Angiotensin–Neprilysin Inhibition in Heart Failure with Preserved Ejection Fraction: A Meta-Analysis of Randomized Controlled Trials

•ARNIs reduce NT-proBNP levels and significantly improve KCCQ score.•ARNIs reduce likelihood of hypotension and ≥50% decline in eGFR compared to control.•ARNIs do not improve cardiovascular mortality or all-cause mortality.•ARNIs do not improve HF hospitalization or NYHA class. The effect of sacubit...

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Veröffentlicht in:Current problems in cardiology 2024-01, Vol.49 (1 Pt C), p.102167-102167, Article 102167
Hauptverfasser: Mattumpuram, Jishanth, Maniya, Muhammad Talha, Fernandes, Craig Albert Luke, Sohail, Chaudhry Saad, Ahmed, Aymen, Khan, Rafay, Ali, Kamran
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Sprache:eng
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Zusammenfassung:•ARNIs reduce NT-proBNP levels and significantly improve KCCQ score.•ARNIs reduce likelihood of hypotension and ≥50% decline in eGFR compared to control.•ARNIs do not improve cardiovascular mortality or all-cause mortality.•ARNIs do not improve HF hospitalization or NYHA class. The effect of sacubitril/valsartan on patients with heart failure (HF) with preserved ejection fraction (HFpEF) is a topic of ongoing debate. Medline was queried from inception through the last week of May 2023 for randomized studies assessing the effects of sacubitril/valsartan in patients with HFpEF. For continuous outcomes, we pooled either the geometric mean ratios (gMR) or weighted mean difference (WMD) with 95% confidence intervals (CI). For dichotomous outcomes, we pooled Risk ratios (RR) with 95% CI. Four trials were included (N=8,129). Compared to the control, sacubitril/valsartan was associated with a reduction in NT-proBNP levels (gMR: 0.84, 95% CI 0.80, 0.88) and improvement in KCCQ score (WMD: 0.85, 95% CI: 0.02, 1.67). We observed no differences for HF hospitalization (RR: 0.90, 95% CI: 0.79, 1.01), cardiovascular mortality (RR: 0.83, 95% CI: 0.52, 1.32), all-cause mortality (RR: 0.99, 95% CI: 0.86-1.13) and improvement (RR: 1.15, 95% CI: 0.93, 1.42) or worsening (RR: 0.92, 95% CI: 0.78, 1.09) of NYHA class between the sacubitril/valsartan and comparator group. Sacubitril/valsartan was generally safe, and patients were less likely to have a ≥50% decline in eGFR compared to control (RR: 0.60, 95% CI: 0.39, 0.92). Pooled analysis suggests that sacubitril/valsartan reduces natriuretic peptide levels and improves the quality of life in patients with HFpEF, which may translate into better clinical outcomes as observed by a numerical trend towards improvement in major HF outcomes with sacubitril/valsartan therapy.
ISSN:0146-2806
1535-6280
DOI:10.1016/j.cpcardiol.2023.102167