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Add-on therapy of herbal formulation rich in standardized fenugreek seed extract in type 2 diabetes mellitus patients with insulin therapy: An efficacy and safety study

机译:富含标准化胡芦巴种子提取物的草药制剂对2型糖尿病胰岛素治疗的附加治疗:疗效和安全性研究

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摘要

Objective: To assess the safety and efficacy of herbal formulation rich in standardized fenugreek seed extract (IND-2) add-on therapy in type 2 diabetes mellitus (T2DM) patients who were on insulin treatment in prospective, single arm, open-label, uncontrolled, multicentre trial. Methods: T2DM patients (n=30) with aged 18-80 years who were stabilized on insulin treatment with fasting blood sugar (FBS) level between 100-140 mg/dL received IND-2 capsules (700 mg, thrice a day) for 16 weeks. The primary endpoints were an assessment of FBS at week 2, 4, 6, 8, 12 and 16. Secondary end-points include post-prandial blood sugar level, glycosylated Hb (HbA1c), reduction in the dose of insulin and number of hypoglycemic attacks, and improvement in lipid profile at various weeks. Safety and adverse events (AEs) were also assessed during the study. Results: Study was completed in twenty T2DM patients, and there was no significant reduction in FBS and post-prandial blood sugar level after add-on therapy of IND-2. However, add-on therapy of IND-2 significantly reduced (P<0.01) the HbA1c values, requirements of insulin and hypoglycemic events as compared with baseline. Total cholesterol, high-density lipoproteins-cholesterol, and low-density lipoprotein-cholesterol levels were significantly increased (P<0.01) after IND-2 add-on therapy. Body weight and safety outcomes did not differ significantly in IND-2 add-on therapy group at week 16. Additionally, add-on therapy of IND-2 did not produce any serious adverse events. Conclusions: The results of present investigation suggest that add-on therapy of IND-2 with insulin in T2DM patients improves glycaemic control through a decrease in levels of HbA1c and number of insulin doses needed per day without an increase in body weight and risk of hypoglycemia. Thus, IND-2 may provide a safe and well-tolerated add-on therapy option for the management of T2DM.
机译:目的:评估富含标准化胡芦巴种子提取物(IND-2)的中草药制剂在前瞻性,单臂,开放标签治疗,接受胰岛素治疗的2型糖尿病(T2DM)患者中的安全性和有效性不受控制的多中心审判。方法:年龄在18-80岁的2型糖尿病患者(n = 30)接受100-140 mg / dL空腹血糖(FBS)胰岛素治疗稳定后,接受IND-2胶囊(700毫克,每天三次)治疗。 16周。主要终点是在第2、4、6、8、12和16周时对FBS的评估。次要终点包括餐后血糖水平,糖基化Hb(HbA1c),胰岛素剂量减少和降糖次数发作,并在不同星期改善脂质分布。在研究期间还评估了安全性和不良事件(AE)。结果:这项研究在20名T2DM患者中完成,并且在IND-2联合治疗后FBS和餐后血糖水平均没有显着降低。但是,与基线相比,IND-2的附加治疗显着降低(P <0.01)HbA1c值,胰岛素需求和降血糖事件。加入IND-2后,总胆固醇,高密度脂蛋白胆固醇和低密度脂蛋白胆固醇水平显着增加(P <0.01)。在第16周时,IND-2附加治疗组的体重和安全性结果无显着差异。此外,IND-2附加治疗未产生任何严重的不良事件。结论:本研究的结果表明,在T2DM患者中用胰岛素补充治疗IND-2可以通过降低HbA1c水平和每天所需的胰岛素剂量数来改善血糖控制,而不会增加体重和低血糖风险。因此,IND-2可以为T2DM的管理提供安全且耐受良好的附加疗法。

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  • 来源
    《亚太热带生物医学杂志(英文版)》 |2018年第9期|446-455|共10页
  • 作者单位

    Department of Scientific Affairs,Indus Biotech Private Limited,1,Rahul Residency,Off Salunke Vihar Road,Kondhwa,Pune - 411048,India;

    Ruby Hall Clinic,40,Sassoon Road,Pune 411001,India;

    Tulip,Opp. Camp Education Society's High School,Camp,Pune-411001,India;

    Department of Scientific Affairs,Indus Biotech Private Limited,1,Rahul Residency,Off Salunke Vihar Road,Kondhwa,Pune - 411048,India;

    Department of Scientific Affairs,Indus Biotech Private Limited,1,Rahul Residency,Off Salunke Vihar Road,Kondhwa,Pune - 411048,India;

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