目前2型糖尿病的治疗指南和糖化血红蛋白目标:哪些患者最有可能从固定比例的基础胰岛素-胰高血糖素样肽-1受体激动剂组合中获益?

IF 5.4 2区 医学 Q1 ENDOCRINOLOGY & METABOLISM
Kevin Cowart, Nicholas W Carris
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引用次数: 0

摘要

基础胰岛素和胰高血糖素样肽-1受体激动剂(GLP-1 RAs)有两种固定比例组合(FRCs)可用于治疗2型糖尿病(T2D),即利拉鲁肽与去葡糖苷胰岛素和利西塞那肽与甘精胰岛素。FRCs为基础胰岛素和GLP-1 RA的使用提供了一种方便的策略,利用单次注射的互补机制,最大限度地减少治疗负担,改善血糖控制,同时减轻体重增加。对于大多数T2D患者,使用FRC的糖化血红蛋白(HbA1c)目标是
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Current treatment guidelines and glycated haemoglobin goals for type 2 diabetes: Which patients are most likely to benefit from fixed-ratio basal insulin glucagon-like peptide-1 receptor agonist combinations?

Basal insulin and glucagon-like peptide-1 receptor agonists (GLP-1 RAs) are available in two fixed-ratio combinations (FRCs) for the treatment of type 2 diabetes (T2D), insulin degludec with liraglutide and insulin glargine with lixisenatide. FRCs offer a convenient strategy to administer basal insulin and a GLP-1 RA, taking advantage of complementary mechanisms in a single injection to minimize treatment burden and improve glycemic control while mitigating weight gain. For most, a glycated haemoglobin (HbA1c) goal for patients with T2D using a FRC would be <7%, though it can be adjusted based on patient-specific factors. An HbA1c goal of <6.5% is less likely to be appropriate for patients requiring basal insulin, which is included in the FRCs. Ideal candidates for FRCs are those (1) taking oral antihyperglycemic medications only with an HbA1c <10% and <2% away from goal, (2) those on basal insulin and above HbA1c goal, (3) those unwilling or unable to initiate or manage multiple daily injections (i.e., basal-bolus insulin therapy) and (4) those tolerating a GLP-1 RA who require basal insulin to achieve glycemic goals.

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来源期刊
Diabetes, Obesity & Metabolism
Diabetes, Obesity & Metabolism 医学-内分泌学与代谢
CiteScore
10.90
自引率
6.90%
发文量
319
审稿时长
3-8 weeks
期刊介绍: Diabetes, Obesity and Metabolism is primarily a journal of clinical and experimental pharmacology and therapeutics covering the interrelated areas of diabetes, obesity and metabolism. The journal prioritises high-quality original research that reports on the effects of new or existing therapies, including dietary, exercise and lifestyle (non-pharmacological) interventions, in any aspect of metabolic and endocrine disease, either in humans or animal and cellular systems. ‘Metabolism’ may relate to lipids, bone and drug metabolism, or broader aspects of endocrine dysfunction. Preclinical pharmacology, pharmacokinetic studies, meta-analyses and those addressing drug safety and tolerability are also highly suitable for publication in this journal. Original research may be published as a main paper or as a research letter.
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