Institute for Clinical Research and Development, Mainz, Germany.
Diabetes Technol Ther. 2011 Jun;13(6):637-43. doi: 10.1089/dia.2010.0233. Epub 2011 Apr 2.
Dyslipidemia in patients with type 2 diabetes is characterized by elevated triglyceride levels, decreased high-density lipoprotein (HDL) cholesterol, and a predominance of small dense low-density lipoprotein (LDL) particles. Also, patients suffer from β-cell dysfunction, chronic systemic inflammation, increased hormonal visceral adipose tissue activity, and an increased risk of cardiovascular events. The aim of our study was to investigate the effect of a fixed pioglitazone + metformin (PM) combination (vs. glimepiride + metformin [GM]) on diabetic dyslipidemia.
A total of 288 type 2 diabetes patients completed this double-blind parallel study (187 men, 101 women; age [mean ± SD], 59 ± 10 years; body mass index, 32.6 ± 5.1 kg/m(2); hemoglobin A1c [HbA1c], 7.3 ± 0.8%). They were randomized to PM or GM for 6 months. Observation parameters at baseline and end point included HDL, LDL, triglycerides, fasting insulin, fasting glucose, total adiponectin, intact proinsulin, and high-sensitivity C-reactive peptide (hsCRP).
HDL increased in the PM group by 0.08 ± 0.25 mmol/L (GM, -0.01 ± 0.2.8 mmol/L; P < 0.001 vs. PM), whereas LDL increased in both groups (GM, 0.25 ± 0.90 mmol/L; PM, 0.29 ± 0.66 mmol/L; difference not significant between groups). Improvements were seen for triglycerides (PM, -0.47 ± 1.30; GM, -0.19 ± 1.39 mmol/L), HbA1c (PM, -0.8 ± 0.9%; GM, -1.0 ± 0.9%), and glucose (PM, -1.2 ± 2.1; GM, -1.2 ± 2.2 mmol/L). Decreases in fasting insulin (PM, -5.2 ± 11.9; GM, -0.1 ± 9.8 μU/mL; P < 0.001 between groups), hsCRP (PM, -0.9 ± 1.9; GM, 0.0 ± 1.8 mg/L; P < 0.001), and fasting intact proinsulin (PM, -5.5 ± 11.1; GM, -0.1 ± 10.0 pmol/L; P < 0.001) and an increase in adiponectin (PM, +6.8 ± 6.4 mg/L; GM, +0.7 ± 2.7 mg/L; P < 0.001) were seen in the PM arm, only.
With comparable glycemic control, the fixed PM combination was more efficacious on HDL cholesterol improvement than the GM combination. Additional positive effects were observed for biomarkers of lipid metabolism, β-cell function, activity of the visceral adipose tissue, and chronic systemic inflammation.
2 型糖尿病患者的血脂异常表现为甘油三酯水平升高、高密度脂蛋白(HDL)胆固醇降低以及小而密的低密度脂蛋白(LDL)颗粒增多。此外,患者还伴有β细胞功能障碍、慢性全身炎症、激素性内脏脂肪组织活性增加以及心血管事件风险增加。我们的研究旨在探讨固定吡格列酮+二甲双胍(PM)联合用药(与格列美脲+二甲双胍[GM]相比)对糖尿病血脂异常的影响。
共有 288 例 2 型糖尿病患者完成了这项双盲平行研究(男性 187 例,女性 101 例;年龄[平均值±标准差],59±10 岁;体重指数,32.6±5.1kg/m2;糖化血红蛋白[HbA1c],7.3±0.8%)。他们被随机分配至 PM 或 GM 组,治疗 6 个月。基线和终点的观察参数包括 HDL、LDL、甘油三酯、空腹胰岛素、空腹血糖、总脂联素、完整胰岛素原和高敏 C 反应蛋白(hsCRP)。
PM 组的 HDL 升高了 0.08±0.25mmol/L(GM 组降低了 0.01±0.25mmol/L,P<0.001),而两组的 LDL 均升高(GM 组升高了 0.25±0.90mmol/L,PM 组升高了 0.29±0.66mmol/L,两组间差异无统计学意义)。甘油三酯(PM 组降低了 0.47±1.30mmol/L,GM 组降低了 0.19±1.39mmol/L)、HbA1c(PM 组降低了 0.8±0.9%,GM 组降低了 1.0±0.9%)和血糖(PM 组降低了 1.2±2.1mmol/L,GM 组降低了 1.2±2.2mmol/L)均有改善。空腹胰岛素(PM 组降低了 5.2±11.9μU/mL,GM 组降低了 0.1±9.8μU/mL,两组间差异具有统计学意义,P<0.001)、hsCRP(PM 组降低了 0.9±1.9mg/L,GM 组无变化 0.0±1.8mg/L,P<0.001)和空腹完整胰岛素原(PM 组降低了 5.5±11.1pmol/L,GM 组降低了 0.1±10.0pmol/L,P<0.001)水平降低,脂联素(PM 组增加了 6.8±6.4mg/L,GM 组增加了 0.7±2.7mg/L,P<0.001)水平升高,这些改善仅见于 PM 组。
在血糖控制相当的情况下,固定 PM 联合用药在改善 HDL 胆固醇方面比 GM 联合用药更有效。此外,还观察到对脂质代谢、β细胞功能、内脏脂肪组织活性和慢性全身炎症的生物标志物有额外的积极影响。