Tjokroprawiro Askandar, Murtiwi Sri, Tjandrawinata Raymond R
J Complement Integr Med. 2016 Dec 1;13(4):413-420. doi: 10.1515/jcim-2016-0031.
BackgroundDLBS3233, a combined bioactive fraction of Cinnamomum burmanii and Lagerstroemia speciosa, has preclinically demonstrated its beneficial effects on glucose and lipid metabolism through the upregulation of insulin-signal transduction. This study evaluated the clinical efficacy of an add-on therapy with DLBS3233 in type-2 diabetes mellitus subjects inadequately controlled by metformin and other oral antidiabetes. MethodsThis was an open and prospective clinical study for 12 weeks of therapy, involving type-2 diabetes mellitus patients who had been treated with two oral antidiabetic agents for at least 3 months prior to screening, yet, with HbA1c level was still beyond 7.0 %. DLBS3233 was given orally at the dose of 100 mg once daily in addition to their baseline oral antidiabetes medication. The primary end point was the reduction of HbA1c level; and the secondary end points were changes of fasting and 1-h postprandial glucose, homeostatic model assessment-insulin resistance, adiponectin, and lipid profile, from their respective baseline. Results After 12 weeks of treatment, the HbA1c level was reduced by 0.65±1.58 % (p=0.001) from baseline (9.67±2.11 %); while the 1-h-PG level was reduced by -1.45±3.89 mmol/L (p=0.021) from baseline (15.29±4.49 mmol/L). Insulin sensitivity, lipid profile and adiponectin level were improved to a considerable extent. DLBS3233 did not adversely affect body weight, liver, and renal function. Most adverse events observed were tolerably mild and they all had been resolved by the end of the study. ConclusionsThe add-on oral antidiabetes therapy with DLBS3233 at the dose of 100 mg once daily helped type-2 diabetes mellitus patients to improve their glycemic control, enhance insulin sensitivity, lipid profile, and adiponectin level. In addition, DLBS3233 treatment concomitantly with other oral antidiabetic agents was proven safe and tolerable in type-2 diabetes subjects.
DLBS3233是阴香和紫薇的一种联合生物活性成分,临床前研究表明其可通过上调胰岛素信号转导对葡萄糖和脂质代谢产生有益作用。本研究评估了在接受二甲双胍和其他口服抗糖尿病药物治疗但控制不佳的2型糖尿病患者中,加用DLBS3233进行治疗的临床疗效。
这是一项为期12周的开放、前瞻性临床研究,纳入在筛查前至少3个月接受两种口服抗糖尿病药物治疗但糖化血红蛋白(HbA1c)水平仍超过7.0%的2型糖尿病患者。除基线口服抗糖尿病药物外,给予DLBS3233口服,剂量为每日1次,每次100mg。主要终点是HbA1c水平的降低;次要终点是空腹及餐后1小时血糖、稳态模型评估胰岛素抵抗、脂联素和血脂谱相对于各自基线水平的变化。
治疗12周后,HbA1c水平较基线(9.67±2.11%)降低了0.65±1.58%(p=0.001);餐后1小时血糖水平较基线(15.29±4.49mmol/L)降低了-1.45±3.89mmol/L(p=0.021)。胰岛素敏感性、血脂谱和脂联素水平有相当程度的改善。DLBS3233对体重、肝脏和肾功能无不良影响。观察到的大多数不良事件为轻度且可耐受,在研究结束时均已缓解。
每日1次、每次100mg的DLBS3233加用口服抗糖尿病药物治疗有助于2型糖尿病患者改善血糖控制、增强胰岛素敏感性、改善血脂谱和提高脂联素水平。此外,在2型糖尿病患者中,DLBS3233与其他口服抗糖尿病药物联合治疗被证明是安全且可耐受的。