Babish John G, Dahlberg Clinton J, Ou Joseph J, Keller William J, Gao Wei, Kaadige Mohan R, Brabazon Holly, Lamb Joseph, Soudah Hani C, Kou Xiaolan, Zhang Zhe, Pacioretty Linda M, Tripp Matthew L
a Bionexus, Ltd., 53 Brown Road, Suite B, Ithaca, NY 14850, USA.
b Hughes Center for Research and Innovation, Nature's Sunshine Products, 2500 Executive Parkway, Lehi, UT 84043, USA.
Can J Physiol Pharmacol. 2016 Dec;94(12):1257-1266. doi: 10.1139/cjpp-2016-0062. Epub 2016 May 31.
We examined the clinical safety and efficacy of F105 in 11 subjects with moderate dyslipidemia. F105 is a combination of bergamot fruit extract (Citrus bergamia, BFE) and 9 phytoextracts selected for their ability to improve the antioxidant and anti-inflammatory activity of BFE. In vitro F105 exhibited a synergistic inhibition of oxygen radical absorbing capacity, peroxynitrite formation, and myeloperoxidase activity. Following 12 weeks of F105 daily, no treatment-related adverse events or changes in body mass were seen. Statistically significant changes were noted in total cholesterol (-7.3%), LDL-cholesterol (-10%), non-HDL cholesterol (-7.1%), cholesterol/HDL (-26%), and apolipoprotein B (-2.8%). A post hoc analysis of 8 subjects with HbA1c > 5.4 and HOMA-IR score > 2 or elevated triglycerides revealed additional statistically significant changes in addition to those previously observed in all subjects including triglycerides (-27%), oxLDL (-19%), LDL/HDL (-25%), triglycerides/HDL (-27%), oxLDL/HDL (-25%), and PAI-1 (-37%). A follow-up case report of a 70-year-old female patient, nonresponsive to statin therapy and placed on F105 daily, demonstrated improved cardiometabolic variables over 12 weeks similar to the subgroup. In summary, F105 was clinically well-tolerated and effective for ameliorating dyslipidemia in subjects with moderate cardiometabolic risk factors, particularly in the individuals with HbA1c > 5.4%.
我们研究了F105对11名中度血脂异常患者的临床安全性和疗效。F105是佛手柑果实提取物(Citrus bergamia,BFE)与9种植物提取物的组合,这些植物提取物因其能提高BFE的抗氧化和抗炎活性而被选用。在体外,F105对氧自由基吸收能力、过氧亚硝酸盐形成和髓过氧化物酶活性表现出协同抑制作用。每日服用F105 12周后,未观察到与治疗相关的不良事件或体重变化。总胆固醇(-7.3%)、低密度脂蛋白胆固醇(-10%)、非高密度脂蛋白胆固醇(-7.1%)、胆固醇/高密度脂蛋白(-26%)和载脂蛋白B(-2.8%)有统计学显著变化。对8名糖化血红蛋白>5.4且胰岛素抵抗指数>2或甘油三酯升高的受试者进行的事后分析显示,除了之前在所有受试者中观察到的变化外,还有其他统计学显著变化,包括甘油三酯(-27%)、氧化低密度脂蛋白(-19%)、低密度脂蛋白/高密度脂蛋白(-25%)、甘油三酯/高密度脂蛋白(-27%)、氧化低密度脂蛋白/高密度脂蛋白(-25%)和纤溶酶原激活物抑制剂-1(-37%)。一名70岁女性患者的随访病例报告显示,该患者对他汀类药物治疗无反应,改为每日服用F105,12周内心血管代谢变量得到改善,与该亚组情况相似。总之,F105在临床上耐受性良好,对改善具有中度心血管代谢危险因素的受试者的血脂异常有效,尤其是对糖化血红蛋白>5.4%的个体。