慢性肾病、透析和肾移植受者血脂异常的处理

Jai Prakash Ojha
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引用次数: 1

摘要

血脂异常是慢性肾脏疾病(CKD)患者,透析和肾移植接受者的一种公认的代谢紊乱。血清胆固醇水平升高在动脉粥样硬化的发生发展中具有明确的作用,血清LDL胆固醇升高作为冠心病发生的危险因素之间的相关性已被牢固确立。HMG-CoA还原酶抑制剂(他汀类药物)是目前治疗高胆固醇血症的首选药物。他汀类药物治疗可有效降低总胆固醇和低密度脂蛋白胆固醇水平,适度降低甘油三酯(TGs)水平,对高密度脂蛋白胆固醇水平升高作用不大。他汀类药物治疗可降低肾功能正常的冠心病患者的发病率和死亡率。然而,他汀类药物治疗对CKD和晚期ESRD患者CVD发病率和死亡率的有益影响存在争议。他汀类药物治疗可降低早期CKD患者(尚不需要透析)的心血管疾病死亡率,并推荐用于早期CKD患者。然而,最近来自AURORA和SHARP研究的结果显示,他汀类药物治疗对晚期CKD患者或长期透析患者的CV死亡率没有好处。这可能是因为在ESRD和/或透析患者中观察到的CVD中,冠状动脉粥样硬化性疾病只占一小部分。此外,晚期CKD导致HDL的结构和功能异常,胆固醇和乳糜微粒代谢受损,导致这类患者动脉粥样硬化和心血管疾病加速。总的来说,这些异常在很大程度上与胆固醇生物合成无关,因此他汀类药物治疗无法纠正。因此,ESRD患者的降脂治疗应个体化。阿托伐他汀和瑞舒伐他汀是现有的他汀类降胆固醇药物中最有效的药物,但也是最昂贵的。辛伐他汀(20mg /天)应该被认为是大多数慢性肾病患者的首选药物,因为它更便宜。普伐他汀和氟伐他汀是移植患者达到目标胆固醇水平最合适的药物,因为它们降低了药物相互作用的风险。
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Management of dyslipidemia in CKD, dialysis and renal transplant recipient

Dyslipidemia is a well-established metabolic disorder in patients with chronic kidney diseases (CKD), on dialysis and renal transplant recipient. The elevated serum cholesterol levels have a definite role in the development and progression of atherosclerosis and the correlation between elevated serum LDL cholesterol as a risk factor for development of CHD has been firmly established. The HMG-CoA reductase inhibitors (statins) are the current drugs of choice for the treatment of hypercholesterolemia. The treatment with statins effectively lower total and LDL-cholesterol levels, moderately decreases triglycerides (TGs) levels, and have a little effect in increasing HDL-cholesterol levels. The statins therapy reduces the morbidity and mortality associated with CHD in patients with normal renal function. However, the beneficial effect of statin therapy on CVD morbidity and mortality in patients with CKD and advanced ESRD are controversial. Statin therapy reduces CVD mortality in patient with early CKD (not yet requiring dialysis) and their use is recommended for patients with early CKD. However, the recent results from the AURORA and SHARP studies have revealed statins treatment provide no CV mortality benefit in patient with advanced CKD or on long-term dialysis. This may be because athermatous coronary artery disease account for a small proportion of the CVD observed in patients with ESRD and/or on dialysis. In addition, advanced CKD result in structural and functional abnormalities of HDL, impaired cholesterol and chylomicron metabolism which leads to accelerated atherosclerosis and CVD in such patients. Collectively, these abnormalities are largely independent of cholesterol biosynthesis, and consequently are not corrected by statin therapy. Therefore lipid lowering therapy in patient with ESRD should be individualized. Atorvastatin and Rosuvastatin are most potent agents among the available statins in cholesterol lowering but are the most expensive. Simvastatin (20 mg/day) should be considered the drug of choice for most patients with chronic kidney disease because it is less expensive. Pravastatin and fluvastatin are the most suitable agents for transplant patients to achieve target cholesterol levels because of the reduced risk of drug interactions.

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