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GLP-1 Receptor Agonists Are Associated with Reduced Ascending Aorta Dilatation in Patients with Type 2 Diabetes: A
Celestino Sardu1,2, Ludovica Vittoria Marfella1, Carlo Fumagalli1
1Department of Advanced Medical and Surgical Sciences, University of Campania "Luigi Vanvitelli", 80126 Naples, Italy.
Abstract:
The aim was to assess the impact of glucagon-like peptide-1 receptor agonists (GLP-1 RA) treatment on the progression of ascending aorta dilatation in patients with type 2 diabetes mellitus (T2DM). A total of 127 T2DM patients with subclinical ascending aortic dilatation (35-45 mm) were prospectively enrolled. Fifty-seven initiated GLP-1 RA therapy (liraglutide, semaglutide, or dulaglutide), while 70 continued on standard care. Ascending aortic diameter was measured by computed tomography angiography (CTA) at baseline and 24 months, alongside circulating markers of vascular remodeling: matrix metalloproteinase-9 (MMP-9), tissue inhibitor of metalloproteinases-1 (TIMP-1), C-reactive protein (CRP), and osteoprotegerin (OPG). Progression of aortic dilatation was significantly lower in the GLP-1 RA group compared with controls (+0.36 ± 0.20 mm vs. +1.05 ± 0.28 mm; p < 0.001). Therapy correlated with decreased MMP-9 and CRP (p < 0.01) and increased TIMP-1 and OPG (p < 0.05). The use of GLP-1 RA was an independent predictor of low progression, even in multivariate models after adjusting for demographic, metabolic, and biomarker data. GLP-1 RA therapy was associated with reduced progression of ascending aortic dilatation in T2DM, supporting a potential vasoprotective role beyond glucose lowering.
Insights
Glucagon-like peptide-1 receptor agonists (GLP-1 RA) slow ascending aorta dilatation in type 2 diabetes mellitus (T2DM) patients. This treatment may offer vasoprotective benefits beyond blood sugar control.
Area of Science:
- Cardiovascular Medicine
- Endocrinology
- Diabetes Research
Background:
- Ascending aorta dilatation is a concern in type 2 diabetes mellitus (T2DM).
- Glucagon-like peptide-1 receptor agonists (GLP-1 RA) are used for T2DM management.
- The vascular effects of GLP-1 RA beyond glycemic control are under investigation.
Purpose of the Study:
- To evaluate the impact of GLP-1 RA therapy on the progression of subclinical ascending aortic dilatation in T2DM patients.
- To explore potential vasoprotective mechanisms of GLP-1 RA in this context.
Main Methods:
- Prospective study of 127 T2DM patients with subclinical ascending aortic dilatation.
- Comparison between patients initiating GLP-1 RA (liraglutide, semaglutide, dulaglutide) and those on standard care.
- Measurement of ascending aortic diameter via computed tomography angiography (CTA) at baseline and 24 months.
- Assessment of vascular remodeling markers: MMP-9, TIMP-1, CRP, and OPG.
Main Results:
- Significantly lower progression of aortic dilatation in the GLP-1 RA group compared to controls (+0.36 mm vs. +1.05 mm; p < 0.001).
- GLP-1 RA therapy correlated with reduced MMP-9 and CRP levels.
- GLP-1 RA therapy correlated with increased TIMP-1 and OPG levels.
- GLP-1 RA use was an independent predictor of slower aortic dilatation progression.
Conclusions:
- GLP-1 RA therapy is associated with reduced progression of ascending aortic dilatation in T2DM patients.
- These findings suggest a potential vasoprotective role for GLP-1 RA, independent of glucose-lowering effects.
- GLP-1 RA may represent a therapeutic option to mitigate cardiovascular risk in T2DM patients with aortic dilatation.
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