Li Yingji, Liu Yang, Wang Rongfei, Ao Ran, Xiang Feng, Zhang Xu, Wang Xiangqing, Yu Shengyuan
Department of Neurology, The First Medical Center of Chinese PLA General Hospital, Beijing, China.
J Mov Disord. 2024 Jul;17(3):282-293. doi: 10.14802/jmd.23145. Epub 2024 Apr 11.
Sialidosis type 2 has variants that are both catalytically inactive (severe), while sialidosis type 1 has at least one catalytically active (mild) variant. This study aimed to discuss the structural changes associated with these variants in a newly reported family carrying N-acetyl-α-neuraminidase-1 (NEU1) variants and explore the clinical characteristics of different combinations of variants in sialidosis type 1.
First, whole-exome sequencing and detailed clinical examinations were performed on the family. Second, structural analyses, including assessments of energy, flexibility and polar contacts, were conducted for several NEU1 variants, and a sialidase activity assay was performed. Third, previous NEU1 variants were systematically reviewed, and the clinical characteristics of patients in the severe-mild and mild-mild groups with sialidosis type 1 were analyzed.
We report a novel family with sialidosis type 1 and the compound heterozygous variants S182G and V143E. The newly identified V143E variant was predicted to be a mild variant through structural analysis and was confirmed by a sialidase activity assay. Cherry-red spots were more prevalent in the severe-mild group, and ataxia was more common in the mild-mild group. Impaired cognition was found only in the severe-mild group. Moreover, patients with cherry-red spots and abnormal electroencephalographies and visual evoked potentials had a relatively early age of onset, whereas patients with myoclonus had a late onset.
Changes in flexibility and local polar contacts may be indicators of NEU1 pathogenicity. Sialidosis type 1 can be divided into two subgroups according to the variant combinations, and patients with these two subtypes have different clinical characteristics.
2型涎酸沉积症具有催化失活(严重)的变异体,而1型涎酸沉积症具有至少一种催化活性(轻度)的变异体。本研究旨在探讨一个新报道的携带N-乙酰-α-神经氨酸酶-1(NEU1)变异体的家系中与这些变异体相关的结构变化,并探索1型涎酸沉积症中不同变异体组合的临床特征。
首先,对该家系进行全外显子测序和详细的临床检查。其次,对几种NEU1变异体进行结构分析,包括能量、柔韧性和极性接触评估,并进行唾液酸酶活性测定。第三,系统回顾既往的NEU1变异体,并分析1型涎酸沉积症严重-轻度和轻度-轻度组患者的临床特征。
我们报道了一个患有1型涎酸沉积症且携带复合杂合变异体S182G和V143E的新家族。通过结构分析预测新鉴定的V143E变异体为轻度变异体,并经唾液酸酶活性测定证实。樱桃红斑在严重-轻度组中更常见,共济失调在轻度-轻度组中更常见。仅在严重-轻度组中发现认知障碍。此外,有樱桃红斑且脑电图和视觉诱发电位异常的患者发病年龄相对较早,而肌阵挛患者发病较晚。
柔韧性和局部极性接触的变化可能是NEU1致病性的指标。1型涎酸沉积症可根据变异体组合分为两个亚组,这两个亚型的患者具有不同的临床特征。