University of Leeds, Leeds Institute of Cardiovascular and Metabolic Medicine, Leeds, United Kingdom.
National Heart, Lung, and Blood Institute, National Institutes of Health, Department of Health and Human Services, Bethesda, Maryland, USA.
J Am Coll Cardiol. 2024 Aug 6;84(6):540-557. doi: 10.1016/j.jacc.2024.04.064.
Type 2 diabetes (T2D) is characterized by insulin resistance (IR) and dysregulated insulin secretion. Glucagon-like peptide-1 receptor agonist liraglutide promotes insulin secretion, whereas thiazolidinedione-pioglitazone decreases IR.
This study aimed to compare the efficacies of increasing insulin secretion vs decreasing IR strategies for improving myocardial perfusion, energetics, and function in T2D via an open-label randomized crossover trial.
Forty-one patients with T2D (age 63 years [95% CI: 59-68 years], 27 [66%] male, body mass index 27.8 kg/m) [95% CI: 26.1-29.5 kg/m)]) without cardiovascular disease were randomized to liraglutide or pioglitazone for a 16-week treatment followed by an 8-week washout and a further 16-week treatment with the second trial drug. Participants underwent rest and dobutamine stress phosphorus magnetic resonance spectroscopy and cardiovascular magnetic resonance for measuring the myocardial energetics index phosphocreatine to adenosine triphosphate ratio, myocardial perfusion (rest, dobutamine stress myocardial blood flow, and myocardial perfusion reserve), left ventricular (LV) volumes, systolic and diastolic function (mitral in-flow E/A ratio), before and after treatment. The 6-minute walk-test was used for functional assessments.
Pioglitazone treatment resulted in significant increases in LV mass (96 g [95% CI: 68-105 g] to 105 g [95% CI: 74-115 g]; P = 0.003) and mitral-inflow E/A ratio (1.04 [95% CI: 0.62-1.21] to 1.34 [95% CI: 0.70-1.54]; P = 0.008), and a significant reduction in LV concentricity index (0.79 mg/mL [95% CI: 0.61-0.85 mg/mL] to 0.73 mg/mL [95% CI: 0.56-0.79 mg/mL]; P = 0.04). Liraglutide treatment increased stress myocardial blood flow (1.62 mL/g/min [95% CI: 1.19-1.75 mL/g/min] to 2.08 mL/g/min [95% CI: 1.57-2.24 mL/g/min]; P = 0.01) and myocardial perfusion reserve (2.40 [95% CI: 1.55-2.68] to 2.90 [95% CI: 1.83-3.18]; P = 0.01). Liraglutide treatment also significantly increased the rest (1.47 [95% CI: 1.17-1.58] to 1.94 [95% CI: 1.52-2.08]; P =0.00002) and stress phosphocreatine to adenosine triphosphate ratio (1.32 [95% CI: 1.05-1.42] to 1.58 [95% CI: 1.19-1.71]; P = 0.004) and 6-minute walk distance (488 m [95% CI: 458-518 m] to 521 m [95% CI: 481-561 m]; P = 0.009).
Liraglutide treatment resulted in improved myocardial perfusion, energetics, and 6-minute walk distance in patients with T2D, whereas pioglitazone showed no effect on these parameters (Lean-DM [Targeting Beta-cell Failure in Lean Patients With Type 2 Diabetes]; NCT04657939).
2 型糖尿病(T2D)的特征是胰岛素抵抗(IR)和胰岛素分泌失调。胰高血糖素样肽-1 受体激动剂利拉鲁肽可促进胰岛素分泌,而噻唑烷二酮吡格列酮则可降低 IR。
本研究旨在通过一项开放标签的随机交叉试验,比较增加胰岛素分泌与降低 IR 策略对 T2D 患者改善心肌灌注、能量和功能的疗效。
41 例 T2D 患者(年龄 63 岁[95%CI:59-68 岁],27 例[66%]男性,体重指数 27.8kg/m)[95%CI:26.1-29.5kg/m)])无心血管疾病,随机分为利拉鲁肽或吡格列酮治疗 16 周,随后洗脱 8 周,再用第二种试验药物治疗 16 周。在治疗前后,参与者进行静息和多巴酚丁胺负荷磷磁共振光谱和心血管磁共振检查,以测量心肌能量指数磷酸肌酸与三磷酸腺苷的比值、心肌灌注(静息、多巴酚丁胺负荷心肌血流和心肌灌注储备)、左心室(LV)容积、收缩和舒张功能(二尖瓣流入 E/A 比值)。6 分钟步行试验用于评估功能。
吡格列酮治疗可显著增加 LV 质量(96g[95%CI:68-105g]增加至 105g[95%CI:74-115g];P=0.003)和二尖瓣流入 E/A 比值(1.04[95%CI:0.62-1.21]增加至 1.34[95%CI:0.70-1.54];P=0.008),并显著降低 LV 向心性指数(0.79mg/mL[95%CI:0.61-0.85mg/mL]降至 0.73mg/mL[95%CI:0.56-0.79mg/mL];P=0.04)。利拉鲁肽治疗可增加应激心肌血流(1.62mL/g/min[95%CI:1.19-1.75mL/g/min]增加至 2.08mL/g/min[95%CI:1.57-2.24mL/g/min];P=0.01)和心肌灌注储备(2.40[95%CI:1.55-2.68]增加至 2.90[95%CI:1.83-3.18];P=0.01)。利拉鲁肽治疗还可显著增加静息(1.47[95%CI:1.17-1.58]增加至 1.94[95%CI:1.52-2.08];P=0.00002)和应激磷酸肌酸与三磷酸腺苷的比值(1.32[95%CI:1.05-1.42]增加至 1.58[95%CI:1.19-1.71];P=0.004)和 6 分钟步行距离(488m[95%CI:458-518m]增加至 521m[95%CI:481-561m];P=0.009)。
利拉鲁肽治疗可改善 T2D 患者的心肌灌注、能量和 6 分钟步行距离,而吡格列酮对这些参数无影响(Lean-DM[针对 2 型糖尿病瘦患者的β细胞衰竭];NCT04657939)。