Yao Ling, Li Yuanyuan, Wang Ping, Xu Chan, Yu Zihua
Department of Nephrology, Rheumatology and Immunology, Fujian Children's Hospital, College of Clinical Medicine for Obstetrics & Gynecology and Pediatrics, Fujian Medical University, 966 Heng Yu Road, Jin'an District, Fuzhou, 350014, Fujian, People's Republic of China.
Department of Pediatrics, The Military Hospital of 92435 Unit of PLA, Ningde, 352103, China.
Pediatr Nephrol. 2025 Mar;40(3):629-649. doi: 10.1007/s00467-024-06494-3. Epub 2024 Sep 27.
Nucleoporins (Nups) are a class of proteins that assemble to form nuclear pore complexes, which are related to nucleocytoplasmic transport, gene expression, and the cell cycle. Pathogenic variants in six genes encoding Nups, NUP85, NUP93, NUP107, NUP133, NUP160, and NUP205, cause monogenic steroid-resistant nephrotic syndrome (SRNS), referred to as nucleoporin-associated SRNS. In this paper, we review the epidemiology, structure and function of Nups, pathogenesis, phenotypes and genotypes, and management of nucleoporin-associated SRNS as well as implications for genetic counseling. Affected individuals exhibit autosomal recessive isolated and syndromic SRNS, whose extrarenal manifestations include neurological disorders, growth and development disorders, cardiovascular disorders, and congenital malformations. The median ages at onset of NUP85-, NUP93-, NUP107-, NUP133-, NUP160-, and NUP205-associated SRNS are 7, 3, 4.1, 9, 7, and 2 years, respectively. Kidney biopsies reveal focal segmental glomerulosclerosis in 89% of patients. Most affected individuals are resistant to immunosuppressants. For the six subtypes of nucleoporin-associated SRNS, patients show progression to kidney failure at median ages of 8.5, 3.7, 6.9, 13, 15, and 7 years, respectively. Only two patients with NUP93-associated SRNS with nephrotic syndrome relapse post-transplant have been reported, and the recurrence rate is 12.5%. Next-generation sequencing using a targeted gene panel is recommended in cases of suspected nucleoporin-associated SRNS for genetic diagnosis. Renin-angiotensin-aldosterone system inhibitors are recommended for patients with nucleoporin-associated SRNS. Once genetic diagnosis is confirmed, immunosuppressant discontinuation should be considered, and kidney transplant is preferred when patients progress to kidney failure. Genetic counselling should be provided for asymptomatic siblings and future siblings of an affected individual. Further studies on the pathogenesis of nucleoporin-associated SRNS are needed to seek new therapeutic interventions.
核孔蛋白(Nups)是一类组装形成核孔复合体的蛋白质,其与核质运输、基因表达及细胞周期相关。编码Nups的六个基因NUP85、NUP93、NUP107、NUP133、NUP160和NUP205中的致病性变异可导致单基因类固醇抵抗性肾病综合征(SRNS),即核孔蛋白相关SRNS。在本文中,我们综述了核孔蛋白的流行病学、结构与功能、发病机制、表型与基因型、核孔蛋白相关SRNS的管理以及对遗传咨询的意义。受影响个体表现为常染色体隐性孤立性和综合征性SRNS,其肾外表现包括神经障碍、生长发育障碍、心血管疾病和先天性畸形。NUP85、NUP93、NUP107、NUP133、NUP160和NUP205相关SRNS的中位发病年龄分别为7岁、3岁、4.1岁、9岁、7岁和2岁。肾活检显示89%的患者为局灶节段性肾小球硬化。大多数受影响个体对免疫抑制剂耐药。对于核孔蛋白相关SRNS的六个亚型,患者分别在8.5岁、3.7岁、6.9岁、13岁、15岁和7岁时进展为肾衰竭。仅报道了两例移植后肾病综合征复发的NUP93相关SRNS患者,复发率为12.5%。对于疑似核孔蛋白相关SRNS的病例,建议使用靶向基因panel进行二代测序以进行基因诊断。对于核孔蛋白相关SRNS患者,建议使用肾素-血管紧张素-醛固酮系统抑制剂。一旦确诊基因诊断,应考虑停用免疫抑制剂,当患者进展为肾衰竭时,优先考虑肾移植。应为受影响个体的无症状同胞和未来同胞提供遗传咨询。需要对核孔蛋白相关SRNS的发病机制进行进一步研究以寻求新的治疗干预措施。