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首页> 外文期刊>Renal failure. >Efficacy of leflunomide combined with prednisone for the treatment of PLA2R-associated primary membranous nephropathy
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Efficacy of leflunomide combined with prednisone for the treatment of PLA2R-associated primary membranous nephropathy

机译:leflunomide联合泼尼松治疗PLA2R相关原代膜肾病的疗效

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Objective: To evaluate the clinical efficacy and safety of leflunomide (LEF) combined with prednisone for the treatment of PLA2R-associated primary membranous nephropathy (PMN) and changes in anti-PLA2R antibody titers after treatment. Methods: Sixty patients with nephrotic syndrome, biopsy-proven MN and anti-PLA2R antibody positivity were included in this study conducted from December 2017 to February 2019. The patients were randomly divided into an experimental group (n?=?30) and a control group (n?=?30). The patients in the experimental group were treated with LEF combined with prednisone, whereas the patients in the control group were treated with cyclophosphamide (CTX) combined with prednisone. We assessed 24-h urinary protein and serum albumin levels, kidney function markers, blood lipid levels and anti-PLA2R antibody titers before and after treatment. Adverse reactions during treatment were recorded. Results: After 16?weeks of treatment, there were 2 cases of complete remission and 6 cases of partial remission in the experimental group, with a total effective rate of 26.67%. In the control group, there were 4 cases of complete remission and 8 cases of partial remission, with a total effective rate of 40% (p??.05). After 24?weeks of treatment, the total effective rates of the experimental and control groups were 66.67% and 76.67%, respectively (p??.05). There were no significant differences in 24-h urinary protein, serum albumin, kidney function marker or blood lipid levels between the two groups after treatment (p??.05). However, there were fewer adverse reactions in the experimental group than in the control group (p??.05). After treatment, serum anti-PLA2R antibody titers were clearly decreased in patients with complete remission and partial remission (p??.05), but these levels remained relatively high in patients without remission (p??.05). Conclusion: LEF combined with prednisone has a certain efficacy for the treatment of PLA2R-associated PMN and provokes few adverse reactions. A large-sample randomized double-blind controlled study with a long follow-up period is needed to verify the efficacy of LEF combined with prednisone.
机译:目的:评价Leflunomide(LEF)与泼尼松治疗PLA2R相关原代膜肾病(PMN)的临床疗效和安全性及治疗后抗PLA2R抗体滴度的变化。方法:2017年12月至2019年2月的这项研究中纳入了60例肾病综合征,活检验证的Mn和抗PLA2R抗体阳性。患者随机分为实验组(N?= 30)和控制组(n?=?30)。实验组中的患者用lef与泼尼松合并处理,而对照组的患者用环磷酰胺(CTX)与泼尼松组合处理。我们在治疗之前和之后评估了24-H尿蛋白和血清白蛋白水平,肾功能标记,血脂水平和抗PLA2R抗体滴度。记录治疗期间的不良反应。结果:治疗16个周后,实验组中有2例完全缓解和6例部分缓解,总有效率为26.67%。在对照组中,有4例完全缓解和病例缓解8例,总有效率为40%(p?>〜05)。在治疗24周后,实验和对照组的总有效率分别为66.67%和76.67%(P?> 05)。在处理后两组之间的24-H尿蛋白,血清白蛋白,肾功能标记或血脂水平无显着差异(p?>〜05)。然而,实验组中的不良反应少于对照组(P?<β.05)。治疗后,在完全缓解和部分缓解的患者中,血清抗PLA2R抗体滴度明显降低(P?<β.05),但在没有缓解的患者中,这些水平仍然相对较高(P?> 05)。结论:与泼尼松结合的液体对PLA2R相关PMN的治疗具有一定的功效,并引起少数不良反应。需要具有长随访期的大型随机双盲对照研究,以验证lef与泼尼松的功效。

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