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首页> 外文期刊>Clinical nephrology >Clinical, biochemical and pathological predictors of poor response to intravenous cyclophosphamide in patients with proliferative lupus nephritis.
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Clinical, biochemical and pathological predictors of poor response to intravenous cyclophosphamide in patients with proliferative lupus nephritis.

机译:增生性狼疮肾炎患者对静脉给予环磷酰胺反应不良的临床,生化和病理学预测指标。

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BACKGROUND: Reports in the literature on the outcome of lupus nephritis (LN) treated with intravenous (i.v.) cyclophosphamide have varied considerably. Previous studies have suggested that less than 25% of patients with LN will progress to end stage renal failure (ESRD) after 5 years. In addition it has been reported that serum creatinine and chronic histologic changes on kidney biopsy are useful markers of renal prognosis. Whether treatment with cyclophosphamide alters the predictive value of these markers in LN patients is not clear. The aim of this study was to review our experience of treating a large cohort of patients with LN treated with i.v. cyclophosphamide and to identify biochemical and histological features at the time renal biopsy which predict outcome in these patients. DESIGN: We retrospectively reviewed our experience with 43 consecutive patients who met criteria for either World Health Organization (WHO) classification III (focal proliferative) or IV (diffuse proliferative) LN and weretreated with monthly i.v. cyclophosphamide. Biochemical indices of renal function and lupus disease activity were recorded. Renal biopsies, performed within two months of commencing therapy, were reviewed by two experienced pathologists and classified according to WHO classification as well as activity and chronicity index. The primary outcome variable for the analysis was the development of ESRD. RESULTS: Patients were followed for a mean of 2 years after renal biopsy. The mean dose of cyclophosphamide received by patients was 8.3 g. One patient died during follow up and 22 (51%) progressed to ESRD. A higher serum creatinine (p = 0.003) and higher score for interstitial fibrosis (p = 0.001) were associated with shorter renal survival. There was no significant association between activity index or its components or in the total chronicity score and survival free from the need for dialysis. CONCLUSION: In our experience more than half of patients treated with i.v. cyclophosphamide for LN progress to ESRD and ahigh serum Cr and a high degree of interstitial fibrosis on renal biopsy before treatment are associated with a worse renal prognosis.
机译:背景:文献中关于用静脉内(i.v.)环磷酰胺治疗狼疮性肾炎(LN)结局的报道差异很大。先前的研究表明,不到25%的LN患者在5年后会发展为终末期肾衰竭(ESRD)。此外,据报道血清肌酐和肾脏活检的慢性组织学变化是肾预后的有用标志。尚不清楚环磷酰胺治疗是否会改变LN患者中这些标志物的预测价值。这项研究的目的是回顾我们治疗接受i.v.治疗的大量LN患者的经验。环磷酰胺,并在肾活检时确定可预测这些患者预后的生化和组织学特征。设计:我们回顾性回顾了连续43例患者的经验,这些患者符合世界卫生组织(WHO)III级(局部增生)LN或IV级(弥散增生)LN的标准,并每月接受静脉输液治疗。环磷酰胺。记录肾功能和狼疮疾病活动的生化指标。由两名经验丰富的病理学家对开始治疗后两个月内进行的肾脏活检进行了检查,并根据WHO分类以及活动和慢性指数进行了分类。分析的主要结果变量是ESRD的发展。结果:肾活检后平均随访2年。患者接受的环磷酰胺平均剂量为8.3 g。一名患者在随访期间死亡,其中22名(51%)进展为ESRD。较高的血清肌酐(p = 0.003)和较高的间质纤维化评分(p = 0.001)与较短的肾脏生存期相关。在没有进行透析的情况下,活动指数或其组成部分或总慢性评分与生存率之间无显着关联。结论:根据我们的经验,超过一半的接受i.v.治疗的患者LN环磷酰胺进展为ESRD,血清Cr较高,治疗前肾脏活检组织间质纤维化程度高,与肾预后不良有关。

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