Borderline hyperlipidemia: preventive supplementation with berberine phospholipids to prevent early atherosclerosis evolution.

Maria R Cesarone, Shu Hu, Gianni Belcaro, Umberto Cornelli, Beatrice Feragalli, Marcello Corsi, Valeria Scipione, Claudia Scipione, Roberto Cotellese, Morio Hosoi, David Cox, Francesca Coppa Zuccari
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Abstract

Background: The aim of this pilot, efficacy supplement registry was to use a supplementary management with berberine to control hyperlipidemia. Berberine (Berbevis as Sophy® tablets) was used to control lipids and to evaluate the early evolution of subclinical atherosclerosis in subjects (otherwise healthy, not using drugs) with borderline hyperlipidemia.

Methods: One group used berberine supplementation and a standard management (SM), while a second comparative group used only SM.

Results: No side effects were observed during the 6 months of berberine supplementation. No tolerability problems were reported. All subjects completed the registry. The groups resulted comparable. At 3 and 6 months the average total cholesterol was decreased more with berberine (P<0.05) and HDL was significantly improved (P<0.5). Triglycerides decreased in the berberine groups (P<0.05), more than in controls. Oxidative stress was significantly more decreased with berberine supplementation (P<0.05). Homocysteine (within normal values) were significantly decreased at 3 and 6 months (P<0.05). Fasting glucose was decreased in the berberine group - at 3 and 6 months - in comparison with controls (P<0.05). Also, glycosylated hemoglobin was reduced with berberine (P<0.05) more than in the SM group. Body weight was also significantly more decreased (P<0.05) with berberine supplementation. The fat proportion also decreased significantly more (P<0.05) with the supplement (P<0.05) than in controls only using the SM. Technical athero-specific measurements: the intima-media thickness (IMT) at the carotids (high-resolution ultrasound) in all subjects was stable with berberine and did not significantly change in 6 months. In SM controls the IMT increase was significant superior at 6 months (P<0.05); more time is needed in this type of observations in subjects with minimal initial alterations at the carotid bifurcations. Endothelial function: after occlusion in normal subjects, with normal arteries, reactive hyperemia (RH) - generally - increases section/flow of more than 30% (up to 50%). The included subjects at the first observation, had a minimal increase in RH after occlusion, as an expression of endothelial dysfunction associated to the hyperlipidemia. RH was significantly increased (P<0.05) with berberine, in comparison with controls, at 3 and 6 months.

Conclusions: This pilot, concept registry indicates that oral berberine administration is effective in reducing lipids (also decreasing weight, fat percentage and fasting glucose) in otherwise healthy subjects not using other drugs. A longer study, with more advanced hyperlipidemic subjects is suggested. Predictive analytics suggests that a 12-month study with 100 patients, in more advanced hyperlipidemics, also evaluating the carotid intima-media thickness for the analysis of vascular benefits, may produce a stronger clinical evaluation for this product.

边缘性高脂血症:预防补充小檗碱磷脂以防止早期动脉粥样硬化演变。
背景:本试验的目的,疗效补充登记是使用黄连素辅助管理来控制高脂血症。小檗碱(Berbevis™as Sophy®片剂)用于控制脂质和评估边缘型高脂血症受试者(其他健康,不使用药物)亚临床动脉粥样硬化的早期演变。方法:一组使用小檗碱补充和标准管理(SM),而第二组只使用SM。结果:服用黄连素6个月无不良反应。无耐受性问题报告。所有受试者都完成了登记。各组结果具有可比性。在第3个月和第6个月时,小檗碱降低平均总胆固醇的效果更好(结论:该试点概念注册表明,在不使用其他药物的健康受试者中,口服小檗碱可有效降低脂质(也可降低体重、脂肪百分比和空腹血糖)。建议对高脂血症患者进行更长期的研究。预测分析表明,对100例晚期高脂血症患者进行为期12个月的研究,同时评估颈动脉内膜-中膜厚度以分析血管益处,可能会对该产品产生更强有力的临床评价。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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