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Glucagon-like peptide-1 receptor agonists modestly reduced blood pressure among patients with and without diabetes mellitus: A meta-analysis and meta-regression.
Rivera, Frederick Berro; Lumbang, Grace Nooriza O; Gaid, Danielle Rose Magno; Cruz, Linnaeus Louisse A; Magalong, John Vincent; Bantayan, Nathan Ross B; Lara-Breitinger, Kyla M; Gulati, Martha; Bakris, George.
  • Rivera FB; Department of Medicine, Lincoln Medical Center, New York, New York, USA.
  • Lumbang GNO; Cebu Institute of Medicine, Cebu City, Philippines.
  • Gaid DRM; Cebu Institute of Medicine, Cebu City, Philippines.
  • Cruz LLA; University of the Philippines College of Medicine, Manila, Philippines.
  • Magalong JV; University of the Philippines College of Medicine, Manila, Philippines.
  • Bantayan NRB; University of the Philippines College of Medicine, Manila, Philippines.
  • Lara-Breitinger KM; Department of Cardiovascular Medicine, Mayo Clinic, Rochester, Minnesota, USA.
  • Gulati M; Department of Cardiology, Barbra Streisand Women's Heart Center, Cedars-Sinai Smidt Heart Institute, Los Angeles, California, USA.
  • Bakris G; Department of Medicine, University of Chicago, Chicago, Illinois, USA.
Diabetes Obes Metab ; 26(6): 2209-2228, 2024 Jun.
Article en En | MEDLINE | ID: mdl-38505997
ABSTRACT

AIM:

The cardiovascular benefits provided by glucagon-like peptide-1 receptor agonists (GLP-1RAs) extend beyond weight reduction and glycaemic control. One possible mechanism may relate to blood pressure (BP) reduction. We aim to quantify the BP-lowering effects of GLP1-RAs.

METHODS:

A comprehensive database search for placebo-controlled randomized controlled trials on GLP-1RA treatment was conducted until December 2023. Data extraction and quality assessment were carried out, employing a robust statistical analysis using a random effects model to determine outcomes with a mean difference (MD) in mmHg and 95% confidence intervals (CIs). The primary endpoint was the mean difference in systolic BP (SBP) and diastolic BP. Subgroup analyses and meta-regressions were done to account for covariates.

RESULTS:

Compared with placebo, GLP-1RAs modestly reduced SBP [semaglutide MD -3.40 (95% CI -4.22 to -2.59, p < .001); liraglutide MD -2.61 (95% CI -3.48 to -1.74, p < .001); dulaglutide MD -1.46 (95% CI -2.20 to -0.72, p < .001); and exenatide MD -3.36 (95% CI -3.63 to -3.10, p < .001)]. This benefit consistently increased with longer treatment durations. Diastolic BP reduction was only significant in the exenatide group [MD -0.94 (95% CI -1.78 to -0.1), p = .03]. Among semaglutide cohorts, mean changes in glycated haemoglobin and mean changes in body mass index were directly associated with SBP reduction.

CONCLUSION:

Patients on GLP-1RA experienced modest SBP lowering compared with placebo. This observed effect was associated with weight/body mass index reduction and better glycaemic control, which suggests that BP-lowering is an indirect effect of GLP-1RA and unlikely to be responsible for the benefits.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Presión Sanguínea / Diabetes Mellitus Tipo 2 / Receptor del Péptido 1 Similar al Glucagón / Hipoglucemiantes Límite: Humans Idioma: En Año: 2024 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Presión Sanguínea / Diabetes Mellitus Tipo 2 / Receptor del Péptido 1 Similar al Glucagón / Hipoglucemiantes Límite: Humans Idioma: En Año: 2024 Tipo del documento: Article