Department of Pediatrics, Kobe University Graduate School of Medicine, 7-5-1 Kusunoki-cho, Chuo-ku, Kobe, 650-0017, Japan.
Department of Nephrology, Hyogo Prefectural Kobe Children's Hospital, 1-6-7 Minatojima-minamimachi, Chuo-ku, Kobe, 650-0047, Japan.
Pediatr Nephrol. 2022 Aug;37(8):1845-1853. doi: 10.1007/s00467-021-05395-z. Epub 2022 Jan 11.
Cases of Henoch-Schönlein purpura nephritis (HSPN) with moderate severity were demonstrated to achieve good prognosis after treatment with renin-angiotensin system (RAS) inhibitors. However, some patients required additional treatment for recurrence after remission. This study aimed to clarify the effect of RAS inhibitors in HSPN cases with moderate severity, including the proportion of cases with recurrence and their response to additional treatment.
Among 126 patients diagnosed with HSPN between 1996 and 2019, 71 patients with clinicopathologically diagnosed HSPN of moderate severity, defined as ISKDC grade II-IIIa and serum albumin ≥ 2.5 g/dL, were investigated.
Proteinuria became negative after RAS inhibitor treatment alone in all 71 cases. However, 16 (22.5%) had recurrence. Eleven recurrent cases achieved negative proteinuria again following additional treatment. At the last follow-up (median 46.5 months; IQR, 23.2-98.2), 5 patients had persistent mild proteinuria; no patients had estimated glomerular filtration rate < 90 mL/min/1.73 m. The pathological findings in all recurrent cases were ISKDC grade IIIa. The 16 recurrent cases had significantly higher proportions of glomeruli with global/segmental sclerosis (25.0 vs. 0%, P < 0.001) and tubular atrophy/interstitial fibrosis (37.5 vs. 12.7%, P =0.0 24) than 55 cases without recurrence.
Japanese childhood HSPN cases with moderate severity had good outcomes without need for corticosteroids or immunosuppressants, when prescribed RAS inhibitor treatment. Even in recurrent cases, abnormal proteinuria was transient, and prognosis was excellent. A higher resolution version of the Graphical abstract is available as Supplementary information.
肾素-血管紧张素系统(RAS)抑制剂治疗后,中重度过敏性紫癜肾炎(HSPN)病例预后良好。然而,一些患者在缓解后复发需要额外治疗。本研究旨在阐明 RAS 抑制剂在中重度 HSPN 病例中的作用,包括复发病例的比例及其对额外治疗的反应。
在 1996 年至 2019 年间诊断为 HSPN 的 126 例患者中,有 71 例经临床病理诊断为中重度 HSPN,定义为 ISKDC 分级 II-IIIa 和血清白蛋白≥2.5g/dL。
71 例患者单独使用 RAS 抑制剂治疗后蛋白尿均转为阴性。然而,有 16 例(22.5%)复发。11 例复发病例在追加治疗后再次出现阴性蛋白尿。最后一次随访(中位数 46.5 个月;IQR,23.2-98.2)时,5 例患者仍有持续性轻度蛋白尿;无患者肾小球滤过率<90ml/min/1.73m。所有复发病例的病理发现均为 ISKDC 分级 IIIa。与 55 例无复发病例相比,16 例复发病例的肾小球全球/节段硬化比例(25.0%比 0%,P<0.001)和肾小管萎缩/间质纤维化比例(37.5%比 12.7%,P=0.024)明显更高。
日本儿童中重度 HSPN 病例在使用 RAS 抑制剂治疗时,无需使用皮质类固醇或免疫抑制剂即可获得良好的疗效。即使在复发病例中,异常蛋白尿也是短暂的,预后极好。详细图表可作为补充信息提供。