PMID- 32743714 OWN - NLM STAT- MEDLINE DCOM- 20211025 LR - 20211025 IS - 1573-7322 (Electronic) IS - 1382-4147 (Linking) VI - 26 IP - 1 DP - 2021 Jan TI - Effect of beta-blockers on heart failure severity in patients with heart failure with preserved ejection fraction: a meta-analysis of randomized controlled trials. PG - 165-171 LID - 10.1007/s10741-020-10013-5 [doi] AB - Patients with heart failure with preserved ejection fraction (HFpEF) are often elderly and likely to have cardiac comorbidities such as coronary artery disease (CAD) and atrial fibrillation (AF). The primary chronic symptom of HFpEF patients is severe exercise intolerance. The inability to adequately increase heart rate during exercise is commonly present in HFpEF patients and contributes to their exercise intolerance. Although beta-blockers are frequently used for the treatment of myocardial ischemia and tachycardia in HFpEF patients, there is a concern that slowing heart rate by beta-blockers may worsen chronotropic incompetence and further exacerbate their symptoms. Although the effect of beta-blockers on heart failure severity in HFpEF patients has been examined in randomized controlled trials (RCTs), results are inconsistent due partly to limited power. We aimed to conduct a meta-analysis of RCTs on the effect of beta-blockers on heart failure severity in HFpEF patients. The search of electronic databases identified 5 RCTs including 538 patients. In pooled analyses, beta-blockers did not significantly change the New York Heart Association (NYHA) class, exercise capacity expressed as metabolic equivalents, or plasma B-type natriuretic peptide (BNP) levels compared with control but with substantial heterogeneity across trials. In meta-regression analyses, the higher proportion of CAD or AF in the included trials was associated with a decrease in NYHA class and BNP levels and with an increase in exercise capacity. Thus, we found no clear beneficial effect of beta-blockers on heart failure severity in HFpEF patients. However, beta-blockers may be beneficial in HFpEF patients with CAD or AF. FAU - Fukuta, Hidekatsu AU - Fukuta H AUID- ORCID: 0000-0002-9577-6586 AD - Core Laboratory, Nagoya City University Graduate School of Medical Sciences, 1 Kawasumi Mizuho-cho Mizuho-ku, Nagoya, 467-8601, Japan. fukuta-h@med.nagoya-cu.ac.jp. FAU - Goto, Toshihiko AU - Goto T AD - Department of Cardiology, Nagoya City University Graduate School of Medical Sciences, Nagoya, Japan. FAU - Wakami, Kazuaki AU - Wakami K AD - Department of Cardiology, Nagoya City University Graduate School of Medical Sciences, Nagoya, Japan. FAU - Kamiya, Takeshi AU - Kamiya T AD - Department of Medical Innovation, Nagoya City University Graduate School of Medical Sciences, Nagoya, Japan. FAU - Ohte, Nobuyuki AU - Ohte N AD - Department of Cardiology, Nagoya City University Graduate School of Medical Sciences, Nagoya, Japan. LA - eng PT - Journal Article PT - Meta-Analysis PT - Review PL - United States TA - Heart Fail Rev JT - Heart failure reviews JID - 9612481 RN - 0 (Adrenergic beta-Antagonists) SB - IM MH - Adrenergic beta-Antagonists/therapeutic use MH - Aged MH - *Atrial Fibrillation MH - *Heart Failure/complications/drug therapy MH - Humans MH - Randomized Controlled Trials as Topic MH - Stroke Volume OTO - NOTNLM OT - Beta-blockers OT - Heart failure OT - Meta-analysis OT - Pharmacotherapy OT - Randomized controlled trial EDAT- 2020/08/04 06:00 MHDA- 2021/10/26 06:00 CRDT- 2020/08/04 06:00 PHST- 2020/08/04 06:00 [pubmed] PHST- 2021/10/26 06:00 [medline] PHST- 2020/08/04 06:00 [entrez] AID - 10.1007/s10741-020-10013-5 [pii] AID - 10.1007/s10741-020-10013-5 [doi] PST - ppublish SO - Heart Fail Rev. 2021 Jan;26(1):165-171. doi: 10.1007/s10741-020-10013-5.