首页> 外文OA文献 >A Randomized, Double-Blinded, Placebo-Controlled, Clinical Study of the Effects of a Nutraceutical Combination (LEVELIP DUO®) on LDL Cholesterol Levels and Lipid Pattern in Subjects with Sub-Optimal Blood Cholesterol Levels (NATCOL Study)
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A Randomized, Double-Blinded, Placebo-Controlled, Clinical Study of the Effects of a Nutraceutical Combination (LEVELIP DUO®) on LDL Cholesterol Levels and Lipid Pattern in Subjects with Sub-Optimal Blood Cholesterol Levels (NATCOL Study)

机译:一种随机,双盲,安慰剂控制,营养素组合(LevelIPDuo®)对具有次优血胆固醇水平的LDL胆固醇水平和脂质模式的影响的临床研究(Natcol研究)

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摘要

Phytosterols and red yeast rice are largely studied cholesterol-lowering nutraceuticals, respectively inhibiting the bowel absorption and liver synthesis of cholesterol. Our aim was to test the effect of combined nutraceutical-containing phytosterols and red yeast rice vs. a placebo on the lipid profile. We performed a parallel arms, double-blind, placebo-controlled clinical trial, randomizing 88 moderately hypercholesterolemic subjects to treatment with a combined nutraceutical containing phytosterols (800 mg) and red yeast rice, standardized to contain 5 mg of monacolins from Monascus purpureus, with added niacin (27 mg) and policosanols (10 mg) (LEVELIP DUO®), or placebo. The mean LDL-Cholesterol (LDL-C) change at Week 8 was −32.5 ± 30.2 mg/dL (−19.8%) in the combined nutraceutical group and 2.5 ± 19.4 mg/dL (2.3%) in the placebo group. The estimated between-group difference of −39.2 mg/dL (95% CI: −48.6; −29.8) indicates a statistically significant difference between treatments in favor of the combined nutraceutical (p < 0.0001). Total Cholesterol (TC), non-HDL cholesterol (non-HDL-C), Apolipoprotein B, TC/HDL-C and LDL-C/HDL-C improved in a similar way in the combined nutraceutical group only. No significant changes in other clinical and laboratory parameters were observed. In conclusion, the tested combined nutraceutical was well tolerated, while significantly reducing the plasma levels of LDL-C, TC, non-HDL-C, ApoB, TC/HDL-C and LDL-C/HDL-C ratios in mildly hypercholesterolemic patients. Trial registration (ClinicalTrials.gov): NCT03739242.
机译:植物甾醇和红酵母大米主要研究了降低胆固醇的营养制品,分别抑制胆固醇的肠道吸收和肝脏合成。我们的目的是测试含营养素植物植物甾醇和红酵母水稻与脂质型材的安慰剂的影响。我们进行了平行的武器,双盲,安慰剂控制的临床试验,随机化88个适度的高胆固醇受试者以含有含有植物植物甾醇(800mg)和红酵母大米的组合治疗,标准化为含有5毫克的莫斯科斯紫癜的单甘油蛋白。添加烟酸(27mg)和萘糖醇(10mg)(SextIPDuo®)或安慰剂。在第8周的平均LDL-胆固醇(LDL-C)的变化为-32.5±30.2mg / dl(-19.8%),在安慰剂组中为2.5±19.4mg / dl(2.3%)。估计的-39.2mg / dl(95%Ci:-48.6; -29.8)之间的组差异表明治疗有利于组合的营养素(P <0.0001)之间的统计学上显着差异。总胆固醇(TC),非HDL胆固醇(非HDL-C),载脂蛋白B,TC / HDL-C和LDL-C / HDL-C仅在组合的营养群组中以类似的方式改善。没有观察到其他临床和实验室参数的显着变化。总之,测试的组合营养素耐受良好,同时在轻微的高胆固醇患者中显着降低LDL-C,TC,非HDL-C,APOB,TC / HDL-C和LDL-C / HDL-C比率的血浆水平。试验登记(ClinicalTrials.gov):NCT03739242。

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