Albarracin Cesar A, Fuqua Burcham C, Evans Joseph L, Goldfine Ira D
Alpha Therapy Center, 4626 Weber Road, Suite 100, Corpus Christi, TX 78411, USA.
Diabetes Metab Res Rev. 2008 Jan-Feb;24(1):41-51. doi: 10.1002/dmrr.755.
Chromium and biotin play essential roles in regulating carbohydrate metabolism. This randomized, double-blind, placebo-controlled study evaluated the efficacy and safety of the combination of chromium picolinate and biotin on glycaemic control.
Four hundred and forty-seven subjects with poorly controlled type 2 diabetes (HbA(1c) > or = 7.0%) were enrolled and received either chromium picolinate (600 microg Cr(+3)) with biotin (2 mg), or matching placebo, for 90 days in combination with stable oral anti-diabetic agents (OADs). Major endpoints were reductions in HbA(1c), fasting glucose, and lipids. Safety and tolerability were assessed.
Change in HbA(1c) was significantly different between treatment groups (p = 0.03). HbA(1c) in the chromium picolinate/biotin group decreased 0.54%. The decrease in HbA(1c) was most pronounced in chromium picolinate/biotin subjects whose baseline HbA(1c) > or = 10%, and highly significant when compared with placebo (-1.76% vs - 0.68%; p = 0.005). Fasting glucose levels were reduced in the entire chromium picolinate/biotin group versus placebo (-9.8 mg/dL vs 0.7 mg/dL; p = 0.02). Reductions in fasting glucose were also most marked in those subjects whose baseline HbA(1c) > or = 10.0%, and significant when compared to placebo (-35.8 mg/dL vs. 16.2 mg/dL; p = 0.01). Treatment was well tolerated with no adverse effects dissimilar from placebo.
These results suggest that the chromium picolinate/biotin combination, administered as an adjuvant to current prescription anti-diabetic medication, can improve glycaemic control in overweight to obese individuals with type 2 diabetes; especially those patients with poor glycaemic control on oral therapy.
铬和生物素在调节碳水化合物代谢中发挥着重要作用。这项随机、双盲、安慰剂对照研究评估了吡啶甲酸铬和生物素联合使用对血糖控制的疗效和安全性。
招募了447名2型糖尿病控制不佳(糖化血红蛋白≥7.0%)的受试者,给予吡啶甲酸铬(600微克三价铬)和生物素(2毫克)或匹配的安慰剂,为期90天,并联合稳定的口服抗糖尿病药物(OADs)。主要终点是糖化血红蛋白、空腹血糖和血脂的降低。评估了安全性和耐受性。
治疗组之间糖化血红蛋白的变化有显著差异(p = 0.03)。吡啶甲酸铬/生物素组的糖化血红蛋白降低了0.54%。在基线糖化血红蛋白≥10%的吡啶甲酸铬/生物素受试者中,糖化血红蛋白的降低最为明显,与安慰剂相比具有高度显著性(-1.76%对-0.68%;p = 0.005)。整个吡啶甲酸铬/生物素组的空腹血糖水平相对于安慰剂有所降低(-9.8毫克/分升对0.7毫克/分升;p = 0.02)。空腹血糖的降低在基线糖化血红蛋白≥10.0%的受试者中也最为显著,与安慰剂相比具有显著性(-35.8毫克/分升对16.2毫克/分升;p = 0.01)。治疗耐受性良好,没有与安慰剂不同的不良反应。
这些结果表明,作为当前处方抗糖尿病药物的辅助药物,吡啶甲酸铬/生物素联合使用可以改善超重至肥胖的2型糖尿病患者的血糖控制;特别是那些口服治疗血糖控制不佳的患者。