 16 名肌萎缩侧索硬化伴额颞叶痴呆(ALS/FTD)患者。此外,为了比较,研究纳入了 29 名健康老年人作为对照组(HC)。所有患者均接受了详细的语言和神经心理学评估。在 156 名患者中,进行了基于图谱的体积测量。鼓掌征见于所有患者组(PSP 组 40%,CBS 组 29.5%,ALS/FTD 组 25%,PPA 组 13.3%,bvFTD 组 9.0%),但健康对照组未见此征。PSP 患者中发生率最高。与 bvFTD、PPA 和 HC 相比,PSP 患者的鼓掌征更为常见。而其他组之间比较并未显示鼓掌征的发生率有显著差异。鼓掌征与多项神经心理学检查结果高度相关,特别是与执行功能、视空间功能和语言功能以及疾病严重程度的测量结果相关。TCT 评分与腹侧间脑和苍白球的体积呈负相关。此外,出现鼓掌征的患者腹侧间脑和苍白球的体积明显较小。本研究证实了鼓掌征在 bvFTD、PSP 和 CBS 中的存在,并将 PPA 和 ALS/FTD 纳入这些疾病。虽然仍提示 PSP,但在临床上必须谨慎解读。根据与各种认知测量的相关性,我们认为鼓掌征提示疾病严重程度。此外,我们认为鼓掌征代表苍白球和底丘脑核的功能障碍,这些结构已知在反应抑制中发挥重要作用。