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单用泼尼松或联合吗替麦考酚酯治疗C3肾小球肾炎的疗效 被引量:7

Prednisone alone or combine with mycophenolate mofetil in treatment of C3 glomerulonephritis
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摘要 目的:探索两种方案治疗C3肾小球肾炎(C3GN)的疗效。方法:回顾性分析东部战区总医院国家肾脏疾病临床医学研究中心经肾活检明确诊断为C3GN的病例,比较泼尼松联合吗替麦考酚酯(Pred+MMF)与单用泼尼松(Pred)两种治疗方案肾脏缓解率和预后的差别。结果:(1)Pred+MMF治疗组8例,男女比例3∶5,中位年龄19岁(16~27岁),Pred治疗组19例,男女比例11∶8,中位年龄33岁(19~45岁)。两组基线临床资料和组织形态学特点无统计学差异;(2)Pred+MMF组中位随访时间43月,肾脏缓解率37.5%,1例进展至随访终点,Pred组中位随访时间41.5月,肾脏缓解率52.9%,2例进展至随访终点;两组肾脏缓解率和预后均无统计学差异;(3)11例进行了补体相关抗体检测,仅1例C3肾炎因子阳性,3例行补体相关基因检测,未发现突变。(4)两组分别有1例出现感染。结论:Pred+MMF对部分C3GN治疗有效,但疗效并不优于单纯Pred治疗。 Objective:To evaluate the therapeutic efficacy of prednisone with mycophenolate mofetil(Pred+MMF) and prednisone(Pred) alone in patients with C3 glomerulonephritis(C3 GN). Methodology:we conducted a retrospective analysis of patients with C3 GN confirmed by renal biopsy,8 patients received Pred+MMF treatment,19 patients received Pred treatment.We compared remission and prognosis of two groups. Results:(1) there were 3 males and 5 females with median age of 19(16~27) years old in Pred+MMF group.11 males and 8 females were treated with Pred alone,with the median age of 33(19~45) years old.There were no significant differences in baseline clinical data and histomorphological features between the two groups.(2) The median follow-up time was 43.5% in the Pred+MMF group,and the renal remission rate was 37.5%.One patient reached the primary endpoint.The median follow-up time in the Pred group was 41.5 months.The renal remission rate was 52.9%,and 2 patients reached the primary endpoint.There was no significant difference in renal remission rate and prognosis between the two groups.(3) 1/11 patients were positive for C3 Nef.Three patients underwent genetic testing,none of them with genetic variants in complement genes(4) There were few adverse reactions of immunosuppressive agents,and one patient in each group had infection. Conclusion:Pred+MMF is effective in the treatment of some C3 GN,but the curative effect is not better than prednisone regimen alone.
作者 徐峰 程震 梁丹丹 梁少姗 曾彩虹 刘志红 XU Feng;CHENG Zhen;LIANG Dandan;LIANG Shaoshan;ZENG Caihong;LIU Zhihong(The Second Military Medical University,National Cliriical Research Center of Kidney Diseases Jingling Hospital,Nanjing 210016,China)
出处 《肾脏病与透析肾移植杂志》 CAS CSCD 北大核心 2019年第1期7-12,共6页 Chinese Journal of Nephrology,Dialysis & Transplantation
基金 国家重点研发计划(2016YFC0904103) 江苏省科技计划项目(BE2016747)
关键词 C3肾小球肾炎 吗替麦考酚酯 泼尼松 治疗 C3 glomerulonephritis mycophenolate mofetil prednisone treatment
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  • 1Sethi S,Fervenza FC.Membranoproliferative glomerulonephritis-- a new look at an old entity[J].N Engl J Med,2012,366(12):1119-1131.
  • 2Servais A,No?l LH,Roumenina LT,et al.Acquired and geneticcomplement abnormalities play a critical role in dense depositdisease and other C3 glomerulopathies[J].Kidney Int,2012,82(4):454-463.
  • 3Zhang Y,Meyer NC,Wang K,et al.Causes of alternative pathwaydysregulation in dense deposit disease[J].Clin J Am SocNephrol,2012,7(2):265-274.
  • 4Barbour TD,Pickering MC,Cook HT.Dense deposit diseaseand C3 glomerulopathy[J].Semin Nephrol,2013,33(6):493-507.
  • 5Martínez-Barricarte R,Heurich M,Valdes-Ca?edo F,et al.Human C3 mutation reveals a mechanism of dense depositdisease pathogenesis and provides insights into complementactivation and regulation[J].J Clin Invest,2010,120(10):3702-3712.
  • 6Habbig S,Mihatsch MJ,Heinen S,et al.C3 depositionglomerulopathy due to a functional factor H defect[J].KidneyInt,2009,75(11):1230-1234.
  • 7Levy M,Halbwachs-Mecarelli L,Gubler MC,et al.H deficiencyin two brothers with atypical dense in tramembranous depositdisease[J].Kidney Int,1986,30(6):949-956.
  • 8Dragon-Durey MA,Frémeaux-Bacchi V,Loirat C,et al.Heterozygous and homozygous factor h deficiencies associatedwith hemolytic uremic syndrome or membranoproliferativeglomerulonephritis:report and genetic analysis of 16 cases[J].JAm Soc Nephrol,2004,15(3):787-795.
  • 9Pickering MC,Goicoechea de Jorge E,Martínez-Barricarte R,et al.Spontaneous hemolytic uremic syndrome triggered bycomplement factor H lacking surface recognition domains[J].JExp Med,2007,204(6):1249-1256.
  • 10Clark SJ,Ridge LA,Herbert AP,et al.Tissue-specific hostrecognition by complement factor H is mediated by differentialactiv ities of its glycosaminoglycan-binding regions[J].JImmunol,2013,190(5):2049-2057.

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