Ormiston Cameron K, Pazargadi Aryana, Rosander Ashley, Ceballos Guillermo, Villarreal Francisco, Taub Pam R
Division of Cardiovascular Medicine, Department of Medicine, University of California, San Diego, La Jolla, California, USA.
Department of Medical Education, Icahn School of Medicine at Mount Sinai, New York, New York, USA.
Clin Transl Sci. 2025 May;18(5):e70236. doi: 10.1111/cts.70236.
Statins play an instrumental role in reducing and managing atherosclerotic cardiovascular disease (ASCVD) but can be difficult to tolerate due to muscle-associated side effects. There remains an unmet need for strategies that improve statin tolerance and synergize their effect on atherogenic lipids. (-)-Epicatechin (Epi) is a natural flavonoid that can improve lipid biomarkers and mitochondrial function. This study explored the capacity of Epi to augment statin's beneficial effects on lipid profile and ASCVD risk parameters. In total, 19 patients completed a randomized, double-blind placebo-controlled trial. The study consisted of two cohorts. Cohort 1 consisted of healthy patients with elevated low-density lipoprotein (LDL) > 100 mg/dL and was used to determine appropriate Epi dosing. Cohort 2 consisted of patients with metabolic syndrome. Patients were randomized into statin-only (n = 8; 5 in Cohort 2) or statin + Epi (n = 11; 8 in Cohort 2) for 3 months. VO max and lipid biomarkers were assessed at baseline and at the end of 3 months. Final analysis included Cohort 2 only. The statin + Epi group saw significant beneficial changes in total cholesterol (p = 0.002) and non-HDL cholesterol (p = 0.007). There was a significantly larger increase in HDL (p = 0.037) and significantly greater decrease in LDL particle number (p = 0.0003) and small LDL particle number (p = 0.003) among the statin + Epi group compared to statin-only. Ten-year ASCVD risk was significantly lower at end-of-study for the statin + Epi arm compared to statin-only (p < 0.05). No VO max differences were found. This is the first proof-of-concept study to show combination therapy of a statin with Epi is safe and effective in augmenting statin-associated improvements in lipid biomarkers. Trial Registration: ClinicalTrials.gov: NCT02490527.
他汀类药物在降低和管理动脉粥样硬化性心血管疾病(ASCVD)方面发挥着重要作用,但由于肌肉相关的副作用,可能难以耐受。目前仍需要能够提高他汀类药物耐受性并增强其对致动脉粥样硬化脂质作用的策略。(-)-表儿茶素(Epi)是一种天然黄酮类化合物,可改善脂质生物标志物和线粒体功能。本研究探讨了Epi增强他汀类药物对脂质谱和ASCVD风险参数有益作用的能力。共有19名患者完成了一项随机、双盲、安慰剂对照试验。该研究包括两个队列。队列1由低密度脂蛋白(LDL)>100mg/dL升高的健康患者组成,用于确定合适的Epi剂量。队列2由代谢综合征患者组成。患者被随机分为仅服用他汀类药物组(n = 8;队列2中有5人)或他汀类药物+Epi组(n = 11;队列2中有8人),为期3个月。在基线和3个月末评估最大摄氧量(VO max)和脂质生物标志物。最终分析仅包括队列2。他汀类药物+Epi组的总胆固醇(p = 0.002)和非高密度脂蛋白胆固醇(p = 0.007)有显著的有益变化。与仅服用他汀类药物组相比,他汀类药物+Epi组的高密度脂蛋白增加显著更大(p = 0.037),低密度脂蛋白颗粒数量(p = 0.0003)和小低密度脂蛋白颗粒数量(p = 0.003)减少显著更大。与仅服用他汀类药物组相比,他汀类药物+Epi组在研究结束时的10年ASCVD风险显著更低(p < 0.05)。未发现最大摄氧量有差异。这是第一项概念验证研究,表明他汀类药物与Epi联合治疗在增强他汀类药物相关的脂质生物标志物改善方面是安全有效的。试验注册:ClinicalTrials.gov:NCT02490527。