Celik Sultan, Doesch Andreas, Erbel Christian, Blessing Erwin, Ammon Kerstin, Koch Achim, Katus Hugo A, Dengler Thomas J
Department of Cardiology, University of Heidelberg, Heidelberg, Germany.
Transplantation. 2008 Jul 27;86(2):245-50. doi: 10.1097/TP.0b013e318177281e.
Hyperlipidemia is an important complication after organ transplantation and may contribute to the development of posttransplant-accelerated coronary artery disease. Immunosuppressive therapy, especially mammalian target of rapamycin inhibitors, induces a considerable increase in cholesterol and triglyceride plasma levels. Omega-3 fatty acids (FAs) exert cardioprotective effects supporting a therapeutic role in cardiovascular conditions.
An observational study of omega-3 FAs 4 g/day was performed in 15 heart transplant recipients with hypertriglyceridemia. Six patients received rapamycin, and nine received everolimus. Apart from one patient the immunosuppressive therapy was combined with mycophenolate mofetil, only one patient received steroids; two patients presented with diabetes.
Mean triglyceride levels before heart transplantation (HTx) were 137+/-54 mg/dL. After HTx, before sirolimus or everolimus treatment triglyceride level had increased to 188+/-67 mg/dL (P<0.05). Treatment with sirolimus or everolimus induced an increase in triglycerides to 354+/-107 mg/dL (P<0.001). Subsequent treatment with omega-3 FAs for 4 months resulted in a marked decrease in triglycerides to 226+/-74 mg/dL (P<0.001). All patients (100%) showed a reduction in triglyceride by more than 20% (responders). In 10 of 15 patients available 12-month data confirmed the long-term efficacy of omega-3 FAs treatment. There were no adverse events or any discontinuations; no changes in immunosuppression were required.
Treatment with mammalian target of rapamycin inhibitors after HTx induces marked increase in serum levels of triglycerides. Omega-3 FAs significantly lower triglyceride levels and seem to be effective, safe, and well-tolerated in sirolimus- or everolimus-treated heart transplant recipients.
高脂血症是器官移植后的重要并发症,可能促使移植后加速性冠状动脉疾病的发展。免疫抑制治疗,尤其是雷帕霉素靶蛋白抑制剂,会导致血浆胆固醇和甘油三酯水平显著升高。ω-3脂肪酸(FAs)具有心脏保护作用,支持其在心血管疾病中的治疗作用。
对15例患有高甘油三酯血症的心脏移植受者进行了一项关于每日服用4克ω-3 FAs的观察性研究。6例患者接受雷帕霉素治疗,9例接受依维莫司治疗。除1例患者外,免疫抑制治疗均与霉酚酸酯联合使用,仅1例患者接受类固醇治疗;2例患者患有糖尿病。
心脏移植(HTx)前平均甘油三酯水平为137±54毫克/分升。HTx后,在使用西罗莫司或依维莫司治疗前,甘油三酯水平已升至188±67毫克/分升(P<0.05)。使用西罗莫司或依维莫司治疗后,甘油三酯升至354±107毫克/分升(P<0.001)。随后使用ω-3 FAs治疗4个月,甘油三酯显著降至226±74毫克/分升(P<0.001)。所有患者(100%)甘油三酯降低超过20%(有反应者)。15例患者中有10例有12个月的数据,证实了ω-3 FAs治疗的长期疗效。未发生不良事件或任何停药情况;无需改变免疫抑制方案。
HTx后使用雷帕霉素靶蛋白抑制剂治疗可导致血清甘油三酯水平显著升高。ω-3 FAs可显著降低甘油三酯水平,在接受西罗莫司或依维莫司治疗的心脏移植受者中似乎有效、安全且耐受性良好。