Department of Internal Medicine, Copenhagen University Hospital, Glostrup, Denmark; Department of Internal Medicine, Copenhagen University Hospital, Amager, Denmark.
Department of Cardiology, Copenhagen University Hospital, Bispebjerg, Denmark.
Atherosclerosis. 2019 Sep;288:60-66. doi: 10.1016/j.atherosclerosis.2019.07.007. Epub 2019 Jul 5.
Atherosclerosis in obesity and type 2 diabetes (T2DM) is associated with low-grade inflammation (LGI) and dyslipidemia, where especially small, dense lipoprotein particles are atherogenic. The glucagon-like peptide-1 receptor agonist, liraglutide, reduces cardiovascular events by poorly understood mechanisms. We investigated the effect of liraglutide combined with metformin on LGI and lipoprotein density profiles in patients with stable coronary artery disease (CAD) and newly diagnosed T2DM.
We conducted a randomized, double-blind, placebo-controlled, cross-over trial over a 12 + 12-week period, with ≥2-week wash-out.
liraglutide/metformin vs. placebo/metformin. Lipoproteins were separated by continuous density gradient ultracentrifugation, and LDL divided into five subfractions between 226 and 270 Å, considering particle size ≤255 Å as the atherogenic pattern. Plasma C-reactive protein and tumor necrosis factor-α were assessed by the enzyme-linked immunosorbent-assay.
28 out of 41 randomized patients completed all visits. Intention-to-treat analysis was performed but one patient had statin dosage and was excluded from the analysis. 95% of the patients were on statin therapy. Overall, liraglutide did not affect lipid subfractions or markers of LGI compared to placebo. The combination of liraglutide and metformin reduced the total LDL subfractions, primarily by reducing the most atherogenic subfraction LDL, and reduced CRP but not TNF-α. Explorative analyses suggested that the subfraction LDL during the wash-out period rebounded significantly at least in a per-protocol analysis of the sub-group of patients starting the liraglutide therapy.
In patients with CAD and newly diagnosed T2DM on stable statin therapy, liraglutide combined with metformin may improve the atherogenic LDL lipid profile and CRP.
肥胖和 2 型糖尿病(T2DM)患者的动脉粥样硬化与低度炎症(LGI)和血脂异常有关,其中小而密的脂蛋白颗粒尤其具有致动脉粥样硬化作用。胰高血糖素样肽-1 受体激动剂利拉鲁肽通过尚未完全明确的机制降低心血管事件的发生风险。我们研究了利拉鲁肽联合二甲双胍对稳定型冠状动脉疾病(CAD)和新诊断的 T2DM 患者 LGI 和脂蛋白密度谱的影响。
我们进行了一项随机、双盲、安慰剂对照、交叉试验,持续 12+12 周,洗脱期≥2 周。
利拉鲁肽/二甲双胍与安慰剂/二甲双胍。通过连续密度梯度超速离心分离脂蛋白,将 LDL 分为 226 至 270Å 之间的五个亚组分,考虑到粒径≤255Å 的 LDL 为致动脉粥样硬化模式。通过酶联免疫吸附试验评估血浆 C 反应蛋白和肿瘤坏死因子-α。
41 名随机患者中有 28 名完成了所有访视。进行了意向治疗分析,但有 1 名患者他汀类药物剂量发生变化,因此被排除在分析之外。95%的患者正在接受他汀类药物治疗。总体而言,与安慰剂相比,利拉鲁肽对脂质亚组分或 LGI 标志物没有影响。与安慰剂相比,利拉鲁肽联合二甲双胍可减少总 LDL 亚组分,主要是通过减少最具致动脉粥样硬化作用的 LDL 亚组分,同时降低 CRP,但不降低 TNF-α。探索性分析表明,在至少基于意向治疗方案的亚组患者的利拉鲁肽治疗开始的洗脱期内,LDL 亚组分明显反弹。
在稳定他汀类药物治疗的 CAD 和新诊断的 T2DM 患者中,利拉鲁肽联合二甲双胍可能改善致动脉粥样硬化的 LDL 血脂谱和 CRP。