激素联合RAAS抑制剂治疗IgA肾病有效性和安全性的研究

    Effectiveness and safety of glucocorticoid combined with RAAS inhibitors for treatment of IgA nephropathy

    • 摘要: 目的 回顾性比较单纯肾素-血管紧张素-醛固酮系统(renin-angiotensin-aldosterone system,RAAS)抑制剂和RAAS抑制剂联合激素治疗IgA肾病的临床疗效和安全性。方法 选取2009年6月至2016年6月在瑞金医院明确诊断为IgA肾病、eGFR≥45 mL·min-1·(1.72 m2-1、24 h尿蛋白定量>0.5 g/d的263例患者,分为单纯RAAS抑制剂组和RAAS抑制剂联合激素组,比较不同治疗方案患者临床生化指标、病理分型、不良事件、预后等资料。结果 RAAS抑制剂联合激素组在尿蛋白减少及肾功能改善方面均优于单纯RAAS抑制剂组(P<0.05),短期内(6个月)感染发生率更高(21.4%比9.9%,P<0.05),但在随访终末,不良事件发生率更低(9.8%比28.0%,P<0.001),Kaplan-Meier生存分析显示即使在24 h尿蛋白定量0.5~1.0 g/d患者中使用联合治疗的长期预后也优于单纯治疗组。在多因素COX生存分析认为使用联合治疗方案(HR 0.304,95%CI 0.148~0.627)、治疗6个月达到完全缓解(HR 0.369,95%CI 0.171~0.798)以及病理类型中T1/0(HR 3.513,95%CI 1.536~8.035)是影响预后的独立因素。结论 RAAS抑制剂联合激素可有效缓解蛋白尿、改善肾功能,且长期不良事件发生率更低;激素联合治疗、6个月尿蛋白完全缓解是影响肾脏预后的独立保护因素,T1/0则是影响肾脏预后的独立危险因素。

       

      Abstract: Objective To retrospectively compare the clinical efficacy and safety of RAAS inhibitor and combination of RAAS inhibitor with glucocorticoid for treatment of IgA nephropathy. Methods A total of 263 patients diagnosed with IgA nephropathy by renal biopsy in Ruijin Hospital from June 2009 to June 2016,with eGFR ≥ 45 mL·min-1·(1.72 m2)-1 and 24-hour urinary protein > 0.5 g/d,were collected and divided into simple RAAS inhibitor group and RAAS combined with glucocorticoid group.The clinical biochemical indicators,pathological parameters,adverse events and prognosis were compared between various regimes. Results The RAAS inhibitor combined with glucocorticoid group was superior to the simple RAAS inhibitor group in terms of urinary protein reduction and renal function improvement(P<0.05),and had a higher incidence of infection in the short term(6 months)(21.4% vs. 9.9%,P<0.05),but a lower incidence of adverse events(9.8% vs. 28%,P<0.01).Kaplan-Meier survival analysis showed that the long-term prognosis of the combination therapy is better than that of the simple treatment groupeven in patients with 24-hour urinary protein 0.5~1.0 g/d.Multivariate Cox regression model showed that the combination therapy(HR 0.304,95% CI 0.148~0.627),complete remission of 24-hour urine protein in 6 months of treatment(HR 0.369,95% CI 0.171~0.798),and T1/0 in pathological type(MEST-C scores)(HR3.513,95% CI 1.536~8.035)were independent risk factors for prognosis. Conclusions A combination of RAAS inhibitor with glucocorticoid can effectively improve proteinuria and eGTR,and has a lover incidence of adverse events.Glucocorticoid combination therapy,complete remission of urinary protein in 6 months of treatment is independent protective factors for renal prognosis,while T1/0 is the independent risk factor.

       

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