Blood pressure effects of SGLT2 inhibitors and GLP‐1 receptor agonists: Mechanisms, trial evidence and Real‐world data

Sodium-glucose cotransporter 2 inhibitors (SGLT2is) and glucagon-like peptide-1 receptor agonists (GLP-1 RAs) have transformed the management of type 2 diabetes, obesity and cardiorenal disease. Beyond their established glycaemic and weight-lowering effects, both drug classes consistently lower blood pressure (BP), a benefit that remains relatively underrecognized. This review provides an integrated synthesis of trial evidence, real-world data and meta-analyses examining the antihypertensive effects of SGLT2is and GLP-1 RAs. Across cardiovascular, heart failure, renal and obesity trials, modest but clinically meaningful BP reductions have been observed in diverse populations, including individuals without diabetes. These effects appear largely independent of glycaemic control and offer additive value in high-risk patients with overlapping comorbidities. The totality of evidence supports the strategic incorporation of these agents into future antihypertensive frameworks, warranting further investigation in dedicated blood pressure-focused trials.

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Publication Details

Journal
British Journal of Clinical Pharmacology
Published
2025-12-04
DOI
https://doi.org/10.1002/bcp.70378
Citations
1
Primary Topic
Diabetes Treatment and Management
Type
article
Field-Weighted Citation Impact
1.29
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article

Blood pressure effects of SGLT2 inhibitors and GLP‐1 receptor agonists: Mechanisms, trial evidence and Real‐world data

Joseph E. Blais, Josipa Radić, Marijana Vučković, Andrej Belančić et al.
1 citations
British Journal of Clinical Pharmacology
Diabetes Treatment and Management
1.29
article

Blood pressure effects of SGLT2 inhibitors and GLP‐1 receptor agonists: Mechanisms, trial evidence and Real‐world data

Joseph E. Blais, Josipa Radić, Marijana Vučković, Andrej Belančić, Yusuf Ziya Şener, Mislav Radić, Emina Karahmet Sher, Almir Fajkić
article en
1 citations

Abstract

Sodium-glucose cotransporter 2 inhibitors (SGLT2is) and glucagon-like peptide-1 receptor agonists (GLP-1 RAs) have transformed the management of type 2 diabetes, obesity and cardiorenal disease. Beyond their established glycaemic and weight-lowering effects, both drug classes consistently lower blood pressure (BP), a benefit that remains relatively underrecognized. This review provides an integrated synthesis of trial evidence, real-world data and meta-analyses examining the antihypertensive effects of SGLT2is and GLP-1 RAs. Across cardiovascular, heart failure, renal and obesity trials, modest but clinically meaningful BP reductions have been observed in diverse populations, including individuals without diabetes. These effects appear largely independent of glycaemic control and offer additive value in high-risk patients with overlapping comorbidities. The totality of evidence supports the strategic incorporation of these agents into future antihypertensive frameworks, warranting further investigation in dedicated blood pressure-focused trials.

British Journal of Clinical Pharmacology
University of Sarajevo (BA), University of Rijeka (HR), Gaziantep Children's Hospital (TR), Nottingham Trent University (GB), University of Hong Kong (HK), University of Split (HR)
Openalex Percentile: Top 13%
Diabetes Treatment and Management
1.29
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Blood pressure effects of SGLT2 inhibitors and GLP‐1 receptor agonists: Mechanisms, trial evidence and Real‐world data — Joseph E. Blais, Josipa Radić, et al. · British Journal of Clinical Pharmacology (2025) | TGRS Research Map | TGRS