Osorio J M, Bravo J, Pérez A, Ferreyra C, Osuna A
Department of Nephrology, Hospital Universitario Virgen de las Nieves, Granada, Spain.
Transplant Proc. 2010 Oct;42(8):2910-3. doi: 10.1016/j.transproceed.2010.08.016.
Hypomagnesemia, a frequent disorder in renal transplant patients related to the use of calcineurin inhibitors (CNIs), plays a causal role in insulin resistance and type 2 diabetes. Recently, hypomagnesemia has been identified as an independent predictor of new-onset diabetes after transplant (NODAT). The objective of this study was to investigate the influence of various immunosuppressive regimens on magnesemia in relation to the development of NODAT. We performed a retrospective study in 589 nondiabetic subjects who underwent serum magnesium measurements (mg/dL) on days 7 and 15 as well as at 1, 2, 3, 6, 9, and 12 months after transplantation. NODAT was diagnosed during the first year using American Diabetes Association criteria. The overall mean magnesemia was lower among CNI compared with non-CNI patients (1.73±0.25 vs 1.98±0.23; P=.000) and in patients on tacrolimus versus cyclosporine (1.72±0.24 vs 1.80±0.26; P=.007). It was higher in patients who received anti-CD25 antibodies with delayed CNI introduction (1.83±0.28 vs 1.71±0.23; P=.000). The use of CNIs and delayed CNI introduction were identified as independent factors related to magnesemia. No differences in magnesemia were observed among patients who developed NODAT versus the non-NODAT cohort. The incidence of NODAT was higher among patients on tacrolimus versus cyclosporine (26.8% vs 18.1%; P=.026), but no differences were found between the serum Mg tertiles at any time during the study or between mean magenesemia tertiles. In conclusion, despite the fact that CNI patients showed lower magnesemia and the group of tacrolimus, the lowest magnesemia and the highest incidence of NODAT, our study did not demonstrate a relationship between the Mg levels and the occurrence of NODAT. Patients treated with anti-CD25 antibodies and delayed CNI introduction maintained higher magnesemia during the first year after transplant.
低镁血症是肾移植患者中常见的一种与使用钙调神经磷酸酶抑制剂(CNIs)相关的病症,在胰岛素抵抗和2型糖尿病中起因果作用。最近,低镁血症已被确定为移植后新发糖尿病(NODAT)的独立预测因素。本研究的目的是调查各种免疫抑制方案对与NODAT发生相关的血镁的影响。我们对589名非糖尿病受试者进行了一项回顾性研究,这些受试者在移植后第7天和第15天以及1、2、3、6、9和12个月进行了血清镁测量(mg/dL)。使用美国糖尿病协会标准在第一年诊断NODAT。与非CNI患者相比,CNI患者的总体平均血镁较低(1.73±0.25对1.98±0.23;P = 0.000),使用他克莫司的患者与使用环孢素的患者相比也是如此(1.72±0.24对1.80±0.26;P = 0.007)。在延迟引入CNI的情况下接受抗CD25抗体治疗的患者血镁较高(1.83±0.28对1.71±0.23;P = 0.000)。使用CNIs和延迟引入CNI被确定为与血镁相关的独立因素。在发生NODAT的患者与未发生NODAT的队列之间,未观察到血镁差异。使用他克莫司的患者中NODAT的发生率高于使用环孢素的患者(26.8%对18.1%;P = 0.026),但在研究期间的任何时间,血清镁三分位数之间或平均血镁三分位数之间均未发现差异。总之,尽管CNI患者的血镁较低,且他克莫司组的血镁最低且NODAT发生率最高,但我们的研究并未证明镁水平与NODAT的发生之间存在关联。接受抗CD25抗体治疗并延迟引入CNI的患者在移植后的第一年维持较高的血镁水平。