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遗传性痉挛性截瘫患者的临床分析

Clinical analysis in patients with hereditary spastic paraplegia.

作者信息

Kang You-Ri, Nam Tai-Seung, Kim Jae-Myung, Kang Kyung Wook, Choi Seong-Min, Lee Seung-Han, Kim Byeong C, Kim Myeong-Kyu

机构信息

Department of Neurology, Chonnam National University Hospital, Gwangju, Republic of Korea.

Department of Neurology, Chonnam National University Medical School, Gwangju, Republic of Korea.

出版信息

Front Neurol. 2023 Jun 15;14:1198728. doi: 10.3389/fneur.2023.1198728. eCollection 2023.

Abstract

BACKGROUND

To analyze the clinical phenotype of hereditary spastic paraplegia (HSP) caused by mutations (SPG11-HSP).

METHODS

Among the 17 patients with sporadic HSP who performed whole exome sequencing analysis, six were diagnosed with SPG11-HSP. The clinical and radiologic findings and the results of the electrodiagnostic and neuropsychologic tests were reviewed retrospectively.

RESULTS

The median age at onset was 16.5 years (range, 13-38 years). Progressive spastic paraparesis was a core feature, and the median spastic paraplegia rating scale score was 24/52 (range, 16-31 points). Additional major symptoms were pseudobulbar dysarthria, intellectual disability, bladder dysfunction, and being overweight. Minor symptoms included upper limbs rigidity and sensory axonopathy. The median body mass index was 26.2 kg/m (range, 25.2-32.3 kg/m). The thin corpus callosum (TCC) was predominant at the rostral body or anterior midbody, and the ears of the lynx sign was seen in all. The follow-up MRI showed the worsening of periventricular white matter (PVWM) signal abnormalities with ventricular widening or the extension of the TCC. Motor evoked potentials (MEP) to the lower limbs showed an absent central motor conduction time (CMCT) in all subjects. The upper limb CMCT was initially absent in three subjects, although it became abnormal in all at the follow-up. The mini-mental state examination median score was 27/30 (range, 26-28) with selective impairment of the attention/calculation domain. The median score of the full-scale intelligence quotient was 48 (range, 42-72) on the Wechsler Adult Intelligence Scale test.

CONCLUSION

Attention/calculation deficits and being overweight as well as pseudobulbar dysarthria were common additional symptoms in patients with SPG11-HSP. The rostral body and anterior midbody of the corpus callosum were preferentially thinned, especially in the early stage of the disease. The TCC, PVWM signal changes, and MEP abnormality worsened as the disease progressed.

摘要

背景

分析由突变(SPG11-HSP)引起的遗传性痉挛性截瘫(HSP)的临床表型。

方法

在17例进行全外显子组测序分析的散发性HSP患者中,6例被诊断为SPG11-HSP。对临床和影像学表现以及电诊断和神经心理学测试结果进行回顾性分析。

结果

发病年龄中位数为16.5岁(范围13 - 38岁)。进行性痉挛性截瘫是核心特征,痉挛性截瘫评定量表评分中位数为24/52(范围16 - 31分)。其他主要症状包括假性球麻痹性构音障碍、智力障碍、膀胱功能障碍和超重。次要症状包括上肢僵硬和感觉轴索性神经病。体重指数中位数为26.2kg/m(范围25.2 - 32.3kg/m)。胼胝体变薄(TCC)主要位于胼胝体体部前部或中部前方,所有患者均可见“猞猁耳征”。随访MRI显示脑室周围白质(PVWM)信号异常随着脑室扩大或胼胝体变薄范围扩大而加重。所有受试者下肢运动诱发电位(MEP)均显示中枢运动传导时间(CMCT)缺失。3例受试者上肢CMCT最初缺失,不过随访时所有患者上肢CMCT均变得异常。简易精神状态检查评分中位数为27/30(范围26 - 28),注意力/计算领域存在选择性损害。韦氏成人智力量表测试全量表智商评分中位数为48(范围42 - 72)。

结论

注意力/计算缺陷、超重以及假性球麻痹性构音障碍是SPG11-HSP患者常见的附加症状。胼胝体体部前部和中部前方优先变薄,尤其是在疾病早期。随着疾病进展,胼胝体变薄、脑室周围白质信号改变和运动诱发电位异常加重。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef05/10310533/17422fd039c3/fneur-14-1198728-g001.jpg

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