Department of Clinical Medicine, University of Bergen, Bergen, Norway.
Department of Medicine, Haukeland University Hospital, Bergen, Norway.
BMC Nephrol. 2024 Jan 29;25(1):42. doi: 10.1186/s12882-024-03481-6.
Despite several clinical trials, the use of corticosteroid therapy for treating immunoglobulin A nephropathy (IgAN) remains controversial. We aimed to describe the use of corticosteroid therapy combined with supportive therapy in Norwegian patients with IgAN who had progressed to end-stage kidney disease.
We conducted a retrospective cohort study using data from the Norwegian Renal Registry. Overall, 143 patients with primary IgAN who progressed to end-stage kidney disease were divided into two groups: the corticosteroid group, who had been treated with corticosteroids and supportive therapy, and the non-corticosteroid group, which had underwent only supportive therapy. The kidney function, time to end-stage kidney disease, and adverse effects were described. The observation period lasted from the diagnostic kidney biopsy until the initiation of kidney replacement therapy.
Of the 143 included patients, 103 underwent supportive therapy alone, and 40 were treated with corticosteroids. Most patients (94%) were treated with renin-angiotensin-system blockade, and all patients reached end-stage kidney disease after a median of 5 years (interquartile range; 2-9 years). Time from diagnosis until end-stage kidney disease was similar in the two study groups (p = 0.98). During 6 months of corticosteroid therapy, median eGFR declined from 21 (interquartile range; 13-46) mL/min/1.73 m to 20 (interquartile range; 12-40) mL/min/1.73 m, and median proteinuria decreased from 5.5 g/24 h to 3.0 g/24 h. Most patients (87.5%) treated with corticosteroids reported adverse events. In our linear regression analysis investigating the time to ESKD, we found that age (β = -0.079, p = 0.008) and proteinuria at diagnosis (β = -0.50, p = 0.01) exhibited statistically significant associations with a delay in the progression to ESKD.
In this cohort of Norwegian patients with IgAN, corticosteroid therapy did not affect the time from diagnosis until end-stage kidney disease among a cohort of patients who all reached end-stage kidney disease. The treatment was also associated with adverse effects.
尽管进行了多项临床试验,皮质类固醇治疗免疫球蛋白 A 肾病(IgAN)的应用仍存在争议。我们旨在描述在已进展为终末期肾病的挪威 IgAN 患者中,皮质类固醇治疗联合支持治疗的应用情况。
我们使用挪威肾脏登记处的数据进行了一项回顾性队列研究。共有 143 名原发性 IgAN 患者进展为终末期肾病,分为皮质类固醇组和非皮质类固醇组。皮质类固醇组接受皮质类固醇和支持治疗,非皮质类固醇组仅接受支持治疗。描述了肾功能、到达终末期肾病的时间和不良反应。观察期从诊断性肾活检开始持续到开始肾脏替代治疗。
在纳入的 143 名患者中,有 103 名仅接受支持治疗,40 名接受皮质类固醇治疗。大多数患者(94%)接受了肾素-血管紧张素系统阻断治疗,所有患者在中位数 5 年(四分位距:2-9 年)后达到终末期肾病。两组研究患者从诊断到终末期肾病的时间相似(p=0.98)。在 6 个月的皮质类固醇治疗期间,eGFR 中位数从 21(四分位距:13-46)mL/min/1.73 m 降至 20(四分位距:12-40)mL/min/1.73 m,尿蛋白中位数从 5.5 g/24 h 降至 3.0 g/24 h。大多数接受皮质类固醇治疗的患者(87.5%)报告了不良反应。在我们针对 ESKD 时间的线性回归分析中,我们发现年龄(β=-0.079,p=0.008)和诊断时的蛋白尿(β=-0.50,p=0.01)与进展为 ESKD 的时间延迟有统计学显著关联。
在本队列研究中,挪威 IgAN 患者中皮质类固醇治疗并未影响所有患者均进展为终末期肾病的队列中从诊断到终末期肾病的时间。该治疗还与不良反应有关。