Satirapoj Bancha, Chueaboonchai Thapana, Nata Naowanit, Supasyndh Ouppatham
Division of Nephrology, Department of Medicine, Phramongkutklao Hospital and College of Medicine, Bangkok, Thailand.
Glomerular Dis. 2025 Mar 20;5(1):191-199. doi: 10.1159/000545382. eCollection 2025 Jan-Dec.
Despite optimization of renin-angiotensin-aldosterone system (RAAS) inhibition, patients with IgA nephropathy remain at risk for kidney failure. The effect of steroids on kidney outcomes in IgA nephropathy with different renal pathologic lesions has been uncertain.
This study aimed to evaluate the efficacy of steroid treatment in IgA nephropathy patients classified according to the Oxford-MEST-C classification.
We retrospectively studied 67 patients with biopsy-proven IgA nephropathy who were receiving optimized RAAS inhibitor therapy and had persistent proteinuria >1 g/day between January 2016 and December 2020. Clinical parameters, including estimated glomerular filtration rate (GFR) decline, were compared between the corticosteroid and supportive treatment groups.
Overall, 68.7% of patients received treatment with corticosteroids. The median estimated GFR decline was significantly lower in the steroid group compared to the controls {-0.65 (interquartile range [IQR] -3.45 to 7) vs. -5.75 (IQR -10.65 to -0.7) mL/min/1.73 m/year, = 0.025}. The slope of estimated GFR was also significantly different between the steroid and control groups in patients with a baseline GFR >50 mL/min/1.73 m (3.90 ± 11.42 vs. -9.31 ± 5.08 mL/min/1.73 m/year, = 0.011), mesangial hypercellularity M0 score (4.69 ± 11.37 vs. -2.63 ± 6.42 mL/min/1.73 m/year, = 0.049), and C0 score (2.48 ± 12.63 vs. -5.58 ± 8.4 mL/min/1.73 m/year, = 0.026). Additionally, rapid GFR decline (>5 mL/min/1.73 m/year) occurred in 9 patients (19.6%) in the steroid group compared with 11 participants (52.4%) in the control group ( = 0.006).
Corticosteroid therapy, in addition to optimized RAAS inhibition, lowers the risk of kidney disease progression in patients with IgA nephropathy, particularly those with a baseline GFR >50 mL/min/1.73 m and those classified with Oxford scores M0 and C0.
尽管肾素 - 血管紧张素 - 醛固酮系统(RAAS)抑制治疗已得到优化,但IgA肾病患者仍有肾衰竭风险。类固醇对不同肾脏病理病变的IgA肾病患者肾脏结局的影响尚不确定。
本研究旨在评估根据牛津 - MEST - C分类的IgA肾病患者中类固醇治疗的疗效。
我们回顾性研究了67例经活检证实为IgA肾病的患者,这些患者在2016年1月至2020年12月期间接受优化的RAAS抑制剂治疗且持续蛋白尿>1g/天。比较了皮质类固醇治疗组和支持治疗组的临床参数,包括估计肾小球滤过率(GFR)下降情况。
总体而言,68.7%的患者接受了皮质类固醇治疗。与对照组相比,类固醇组的估计GFR下降中位数显著更低{-0.65(四分位间距[IQR] -3.45至7)vs. -5.75(IQR -10.65至 -0.7)mL/min/1.73m²/年,P = 0.025}。在基线GFR>50 mL/min/1.73m²的患者中,类固醇组和对照组之间的估计GFR斜率也有显著差异(3.90±11.42 vs. -9.31±5.08 mL/min/1.73m²/年,P = 0.011),系膜细胞增生M0评分(4.69±11.37 vs. -2.63±6.42 mL/min/1.73m²/年,P = 0.049),以及C0评分(2.48±12.63 vs. -5.58±8.4 mL/min/1.73m²/年,P = 0.026)。此外,类固醇组有9例患者(19.6%)出现快速GFR下降(>5 mL/min/1.73m²/年),而对照组有11例参与者(52.4%)出现快速GFR下降(P = 0.006)。
除了优化的RAAS抑制治疗外,皮质类固醇治疗可降低IgA肾病患者肾脏疾病进展的风险,特别是那些基线GFR>50 mL/min/1.73m²以及牛津评分M0和C0的患者。