Effects of simvastatin and ezetimibe on interleukin-6 and high-sensitivity C-reactive protein.

Heiner K Berthold, Kaspar Berneis, Christos S Mantzoros, Wilhelm Krone, Ioanna Gouni-Berthold
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引用次数: 17

Abstract

Objectives: Statins decrease cardiovascular events mainly by lowering cholesterol but anti-inflammatory effects also play a role. The effects of the cholesterol absorption inhibitor ezetimibe on markers of inflammation remain unclear. We performed an exploratory post-hoc analysis whether these drugs influence the pro-inflammatory markers interleukin-6 and high-sensitivity C-reactive protein in subjects with very-low cardiovascular risk.

Design: Single center, randomized, parallel 3-group study in 72 healthy men without apparent cardiovascular disease (age 32 ± 9 years, BMI 25.7 ± 3.2 kg/m(2)). Each group of 24 subjects received a 14-day treatment with either simvastatin 40 mg, ezetimibe 10 mg, or their combination.

Results: Baseline IL-6 and hsCRP concentrations in the total cohort were 0.72 ± 0.57 ng/l and 0.40 ± 0.65 mg/l, respectively, with no differences between the 3 groups. Median changes (interquartile range) in IL-6 and hsCRP concentrations were -22% (-43 to 0%) and -30% (-44 to +19%) after simvastatin, -5% (-36 to +30%) and +9% (-22 to +107%) after ezetimibe, and +15% (-15 to +86%) and +1 (-30 to +49%) after the combination. Using a generalized linear model, the multivariable adjusted overall P-values for these changes were 0.008 (IL-6) and 0.1 (hsCRP).

Conclusions: Simvastatin decreases the pro-inflammatory markers IL-6 and almost significantly hsCRP while ezetimibe monotherapy or the combination with simvastatin has no effect.

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辛伐他汀和依折替米布对白细胞介素-6和高敏c反应蛋白的影响。
目的:他汀类药物主要通过降低胆固醇来减少心血管事件,但抗炎作用也起作用。胆固醇吸收抑制剂依折替米比对炎症标志物的影响尚不清楚。我们进行了一项探索性事后分析,这些药物是否会影响极低心血管风险受试者的促炎标志物白介素-6和高敏c反应蛋白。设计:单中心、随机、平行3组研究,72名无明显心血管疾病的健康男性(年龄32±9岁,BMI 25.7±3.2 kg/m(2))。每组24名受试者接受为期14天的辛伐他汀40mg、依折替米贝10mg或两者联合治疗。结果:整个队列中IL-6和hsCRP的基线浓度分别为0.72±0.57 ng/l和0.40±0.65 mg/l,三组间无差异。IL-6和hsCRP浓度的中位变化(四分位数范围)辛伐他汀组为-22%(-43 ~ 0%)和-30%(-44 ~ +19%),依折替米贝组为-5%(-36 ~ +30%)和+9%(-22 ~ +107%),联合用药组为+15%(-15 ~ +86%)和+1(-30 ~ +49%)。使用广义线性模型,这些变化的多变量调整总p值为0.008 (IL-6)和0.1 (hsCRP)。结论:辛伐他汀可显著降低促炎标志物IL-6和hsCRP,而依折替米贝单药或与辛伐他汀联用无明显作用。
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