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Endocrine Abstracts (2019) 63 P562 | DOI: 10.1530/endoabs.63.P562

ECE2019 Poster Presentations Diabetes, Obesity and Metabolism 2 (100 abstracts)

The role of glucagon like peptide - 1 (GLP-1) receptor agonists in the treatment of type 2 diabetes mellitus

Vaishnavi Menon


King’s College London, London, UK.


Background and Aims: Type 2 diabetes mellitus (T2DM) is multifactorial, affected by obesity, blood pressure (BP) and cardiovascular disease (CVD). The therapeutic effects of GLP-1 in managing BP and increasing satiety promoting weight loss prove beneficial against these risk factors. This literature review aims to assess current evidence on the efficacy of GLP-1 receptor agonists (GLP-1RA) for T2DM treatment.

Methods: A PubMed literature search over the preceding 5 years was carried out using keywords including GLP-1 receptor agonists and obesity, hypertension and CVD. A total of 7 studies were analysed.

Results: Obesity: A meta-analysis showed a 3 kg weight reduction by GLP-1RA compared to other active therapies. The SCALE diabetes study confirmed that Liraglutide 3.0mg brought about a 6.0% weight reduction. Liraglutide use sufficiently reduced HbA1c (−1.3) that 57.0% of patients achieved target HbA1c of ≤6.5% compared to placebo (−0.3 HbA1c reduction, 15.0% HbA1c ≤6.5%), and significantly reduced the use of other antiglycaemic drugs also.

BP control: Mice studies showed atrial GLP-1 receptor stimulation promoted secretion of atrial natriuretic peptide and lowering of BP. A 12 week treatment of Liraglutide in obese T2DM patients also lowered BP (−5.30; 95% CI, −7.90 to −2.60; P<0.001) and increased weight loss (−5.03; 95% CI, −5.81 to −3.80; P<0.001).

CV effects: ELIXA study showed no significant change (P=0.81) in heart failure risk with Lixisenatide (hazard ratio 0.96; 95% CI, 0.89 to 1.17) or rate of death (hazard ratio 0.94; 95% CI, 0.75 to 1.23) compared to placebo. LEADER and SUSTAIN-6 studies showed significant reductions in CV risk using Liraglutide (0.87; 95% CI, 0.78 to 0.97; P=0.01) and Semiglutide (0.74; 95% CI, 0.58 to 0.95; P<0.001) respectively, along with reductions in HbA1c, body weight and BP therefore providing cardiac protection.

Conclusion: GLP-1RA, by appetite regulation and BP control, could slow down progression of T2DM and death by CVD. The studies explored in this review suggest that GLP-1RA could have a place much earlier in T2DM treatment than where current guidelines suggest. Further research to assess long term outcomes is recommended.

Volume 63

21st European Congress of Endocrinology

Lyon, France
18 May 2019 - 21 May 2019

European Society of Endocrinology 

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