# Sustained Effects of Glucagon-Like Peptide-1 (GLP-1) Agonists on Blood Pressure in Obesity and Type 2 Diabetes: A Longitudinal Case Study

**Authors:** Jimmy Joseph

PMC · DOI: 10.7759/cureus.88893 · 2025-07-28

## TL;DR

This case study shows that GLP-1 agonists can help lower blood pressure and improve other health markers in obese patients with type 2 diabetes over 18 months.

## Contribution

Demonstrates sustained antihypertensive effects of GLP-1 RAs in a real-world patient with T2DM and obesity.

## Key findings

- Blood pressure remained consistently ≤130/80 mmHg for 18 months without antihypertensive therapy.
- HbA1c and weight were significantly reduced and maintained over the study period.
- Lipid parameters remained stable without additional pharmacological intervention.

## Abstract

Glucagon-like peptide-1 receptor agonists (GLP-1 RAs) confer multiple cardiometabolic benefits beyond glycemic control, including weight reduction and potential cardiovascular protection. This case presents an 18-month follow-up of a 48-year-old obese male with type 2 diabetes mellitus (T2DM) and hypertension, who achieved sustained blood pressure (BP) control and lipid stability on semaglutide following discontinuation of triple antihypertensive therapy. At baseline, the patient had a BMI of 38 kg/m², BP of 156/96 mmHg, and an elevated glycosylated hemoglobin (HbA1c). Semaglutide was initiated at 0.25 mg weekly and titrated to 1 mg over six months. The patient exhibited progressive improvements in glycemic control, body weight, and BP, with HbA1c reduction and weight loss sustained over 18 months. Notably, BP remained consistently ≤130/80 mmHg, and lipid parameters remained stable without additional pharmacotherapy. This case underscores the potential of GLP-1 RAs to exert antihypertensive effects, possibly through weight loss, vascular endothelial function enhancement, and modulation of the renin-angiotensin-aldosterone system (RAAS). These findings support the evolving role of GLP-1 RAs as a multifaceted therapeutic option in managing T2DM with coexisting cardiovascular risk factors.

## Linked entities

- **Chemicals:** semaglutide (PubChem CID 56843331)
- **Diseases:** type 2 diabetes mellitus (MONDO:0005148), obesity (MONDO:0011122)

## Full-text entities

- **Genes:** REN (renin) [NCBI Gene 5972] {aka ADTKD4, HNFJ2, RTD}, GLP1R (glucagon like peptide 1 receptor) [NCBI Gene 2740] {aka GLP-1, GLP-1-R, GLP-1R}, GCG (glucagon) [NCBI Gene 2641] {aka GLP-1, GLP1, GLP2, GRPP}
- **Diseases:** hypertension (MESH:D006973), Obesity (MESH:D009765), T2DM (MESH:D003924), weight (MESH:D015431)
- **Chemicals:** aldosterone (MESH:D000450), glycosylated (-), lipid (MESH:D008055)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12329614/full.md

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Source: https://tomesphere.com/paper/PMC12329614