Department of Liver and Vascular Surgery, Center of Liver Transplantation, West China Hospital, Sichuan University, Chengdu, 610041 Sichuan, China.
Dig Dis Sci. 2012 Jan;57(1):204-9. doi: 10.1007/s10620-011-1817-5. Epub 2011 Jul 9.
The arrival of tacrolimus has drastically improved AALDLT recipients' survival. However, little data of tacrolimus have been reported concerning its effects on lipid metabolism for AALDLT recipients.
Out aim was to investigate the relationship between tacrolimus blood concentration and lipid metabolism in AALDLT recipients.
The pre and postoperative data of 77 adult patients receiving AALDLT between 2002 and December 2007 were retrospectively reviewed. The postoperative immune suppressive regimen was prednisone with tacrolimus ± mycophenolate mofetil. Prednisone was withdrawn within the first postoperative month. Blood lipids and tacrolimus concentration were detected at the first, third, and sixth month during follow-up. Episodes of acute rejection were diagnosed based on biopsy.
Overall prevalence of post-transplantation hyperlipidemia was 29.9% (23/77) at the sixth postoperative month. The patients were divided into two groups, the hyperlipidemia group and the ortholipidemia group. In the 23 patients with hyperlipidemia, 15 (65%) were hypercholesterolemia, five (22%) were hypertriglyceridemia, and three (13%) patients had both hypercholesterolemia and hypertriglyceridemia. In univariate analysis, only tacrolimus blood concentration at the third and sixth post-transplantation months showed significant difference (8.7 ± 2.1 vs. 6.9 ± 3.2, p = 0.013; 9.2 ± 2.7 vs. 7.3 ± 3.8, p = 0.038, respectively). In multivariate logistic analysis, only two factors appear to be risk factors, namely, tacrolimus blood concentration at the third and sixth post-transplantation months (8.7 ± 2.1 vs. 6.9 ± 3.2, p = 0.043; 9.2 ± 2.7 vs. 7.3 ± 3.8 p = 0.035, respectively).
Higher tacrolimus blood concentration was related to hyperlipidemia at an early postoperative period. This indicates that tacrolimus blood concentration should be controlled as low as possible in the premise that there is no risk of rejection to minimize post-transplant hyperlipidemia after AALDLT.
他克莫司的出现极大地提高了 AALDLT 受者的生存率。然而,对于 AALDLT 受者,关于他克莫司对脂代谢影响的数据很少。
本研究旨在探讨 AALDLT 受者他克莫司血药浓度与脂代谢的关系。
回顾性分析 2002 年至 2007 年 12 月期间接受 AALDLT 的 77 例成人患者的术前和术后数据。术后免疫抑制方案为泼尼松联合他克莫司±霉酚酸酯。泼尼松在术后第一个月内停用。在随访期间的第 1、3 和 6 个月检测血脂和他克莫司浓度。根据活检诊断急性排斥反应发作。
术后 6 个月时,总体移植后高脂血症的发生率为 29.9%(23/77)。将患者分为高脂血症组和正常血脂组。在 23 例高脂血症患者中,15 例(65%)为高胆固醇血症,5 例(22%)为高三酰甘油血症,3 例(13%)患者同时患有高胆固醇血症和高三酰甘油血症。单因素分析显示,仅移植后第 3 个月和第 6 个月的他克莫司血药浓度有显著差异(8.7±2.1 与 6.9±3.2,p=0.013;9.2±2.7 与 7.3±3.8,p=0.038)。多因素 logistic 分析显示,仅两个因素似乎是危险因素,即移植后第 3 个月和第 6 个月的他克莫司血药浓度(8.7±2.1 与 6.9±3.2,p=0.043;9.2±2.7 与 7.3±3.8,p=0.035)。
较高的他克莫司血药浓度与术后早期的高脂血症有关。这表明,在没有排斥风险的前提下,应尽可能将他克莫司的血药浓度控制在较低水平,以最大限度地减少 AALDLT 后的移植后高脂血症。