Agrwal Shipra, Mantan Mukta, Dabas Aashima, Batra Vineeta V
Department of Pediatrics, Army College of Medical Sciences, New Delhi, India.
Department of Pediatrics, Maulana Azad Medical College and Lok Nayak Hospital, New Delhi, India.
Indian J Nephrol. 2022 Jul-Aug;32(4):320-326. doi: 10.4103/ijn.ijn_258_21. Epub 2022 Jul 16.
Steroid-resistant nephrotic syndrome (SRNS) is a rare condition that accounts for about 10% to 20% of all nephrotic syndromes in children. While calcineurin inhibitors induce remission in the majority, the data on long-term outcomes are limited. This retrospective study aimed to look at the clinical profile, biopsy findings, and long-term treatment outcomes in children with SRNS.
The records of all children (1-18 years) with SRNS with biopsy findings of minimal change disease (MCD), focal segmental glomerulosclerosis (FSGS), or mesangioproliferative glomerulonephritis, who received treatment for a minimum period of 12 months and were in follow-up during the years 2007-2018 at a tertiary care teaching hospital were retrieved. The clinical, histopathological, and biochemical factors and treatment outcomes were recorded and analyzed.
Ninety-one (72 boys) children with a median (interquartile range [IQR]) age of onset of nephrotic syndrome as 48 (24-87) months were included. MCD and FSGS were the most common histopathological types (57.1% and 36.3%, respectively) and 62 (68.1%) patients had late steroid resistance. Calcineurin inhibitors (CNIs) were used in 86.8% of the children, and response rates with cyclosporine and tacrolimus for complete remission (CR) were 80% and 73.7%, respectively, with median (IQR) time to response being 3 (2-4) months. The presence of MCD on histology and the use of CNIs were significantly associated with CR ( < 0.01). At a median (IQR) follow-up of 5 (3-7) years, 76 (83.5%) children had either CR or partial remission, four (4.4%) developed chronic kidney disease and five (5.5%) died (three due to end-stage renal disease and two of infective complications).
SRNS children with MCD on biopsy, late resistance, and response to CNIs have better long-term outcomes. Most patients respond to CNIs within the first 6 months of use and need therapy for at least 24 to 36 months.
激素抵抗型肾病综合征(SRNS)是一种罕见疾病,约占儿童所有肾病综合征的10%至20%。虽然钙调神经磷酸酶抑制剂能使大多数患者缓解,但关于长期预后的数据有限。这项回顾性研究旨在观察SRNS患儿的临床特征、活检结果及长期治疗效果。
检索了一家三级护理教学医院在2007年至2018年期间接受治疗至少12个月且处于随访中的所有SRNS患儿(1至18岁)的记录,这些患儿的活检结果为微小病变病(MCD)、局灶节段性肾小球硬化(FSGS)或系膜增生性肾小球肾炎。记录并分析临床、组织病理学、生化因素及治疗效果。
纳入了91名(72名男孩)肾病综合征发病年龄中位数(四分位间距[IQR])为48(24 - 87)个月的患儿。MCD和FSGS是最常见的组织病理学类型(分别为57.1%和36.3%),62名(68.1%)患者存在晚期激素抵抗。86.8%的患儿使用了钙调神经磷酸酶抑制剂(CNIs),环孢素和他克莫司的完全缓解(CR)率分别为80%和73.7%,缓解的中位(IQR)时间为3(2 - 4)个月。组织学上存在MCD以及使用CNIs与CR显著相关(<0.01)。在中位(IQR)随访5(3 - 7)年时,76名(83.5%)患儿达到CR或部分缓解,4名(4.4%)发展为慢性肾脏病,5名(5.5%)死亡(3名死于终末期肾病,2名死于感染性并发症)。
活检为MCD、存在晚期抵抗且对CNIs有反应的SRNS患儿长期预后较好。大多数患者在使用CNIs的前6个月内有反应,且需要至少24至36个月的治疗。