Sadoni S, Kaczmarek I, Delgado O, Schmöckel M, Reichart B, Meiser B
Department of Cardiac Surgery, Grosshadern University Hospital, Ludwig-Maximilians-University, Munich, Germany.
Transplant Proc. 2007 Mar;39(2):558-9. doi: 10.1016/j.transproceed.2006.12.009.
Statins reduce the risk for transplant vasculopathy and mortality among heart transplant recipients. Interactions between commonly used statins (ie, simvastatin, atorvastatin) and immunosuppressant drugs lead to side effects or withdrawal of statin therapy. Fluvastatin shows fewer interactions with the immunosuppressant agents because it is not metabolized via the cytochrome P-450 3A4 pathway like most immunosuppressants, steroids, or other statins. This study investigated the impact of a switch from other statins to fluvastatin in heart transplant recipients who revealed elevated creatine-kinase levels.
A total of 23 heart transplant patients with elevated creatine-kinase levels were included in this study. Statins were replaced with an equal dosage of fluvastatin. We measured on the day of replacement as well as there after at 3, 6, 9, and 12 months creatine-kinase, lipid status, ALT, AST, and creatinine levels.
After 6 months creatine-kinase showed a significant reduction of 25% (P < .05) and after 9 months of 38% (P < .05). The HDL-cholesterol levels were significantly reduced at 6 months (8%; P < .05) and 9 months (23%; P < .05). At 3 months, triglyceride levels were significantly elevated (18%; P < .05). No differences were observed in ALT, AST, creatinine, total, and LDL-cholesterol at any time.
A conversion from commonly used statins to fluvastatin in heart transplant patients with elevated creatine-kinase was safe, leading to a significant reduction in creatine-kinase levels. Except for an initial raise in triglycerides and a lowering of HDL-cholesterol, no changes in lipid status were seen. This conversion might help to maintain lipid-lowering therapy in transplant recipients who show side effects using conventional statins.
他汀类药物可降低心脏移植受者发生移植血管病变的风险及死亡率。常用他汀类药物(即辛伐他汀、阿托伐他汀)与免疫抑制剂之间的相互作用会导致副作用或他汀类药物治疗中断。氟伐他汀与免疫抑制剂的相互作用较少,因为它不像大多数免疫抑制剂、类固醇或其他他汀类药物那样通过细胞色素P - 450 3A4途径代谢。本研究调查了在肌酸激酶水平升高的心脏移植受者中从其他他汀类药物转换为氟伐他汀的影响。
本研究共纳入23例肌酸激酶水平升高的心脏移植患者。将他汀类药物替换为等量的氟伐他汀。我们在替换当天以及之后的3、6、9和12个月测量肌酸激酶、血脂状况、谷丙转氨酶、谷草转氨酶和肌酐水平。
6个月后肌酸激酶显著降低25%(P < 0.05),9个月后降低38%(P < 0.05)。高密度脂蛋白胆固醇水平在6个月时显著降低(8%;P < 0.05),9个月时降低23%(P < 0.05)。3个月时,甘油三酯水平显著升高(18%;P < 0.05)。在任何时间点,谷丙转氨酶、谷草转氨酶、肌酐、总胆固醇和低密度脂蛋白胆固醇均未观察到差异。
在肌酸激酶水平升高的心脏移植患者中,从常用他汀类药物转换为氟伐他汀是安全的,可导致肌酸激酶水平显著降低。除了最初甘油三酯升高和高密度脂蛋白胆固醇降低外,血脂状况未见变化。这种转换可能有助于在使用传统他汀类药物出现副作用的移植受者中维持降脂治疗。