Organ Transplantation Unit, Tel Aviv Sourasky Medical Center and Sackler Faculty of Medicine, Tel Aviv University, 6th Weizman St, 6423906, Tel Aviv, Israel.
Nephrology Department, Tel-Aviv Sourasky Medical Center and Sackler Faculty of Medicine, Tel-Aviv University, 6th Weizman St, 6423906, Tel Aviv, Israel.
BMC Nephrol. 2019 Jan 31;20(1):30. doi: 10.1186/s12882-019-1214-4.
Only few studies of living kidney donors have included controls that were similarly healthy, including excellent kidney function.
In this study, we aimed to estimate long term metabolic and renal outcome in a cohort of 211 living donors compared to two control groups: paired-matched controls, and another control group of 2534 healthy individuals with excellent kidney function.
Donors presented with higher estimated Glomerular Filtration Rate (eGFR): (97.6 ± 15.2 vs 96.1 ± 12.2 vs 94.5 ± 12.4 ml/min/1.73m) and lower urine albumin to creatinine ratio (UACR) (4.3 ± 5.9 vs 5.9 ± 6.1 vs 6.1 ± 6.9 mg/g) for donors, matched controls and healthy controls, respectively (p < 0.001). In a mean follow up period of 5.5 for donors, donors presented with positive eGFR slopes during the first 3 years post donation, followed by negative slopes, compared to constantly negative slopes presented in the control group (p < 0.05). The variables related to the slope were being a donor, baseline eGFR, Body Mass Index (BMI) and age but not eGFR on the last day of follow-up or increased delta UACR. There was a significant increase in UACR in donors, as well as a higher rate of albuminuria, associated with a longer time since donation, higher pre-donation UACR and higher pre-donation BMI. Healthy controls had a lower BMI at baseline and gained less weight during the follow up period. Donors and controls had similar incidence of new onset diabetes mellitus and hypertension, as well as similar delta systolic and diastolic blood pressure. Donors were more likely to develop new onset metabolic syndrome, even after adjustment for age, gender and BMI. The higher incidence of metabolic syndrome resulted mainly from increased triglycerides and impaired fasting glucose criteria. However, prevalence of major cardiovascular events was not higher in this group.
Donors are at increased risk to develop features of the metabolic syndrome in addition to the expected mild reduction of GFR and increased urine albumin excretion. Future studies are needed to explore whether addressing those issues will impact post donation morbidity and mortality.
仅有少数关于活体供肾者的研究纳入了同样健康、包括肾功能良好的对照组。
在这项研究中,我们旨在比较 211 名活体供者与两组对照者(配对对照者和 2534 名肾功能良好的健康个体对照者)的长期代谢和肾脏结局,以评估长期代谢和肾脏结局。
与配对对照组和健康对照组相比,供者的估计肾小球滤过率(eGFR)更高(97.6±15.2 比 96.1±12.2 比 94.5±12.4 ml/min/1.73m),尿白蛋白与肌酐比值(UACR)更低(4.3±5.9 比 5.9±6.1 比 6.1±6.9 mg/g)(p<0.001)。在供者平均随访 5.5 年期间,与对照组持续负斜率相比,供者在捐献后前 3 年呈正 eGFR 斜率,随后呈负斜率(p<0.05)。与斜率相关的变量是供者、基线 eGFR、体重指数(BMI)和年龄,但不是最后一天的 eGFR 或 UACR 增加量。供者的 UACR 显著增加,并且随着捐献时间的延长、较高的预捐献 UACR 和较高的预捐献 BMI,蛋白尿的发生率也更高。健康对照组的 BMI 较低,且在随访期间体重增加较少。供者和对照组新发糖尿病和高血压的发生率相似,收缩压和舒张压的变化也相似。供者发生新的代谢综合征的可能性更高,即使在调整年龄、性别和 BMI 后也是如此。代谢综合征的发生率较高主要是由于甘油三酯增加和空腹血糖受损标准。然而,该组主要心血管事件的发生率并未升高。
除了预计的肾小球滤过率轻度下降和尿白蛋白排泄增加外,供者发生代谢综合征特征的风险增加。需要进一步研究以探讨解决这些问题是否会影响捐后发病率和死亡率。