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首页> 外文期刊>BMC Nephrology >Membranous nephropathy: a retrospective observational study of membranous nephropathy in north east and central London
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Membranous nephropathy: a retrospective observational study of membranous nephropathy in north east and central London

机译:膜肾病:东北和伦敦东北膜肾病的回顾性观察研究

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Background Membranous nephropathy (MN) is the leading cause of nephrotic syndrome in adults. MN is a clinically heterogeneous disease and it is difficult to accurately predict outcomes (including end stage renal failure) at presentation and whom to treat with potentially toxic therapies. We aimed to identify factors predicting outcome in MN in our cohort from two large tertiary London units by undertaking a retrospective data analysis of 148 biopsy-proven MN patients from North East and Central London between 1995 and 2015. Methods Review of clinical and biochemistry databases. Results Surprisingly, patients that reached end stage renal failure (ESRF) had a less severe nephrosis compared to those that did not develop ESRF; serum albumin 33 g/L (3.3?g/dL) versus 24?g/L (2.4?g/dL), p =?0.002 and urinary protein creatinine ratio (uPCR) 550?mg/mmol (5500?mg/g) versus 902?mg/mmol (9020?mg/g), p =?0.0124. The correlation with ESRF was strongest with the presenting creatinine; 215?μmol/L (2.43?mg/dL) compared to 81?μmol/L (0.92?mg/dL), p 120?μmol/L (1.36?mg/dL; corresponding to an eGFR of ≤60?ml/min in non-Black males) had an increased rate of ESRF and a faster decline. Other traditional risk factors for progression were not significantly associated with ESRF. Black patients presented with higher serum creatinine but no statistically significant difference in the estimated glomerular filtration rate, a higher rate of progression to ESRF and had a poorer response to treatment. Conclusions This ethnically diverse cohort does not demonstrate the traditional risk profile associated with development of ESRF. Thus, careful consideration of therapeutic options is crucial, as current risk modelling cannot accurately predict the risk of ESRF. Further studies are required to elucidate the role of antibodies and risk genes.
机译:背景技术膜状肾病(Mn)是成人肾病综合征的主要原因。 Mn是临床异质疾病,难以准确地预测介绍的结果(包括末期肾功能衰竭),以及用潜在有毒疗法治疗谁。我们旨在通过在1995年至2015年间,通过在伦敦东北和伦敦东北和伦敦东北部和中央综合检查患者的回顾性数据分析来确定预测MN的队列成果的因素。方法对临床和生物化学数据库的方法审查。结果令人惊讶的是,与未发展ESRF的人相比,达到末期肾功能衰竭(ESRF)的患者具有更严重的肾病;血清白蛋白33g / L(3.3?g / dl)与24?g / l(2.4?g / dl),p = 0.002和尿蛋白肌酐比(upcr)550?mg / mmol(5500?mg / g )与902?mg / mmol(9020?mg / g),p = 0.0124。与呈递肌酐与ESRF的相关性最强; 215?μmol/ l(2.43Ωmg/ dl)与81Ωμmol/ l(0.92×mg / dl),p 120?μmol/ l(1.36≤mg/ dl;对应于≤60?ml /的EGFR /在非黑色男性中的最小值)的ESRF率增加,更快地下降。进展的其他传统风险因素与ESRF没有明显相关。黑色患者患有更高的血清肌酐,但估计的肾小球过滤速率没有统计学上显着差异,对ESRF的较高进展速率较高,并对治疗较差。结论这种种族多样化的队列不会展示与ESRF发展相关的传统风险状况。因此,仔细考虑治疗选择至关重要,因为目前的风险建模不能准确地预测ESRF的风险。需要进一步的研究来阐明抗体和风险基因的作用。

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