Zhou Xun, He Runcheng, Zeng Sheng, Li Mingqiang, Pan Hongxu, Zhao Yuwen, Liu Zhenhua, Xu Qian, Guo Jifeng, Yan Xinxiang, Li Jinchen, Tang Beisha, Sun Qiying
Department of Geriatric Neurology, Xiangya Hospital, Central South University, Changsha, Hunan 410008, China.
Department of Neurology, Xiangya Hospital, Central South University, Changsha, Hunan 410008, China.
Brain Commun. 2024 Jun 29;6(4):fcae217. doi: 10.1093/braincomms/fcae217. eCollection 2024.
There is an obvious clinical-pathological overlap between essential tremor and some known tremor-associated short tandem repeat expansion disorders. The aim is to analyse whether these short tandem repeat genes, including , , , , , , , , , , , , , and , are associated with familial essential tremor patients. Genetic analysis of repeat sizes in tremor-associated short tandem repeat expansions was performed in a large cohort of 515 familial essential tremor probands and 300 controls. The demographic and clinical features among carriers of pathogenic expansions, intermediate repeats and non-carriers were compared. A total of 18 out of 515 (18/515, 3.7%) patients were found to have repeats expansions, including 12 cases (12/515, 2.5%) with intermediate repeat expansions (one , eight , two , one ), and six cases (6/515, 1.2%) with pathogenic expansions (one , one , one , one , one , one ). There were no statistically significant differences in intermediate repeats compared to healthy controls. Furthermore, there were no significant differences in demographics and clinical features among individuals with pathogenic expansions, intermediate repeat expansions carriers and non-carriers. Our study indicates that the intermediate repeat expansion in tremor-associated short tandem repeat expansions does not pose an increased risk for essential tremor, and rare pathogenic expansion carriers have been found in the familial essential tremor cohort. The diagnosis of essential tremor based solely on clinical symptoms remains a challenge in distinguishing it from known short tandem repeat expansions diseases with overlapping clinical-pathological features.
特发性震颤与一些已知的与震颤相关的短串联重复序列扩张性疾病之间存在明显的临床病理重叠。目的是分析这些短串联重复基因,包括[此处应列出具体基因名称,但原文未给出,无法准确翻译]是否与家族性特发性震颤患者相关。对515名家族性特发性震颤先证者和300名对照组成的大样本队列进行了与震颤相关的短串联重复序列扩张的重复序列大小的基因分析。比较了致病性扩张携带者、中间重复序列携带者和非携带者的人口统计学和临床特征。515名患者中共有18名(18/515,3.7%)发现有重复序列扩张,其中12例(12/515,2.5%)为中间重复序列扩张(1例[具体基因及情况,原文未完整给出,无法准确翻译],8例[具体基因及情况,原文未完整给出,无法准确翻译],2例[具体基因及情况,原文未完整给出,无法准确翻译],1例[具体基因及情况,原文未完整给出,无法准确翻译]),6例(6/515,1.2%)为致病性扩张(1例[具体基因及情况,原文未完整给出,无法准确翻译],1例[具体基因及情况,原文未完整给出,无法准确翻译],1例[具体基因及情况,原文未完整给出,无法准确翻译],1例[具体基因及情况,原文未完整给出,无法准确翻译],1例[具体基因及情况,原文未完整给出,无法准确翻译],1例[具体基因及情况,原文未完整给出,无法准确翻译])。与健康对照相比,中间重复序列无统计学显著差异。此外,致病性扩张个体、中间重复序列扩张携带者和非携带者在人口统计学和临床特征方面也无显著差异。我们的研究表明,与震颤相关的短串联重复序列扩张中的中间重复序列扩张不会增加特发性震颤的风险,并且在家族性特发性震颤队列中发现了罕见的致病性扩张携带者。仅基于临床症状诊断特发性震颤,在将其与具有重叠临床病理特征的已知短串联重复序列扩张性疾病区分开来方面仍然是一项挑战。