Effects of Liraglutide on Weight Loss, Fat Distribution, and β-Cell Function in Obese Subjects With Prediabetes or Early Type 2 Diabetes.
Diabetes Care · 2017
Last updated 2026-05-28In a study of 62 obese adults with prediabetes or early type 2 diabetes, participants who lost 7% of their body weight either through liraglutide (1.8 mg/day) or lifestyle changes saw similar improvements in blood sugar control. However, those taking liraglutide lost significantly more visceral fat (the fat around organs) than those in the lifestyle group, and their insulin-producing cell function also improved more.
AI summary of the abstract below.
| Journal | Diabetes Care, 2017 |
|---|---|
| Citations | 86 |
| Relative citation ratio | 3.36 |
| NIH percentile | 86 |
| Molecules | liraglutide |
| Conditions studied | Type 2 Diabetes, Obesity |
Abstract
OBJECTIVE: Obesity is associated with an increased risk of type 2 diabetes and cardiovascular complications. The risk depends significantly on adipose tissue distribution. Liraglutide, a glucagon-like peptide 1 analog, is associated with weight loss, improved glycemic control, and reduced cardiovascular risk. We determined whether an equal degree of weight loss by liraglutide or lifestyle changes has a different impact on subcutaneous adipose tissue (SAT) and visceral adipose tissue (VAT) in obese subjects with prediabetes or early type 2 diabetes.
RESEARCH DESIGN AND METHODS: Sixty-two metformin-treated obese subjects with prediabetes or newly diagnosed type 2 diabetes, were randomized to liraglutide (1.8 mg/day) or lifestyle counseling. Changes in SAT and VAT levels (determined by abdominal MRI), insulin sensitivity (according to the Matsuda index), and β-cell function (β-index) were assessed during a multiple-sampling oral glucose tolerance test; and circulating levels of IGF-I and IGF-II were assessed before and after a comparable weight loss (7% of initial body weight).
RESULTS: After comparable weight loss, achieved by 20 patients per arm, and superimposable glycemic control, as reflected by HbA level ( = 0.60), reduction in VAT was significantly higher in the liraglutide arm than in the lifestyle arm ( = 0.028), in parallel with a greater improvement in β-index ( = 0.021). No differences were observed in SAT reduction ( = 0.64). IGF-II serum levels were significantly increased ( = 0.024) only with liraglutide administration, and the increase in IGF-II levels correlated with both a decrease in VAT (ρ = -0.435, = 0.056) and an increase in the β-index (ρ = 0.55, = 0.012).
CONCLUSIONS: Liraglutide effects on visceral obesity and β-cell function might provide a rationale for using this molecule in obese subjects in an early phase of glucose metabolism dysregulation natural history.
Verbatim abstract via PubMed 28912305 ↗
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