首页> 外文期刊>Journal of cardiovascular pharmacology and therapeutics >Effect of rosuvastatin monotherapy and in combination with fenofibrate or omega-3 fatty acids on serum vitamin D levels
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Effect of rosuvastatin monotherapy and in combination with fenofibrate or omega-3 fatty acids on serum vitamin D levels

机译:罗苏伐他汀单一疗法联合非诺贝特或omega-3脂肪酸对血清维生素D水平的影响

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Background: Low levels of 25(OH) vitamin D [25(OH)VitD] have been recognized as a new cardiovascular disease (CVD) risk factor. Statins seem to increase 25(OH)VitD concentration. Aim: To investigate whether combined treatment with the usual dose of rosuvastatin plus fenofibrate or omega-3 fatty acids would increase 25(OH)VitD levels compared with the high-dose rosuvastatin monotherapy in participants with mixed dislipidemia. Methods: We randomly allocated 60 patients with mixed dyslipidemia (low-density lipoprotein cholesterol: >160 mg/dL plus triglycerides: >200 mg/dL) to receive rosuvastatin 40 mg (n = 22), rosuvastatin 10 mg plus fenofibrate 200 mg (n = 21), or rosuvastatin 10 mg plus omega-3 fatty acids 2 g (n = 17) daily for 3 months. Our primary end point was changes in the levels of serum 25(OH)VitD. Results: Rosuvastatin monotherapy was associated with a 53% increase in 25(OH)VitD (from 14.6 [1.0-38.0] to 17.8 [5.3-49.6] ng/mL; P = .000). Rosuvastatin plus micronized fenofibrate and rosuvastatin plus omega-3 fatty acids were associated with increases of 64% (from 14.1 [1.0-48.0] to 18.4 [6.7-52.4] ng/mL, P = .001) and 61% (from 10.4 [6.6-38.4] to 14.0 [9.6-37.6] ng/mL, P = .04), respectively. The changes in 25(OH)VitD after treatment were comparable in the 3 groups. Conclusion: High-dose rosuvastatin monotherapy and the usual dose of rosuvastatin plus fenofibrate or omega-3 fatty acids are associated with significant and similar increases in the 25(OH)VitD levels. This increase may be relevant in terms of CVD risk prevention.
机译:背景:低水平的25(OH)维生素D [25(OH)VitD]被认为是新的心血管疾病(CVD)危险因素。他汀类药物似乎可以增加25(OH)VitD的浓度。目的:研究与高剂量罗苏伐他汀单一疗法相比,混合性血脂异常参与者与常规剂量罗苏伐他汀加非诺贝特或omega-3脂肪酸联合治疗是否会增加25(OH)VitD水平。方法:我们随机分配60名混合血脂异常(低密度脂蛋白胆固醇:> 160 mg / dL加甘油三酸酯:> 200 mg / dL)的患者接受瑞舒伐他汀40 mg(n = 22),瑞舒伐他汀10 mg加非诺贝特200 mg( n = 21),或瑞舒伐他汀10 mg加omega-3脂肪酸2 g(n = 17),持续3个月。我们的主要终点是血清25(OH)VitD水平的变化。结果:瑞舒伐他汀单药治疗与25(OH)VitD增加53%(从14.6 [1.0-38.0] ng至17.8 [5.3-49.6] ng / mL; P = .000)相关。瑞舒伐他汀加微粉非诺贝特和瑞舒伐他汀加omega-3脂肪酸分别增加64%(从14.1 [1.0-48.0]到18.4 [6.7-52.4] ng / mL,P = .001)和61%(从10.4 [ 6.6-38.4]至14.0 [9.6-37.6] ng / mL,P = .04)。 3组治疗后25(OH)VitD的变化相当。结论:大剂量瑞舒伐他汀单药治疗和通常剂量的瑞舒伐他汀加非诺贝特或omega-3脂肪酸与25(OH)VitD水平显着且相似的升高有关。就CVD风险的预防而言,这种增加可能是相关的。

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