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首页> 外文期刊>Clinical nephrology >Combination therapy using prednisolone and cyclophosphamide slows the progression of moderately advanced IgA nephropathy.
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Combination therapy using prednisolone and cyclophosphamide slows the progression of moderately advanced IgA nephropathy.

机译:泼尼松龙和环磷酰胺的联合治疗可减缓中度晚期IgA肾病的进展。

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AIM: We retrospectively examined the effect of combination therapy using prednisolone (PSL) and cyclophosphamide (CPA) on the progression of IgA nephropathy (IgAN) in 45 patients with moderate to severe histological changes. PATIENTS AND METHODS: Patients were recruited from 129 consecutive patients with IgAN seen over 10 years based on semiquantitative histological grading. They were divided into two groups: PSL+CPA group (n = 26, male/female = 11/15, age 40+/-3 years (SEM)) or control group undergone conventional therapy with or without antiplatelet agents (n = 19, male/female = 10/9, age 41+/-3). In PSL+CPA group, PSL and CPA treatment commenced using a dose of 30 and 50 mg/day, respectively. PSL was reduced by 5 mg every month. RESULTS: The clinical parameters at the start of treatment such as age, gender, histological score, blood pressure, urinary protein excretion and serum creatinine concentration (SCr) were not different between the groups. The mean observation period in PSL+CPA group (3.3+/-0.3 years) was not different from the control group (4.0+/-0.7 years). In PSL+CPA group, urinary protein excretion, defined as the ratio of urinary protein to creatinine concentration (UP/UCr), significantly decreased from 3.9+/-0.4 to 1.3 +/-0.2 (p<0.01), whereas it remained high in the control group (3.8+/-0.7 to 2.7+/-0.8). The progression rate (PR), which was determined by the slope of the correlation between time after renal biopsy and reciprocal SCr, was significantly lower in PSL+CPA (0.054+/-0.014) than in the control group (0.172+/-0.032 dl/mg/year, p<0.001). Our results indicated that PSL+CPA combination therapy was effective in slowing the progression of moderately advanced IgAN. CONCLUSION: We suggest that the immunosuppressive treatment with CPA is sometimes necessary to preserve renal function in patients with histologically advanced IgAN.
机译:目的:我们回顾性研究了泼尼松龙(PSL)和环磷酰胺(CPA)联合治疗对45例中度至重度组织学改变患者的IgA肾病(IgAN)进展的影响。病人与方法:根据半定量组织学分级,从连续10年以上的129例IgAN患者中招募患者。他们分为两组:PSL + CPA组(n = 26,男性/女性= 11/15,年龄40 +/- 3岁(SEM))或对照组,接受或不接受抗血小板药物的常规治疗(n = 19 ,男性/女性= 10/9,年龄41 +/- 3)。在PSL + CPA组中,分别以30和50 mg /天的剂量开始PSL和CPA治疗。 PSL每月减少5 mg。结果:两组治疗开始时的临床参数如年龄,性别,组织学评分,血压,尿蛋白排泄和血清肌酐浓度(SCr)无差异。 PSL + CPA组的平均观察期(3.3 +/- 0.3年)与对照组(4.0 +/- 0.7年)没有差异。在PSL + CPA组中,尿蛋白排泄(定义为尿蛋白与肌酐浓度之比(UP / UCr))从3.9 +/- 0.4显着降低至1.3 +/- 0.2(p <0.01),但仍保持较高水平对照组(3.8 +/- 0.7至2.7 +/- 0.8)。 PSL + CPA(0.054 +/- 0.014)显着低于对照组(0.172 +/- 0.032),由肾活检后时间与Scr倒数之间的相关性斜率确定的进展率(PR) dl / mg /年,p <0.001)。我们的结果表明,PSL + CPA联合治疗可有效减缓中度晚期IgAN的进展。结论:我们建议,对于组织学晚期IgAN患者,为了维持肾脏功能,有时需要用CPA进行免疫抑制治疗。

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