Imperial Centre for Cardiovascular Disease Prevention, Imperial College, UK.
Li Ka Shing Knowledge Institute, University of Toronto, Canada.
Eur J Prev Cardiol. 2020 Oct;27(15):1663-1674. doi: 10.1177/2047487320905185. Epub 2020 Feb 23.
Guidelines recommend targeting non-high-density lipoprotein cholesterol to reduce cardiovascular risk. We assessed the impact of baseline triglycerides on non-high-density lipoprotein cholesterol goal attainment in 10 phase 3 trials with alirocumab versus control ( = 4983).
Trials were grouped into four pools based on alirocumab dose (75-150 mg every 2 weeks), control (placebo/ezetimibe) and statin use. Baseline triglyceride quintiles were built within each pool. Non-high-density lipoprotein cholesterol goal attainment (very high risk: <100 mg/dl; moderate/high risk: <130 mg/dl), low-density lipoprotein cholesterol goal attainment (very high risk: <70 mg/dl; moderate/high risk: <100 mg/dl) and changes from baseline in lipid parameters were assessed at Week 24 among baseline triglyceride quintiles.
Higher baseline triglycerides were associated with a worse cardiovascular risk profile. Low-density lipoprotein cholesterol and non-high-density lipoprotein cholesterol increased with higher triglycerides, but the magnitude in non-high-density lipoprotein cholesterol was three- to four-fold higher compared with the increase in low-density lipoprotein cholesterol. Non-high-density lipoprotein cholesterol and low-density lipoprotein cholesterol percentage reductions from baseline with alirocumab were similar regardless of baseline triglycerides. A greater proportion of alirocumab-treated patients attained non-high-density lipoprotein cholesterol and low-density lipoprotein cholesterol goals compared with placebo or ezetimibe. Unlike low-density lipoprotein cholesterol goal attainment, non-high-density lipoprotein cholesterol goal attainment significantly declined with increasing baseline triglycerides ( < 0.05 for trend tests). A single standard deviation increase in baseline log(triglycerides) was significantly associated with lower odds ratios of attaining non-high-density lipoprotein cholesterol goals in the different pools and treatment (alirocumab/placebo/ezetimibe) groups, unlike low-density lipoprotein cholesterol goal attainment.
Individuals with increased triglycerides have higher non-high-density lipoprotein cholesterol levels and lower rates of non-high-density lipoprotein cholesterol goal attainment (unlike low-density lipoprotein cholesterol goal attainment). Alirocumab improves non-high-density lipoprotein cholesterol goal attainment in this population. These results highlight the impact of triglycerides on non-high-density lipoprotein cholesterol and the need for novel therapies targeting triglyceride-related pathways.
指南建议将非高密度脂蛋白胆固醇作为治疗靶点,以降低心血管风险。我们评估了基线甘油三酯对 10 项接受阿利西尤单抗治疗与对照组(n=4983)的 3 期临床试验中达到非高密度脂蛋白胆固醇目标的影响。
根据阿利西尤单抗剂量(每 2 周 75-150mg)、对照组(安慰剂/依折麦布)和他汀类药物使用情况,将试验分为 4 个组。在每个组内构建基线甘油三酯五分位数。评估基线甘油三酯五分位数组内第 24 周时非高密度脂蛋白胆固醇目标达标(极高危:<100mg/dl;中高危:<130mg/dl)、低密度脂蛋白胆固醇目标达标(极高危:<70mg/dl;中高危:<100mg/dl)和脂质参数的基线变化。
基线甘油三酯越高,心血管风险状况越差。随着甘油三酯的升高,低密度脂蛋白胆固醇和非高密度脂蛋白胆固醇也随之升高,但非高密度脂蛋白胆固醇的升高幅度是低密度脂蛋白胆固醇的 3-4 倍。无论基线甘油三酯水平如何,阿利西尤单抗治疗均能使非高密度脂蛋白胆固醇和低密度脂蛋白胆固醇百分比从基线下降。与安慰剂或依折麦布相比,更多的阿利西尤单抗治疗患者达到了非高密度脂蛋白胆固醇和低密度脂蛋白胆固醇目标。与低密度脂蛋白胆固醇目标达标不同,随着基线甘油三酯的升高,非高密度脂蛋白胆固醇目标达标率显著下降(趋势检验 P<0.05)。与低密度脂蛋白胆固醇目标达标不同,基线对数(甘油三酯)每增加一个标准差,与不同组和治疗(阿利西尤单抗/安慰剂/依折麦布)中达到非高密度脂蛋白胆固醇目标的比值比显著相关。
甘油三酯升高的个体具有更高的非高密度脂蛋白胆固醇水平和更低的非高密度脂蛋白胆固醇目标达标率(与低密度脂蛋白胆固醇目标达标不同)。阿利西尤单抗可改善该人群的非高密度脂蛋白胆固醇目标达标率。这些结果突出了甘油三酯对非高密度脂蛋白胆固醇的影响,以及需要针对甘油三酯相关途径的新型治疗方法。