首页> 美国卫生研究院文献>Cardiovascular Diabetology >Design and rationale of the ODYSSEY DM-DYSLIPIDEMIA trial: lipid-lowering efficacy and safety of alirocumab in individuals with type 2 diabetes and mixed dyslipidaemia at high cardiovascular risk
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Design and rationale of the ODYSSEY DM-DYSLIPIDEMIA trial: lipid-lowering efficacy and safety of alirocumab in individuals with type 2 diabetes and mixed dyslipidaemia at high cardiovascular risk

机译:ODYSSEY DM-DYSLIPIDEMIA试验的设计和原理:Alirocumab在具有高心血管风险的2型糖尿病和混合血脂异常患者中的降脂功效和安全性

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摘要

BackgroundType 2 diabetes mellitus (T2DM) is often associated with mixed dyslipidaemia, where non-high-density lipoprotein cholesterol (non-HDL-C) levels may more closely align with cardiovascular risk than low-density lipoprotein cholesterol (LDL-C). We describe the design and rationale of the ODYSSEY DM-DYSLIPIDEMIA study that assesses the efficacy and safety of alirocumab, a proprotein convertase subtilisin/kexin type 9 (PCSK9) inhibitor, versus lipid-lowering usual care in individuals with T2DM and mixed dyslipidaemia at high cardiovascular risk with non-HDL-C inadequately controlled despite maximally tolerated statin therapy. For the first time, atherogenic cholesterol-lowering with a PCSK9 inhibitor will be assessed with non-HDL-C as the primary endpoint with usual care as the comparator.
机译:背景2型糖尿病(T2DM)通常与混合性血脂异常有关,与低密度脂蛋白胆固醇(LDL-C)相比,非高密度脂蛋白胆固醇(non-HDL-C)水平可能与心血管疾病风险更为接近。我们描述了ODYSSEY DM-DYSLIPIDEMIA研究的设计和原理,该研究评估了Alirocumab(一种前蛋白转化酶枯草杆菌蛋白酶/ kexin 9型(PCSK9)抑制剂)相对于高脂血症和T2DM混合血脂异常患者的降脂常规护理的有效性和安全性尽管他汀类药物的耐受性最大,但非HDL-C引起的心血管疾病风险仍未得到充分控制。首次将使用非HDL-C作为主要终点评估使用PCSK9抑制剂降低动脉粥样硬化胆固醇的水平,并通常将其作为对照。

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