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Outcomes of De Novo Allograft Diabetic Nephropathy in Renal Allograft Recipients

机译:De Novo同种异体移植糖尿病性肾病在肾移植受者中的结果。

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Objectives: Despite increased use of diabetogenic immunosuppressive drugs and increased incidence of new-onset diabetes after transplant in renal allograft recipients, there are few case studies on the subject of de novo allograft diabetic nephropathy and interstitial fibrosis/tubular atrophy without specific glomerular changes. We sought to study the outcomes of allograft diabetic nephropathy and interstitial fibrosis/tubular atrophy without specific glomerular changes in patients with new-onset diabetes after transplant. Materials and Methods: We reviewed the case records of all new-onset diabetes after transplant patients who underwent graft biopsy for graft dysfunction from 1992 to 2010. We analyzed the clinical characteristics and outcomes of new-onset diabetes after transplant patients with de novo allograft diabetic nephropathy and interstitial fibrosis/tubular atrophy without specific glomerular changes. Results: Of the 1989 recipients, 421 patients developed new-onset diabetes after transplant and 26 underwent graft biopsy. Of the 26 patients, 9 had histopathologic evidence of de novo allograft diabetic nephropathy, and 17 had interstitial fibrosis/tubular atrophy without specific glomerular changes. The mean duration from transplant to developing novo allograft diabetic nephropathy was 115.2 months (range, 33-192 mo), and from developing new-onset diabetes after transplant to allograft diabetic nephropathy, was 109.66 months (range, 27-188.4 mo). Of the 9 patients with de novo allograft diabetic nephropathy, 3 died (33.3%), 2 reached end-stage renal disease (22.2%), and 4 remained stable (44.4%). Of the 17 with interstitial fibrosis/tubular atrophy, 2 died (11.7%), 5 developed end-stage renal disease (29.4%), and 10 remained stable on triple immuno-suppression and insulin therapy during follow-up (58.8%). Conclusions: De novo allograft diabetic nephropathy is a significant cause of graft and patient loss in renal allograft recipients who develop new-onset diabetes after transplant.
机译:目的:尽管在肾脏同种异体移植患者中增加了使用致糖尿病的免疫抑制药物的使用和移植后新发糖尿病的发生率增加,但很少有关于从头移植同种异体糖尿病性肾病和间质纤维化/肾小管萎缩而无特定肾小球改变的病例研究。我们试图研究同种异体移植糖尿病性肾病和间质纤维化/肾小管萎缩的预后,而新发糖尿病患者的肾小球无特异性改变。资料和方法:我们回顾了1992年至2010年所有因移植物功能障碍而进行了活检的移植患者的所有新发糖尿病的病例记录。我们分析了同种异体移植糖尿病患者移植后新发糖尿病的临床特征和结局肾病和间质纤维化/肾小管萎缩,无特异性肾小球改变。结果:在1989位接受者中,有421位患者在移植后出现了新发糖尿病,其中26位接受了活检。在这26例患者中,有9例具有同种异体移植糖尿病性肾病的组织病理学证据,还有17例间质纤维化/肾小管萎缩,但无特异性肾小球改变。从移植到发展中的同种异体移植糖尿病肾病的平均持续时间为115.2个月(范围33-192 mo),从移植到同种异体糖尿病性肾病的发展为新发糖尿病的平均持续时间为109.66个月(范围27-188.4 mo)。在从头移植的9例糖尿病肾病患者中,有3例死亡(33.3%),有2例达到终末期肾脏疾病(22.2%),而4例保持稳定(44.4%)。在有间质纤维化/肾小管萎缩的17例中,有2例死亡(11.7%),有5例发展为终末期肾病(29.4%),在随访期间有10例在三联免疫抑制和胰岛素治疗下保持稳定(58.8%)。结论:从头移植同种异体糖尿病性肾病是移植后新发糖尿病的肾脏同种异体移植患者移植和患者流失的重要原因。

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