首页> 外文期刊>BMC Nephrology >HMG-CoA reductase inhibitors in kidney transplant recipients receiving tacrolimus: statins not associated with improved patient or graft survival
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HMG-CoA reductase inhibitors in kidney transplant recipients receiving tacrolimus: statins not associated with improved patient or graft survival

机译:HMG-CoA还原酶抑制剂在接受他克莫司治疗的肾移植受者中:他汀类药物与患者或移植物生存期的改善无关

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Background The beneficial effects of early statin use in kidney transplant recipients, especially those on tacrolimus-based immunosuppression, are not well established. We evaluated the predictors of statin use following kidney transplantation and examined its association with patient and allograft survival. Methods We examined 615 consecutive patients who underwent kidney transplant at our institution between January 1998 and January 2002. Statin use was assessed at baseline and 3, 6, 9, and 12 months following kidney transplant. Patients were followed for allograft and patient survival. Results 36% of the 615 kidney transplant recipients were treated with statin treatment. Statin use increased over the course of the study period. Older age, elevated body mass index, higher triglyceride levels, hypercholesterolemia, diabetes, history of myocardial infarction were associated with higher rates of statin use; elevated alkaline phosphatase levels and CMV IgG seropositivity were associated with less statin use. Older age, elevated BMI and hypercholesterolemia remained significant predictors of increased statin use after accounting for covariates using multiple regression. The early use of statins was not associated with improvements in unadjusted patient survival [HR 0.99; 95%CI 0.72-1.37] or graft survival [HR 0.97; 95% CI 0.76-1.24]. The risks of death and graft survival were not consistently reduced with exposure to statin using either adjusted models or propensity scores in Cox Proportional Hazards models. Conclusions In a kidney transplant population primarily receiving tacrolimus-based immunosuppression, early statin use was not associated with significantly improved graft or patient survival.
机译:背景技术在肾脏移植接受者中早期使用他汀类药物的有益作用,尤其是那些基于他克莫司的免疫抑制作用尚不十分清楚。我们评估了他汀类药物在肾脏移植后使用的预测因素,并检查了其与患者和同种异体移植物存活的关系。方法我们对1998年1月至2002年1月间在本机构接受肾移植的615例患者进行了检查。在基线和肾移植后3、6、9和12个月评估了他汀类药物的使用。随访患者同种异体移植和患者生存情况。结果615例肾移植受者中有36%接受了他汀类药物治疗。在研究期间,他汀类药物的使用有所增加。年龄较大,体重指数升高,甘油三酯水平升高,高胆固醇血症,糖尿病,心肌梗塞病史与他汀类药物的使用率增加有关;碱性磷酸酶水平升高和CMV IgG血清阳性与他汀类药物使用量减少相关。使用多元回归分析协变量后,老年,BMI升高和高胆固醇血症仍是他汀类药物使用增加的重要预测指标。他汀类药物的早期使用与未经调整的患者生存率的改善没有关联[HR 0.99; 95%CI 0.72-1.37]或移植物存活率[HR 0.97; 95%CI 0.76-1.24]。使用调整模型或Cox比例危害模型中的倾向评分,未因使用他汀类药物而持续降低死亡和移植物存活的风险。结论在主要接受基于他克莫司的免疫抑制的肾脏移植人群中,早期使用他汀类药物与移植物或患者存活率无明显改善。

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