Pediatric Department, Faculty of Medicine, Tanta University, El-Geesh Street, Tanta, 31527, Egypt.
Eur J Pediatr. 2023 Apr;182(4):1685-1695. doi: 10.1007/s00431-023-04837-0. Epub 2023 Feb 8.
Hydroxychloroquine (HCQ) is an antimalarial agent used to treat mucocutaneous, musculoskeletal, constitutional manifestations of systemic lupus erythematosus (SLE). This study assessed the efficacy and side effects of HCQ in children with proliferative lupus nephritis (LN). This double-blind, randomized, placebo-controlled trial study was conducted on 60 children with proliferative LN classes III and IV treated with steroids and a mycophenolate (MMF) regimen. Patients were categorized into two groups, the HCQ group (n = 30) and the placebo group (n = 30). They were evaluated initially at 6- and a 12-month follow-up by mucocutaneous, ophthalmological examination, and investigations (BUN, creatinine, 24 h proteinuria, triglycerides (TG), cholesterol, Antids-DNA, C3, C4). Disease activity was assessed using the SLE disease activity index (SLEDAI-2 k). After 12 months, TG, cholesterol, 24 h proteinuria, Antids-DNA, and SLEDAI score were significantly decreased in the HCQ group (P: 0.002, 0.012, 0.031, 0.001, respectively). After 12 months, the cumulative probabilities of developing primary end-points (LN partial and complete remission) were 40% and 60% in the HCQ group versus 53.3% and 36.7% in the placebo group (P: 0.002). After 12 months, the HCQ group experienced mucocutaneous alopecia (3.3%), hyperpigmentation (10%), and ophthalmological mild retinal changes (6.7%), but they did not differ significantly from the placebo group. Cunclusion: HCQ improved the disease and LN activity in children with proliferative LN, with documented skin hyperpigmentation and mild retinal changes following HCQ use in a few cases. This study was registered on http://www.
gov/ with trial registration number (TRN): NCT03687905, September 2018 "retrospectively registered."
• Hydroxychloroquine (HCQ) is documented as an adjunctive treatment in children with systemic lupus erythematosus (c-SLE) LN with efficacy in improving lupus musculoskeletal and mucocutaneous manifestations. • Due to the paucity of studies, its effects and side effects in children with LN remain unclear.
• This pilot randomized clinical trial assessed the efficacy and adverse effects of HCQ in children with proliferative LN. • HCQ had numerous advantages for LN, including rapid and sustained remission, antilipidemic effect, and rapid improvement of kidney functions.
评估羟氯喹(HCQ)在儿童增殖性狼疮肾炎(LN)中的疗效和副作用。
这是一项双盲、随机、安慰剂对照试验,纳入了 60 例接受类固醇和霉酚酸酯(MMF)治疗的增殖性 LN Ⅲ和Ⅳ类患儿。患儿被分为 HCQ 组(n=30)和安慰剂组(n=30)。在 6 个月和 12 个月时,通过黏膜皮肤检查、眼科检查和实验室检查(BUN、肌酐、24 小时蛋白尿、甘油三酯(TG)、胆固醇、抗 ds-DNA、C3、C4)对其进行评估。采用狼疮疾病活动指数(SLEDAI-2k)评估疾病活动度。
在 12 个月时,HCQ 组的 TG、胆固醇、24 小时蛋白尿、抗 ds-DNA 和 SLEDAI 评分均显著降低(P 值分别为 0.002、0.012、0.031、0.001)。在 12 个月时,HCQ 组达到主要终点(LN 部分和完全缓解)的累积概率为 40%和 60%,安慰剂组为 53.3%和 36.7%(P=0.002)。在 12 个月时,HCQ 组有 3.3%的患儿出现黏膜皮肤脱发、10%出现皮肤色素沉着过度、6.7%出现轻微的视网膜病变,但与安慰剂组相比差异无统计学意义。
HCQ 改善了增殖性 LN 患儿的疾病和 LN 活动,使用 HCQ 后有皮肤色素沉着过度和少数病例出现轻微视网膜改变的报道。本研究在 http://www.clinicaltrials.gov 上进行了注册(注册号:NCT03687905),于 2018 年 9 月进行了“回顾性注册”。