Zhong Lin, Gao Xiaolan, Wang Yu, Qiu Wenjuan, Han Lianshu, Gu Xuefan, Zhang Huiwen
Pediatric Endocrinology and Genetic Metabolism, Xinhua Hospital, Shanghai Institute for Pediatric Research, Shanghai Jiao Tong University School of Medicine, 1665 Kongjiang Road, Shanghai, 200092, People's Republic of China.
Clin Genet. 2023 Jun;103(6):655-662. doi: 10.1111/cge.14329. Epub 2023 Mar 22.
Mucopolysaccharidosis type II (MPS II) is an X-linked recessive lysosomal storage disease caused by a disease-associated variant in the IDS gene, which encodes iduronate 2-sulfatase (IDS). We aimed to characterize the clinical characteristics and genotypes of the largest cohort of Chinese patients with MPS II and so gain a deeper understanding of natural disease progression. Patients with confirmed MPS II and without treatment were included. The disease was classified as severe in patients with neurological impairment, and as attenuated in patients aged >6 years without neurological impairment. Of the 201 male patients, 78.1% had severe MPS II. Cognitive regression occurred before age 6 years in 94.3% of patients. Of 122 IDS variants identified, 37 were novel. Among the large gene alteration types identified, only the frequency of IDS-IDS2 recombination was significantly higher in severe versus attenuated MPS II (P = 0.032). Some identified point variants could inform the understanding of genotype-phenotype correlations. In conclusion, this study showed that classification of the disease as attenuated should only be made in patients aged >6 years. Our findings expand the understanding of the genotype-phenotype relationship, inform the diagnostic process, and provide an indication of the likely prognosis.
II型黏多糖贮积症(MPS II)是一种X连锁隐性溶酶体贮积病,由IDS基因中的疾病相关变异引起,该基因编码艾杜糖醛酸2-硫酸酯酶(IDS)。我们旨在描述中国最大队列的MPS II患者的临床特征和基因型,从而更深入地了解疾病的自然进展。纳入确诊为MPS II且未接受治疗的患者。若患者有神经功能障碍,则疾病分类为重型;若患者年龄>6岁且无神经功能障碍,则疾病分类为轻型。在201例男性患者中,78.1%患有重型MPS II。94.3%的患者在6岁前出现认知功能衰退。在鉴定出的122个IDS变异中,37个是新发现的。在鉴定出的大基因改变类型中,只有IDS-IDS2重组的频率在重型与轻型MPS II患者中显著更高(P = 0.032)。一些鉴定出的点变异有助于理解基因型-表型相关性。总之,本研究表明,只有年龄>6岁的患者才能分类为轻型。我们的研究结果扩展了对基因型-表型关系的理解,为诊断过程提供了信息,并提示了可能的预后。