Department of Pediatrics, Faculty of Medicine, Saga University, Saga, Japan.
Department of Pediatrics, Nara Medical University, Japan.
Brain Dev. 2024 May;46(5):207-212. doi: 10.1016/j.braindev.2024.03.002. Epub 2024 Mar 6.
Niemann-Pick type C (NPC) is a rare lysosomal storage disease characterized by hepatosplenomegaly and progressive neurological deterioration due to abnormal intracellular cholesterol transport. Cyclic oligosaccharide 2-hydroxypropyl-β-cyclodextrin (HPBCD) is an effective treatment for NPC; however, few reports have shown its long-term efficacy and safety. To demonstrate long-term efficacy and safety of intrathecal HPBCD (IT-HPBCD) treatment for NPC, we herein reports five patients with NPC treated using IT-HPBCD for 4-11 years.
Patients' ages at the onset ranged from 1.5 to 20 years. Notably, all patients showed rapid disease progression despite treatment with miglustat before IT-HPBCD treatment. Similarly, some patients showed transient improvement; however, all patients' conditions stabilized after long-term IT-HPBCD therapy. Mild-to-moderate hearing loss was observed in three patients. Furthermore, long-term treatment with IT-HPBCD may suppress neurological deterioration in patients with NPC; however, patients still experience some disease progression.
Long-term treatment with IT-HPBCD may suppress neurological deterioration in patients with NPC; however, the treatment outcome is dependent on the neurological status at the time of diagnosis, and disease progression is not completely inhibited. Awareness of the disease and newborn screening is needed for earlier disease detection. In addition, further optimization of the treatment protocol and additional treatments are needed to improve patient outcomes.
尼曼-匹克 C 型(NPC)是一种罕见的溶酶体贮积病,其特征为肝脾肿大和进行性神经功能恶化,这是由于异常的细胞内胆固醇转运所致。环糊精 2-羟丙基-β-环糊精(HPBCD)是 NPC 的有效治疗方法;然而,很少有报道显示其长期疗效和安全性。为了证明鞘内注射 HPBCD(IT-HPBCD)治疗 NPC 的长期疗效和安全性,我们在此报告了 5 例 NPC 患者接受 IT-HPBCD 治疗 4-11 年的情况。
患者发病年龄为 1.5-20 岁。值得注意的是,所有患者在接受 IT-HPBCD 治疗前均使用米格列醇治疗,但疾病仍迅速进展。同样,一些患者表现出短暂的改善;然而,所有患者的病情在长期 IT-HPBCD 治疗后稳定。3 名患者出现轻度至中度听力损失。此外,长期 IT-HPBCD 治疗可能抑制 NPC 患者的神经功能恶化;然而,患者仍会经历一些疾病进展。
长期 IT-HPBCD 治疗可能抑制 NPC 患者的神经功能恶化;然而,治疗结果取决于诊断时的神经状态,并且不能完全抑制疾病进展。需要提高对该疾病的认识并进行新生儿筛查,以便更早地发现疾病。此外,需要进一步优化治疗方案并增加其他治疗方法,以改善患者的预后。