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Angiotensin Receptor-Neprilysin Inhibitor Effects on Atherosclerotic Cardiovascular Disease Events: A Meta-Analysis of Randomized Controlled Trials.
Ravani, Lis Victoria; Gewehr, Douglas Mesadri; Calomeni, Pedro; Gauza, Mateus de Miranda; Pereira, Jussara; Cardoso, Rhanderson; Ribeiro, Henrique Barbosa; Bocchi, Edimar.
Affiliation
  • Ravani LV; Department of Medicine, University of São Paulo Medical School, São Paulo, Brazil. Electronic address: lis.ravani@fm.usp.br.
  • Gewehr DM; Curitiba Heart Institute (INCOR Curitiba) and Denton Cooley Institute of Research Science and Technology,Curitiba, Paraná, Brazil.
  • Calomeni P; Department of Medicine, University of São Paulo Medical School, São Paulo, Brazil.
  • Gauza MM; Department of Medicine, Universidade da Região de Joinville, Joinville, Santa Catarina, Brazill.
  • Pereira J; Goiânia General Hospital, Goiânia, Goiás, Brazil.
  • Cardoso R; Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts.
  • Ribeiro HB; Department of Medicine, Universidade da Região de Joinville, Joinville, Santa Catarina, Brazill; Instituto do Coração, Hospital das Clínicas HCFMUSP, Faculdade de Medicina, Universidade de São Paulo, São Paulo, Brazil.
  • Bocchi E; Department of Medicine, Universidade da Região de Joinville, Joinville, Santa Catarina, Brazill; Instituto do Coração, Hospital das Clínicas HCFMUSP, Faculdade de Medicina, Universidade de São Paulo, São Paulo, Brazil.
Am J Cardiol ; 205: 259-268, 2023 10 15.
Article in En | MEDLINE | ID: mdl-37619492
ABSTRACT
Sacubitril-valsartan is an angiotensin receptor-neprilysin inhibitor (ARNI) associated with a decreased risk of death and hospitalization for selected patients with heart failure (HF). However, its association with improved atherosclerotic cardiovascular disease (ASCVD) events remains unclear. We performed a meta-analysis to evaluate the association of ARNI with ASCVD events in patients with HF. We systematically searched PubMed, Embase, Cochrane, and ClinicalTrials.gov for studies comparing ARNIs with angiotensin-converting enzyme inhibitors (ACEIs) or angiotensin receptor blockers (ARBs) in terms of myocardial infarction, stroke, angina pectoris, peripheral artery disease, and the composite end point in patients with HF. A total of 8 randomized controlled trials were included, with 17,541 patients assigned to either the ARNI (8,764 patients) or ACEi/ARB (8,777 patients) groups. The incidence of composite end point (risk ratio [RR] 1.03, 95% confidence interval [CI] 0.93 to 1.13, p = 0.63), myocardial infarction (RR 1.02, 95% CI 0.81 to 1.30, p = 0.85), angina pectoris (RR 0.96, 95% CI 0.80 to 1.17, p = 0.70), and stroke (RR 0.99, 95% CI 0.85 to 1.16, p = 0.93) were not statistically different between the ARNI and ACEi/ARB groups. However, ARNI was associated with a higher incidence of peripheral artery disease (RR 1.63, 95% CI 1.05 to 2.52, p = 0.03). In conclusion, this meta-analysis found no association between ARNI therapy and improved ASCVD events in patients with HF.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Cardiovascular Diseases / Stroke / Atherosclerosis / Peripheral Arterial Disease / Heart Failure / Myocardial Infarction Type of study: Clinical_trials / Systematic_reviews Limits: Humans Language: En Journal: Am J Cardiol Year: 2023 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Cardiovascular Diseases / Stroke / Atherosclerosis / Peripheral Arterial Disease / Heart Failure / Myocardial Infarction Type of study: Clinical_trials / Systematic_reviews Limits: Humans Language: En Journal: Am J Cardiol Year: 2023 Document type: Article
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