Department of Nephrology, Universitair Ziekenhuis Brussel, Brussels, Belgium.
Department of Nephrology, Universitair Ziekenhuis Antwerpen, Antwerpen, Belgium.
Am J Transplant. 2018 Jul;18(7):1726-1734. doi: 10.1111/ajt.14665. Epub 2018 Feb 22.
Tacrolimus (TAC) increases the risk of posttransplant diabetes (PTDM) compared with cyclosporine A (CYC). The present 12-month, multicenter, investigator-driven, prospective, randomized study was designed to assess whether conversion from tacrolimus to CYC can reverse PTDM after renal transplantation. Predominantly white patients with PTDM according to the 2005 American Diabetes Association criteria were randomized to either replacement of TAC with CYC or continuation of their TAC-based regimen after stratification for type of glucose-lowering therapy, steroid therapy, and hepatitis C status. At 12 months, 14 of 41 patients with complete data in the CYC arm (34%; 95%CI 19%-49%) were free of diabetes, whereas this was the case in only 4 of 39 patients (10%; 95%CI 3%-20%) in the TAC arm (P = .01). At 12 months, 39% of patients in the CYC arm were off glucose-lowering medication vs 13% of patients in the TAC arm (P = .01). The CYC group decreased glycated hemoglobin level during the 12-month follow-up, resulting in significantly lower levels compared with the TAC group (6.0 ± 0.9% vs 7.1 ± 1.7% at 12 months; P = .002). In conclusion, replacement of TAC with CYC significantly improves glucose metabolism and has the potential to reverse diabetes during the first year after conversion. (EU Clinical Trials Register No. 2006-001765-42).
他克莫司(TAC)相较于环孢素 A(CYC)会增加移植后糖尿病(PTDM)的风险。本为期 12 个月、多中心、研究者驱动、前瞻性、随机研究旨在评估肾移植后从他克莫司转换为环孢素 A 是否可以逆转 PTDM。根据 2005 年美国糖尿病协会标准,患有 PTDM 的主要为白人患者被随机分为 CYC 组或继续他们的基于 TAC 的方案,同时根据降糖治疗、类固醇治疗和丙型肝炎状态进行分层。在 12 个月时,在 CYC 组中有 14 名患者(34%;95%CI 19%-49%)完全没有糖尿病,而在 TAC 组中只有 4 名患者(10%;95%CI 3%-20%)(P=0.01)。在 12 个月时,CYC 组中有 39%的患者停止使用降糖药物,而 TAC 组中只有 13%的患者(P=0.01)。CYC 组在 12 个月的随访期间糖化血红蛋白水平下降,与 TAC 组相比,水平显著降低(6.0±0.9%比 7.1±1.7%;P=0.002)。总之,用 CYC 替代 TAC 可显著改善葡萄糖代谢,并有可能在转换后的第一年逆转糖尿病。(欧盟临床试验注册编号:2006-001765-42)。