Wanyin Hou, Haiyan Yang, Pei Chen, Chen Tang, Xujie Zhou, Lijun Liu, Li Zhu, Sufang Shi, Jicheng Lv, Hong Zhang
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The primary endpoint was a composite renal outcome [estimated glomerular filtration rate (eGFR) >50% reduction, end-stage kidney disease or renal death]. Secondary endpoints included eGFR decline >30% or >40% and an eGFR slope and time-average proteinuria.</p><p><strong>Results: </strong>Propensity score matching identified 191 individuals for analysis. The primary outcome was significantly better in the early therapy group, with a hazard ratio (HR) of 0.41 [95% confidence interval (CI) 0.17-0.96, <i>P</i> = .041]. Significant benefits were also observed for secondary outcomes, including a lower frequency of >30% and >40% eGFR decline in the early therapy group, with HRs of 0.48 (95% CI 0.24-0.98, <i>P</i> = .04) and 0.34 (95% CI 0.14-0.81, <i>P</i> = .01), respectively. Cox regression confirmed that the timing of steroid initiation (early vs delayed) was a significant factor associated with kidney progression [HR = 0.33 (95% CI 0.14-0.77), <i>P</i> = .01]. The average eGFR slope over 10 years was more favorable in the early therapy group (-1.0 ± 6.0 vs -2.9 ± 6.8 mL/min/1.73 m<sup>2</sup> per year, <i>P</i> = .039). No significant differences in baseline characteristics were found to influence the timing of steroid use in progressive IgAN.</p><p><strong>Conclusions: </strong>Early corticosteroid therapy may help reduce renal decline and preserve long-term kidney function in IgAN patients requiring steroid treatment.</p>","PeriodicalId":10435,"journal":{"name":"Clinical Kidney Journal","volume":"18 5","pages":"sfaf076"},"PeriodicalIF":3.9000,"publicationDate":"2025-03-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12044332/pdf/","citationCount":"0","resultStr":"{\"title\":\"Long-term evaluation of the timing of corticosteroid therapy in an IgA nephropathy cohort.\",\"authors\":\"Wanyin Hou, Haiyan Yang, Pei Chen, Chen Tang, Xujie Zhou, Lijun Liu, Li Zhu, Sufang Shi, Jicheng Lv, Hong Zhang\",\"doi\":\"10.1093/ckj/sfaf076\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Background: </strong>Current proposed KDIGO guidelines suggest systemic corticosteroid therapy to reduce glomerular inflammation in immunoglobulin A nephropathy (IgAN), however the optimal timing for initiating steroid treatment remains a topic of debate. This study evaluates the impact of early versus delayed steroid initiation on long-term outcomes in IgAN patients.</p><p><strong>Methods: </strong>We conducted a retrospective study of 268 IgAN patients treated with corticosteroids for >3 months within 3 years of kidney biopsy. Patients were categorized into early therapy (steroids within 30 days) and delayed therapy (after 30 days). Propensity score matching created matched cohorts. Kaplan-Meier curves and Cox regression assessed outcomes. The primary endpoint was a composite renal outcome [estimated glomerular filtration rate (eGFR) >50% reduction, end-stage kidney disease or renal death]. Secondary endpoints included eGFR decline >30% or >40% and an eGFR slope and time-average proteinuria.</p><p><strong>Results: </strong>Propensity score matching identified 191 individuals for analysis. 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引用次数: 0
摘要
背景:目前提出的KDIGO指南建议全体性皮质类固醇治疗以减少免疫球蛋白A肾病(IgAN)的肾小球炎症,然而,启动类固醇治疗的最佳时机仍然是一个有争议的话题。本研究评估了早期与延迟类固醇起始治疗对IgAN患者长期预后的影响。方法:我们对268例接受皮质类固醇治疗的IgAN患者进行了回顾性研究,这些患者在3年内接受了肾活检。患者分为早期治疗(30天内使用类固醇)和延迟治疗(30天后)。倾向评分匹配创建了匹配的队列。Kaplan-Meier曲线和Cox回归评估结果。主要终点是肾脏综合结局[估计肾小球滤过率(eGFR)降低50%,终末期肾病或肾性死亡]。次要终点包括eGFR下降30%或40%,以及eGFR斜率和时间平均蛋白尿。结果:倾向得分匹配确定了191个个体进行分析。早期治疗组的主要结局明显更好,风险比(HR)为0.41[95%可信区间(CI) 0.17-0.96, P = 0.041]。次要结果也观察到显著的益处,包括早期治疗组eGFR下降>30%和>40%的频率较低,hr分别为0.48 (95% CI 0.24-0.98, P = 0.04)和0.34 (95% CI 0.14-0.81, P = 0.01)。Cox回归证实类固醇起始时间(早期vs延迟)是与肾脏进展相关的重要因素[HR = 0.33 (95% CI 0.14-0.77), P = 0.01]。早期治疗组10年的平均eGFR斜率更有利(-1.0±6.0 vs -2.9±6.8 mL/min/1.73 m2 /年,P = 0.039)。没有发现基线特征的显著差异影响进行性IgAN患者使用类固醇的时机。结论:对于需要类固醇治疗的IgAN患者,早期皮质类固醇治疗可能有助于减少肾功能下降并保持长期肾功能。
Long-term evaluation of the timing of corticosteroid therapy in an IgA nephropathy cohort.
Background: Current proposed KDIGO guidelines suggest systemic corticosteroid therapy to reduce glomerular inflammation in immunoglobulin A nephropathy (IgAN), however the optimal timing for initiating steroid treatment remains a topic of debate. This study evaluates the impact of early versus delayed steroid initiation on long-term outcomes in IgAN patients.
Methods: We conducted a retrospective study of 268 IgAN patients treated with corticosteroids for >3 months within 3 years of kidney biopsy. Patients were categorized into early therapy (steroids within 30 days) and delayed therapy (after 30 days). Propensity score matching created matched cohorts. Kaplan-Meier curves and Cox regression assessed outcomes. The primary endpoint was a composite renal outcome [estimated glomerular filtration rate (eGFR) >50% reduction, end-stage kidney disease or renal death]. Secondary endpoints included eGFR decline >30% or >40% and an eGFR slope and time-average proteinuria.
Results: Propensity score matching identified 191 individuals for analysis. The primary outcome was significantly better in the early therapy group, with a hazard ratio (HR) of 0.41 [95% confidence interval (CI) 0.17-0.96, P = .041]. Significant benefits were also observed for secondary outcomes, including a lower frequency of >30% and >40% eGFR decline in the early therapy group, with HRs of 0.48 (95% CI 0.24-0.98, P = .04) and 0.34 (95% CI 0.14-0.81, P = .01), respectively. Cox regression confirmed that the timing of steroid initiation (early vs delayed) was a significant factor associated with kidney progression [HR = 0.33 (95% CI 0.14-0.77), P = .01]. The average eGFR slope over 10 years was more favorable in the early therapy group (-1.0 ± 6.0 vs -2.9 ± 6.8 mL/min/1.73 m2 per year, P = .039). No significant differences in baseline characteristics were found to influence the timing of steroid use in progressive IgAN.
Conclusions: Early corticosteroid therapy may help reduce renal decline and preserve long-term kidney function in IgAN patients requiring steroid treatment.
期刊介绍:
About the Journal
Clinical Kidney Journal: Clinical and Translational Nephrology (ckj), an official journal of the ERA-EDTA (European Renal Association-European Dialysis and Transplant Association), is a fully open access, online only journal publishing bimonthly. The journal is an essential educational and training resource integrating clinical, translational and educational research into clinical practice. ckj aims to contribute to a translational research culture among nephrologists and kidney pathologists that helps close the gap between basic researchers and practicing clinicians and promote sorely needed innovation in the Nephrology field. All research articles in this journal have undergone peer review.