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Cardiovascular benefits of GLP-1 receptor agonists in patients living with obesity or overweight: a meta-analysis of randomized controlled trials
de Oliveira Almeida, Gustavo; Nienkötter, Thiago Faraco; Balieiro, Caroline Cristine Almeida; Pasqualotto, Eric; Cintra, Júlia Braga; Carvalho, Henrique Champs Porfírio; Silva, Ana Laura Soares; Kabariti, Júlia Camargo; Minucci, Bárbara Silvestre; Bertoli, Edmundo Damiani; Guida, Camila Mota.
Affiliation
  • de Oliveira Almeida, Gustavo; Department of Medicine, Federal University of Triângulo Mineiro. Minas Gerais. BR
  • Nienkötter, Thiago Faraco; University of South Santa Catarina. Santa Catarina. BR
  • Balieiro, Caroline Cristine Almeida; Amazonas State University. Amazonas. BR
  • Pasqualotto, Eric; Federal University of Santa Catarina. Santa Catarina. BR
  • Cintra, Júlia Braga; Department of Medicine, Federal University of Triângulo Mineiro. Minas Gerais. BR
  • Carvalho, Henrique Champs Porfírio; Department of Medicine, Federal University of Triângulo Mineiro. Minas Gerais. BR
  • Silva, Ana Laura Soares; Federal University of Triângulo Mineiro. Minas Gerais. BR
  • Kabariti, Júlia Camargo; Federal University of Triângulo Mineiro. Minas Gerais,. BR
  • Minucci, Bárbara Silvestre; Federal University of Triângulo Mineiro. Minas Gerais. BR
  • Bertoli, Edmundo Damiani; University of South Santa Catarina. Santa Catarina. BR
  • Guida, Camila Mota; Dante Pazzanese Institute of Cardiology. São Paulo. BR
Am. j. cardiovasc. drugs ; maio.2024. ilus
Article in En | CONASS, SES-SP, SESSP-IDPCPROD, SES-SP | ID: biblio-1554136
Responsible library: BR79.1
ABSTRACT

BACKGROUND:

GLP-1 receptor agonists (GLP-1 RAs) have emerged as an effective therapeutic class for weight loss. However, the efficacy of these agents in reducing cardiovascular endpoints among patients living with obesity or overweight is unclear.

METHODS:

We conducted a systematic review and meta-analysis of randomized controlled trials (RCTs) comparing GLP-1 RAs versus placebo in patients with obesity or overweight. We searched PubMed, Cochrane, and Embase databases. A random-effects model was used to calculate risk ratios (RRs) and mean differences (MDs), with 95% confidence intervals (CIs).

RESULTS:

A total of 13 RCTs were included, with 30,512 patients. Compared with placebo, GLP-1 RAs reduced systolic blood pressure (MD - 4.76 mmHg; 95% CI - 6.03, - 3.50; p < 0.001; I2 = 100%) and diastolic blood pressure (MD - 1.41 mmHg; 95% CI - 2.64, - 0.17; p = 0.03; I2 = 100%). GLP-1 RA significantly reduced the occurrence of myocardial infarction (RR 0.72; 95% CI 0.61, 0.85; p < 0.001; I2 = 0%). There were no significant differences between groups in unstable angina (UA; RR 0.84; 95% CI 0.65, 1.07; p = 0.16; I2 = 0%), stroke (RR 0.91; 95% CI 0.74, 1.12; p = 0.38; I2 = 0%), atrial fibrillation (AF; RR 0.49; 95% CI 0.17, 1.43; p = 0.19; I2 = 22%), and deep vein thrombosis (RR 0.30; 95% CI 0.06, 1.40; p = 0.13; I2 = 0%).

CONCLUSIONS:

In patients living with obesity or overweight, GLP-1 RA reduced systolic and diastolic blood pressure and the occurrence of myocardial infarction, with a neutral effect on the occurrence of UA, stroke, AF, and deep vein thrombosis.
Subject(s)

Full text: 1 Collection: 06-national / BR Database: CONASS / SES-SP / SESSP-IDPCPROD Main subject: Glucagon-Like Peptide-1 Receptor Agonists / Obesity Language: En Journal: Am. j. cardiovasc. drugs Year: 2024 Document type: Article

Full text: 1 Collection: 06-national / BR Database: CONASS / SES-SP / SESSP-IDPCPROD Main subject: Glucagon-Like Peptide-1 Receptor Agonists / Obesity Language: En Journal: Am. j. cardiovasc. drugs Year: 2024 Document type: Article