Bergheanu S C, Van Tol A, Dallinga-Thie G M, Liem A, Dunselman P H J, Van der Bom J G, Jukema J W
Leiden University Medical Center, Leiden, The Netherlands.
Curr Med Res Opin. 2007 Sep;23(9):2235-40. doi: 10.1185/030079907X226104.
Paraoxonase-1 (PON-1) is a high-density lipoprotein (HDL) associated enzyme involved in the protective mechanisms of HDL. Our aim was to compare the effect of treatment with rosuvastatin and atorvastatin on serum PON-1 activity.
We performed a prespecified prospective study in 68 patients, part of a larger, multicentre randomized study--RADAR (Rosuvastatin and Atorvastatin in different Dosages And Reverse cholesterol transport). Patients aged 40-80 years, all men, with established cardiovascular disease and high-density lipoprotein cholesterol (HDL-C) < 1.0 mmol/L (< 40 mg/dL) entered a 6-week dietary run-in period before receiving treatment with rosuvastatin 10 mg or atorvastatin 20 mg daily for 6-weeks. Doses were increased after 6 weeks to rosuvastatin 20 mg or atorvastatin 40 mg and after 12 weeks to rosuvastatin 40 mg or atorvastatin 80 mg daily. Serum PON-1 activity and lipid profile were determined at baseline, 6 and 18 weeks.
After 18 weeks, the rosuvastatin arm showed a significant increase of PON-1 activity (6.39 U/L, p = 0.02) whereas this was not observed in the atorvastatin arm (1.84 U/L, p = 0.77). The difference between groups did not reach significance (p = 0.11). Both rosuvastatin and atorvastatin resulted in significant (p = 0.0001) and similar increases in HDL-C after 6 weeks [0.06 mmol/L (2.32 mg/dL) vs. 0.05 mmol/L (1.93 mg/dL)] and after 18 weeks [0.10 mmol/L (3.87 mg/dL) vs. 0.10 mmol/L (3.87 mg/dL)].
Rosuvastatin treatment resulted in a significant increment of serum PON-1 activity with increasing dose while this was not observed with atorvastatin.
对氧磷酶-1(PON-1)是一种与高密度脂蛋白(HDL)相关的酶,参与HDL的保护机制。我们的目的是比较瑞舒伐他汀和阿托伐他汀治疗对血清PON-1活性的影响。
我们在68例患者中进行了一项预先设定的前瞻性研究,这些患者是一项更大的多中心随机研究——RADAR(不同剂量瑞舒伐他汀和阿托伐他汀与逆向胆固醇转运)的一部分。年龄在40-80岁的男性患者,患有确诊的心血管疾病且高密度脂蛋白胆固醇(HDL-C)<1.0 mmol/L(<40 mg/dL),在接受每日10 mg瑞舒伐他汀或20 mg阿托伐他汀治疗6周之前,先进入为期6周的饮食导入期。6周后剂量增加至瑞舒伐他汀20 mg或阿托伐他汀40 mg,12周后剂量增加至瑞舒伐他汀40 mg或阿托伐他汀80 mg每日。在基线、6周和18周时测定血清PON-1活性和血脂谱。
18周后,瑞舒伐他汀组的PON-1活性显著增加(6.39 U/L,p = 0.02),而阿托伐他汀组未观察到这种情况(1.84 U/L,p = 0.77)。两组之间的差异未达到显著水平(p = 0.11)。瑞舒伐他汀和阿托伐他汀在6周后[0.06 mmol/L(2.32 mg/dL)对0.05 mmol/L(1.93 mg/dL)]和18周后[0.10 mmol/L(3.87 mg/dL)对0.10 mmol/L(3.87 mg/dL)]均导致HDL-C显著(p = 0.0001)且相似的升高。
瑞舒伐他汀治疗随着剂量增加导致血清PON-1活性显著增加,而阿托伐他汀未观察到这种情况。