Rosenstock J, Rigby S P, Ford D M, Tao B, Chou H S
Dallas Diabetes and Endocrine Center at Medical City, Dallas, TX, USA.
Summit Research Group, Stow, Ohio, USA.
Horm Metab Res. 2014 May;46(5):348-53. doi: 10.1055/s-0033-1358759. Epub 2013 Dec 19.
Colesevelam has shown efficacy in adults with type 2 diabetes mellitus (T2DM) in combination with metformin-, sulfonylurea-, or insulin-based therapy, lowering hemoglobin A1c (HbA1c) and low-density lipoprotein cholesterol levels. A study was conducted to evaluate colesevelam as monotherapy in drug-naïve patients with T2DM. In this randomized, double-blind, placebo-controlled, parallel-group study, adults with T2DM who had inadequate glycemic control (HbA1c ≥7.5% and ≤9.5%) with diet and exercise alone were randomized to receive colesevelam 3.75 g/day (n=176) or placebo (n=181) for 24 weeks. The primary efficacy variable was HbA1c at week 24. Colesevelam as compared to placebo showed significant reductions from baseline in HbA1c (-2.92 mmol/mol [0.3%]; p=0.01) and fasting plasma glucose (-10.3 mg/dl; p=0.04) at week 24 with last observation carried forward. Colesevelam also significantly reduced low-density lipoprotein cholesterol (-11.2%; p<0.0001), total cholesterol (-5.1%; p=0.0005), non-high-density lipoprotein cholesterol (-7.4%; p=0.0001), and apolipoprotein B (-6.5%; p=0.0001) and increased apolipoprotein A-I (+ 2.4%; p=0.04), and triglycerides (+ 9.7%; p=0.03). Colesevelam monotherapy resulted in statistically significant improvements in glycemic and most lipid parameters in subjects with type 2 diabetes, with no new or unexpected safety and tolerability issues. Modest reductions in HbA1c and low-density lipoprotein cholesterol levels with colesevelam further support its use in combination with other antidiabetes agents when treatment targets for these parameters are close but are not quite achieved.ClinicalTrials.gov identifier: NCT00789737.
考来维仑与二甲双胍、磺脲类药物或胰岛素类疗法联合使用时,已显示出对2型糖尿病(T2DM)成人患者有效,可降低糖化血红蛋白(HbA1c)和低密度脂蛋白胆固醇水平。开展了一项研究,以评估考来维仑在初治T2DM患者中的单药治疗效果。在这项随机、双盲、安慰剂对照、平行组研究中,仅通过饮食和运动血糖控制不佳(HbA1c≥7.5%且≤9.5%)的T2DM成人患者被随机分配接受3.75克/天考来维仑(n = 176)或安慰剂(n = 181)治疗24周。主要疗效变量为第24周时的HbA1c。与安慰剂相比,考来维仑在第24周时,末次观察向前结转,HbA1c较基线显著降低(-2.92毫摩尔/摩尔[0.3%];p = 0.01),空腹血糖降低(-10.3毫克/分升;p = 0.04)。考来维仑还显著降低了低密度脂蛋白胆固醇(-11.2%;p<0.0001)、总胆固醇(-5.1%;p = 0.0005)、非高密度脂蛋白胆固醇(-7.4%;p = 0.0001)和载脂蛋白B(-6.5%;p = 0.0001),并升高了载脂蛋白A-I(+2.4%;p = 0.04)和甘油三酯(+9.7%;p = 0.03)。考来维仑单药治疗使2型糖尿病患者的血糖和大多数血脂参数有统计学意义的改善,且无新的或意外的安全性和耐受性问题。考来维仑使HbA1c和低密度脂蛋白胆固醇水平适度降低,进一步支持在这些参数的治疗目标接近但未完全实现时,将其与其他抗糖尿病药物联合使用。ClinicalTrials.gov标识符:NCT00789737。