Leitão Cristiane B, Cure Pablo, Messinger Shari, Pileggi Antonello, Lenz Oliver, Froud Tatiana, Faradji Raquel N, Selvaggi Gennaro, Kupin Warren, Ricordi Camillo, Alejandro Rodolfo
Diabetes Research Institute, University of Miami Miller School of Medicine, Miami, FL 33136, USA.
Transplantation. 2009 Mar 15;87(5):681-8. doi: 10.1097/TP.0b013e31819279a8.
Proteinuria development and decrease in glomerular filtration rate (GFR) have been observed after successful islet transplantation. The aim of this study was to determine clinical, laboratory, and immunosuppressant-related factors associated with kidney dysfunction in islet transplant recipients.
A retrospective cohort study was conducted in 35 subjects submitted to pancreatic islet transplantation for treatment of unstable type 1 diabetes mellitus. Demographic, anthropometrical, and laboratory data, as well as immunosuppressive and antihypertensive therapy were recorded. Kidney function was assessed by albuminuria and estimated GFR (eGFR), calculated by modification of diet in renal disease formula.
Age was the only independent risk factor for low eGFR (<60 mL/min/1.73 m2) (odds ratio [OR]=1.78 [1.22-2.61]). Low-density lipoprotein cholesterol (OR=2.90 [1.37-6.12]) and previous microalbuminuria (OR=6.42 [1.42-29.11]) were risk factors for transient macroalbuminuria. Interestingly, tacrolimus was a protective factor for macroalbuminuria (OR=0.12 [0.06-0.26]). Six of 30 (20%) normoalbuminuric subjects at baseline progressed to microalbuminuria. No subject developed sustained macroalbuminuria. Surprisingly, overall eGFR remained stable during follow-up (before transplant: 74.0+/-2.0; during immunosuppressive therapy: 75.4+/-2.8; and after withdrawal: 76.3+/-5.3 mL/min/1.73 m2; P>0.05). Even subjects with low eGFR and microalbuminuria at baseline (n=10) maintained stable values posttransplantation (61.13+/-3.25 mL/min/1.73 m2 vs. 63.32+/-4.36 mL/min/1.73 m2, P=0.500).
Kidney function remained stable after islet transplantation alone. The unchanged kidney function found in this sample may be attributed to healthier kidney status at baseline and possibly to prompt treatment of modifiable risk factors. Aggressive treatment of risk factors for nephropathy, such as blood pressure, low-density lipoprotein cholesterol, and careful tacrolimus levels monitorization, should be part of islet transplant recipient care.
成功进行胰岛移植后,已观察到蛋白尿的出现以及肾小球滤过率(GFR)的降低。本研究的目的是确定与胰岛移植受者肾功能不全相关的临床、实验室及免疫抑制剂相关因素。
对35例因治疗不稳定型1型糖尿病而接受胰岛移植的受试者进行了一项回顾性队列研究。记录了人口统计学、人体测量学和实验室数据,以及免疫抑制和抗高血压治疗情况。通过蛋白尿和根据肾病饮食改良公式计算的估计肾小球滤过率(eGFR)评估肾功能。
年龄是低eGFR(<60 mL/分钟/1.73 m²)的唯一独立危险因素(比值比[OR]=1.78 [1.22 - 2.61])。低密度脂蛋白胆固醇(OR=2.90 [1.37 - 6.12])和既往微量白蛋白尿(OR=6.42 [1.42 - 29.11])是短暂性大量蛋白尿的危险因素。有趣的是,他克莫司是大量蛋白尿的保护因素(OR=0.12 [0.06 - 0.26])。30例基线时正常白蛋白尿受试者中有6例(20%)进展为微量白蛋白尿。无受试者出现持续性大量蛋白尿。令人惊讶的是,随访期间总体eGFR保持稳定(移植前:74.0±2.0;免疫抑制治疗期间:75.4±2.8;撤药后:76.3±5.3 mL/分钟/1.73 m²;P>0.05)。即使是基线时eGFR低且有微量白蛋白尿的受试者(n = 10)移植后也保持稳定值(61.13±3.25 mL/分钟/1.73 m²对63.32±4.36 mL/分钟/1.73 m²,P = 0.500)。
单独进行胰岛移植后肾功能保持稳定。本样本中肾功能未变可能归因于基线时更健康的肾脏状态以及可能对可改变危险因素的及时治疗。积极治疗肾病危险因素,如血压、低密度脂蛋白胆固醇,并仔细监测他克莫司水平,应成为胰岛移植受者护理的一部分。