Monoglucosyl rutin, a flavonoid glycoside, improves low-density lipoprotein-cholesterol levels in healthy adults: A randomized controlled trial

Yushi Hashizume, M. Tandia
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Abstract

Background: Atherosclerotic cardiovascular disease (ASCVD) continues to be a significant contributor to global mortality, impacting over 523 million individuals worldwide.  Dyslipidemia stands as one of the foremost risk factors for ASCVD. Thus, prioritizing the reduction of low-density lipoprotein cholesterol (LDL-C) levels is essential in mitigating cardiovascular complications.  Objective: This study aimed to evaluate the lipid-lowering activity of a dietary supplement containing monoglucosyl rutin (MR) in individuals with low to mild hypercholesterolemia. Methods: This was a randomized, placebo-controlled, double-blind, parallel-group study conducted from April 20 to December 24, 2022. The study population included 56 healthy Japanese adult participants with LDL-C levels between 120–139 mg/dL who were randomly allocated to either the MR or placebo groups (n = 28/group) using a computerized random number generator. 200 mg of MR or placebo divided into 3 tablets was given daily; participants were instructed to take 1 tablet with water after each meal for 12 weeks. The main focus was on measuring the serum LDL-C level as the primary outcome, with additional attention given to secondary outcomes such as serum high-density lipoprotein cholesterol (HDL-C), total cholesterol, and nonHDL-C levels. The study also evaluated the percentage of participants achieving serum LDL-C levels below 120 mg/dL after the 12-week intervention.  Assessments were conducted after 4, 8, and 12 weeks of intervention. Results: There were 54 (27 in each group) participants in the per-protocol set (PPS) and 53 (placebo group, 26; MR group, 27) participants in the modified PPS (mPPS). A statistically significant group difference in serum LDL-C levels was observed (P < 0.05), with a 5.0% decrease from preintervention to after 12 weeks. The reduction in LDL-C levels coincided with (statistically significant?) decreases in total cholesterol levels, nonHDL-C levels, and the LDL-C/HDL-C ratio. During the study period, there was no adverse event or concern about the safety of MR. Conclusions: MR has potential as a preventive or therapeutic tool for improving improve long-term health and reducing cardiovascular morbidity. Keywords: monoglucosyl rutin, flavonoid glycoside, low-density lipoprotein cholesterol, hyperlipidemia, lipid profile Trial registration number: UMIN000047790
单葡糖基芦丁是一种黄酮苷,可改善健康成年人的低密度脂蛋白胆固醇水平:随机对照试验
背景:动脉粥样硬化性心血管疾病(ASCVD)仍然是导致全球死亡的重要因素,影响着全球超过 5.23 亿人。 血脂异常是导致动脉粥样硬化性心血管疾病的首要风险因素之一。因此,优先降低低密度脂蛋白胆固醇(LDL-C)水平对于减轻心血管并发症至关重要。研究目的本研究旨在评估含有单葡糖基芦丁(MR)的膳食补充剂对低至轻度高胆固醇血症患者的降脂活性:这是一项随机、安慰剂对照、双盲、平行组研究,于 2022 年 4 月 20 日至 12 月 24 日进行。研究对象包括 56 名健康的日本成年人,他们的低密度脂蛋白胆固醇水平在 120-139 毫克/分升之间,研究人员使用计算机随机数字生成器将他们随机分配到 MR 组或安慰剂组(n = 28/组)。每天服用 200 毫克 MR 或安慰剂,分成 3 片;要求参与者每餐后用水送服 1 片,连续服用 12 周。研究的主要重点是测量血清低密度脂蛋白胆固醇(LDL-C)水平,并关注血清高密度脂蛋白胆固醇(HDL-C)、总胆固醇和非 HDL-C 水平等次要结果。研究还评估了 12 周干预后血清低密度脂蛋白胆固醇(LDL-C)水平低于 120 毫克/分升的参与者比例。 评估分别在干预 4 周、8 周和 12 周后进行:按方案治疗组(PPS)有 54 名参与者(每组 27 人),改良方案治疗组(mPPS)有 53 名参与者(安慰剂组 26 人;MR 组 27 人)。血清 LDL-C 水平的组间差异有统计学意义(P < 0.05),从干预前到 12 周后下降了 5.0%。低密度脂蛋白胆固醇水平降低的同时,总胆固醇水平、非高密度脂蛋白胆固醇水平和低密度脂蛋白胆固醇/高密度脂蛋白胆固醇比率也有所下降(有统计学意义吗?在研究期间,没有发生任何不良事件,也没有人担心 MR 的安全性:关键词:单葡糖基芦丁;黄酮苷;低密度脂蛋白胆固醇;高脂血症;血脂概况试验注册号:UMIN000047790:UMIN000047790
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