Shima Yuko, Nakanishi Koichi, Yoshikawa Norishige
Department of Pediatrics, Wakayama Medical University, Wakayama City, Wakayama, Japan.
Department of Child Health and Welfare (Pediatrics), Graduate School of Medicine, University of the Ryukyus, Nishihara-cho, Okinawa, Japan.
Pediatr Nephrol. 2021 Oct;36(10):3057-3065. doi: 10.1007/s00467-021-04954-8. Epub 2021 Feb 16.
IgA nephropathy (IgAN) is the most common chronic primary glomerulonephritis in both children and adults, and 20-30% of patients with persistent hematuria/proteinuria progress to kidney failure within 20 years. In Japan, most cases of childhood IgAN are detected by school screening programs during the early onset of the disease when hematuria/proteinuria are asymptomatic and kidney function is normal. Therefore, it is possible to follow the detailed clinical course and appropriate therapeutic interventions from early onset of the disease. Data on non-immunosuppressive therapies for children with IgAN are highly limited. The Japanese Pediatric IgA Nephropathy Treatment Study Group was organized in 1989 to conduct clinical trials and accumulate data on treatments for childhood IgAN. In this review, we focus on non-immunosuppressive therapies, notably with renin-angiotensin-aldosterone system (RAAS) inhibitors for childhood IgAN and related clinical trials conducted primarily in Japan. We also describe the anti-inflammatory and antiproteinuric effects of RAAS inhibitors in IgAN, differences in treatment regimens because of the acute and active pathological features of childhood IgAN, adverse events of RAAS inhibitors, other non-immunosuppressive treatment options, and future directions.
IgA肾病(IgAN)是儿童和成人中最常见的慢性原发性肾小球肾炎,20%至30%持续性血尿/蛋白尿患者会在20年内进展为肾衰竭。在日本,大多数儿童IgAN病例是在疾病早期通过学校筛查项目发现的,此时血尿/蛋白尿无症状且肾功能正常。因此,从疾病早期开始就有可能跟踪详细的临床病程并采取适当的治疗干预措施。关于IgAN儿童非免疫抑制疗法的数据非常有限。日本儿童IgA肾病治疗研究小组于1989年成立,旨在开展临床试验并积累儿童IgAN治疗的数据。在本综述中,我们重点关注非免疫抑制疗法,特别是用于儿童IgAN的肾素-血管紧张素-醛固酮系统(RAAS)抑制剂以及主要在日本进行的相关临床试验。我们还描述了RAAS抑制剂在IgAN中的抗炎和抗蛋白尿作用、由于儿童IgAN的急性和活动性病理特征导致的治疗方案差异、RAAS抑制剂的不良事件、其他非免疫抑制治疗选择以及未来方向。