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Prednisolone and azathioprine in IgA nephropathy. A ten-year follow-up study.

机译:泼尼松龙和硫唑嘌呤在IgA肾病中的作用。十年随访研究。

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BACKGROUND: Immunoglobulin A nephropathy (IgAN) is one of the most common primary glomerular diseases. Although its clinical course is usually benign, some patients develop end-stage renal failure (ESRF). The role of immunosuppressive drugs in the treatment of IgAN remains controversial. The effect of treatment with prednisolone and azathioprine and the clinical and histological parameters related to a poor outcome are examined retrospectively in this analysis. METHODS: Seventy-four patients with IgAN and a follow-up period of 10 years were included in this study. Forty-one were treated with prednisolone (initially 60 mg/day) and azathioprine (initially 2 mg/kg BW/day) in gradually reduced doses for 24 +/- 9 months, whereas 33 patients received no immunosuppressive drugs. The clinical course was estimated using the end-points of doubling of baseline serum creatinine and/or ESRF. The contribution of clinical and histological parameters in the clinical outcome was estimated by univariate and multivariateanalyses. RESULTS: The overall clinical courses of both groups of patients showed a rather similar pattern. Doubling of serum baseline creatinine was observed in 9 of 41 treated (22%) and in 10 of 33 untreated (30%), whereas ESRF developed in 6 treated (15%) and 6 untreated patients (18%) (p = NS). However, treated patients with heavy proteinuria (>3 g/24 h) had a significantly better outcome compared to untreated (doubling of serum creatinine in 29 vs. 78% and ESRF in 17 vs. 55%, p < 0.05). Proteinuria (p < 0.01), mean blood pressure (p < 0.02), baseline serum creatinine (p = 0.02) and severity of interstitial myofibroblast expression (p = 0.02) were identified as independent risk factors related to a poor outcome by multivariate analysis. Side effects of treatment were not uncommomn and observed in 10 (24%) patients. CONCLUSION: Treatment with prednisolone and azathioprine is beneficial in ameliorating the clinical course of a subset of IgAN patients with heavy proteinuria or impaired renal function. Patients with advanced renal failure and severe chronic histological lesions should not be treated by this regimen as no benefit is expected and there is a risk of side effects. Copyright 2003 S. Karger AG, Basel
机译:背景:免疫球蛋白A肾病(IgAN)是最常见的原发性肾小球疾病之一。尽管其临床过程通常是良性的,但有些患者会发展为终末期肾衰竭(ESRF)。免疫抑制药物在治疗IgAN中的作用仍存在争议。回顾性分析了泼尼松龙和硫唑嘌呤的治疗效果以及与不良预后相关的临床和组织学参数。方法:该研究纳入了74例IgAN患者,随访期为10年。用泼尼松龙(最初为60 mg /天)和硫唑嘌呤(最初为2 mg / kg BW /天)以逐渐降低的剂量治疗41例,持续24 +/- 9个月,而33例患者未接受免疫抑制药物。使用基线血清肌酐和/或ESRF加倍的终点来估算临床过程。通过单因素和多因素分析评估临床和组织学参数对临床结果的贡献。结果:两组患者的整体临床过程显示出相似的模式。在接受治疗的41名患者中有9名(22%)和未经治疗的33名患者中有10名(30%)观察到血清基线肌酐翻倍,而在接受治疗的6名患者(15%)和未经治疗的6名患者(18%)中出现了ESRF(p = NS) 。然而,重度蛋白尿(> 3 g / 24 h)的治疗患者相比未治疗的患者有明显更好的结局(血清肌酐分别为29%和78%的两倍,ESRF为17%和55%的两倍,p <0.05)。通过多变量分析,蛋白尿(p <0.01),平均血压(p <0.02),基线血清肌酐(p = 0.02)和间质性成纤维细胞表达的严重程度(p = 0.02)被确定为与不良预后相关的独立危险因素。治疗的副作用并不罕见,在10名(24%)患者中观察到。结论:泼尼松龙和硫唑嘌呤治疗可改善部分蛋白尿或肾功能受损的IgAN患者的临床病情。患有晚期肾功能衰竭和严重的慢性组织学病变的患者不应采用该方案治疗,因为预期不会带来任何益处,并且存在发生副作用的风险。版权所有2003 S. Karger AG,巴塞尔

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