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What next after basal insulin? Treatment intensification with lixisenatide in Asian patients with type 2 diabetes mellitus.

J Diabetes · 2017

Last updated 2026-05-28

Asian patients with type 2 diabetes often have early insulin deficiencies and higher blood sugar spikes after meals compared to Western patients. Studies on GLP-1 drugs like lixisenatide are limited in Asian populations, but some evidence suggests they may cause more stomach-related side effects, such as nausea or vomiting. This review explores how combining basal insulin with lixisenatide—a short-acting GLP-1 drug—could help manage blood sugar in Asian patients.

AI summary of the abstract below.

JournalJ Diabetes, 2017
Citations3
Relative citation ratio0.16
NIH percentile11
Molecules lixisenatide
Conditions studied Type 2 Diabetes

Abstract

There is increasing evidence that the pathophysiology of type 2 diabetes mellitus (T2DM) in Asian patients differs from that in Western patients, with early phase insulin deficiencies, increased postprandial glucose excursions, and increased sensitivity to insulin. Asian patients may also experience higher rates of gastrointestinal adverse events associated with glucagon-like peptide-1 receptor agonists (GLP-1RAs), such as nausea and vomiting, compared with their Western counterparts. These factors should be taken into consideration when selecting therapy for basal insulin treatment intensification in Asian patients. However, the majority of studies to establish various agents for treatment intensification in T2DM have been conducted in predominantly Western populations, and the levels of evidence available in Chinese or Asian patients are limited. This review discusses the different mechanisms of action of short-acting, prandial, and long-acting GLP-1RAs in addressing hyperglycemia, and describes the rationale and available clinical data for basal insulin in combination with the short-acting prandial GLP-1RA lixisenatide, with a focus on treatment of Asian patients with T2DM.

Verbatim abstract via PubMed 27976513 ↗

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