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未经治疗的中度高胆固醇血症患者中,植物提取物膳食补充剂大剂量对 LDL-胆固醇的影响:一项随机、双盲、安慰剂对照研究。

Effect on LDL-cholesterol of a large dose of a dietary supplement with plant extracts in subjects with untreated moderate hypercholesterolaemia: a randomised, double-blind, placebo-controlled study.

机构信息

Department of Research, Laboratoire Lescuyer, BP 33, 17442, Aytré Cedex, France.

出版信息

Eur J Nutr. 2013 Dec;52(8):1843-52. doi: 10.1007/s00394-012-0486-2. Epub 2012 Dec 25.

Abstract

PURPOSE

To determine the effect of 4 weeks of supplementation, then, withdrawal of a dietary supplement (DS) containing red yeast rice extract, policosanol and artichoke leaf extract at twice the recommended daily dose (6 tablets, 6-TAB) compared to the usual dose (3-TAB) or to a placebo (PLA), on blood lipid profiles and safety biomarkers.

METHODS

Forty-five healthy subjects (15 per group), with untreated hypercholesterolaemia, were included in this randomised, double-blind, placebo-controlled clinical trial.

RESULTS

After 4 weeks of supplementation, LDL-C was significantly lower in 6-TAB (-0.21 g/l; 95 % CI -0.38 to -0.03 g/l; p = 0.0217) and 3-TAB (-0.25 g/l; 95 % CI -0.42 to -0.07 g/l; p = 0.0071) compared to PLA, although no difference in LDL-cholesterol was observed between the two groups, while no effect was seen on triacylglycerol and HDL-cholesterol. Four weeks after the end of supplementation, no difference in LDL-C was seen between the PLA group and the DS-treated groups. The muscle breakdown biomarkers, as well as biomarkers of liver and renal function, were altered by neither dose of the DS. Acute application of the DS on permeabilised skeletal muscle fibres of rats did not induce deleterious effects on mitochondrial function.

CONCLUSIONS

Supplementation with twice the recommended dose of the DS was effective in reducing LDL-cholesterol and appeared safe, but according to the present results, no additional benefit could be achieved compared to the recommended dose.

摘要

目的

确定补充 4 周,然后停止食用两倍于推荐日剂量(6 片,6-TAB)的红曲米提取物、植物固醇和朝鲜蓟叶提取物的膳食补充剂(DS)与常规剂量(3-TAB)或安慰剂(PLA)相比,对血脂谱和安全生物标志物的影响。

方法

将 45 名未经治疗的高胆固醇血症健康受试者(每组 15 名)纳入这项随机、双盲、安慰剂对照临床试验。

结果

补充 4 周后,6-TAB(-0.21 g/l;95 % CI -0.38 至 -0.03 g/l;p = 0.0217)和 3-TAB(-0.25 g/l;95 % CI -0.42 至 -0.07 g/l;p = 0.0071)组的 LDL-C 明显低于 PLA 组,但两组间 LDL-胆固醇无差异,而三酰甘油和高密度脂蛋白胆固醇无变化。补充结束后 4 周,PLA 组与 DS 治疗组之间的 LDL-C 无差异。两种剂量的 DS 均未改变肌肉分解生物标志物以及肝肾功能生物标志物。DS 对大鼠通透性骨骼肌纤维的急性应用未引起线粒体功能的有害影响。

结论

补充两倍推荐剂量的 DS 可有效降低 LDL-胆固醇,且似乎安全,但根据本研究结果,与推荐剂量相比,不能获得额外的益处。

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