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GLP-1RA 和 SGLT2i 可降低血糖并降低心血管和糖尿病肾病风险。

GLP-1 RAs and SGLT2-Is to Lower Glucose and Reduce the Risk of Cardiovascular and Diabetic Kidney Disease.

机构信息

From the Clinical Assistant Professor, Department of Family Medicine, University of Michigan (LM, JG); Associate Professor, Department of Family Medicine, University of Michigan (LO).

出版信息

J Am Board Fam Med. 2024 May-Jun;37(3):372-382. doi: 10.3122/jabfm.2023.230455R1.

Abstract

The landscape of diabetes management has changed, such that the goal of pharmacotherapy extends beyond glucose-lowering to prioritize risk reduction of cardiovascular disease and diabetic kidney disease. Two newer classes of medications, glucagon-like peptide-1 receptor agonists (GLP-1 RAs) and sodium-glucose cotransporter-2 inhibitors (SGLT2-Is), have become first line therapies for many patients with type 2 diabetes to reduce cardiovascular and renal complications of type 2 diabetes. This review article will describe the mechanism of action, evidence for cardiovascular and kidney outcomes, contraindications, adverse effects, and risk mitigation strategies for the GLP-1 RA and SGLT2-I drug classes. In addition, we will provide a practical approach for primary care clinicians to prescribe, adjust, and combine these medication classes, while considering patient preference, tolerability, comorbidities, cost, and availability.

摘要

糖尿病管理领域已经发生了变化,药物治疗的目标不再仅仅是降低血糖,而是要优先降低心血管疾病和糖尿病肾病的风险。两类较新的药物,胰高血糖素样肽-1 受体激动剂(GLP-1 RAs)和钠-葡萄糖共转运蛋白 2 抑制剂(SGLT2-Is),已成为许多 2 型糖尿病患者的一线治疗药物,以降低 2 型糖尿病的心血管和肾脏并发症。本文将描述 GLP-1 RA 和 SGLT2-I 类药物的作用机制、心血管和肾脏结局的证据、禁忌证、不良反应和风险缓解策略。此外,我们还将为初级保健临床医生提供一种实用的方法,用于开处方、调整和联合使用这些药物类别,同时考虑患者的偏好、耐受性、合并症、成本和可获得性。

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