Cardiology Division, Massachusetts General Hospital, Boston.
Division of Endocrinology, Diabetes, and Hypertension, Brigham and Women's Hospital, Boston, Massachusetts.
JAMA Cardiol. 2020 Oct 1;5(10):1182-1190. doi: 10.1001/jamacardio.2020.1966.
Recent randomized clinical trials have demonstrated that glucagon-like peptide-1 receptor agonists (GLP-1RAs) reduce cardiovascular events in at-risk individuals with type 2 diabetes. Despite these findings, GLP-1RAs are underused in eligible patients, particularly by cardiologists.
To date, randomized clinical trials of albiglutide, dulaglutide, liraglutide, and injectable semaglutide have reported favorable cardiovascular outcomes. Most recently approved for clinical use, oral semaglutide has a favorable safety profile and is currently undergoing regulatory evaluation and further study for cardiovascular outcomes. Professional society guidelines now recommend GLP-1RA therapy for cardiovascular risk mitigation in patients with type 2 diabetes and established atherosclerotic cardiovascular disease (ASCVD) or multiple ASCVD risk factors, independent of glucose control or background antihyperglycemic therapy (other diabetes medications being used). Additional conditions suitable for GLP-1RA therapy include obesity and advanced chronic kidney disease (estimated glomerular filtration rate <30 mL/min/1.73 m2), for which cardiovascular risk-reducing options are limited. Out-of-pocket costs and secondary advantages (eg, weight loss) may inform shared decision-making discussions regarding potential therapies. GLP-1RA therapy has a favorable safety profile. Its most common adverse effect is gastrointestinal upset, which typically wanes during the early weeks of therapy and may be mitigated by starting at the lowest dose and escalating as tolerated. Depending on baseline glycemic control, sulfonylureas and insulin may need to be decreased before GLP-1RA initiation; without concurrent use of insulin or sulfonylureas, GLP-1RAs are not associated with hypoglycemia. Multidisciplinary follow-up and collaborative care with primary care physicians and/or endocrinologists are important.
Findings from this review suggest that GLP-1RAs are safe, are well tolerated, and improve cardiovascular outcomes, largely independent of their antihyperglycemic properties, but they remain underused by cardiologists. This review provides a practical resource for cardiologists for initiating GLP-1RAs and managing the therapy in patients with type 2 diabetes and established ASCVD or high risk for ASCVD.
最近的随机临床试验表明,胰高血糖素样肽-1 受体激动剂(GLP-1RAs)可降低 2 型糖尿病高危人群的心血管事件。尽管有这些发现,但在符合条件的患者中,GLP-1RAs 的使用仍然不足,尤其是在心脏病专家中。
迄今为止,关于阿必鲁肽、度拉糖肽、利拉鲁肽和可注射的司美格鲁肽的随机临床试验报告了有利的心血管结局。最近批准用于临床使用的口服司美格鲁肽具有良好的安全性,目前正在进行监管评估和进一步的心血管结局研究。专业学会指南现在建议在患有 2 型糖尿病和已确诊的动脉粥样硬化性心血管疾病(ASCVD)或多种 ASCVD 危险因素的患者中,无论血糖控制或背景抗高血糖治疗(正在使用的其他糖尿病药物)如何,都应进行 GLP-1RA 治疗以降低心血管风险。适合 GLP-1RA 治疗的其他条件包括肥胖症和晚期慢性肾脏病(估计肾小球滤过率 <30 mL/min/1.73 m2),对于这些条件,心血管风险降低的选择有限。自付费用和次要优势(例如,体重减轻)可能会影响关于潜在治疗方法的共同决策讨论。GLP-1RA 治疗具有良好的安全性。其最常见的不良反应是胃肠道不适,通常在治疗的早期几周内减轻,并且可以通过从最低剂量开始并根据耐受情况逐渐增加剂量来缓解。根据基线血糖控制情况,在开始 GLP-1RA 治疗之前可能需要减少磺酰脲类药物和胰岛素的用量;如果不同时使用胰岛素或磺酰脲类药物,则 GLP-1RAs 不会引起低血糖。多学科随访以及与初级保健医生和/或内分泌科医生的协作护理非常重要。
本综述的结果表明,GLP-1RAs 是安全的,耐受良好,并改善心血管结局,主要与它们的抗高血糖特性无关,但心脏病专家对其使用仍然不足。本综述为心脏病专家在患有 2 型糖尿病和已确诊的 ASCVD 或 ASCVD 高危患者中启动 GLP-1RA 治疗和管理治疗提供了实用资源。