综合营养配方对代谢综合征患者关键炎症调节因子的影响:一项随机双盲研究

F. He, N. Kumar, F. Marotta, Birbal Singh, A. Khokhlov, Manoj Kumar, A. Italia, A. Lorenzetti, Makoto Kantah, R. Catanzaro
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摘要

据报道,大约四分之一的美国成年人和不到六分之一的欧洲成年人受到代谢综合征的影响。衰老似乎与这种现象的持续增加有关,现在清楚地表明,这种现象与低度促炎级联反应有关。血脂异常是涉及这一多方面代谢设置的一个特征因素,这为非化学生物制药干预提供了新的途径。随机选取代谢综合征患者82例(男66例,女16例,年龄38 ~ 69岁)。符合纳入标准的患者被建议坚持标准的均衡饮食,但没有特定的饮食热量限制或生活方式的改变。两组患者分别给予A药1片/餐,B药1片/餐,疗程均为3个月。医生和患者不知道片剂的含量,只知道一种是P3/GB-2016,而另一种看起来很像安慰剂。第三组25名健康、体重正常、没有任何生化异常的受试者作为对照组。在3个月的观察中,第一组患者的平均HbA1c水平呈下降趋势,但在整个研究期间,该组患者的总胆固醇、低密度脂蛋白胆固醇、非高密度脂蛋白胆固醇和甘油三酯均显著下降(p<0.05)。代谢异常患者血清中MIP1α或MIF浓度均显著高于健康对照组(p<0.01)。P3/GB-2016治疗3个月后,两项指标均显著降低(p<0.01)。然而,MCP-1的循环水平显示出数据的广泛分散,并且在最高(n.s.)的受试者中似乎更高。综上所述,P3/GB-2016似乎是一种有效的控制血脂异常的口服药物和代谢综合征管理中的关键调节调节剂。
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Effect of an Integrated Nutraceutical Formula on Key Inflammatory Regulators in Subjects with Metabolic Syndrome Features: A Randomized, Double-Blind Study
About one fourth of all American adults and a bit less than one sixth of Europeans are reported to be affected by metabolic syndrome. Aging seem associated to a consistent increase of this phenomenon which is now clear to be associated with a low-grade pro-inflammatory cascade. Dyslipidemia is a characteristic factor involved in this multifaceted metabolic setting and this provides new avenues to non-chemical biopharmaceutical interventions. Eighty-two patients (66 males and 16 females, 38-69 as age range) with metabolic syndrome were selected randomly. Patients meeting inclusion criteria were advised to adhere to a standard balanced diet but no specific dietary calorie-restriction or life-style modifications. Two matched patients groups were assigned either to 1 tab/ dinner of drug A and another group received 1 tab/dinner of drug B, both for 3 months. Physicians and patients were blinded as for the content of the tablets except being aware that one being P3/GB-2016 while the other a looking alike placebo. A third group of 25 healthy, normal-weight subjects without any biochemical abnormalities served as control. The mean HbA1c level showed a trend decrease in group I at 3-month observation but this group showed a significant decrease of total and LDL cholesterol, non-HDL aliquot and triglycerides throughout the study period (p<0.05). Serum concentration of either MIP1α or MIF were significantly higher in dysmetabolic patients as compared to healthy control (p<0.01). Treatment with P3/GB-2016 proved to significantly decrease both parameters at 3-month observation (p<0.01). Whereas circulating levels of MCP-1 appeared showed a wide dispersion of data and appearing to be higher in those subjects with highest (n.s.). Overall, P3/GB-2016 seems to be an effective oral agent in controlling dyslipidemia and key regulatory modulator within the management of metabolic syndrome.
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