Department of Cardiovascular Surgery and Transplantology, Collegium Medicum, Jagiellonian University, John Paul II Hosptal, Cracow, Poland.
Med Sci Monit. 2010 Nov;16(11):CR563-6.
Heart transplantation is an established treatment for advanced heart failure. Heart transplant recipients experience a number of complications related to pharmacological immunosuppression and infections. Chronic kidney disease (CKD) is an important long-term complication of all forms of organ transplantation other than renal. It has been shown that a GFR <60ml/min is predictive of premature cardiovascular death. The aim of our study was to assess kidney function in relation to the type of immunosuppression regimen used.
MATERIAL/METHODS: We analyzed 169 patients who underwent their first orthotopic heart transplant. The immunosuppressive regimen of prevalent patients consisted of tacrolimus (n=60), cyclosporine (n=109), in combination with mycophenolate mofetil (n=134), azathioprine (n=4), everolimus (n=28) or sirolimus (n=8). GFR was estimated using 3 formulae: CKD-EPI, MDRD and the Cockcroft-Gault. Complete blood count, urea, serum lipids, fasting glucose, creatinine, and NT-proBNP were also analyzed.
In patients treated with tacrolimus, we observed a higher eGFR (all formulae), a greater 24-hour creatinine clearance, and lower serum cholesterol, LDL-cholesterol and triglyceride values than in patients treated with cyclosporine. Patients treated with tacrolimus were younger than those treated with cyclosporine. However, the time elapsed after OHT was similar in both groups. The prevalence of CKD (eGFR <60 ml/min) in the tacrolimus-treated patients was 45%, whereas in the cyclosporine treated group it was 87% (p<0.01).
The prevalence of CKD is high in heart transplant recipients. Tacrolimus-based immunosuppression was associated with better kidney function and more favorable lipid profile. Evaluation of renal function is important in order to select the appropriate strategy by individually tailored therapy to achieve the best possible outcomes.
心脏移植是治疗晚期心力衰竭的一种成熟疗法。心脏移植受者会经历许多与药物免疫抑制和感染相关的并发症。慢性肾脏病(CKD)是除肾脏以外的所有器官移植的一种重要长期并发症。已经表明,GFR<60ml/min 是预测心血管过早死亡的指标。我们研究的目的是评估与所使用的免疫抑制方案类型相关的肾功能。
材料/方法:我们分析了 169 名接受首次原位心脏移植的患者。当时患者的免疫抑制方案包括他克莫司(n=60)、环孢素(n=109),联合霉酚酸酯(n=134)、硫唑嘌呤(n=4)、依维莫司(n=28)或西罗莫司(n=8)。使用 3 种公式:CKD-EPI、MDRD 和 Cockcroft-Gault 估算肾小球滤过率(GFR)。还分析了全血细胞计数、尿素、血清脂质、空腹血糖、肌酐和 NT-proBNP。
在接受他克莫司治疗的患者中,我们观察到更高的 eGFR(所有公式)、更高的 24 小时肌酐清除率以及更低的血清胆固醇、LDL 胆固醇和甘油三酯值,而接受环孢素治疗的患者则较低。接受他克莫司治疗的患者比接受环孢素治疗的患者年轻。然而,两组的 OHT 后时间间隔相似。在接受他克莫司治疗的患者中,CKD(eGFR<60ml/min)的患病率为 45%,而在接受环孢素治疗的患者中为 87%(p<0.01)。
心脏移植受者的 CKD 患病率很高。基于他克莫司的免疫抑制与更好的肾功能和更有利的血脂谱相关。评估肾功能很重要,以便通过个体化治疗选择合适的策略,以获得最佳结果。