Louisville Metabolic and Atherosclerosis Research Center, Inc., Louisville, Kentucky 40213, USA.
Endocr Pract. 2011 Nov-Dec;17(6):933-8. doi: 10.4158/EP11218.OR.
To evaluate the glucose- and lipid-altering efficacy of colesevelam hydrochloride (HCl) when added to background metformin therapy in patients with inadequately controlled type 2 diabetes mellitus (T2DM).
This post hoc analysis included patients with T2DM from 3 randomized, double-blind, placebo-controlled pivotal studies who received metformin as part of their background antidiabetes therapy. In the pivotal studies, patients with T2DM were randomly assigned to receive colesevelam HCl (3.75 g/d) or placebo added to existing metformin (26 weeks), sulfonylurea (26 weeks), or insulin (16 weeks) monotherapy or combination therapy, wherein the combination therapies may have included metformin.
In this pooled analysis of 696 patients with T2DM who were receiving metformin monotherapy or metformin combined with other antidiabetes therapies, 355 were randomly assigned to receive colesevelam HCl and 341 to receive placebo. In comparison with placebo, colesevelam HCl significantly reduced hemoglobin A1c (A1C) and fasting plasma glucose (mean treatment difference: -0.50% and -15.7 mg/dL, respectively; P<.001 for both), as well as significantly reduced levels of low-density lipoprotein cholesterol (LDL-C; mean treatment difference: -16.5%), total cholesterol (TC; -5.8%), non-high-density lipoprotein cholesterol (non-HDL-C; -8.2%), and apolipoprotein (apo) B (-7.6%) (P<.0001 for all). Median triglyceride levels were increased with colesevelam HCl (median treatment difference: +12.8%; P<.0001). In comparison with placebo, colesevelam HCl significantly increased apo A-I (mean treatment difference: +3.3%; P<.0001), whereas the mean increase in HDL-C with colesevelam HCl was not significant. Colesevelam HCl therapy was generally well tolerated.
When added to metformin-including therapy, colesevelam HCl significantly reduced A1C and fasting glucose, as well as levels of LDL-C, TC, non-HDL-C, and apo B in patients with inadequately controlled T2DM.
评估盐酸考来维仑(HCl)在二甲双胍背景治疗中对血糖和血脂的影响,用于治疗血糖控制不佳的 2 型糖尿病(T2DM)患者。
本事后分析纳入了来自 3 项随机、双盲、安慰剂对照的关键性研究的 T2DM 患者,这些患者在背景抗糖尿病治疗中接受了二甲双胍治疗。在关键性研究中,T2DM 患者被随机分配接受盐酸考来维仑(3.75g/d)或安慰剂,添加到现有的二甲双胍(26 周)、磺脲类药物(26 周)或胰岛素(16 周)单药或联合治疗中,其中联合治疗可能包括二甲双胍。
在这项纳入 696 例接受二甲双胍单药或二甲双胍联合其他抗糖尿病治疗的 T2DM 患者的汇总分析中,355 例患者被随机分配接受盐酸考来维仑治疗,341 例患者接受安慰剂治疗。与安慰剂相比,盐酸考来维仑显著降低了糖化血红蛋白(A1C)和空腹血糖(平均治疗差异:-0.50%和-15.7mg/dL,均<.001),还显著降低了低密度脂蛋白胆固醇(LDL-C;平均治疗差异:-16.5%)、总胆固醇(TC;-5.8%)、非高密度脂蛋白胆固醇(非-HDL-C;-8.2%)和载脂蛋白(apo)B(-7.6%)(均<.0001)。用盐酸考来维仑治疗后,中位数甘油三酯水平升高(中位数治疗差异:+12.8%;<.0001)。与安慰剂相比,盐酸考来维仑显著增加了载脂蛋白 A-I(平均治疗差异:+3.3%;<.0001),而盐酸考来维仑治疗后 HDL-C 的平均升高并不显著。盐酸考来维仑治疗通常具有良好的耐受性。
在二甲双胍治疗基础上加用盐酸考来维仑可显著降低血糖控制不佳的 2 型糖尿病患者的 A1C 和空腹血糖,以及 LDL-C、TC、非-HDL-C 和 apo B 水平。