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依折麦布剂量从10毫克换为5毫克对血清脂质水平的影响。

Effect on serum lipid levels of switching dose of ezetimibe from 10 to 5 mg.

作者信息

Baruch Lawrence, Agarwal Sanjay, Gupta Bhanu, Haynos Ann, Eng Calvin

机构信息

James J. Peters Veterans Affairs Medical Center, Bronx, New York, USA.

出版信息

Am J Cardiol. 2009 Jun 1;103(11):1568-71. doi: 10.1016/j.amjcard.2009.01.365. Epub 2009 Apr 22.

Abstract

Although during its initial development, lower doses of ezetimibe reduced low-density lipoprotein (LDL) significantly, ezetimibe is available only in 10-mg form. Compliant patients receiving ezetimibe 10 mg were randomized in a blinded fashion to continue therapy with ezetimibe 10 mg or to convert to a split-tablet 5-mg dose. Lipid panels were collected at baseline and after 4 weeks of therapy. The impact of the 2 ezetimibe dosing strategies on LDL and the achievement of the Adult Treatment Panel III LDL goal was evaluated. One hundred thirty patients receiving ezetimibe 10 mg were screened for eligibility. Thirty-nine of the 130 patients were randomized; 36 patients successfully completed the study. All patients who had achieved their Adult Treatment Panel III LDL goals at baseline remained at their LDL goals after conversion to 5 mg. In conclusion, conversion to the lower dose of ezetimibe did not result in any clinically meaningful or statistically significant changes in any lipid parameter.

摘要

尽管在其最初研发过程中,较低剂量的依折麦布能显著降低低密度脂蛋白(LDL),但依折麦布仅有10毫克剂型。接受10毫克依折麦布治疗的依从性良好的患者被随机分为两组,一组继续接受10毫克依折麦布治疗,另一组转换为5毫克的分服剂量。在基线期和治疗4周后收集血脂指标。评估了两种依折麦布给药策略对LDL的影响以及是否达到成人治疗小组第三次报告(Adult Treatment Panel III)的LDL目标。对130名接受10毫克依折麦布治疗的患者进行了资格筛查。130名患者中有39名被随机分组;36名患者成功完成了研究。所有在基线期达到成人治疗小组第三次报告LDL目标的患者在转换为5毫克剂量后仍保持其LDL目标。总之,转换为较低剂量的依折麦布并未导致任何血脂参数出现具有临床意义或统计学意义的显著变化。

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