Isono Chiharu, Hirano Makito, Sakamoto Hikaru, Ueno Shuichi, Kusunoki Susumu, Nakamura Yusaku
Department of Neurology, Sakai Hospital Kindai University, 2-7-1 Harayamadai, Minami-ku, Sakai, Osaka, 590-0132, Japan.
Department of Neurology, Kindai University Faculty of Medicine, 377-2 Ohnohigashi, Osakasayama, Osaka, 589-8511, Japan.
Dysphagia. 2017 Jun;32(3):420-426. doi: 10.1007/s00455-016-9771-1. Epub 2017 Jan 2.
Spinocerebellar ataxia type 6 (SCA6), an autosomal dominant triplet repeat disease, predominantly affects the cerebellum with a late onset and generally good prognosis. Dysphagia is commonly associated with the outcomes of neurodegenerative diseases such as SCA6. Although the characteristics of dysphagia have been rarely reported in SCA6, our previous study indicated that dysphagia is generally milder in SCA6 than in SCA3, another inherited ataxia with multisystem involvement. However, abnormalities in the pharyngeal phase in SCA6 were indistinguishable from those in SCA3, with no explainable reason. To determine the reason, we repeatedly performed videofluoroscopic examinations (VF) in 14 patients with SCA6. The results showed that the gross progression of dysphagia was apparently slow, but four patients had progressive dysphagia at an early disease stage; dysphagia began within 10 years from the onset of ataxia and rapidly progressed. A common clinical feature of the four patients was a significantly older age at the onset of ataxia (74.0 vs. 60.3 years), associated with significantly shorter triplet repeats. This finding surprisingly indicated that patients who had shorter repeats and thereby later onset and potentially better prognoses were at risk for dysphagia-associated problems. Ischemic changes, homozygous mutation, and diabetes mellitus as well as aging might have contributed to the observed progressive dysphagia. We found that conventionally monitored somatosensory evoked potentials at least partly reflected progressive dysphagia. Despite the small study group, our findings suggest that clinicians should carefully monitor dysphagia in patients with SCA6 who are older at disease onset (>60 years).
6型脊髓小脑共济失调(SCA6)是一种常染色体显性三联体重复疾病,主要影响小脑,起病较晚,预后一般较好。吞咽困难通常与SCA6等神经退行性疾病的预后相关。尽管SCA6中吞咽困难的特征鲜有报道,但我们之前的研究表明,SCA6中的吞咽困难通常比SCA3(另一种累及多系统的遗传性共济失调)中的吞咽困难症状更轻。然而,SCA6中咽期的异常与SCA3中的异常并无差异,且原因不明。为了确定原因,我们对14例SCA6患者反复进行了视频荧光透视检查(VF)。结果显示,吞咽困难的总体进展明显缓慢,但有4例患者在疾病早期出现进行性吞咽困难;吞咽困难在共济失调发病后10年内开始,并迅速进展。这4例患者的一个共同临床特征是共济失调发病时年龄显著较大(74.0岁对60.3岁),且三联体重复序列明显较短。这一发现令人惊讶地表明,重复序列较短、起病较晚且预后可能较好的患者存在吞咽困难相关问题的风险。缺血性改变、纯合突变、糖尿病以及衰老可能导致了观察到的进行性吞咽困难。我们发现,传统监测的体感诱发电位至少部分反映了进行性吞咽困难。尽管研究组规模较小,但我们的研究结果表明,临床医生应仔细监测疾病发病时年龄较大(>60岁)的SCA6患者的吞咽困难情况。