(−)-表儿茶素增强他汀类药物降脂和降低心血管风险评分的作用:概念验证试点研究

IF 3.1 3区 医学 Q2 MEDICINE, RESEARCH & EXPERIMENTAL
Cameron K. Ormiston, Aryana Pazargadi, Ashley Rosander, Guillermo Ceballos, Francisco Villarreal, Pam R. Taub
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引用次数: 0

摘要

他汀类药物在减少和控制动脉粥样硬化性心血管疾病(ASCVD)方面发挥着重要作用,但由于与肌肉相关的副作用,他汀类药物可能难以耐受。对于提高他汀类药物耐受性和协同其对动脉粥样硬化性脂质的影响的策略仍有未满足的需求。(−)-表儿茶素(Epi)是一种天然类黄酮,可以改善脂质生物标志物和线粒体功能。本研究探讨了Epi增强他汀类药物对血脂和ASCVD风险参数的有益作用的能力。总共有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)升高≤100mg /dL的健康患者组成,用于确定Epi的适当剂量。队列2包括代谢综合征患者。患者随机分为仅使用他汀类药物组(n = 8;队列2 5例)或他汀类药物+ Epi (n = 11;8人(队列2),3个月。在基线和3个月结束时评估最大摄氧量和脂质生物标志物。最终分析仅包括队列2。他汀+ Epi组在总胆固醇(p = 0.002)和非高密度脂蛋白胆固醇(p = 0.007)方面有显著的有益变化。他汀+ Epi组HDL升高(p = 0.037), LDL颗粒数降低(p = 0.0003),小LDL颗粒数降低(p = 0.003)。在研究结束时,他汀+肾上腺素组的10年ASCVD风险显著低于单纯他汀组(p <;0.05)。没有发现VO2 max差异。这是第一个概念验证研究,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
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Enhancement of Statin Effects on Lipid Lowering and Reduction of Cardiovascular Risk Score by (−)-Epicatechin in Proof-of-Concept Pilot Study

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. VO2 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 VO2 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

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来源期刊
Cts-Clinical and Translational Science
Cts-Clinical and Translational Science 医学-医学:研究与实验
CiteScore
6.70
自引率
2.60%
发文量
234
审稿时长
6-12 weeks
期刊介绍: Clinical and Translational Science (CTS), an official journal of the American Society for Clinical Pharmacology and Therapeutics, highlights original translational medicine research that helps bridge laboratory discoveries with the diagnosis and treatment of human disease. Translational medicine is a multi-faceted discipline with a focus on translational therapeutics. In a broad sense, translational medicine bridges across the discovery, development, regulation, and utilization spectrum. Research may appear as Full Articles, Brief Reports, Commentaries, Phase Forwards (clinical trials), Reviews, or Tutorials. CTS also includes invited didactic content that covers the connections between clinical pharmacology and translational medicine. Best-in-class methodologies and best practices are also welcomed as Tutorials. These additional features provide context for research articles and facilitate understanding for a wide array of individuals interested in clinical and translational science. CTS welcomes high quality, scientifically sound, original manuscripts focused on clinical pharmacology and translational science, including animal, in vitro, in silico, and clinical studies supporting the breadth of drug discovery, development, regulation and clinical use of both traditional drugs and innovative modalities.
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