PMID- 29180457 OWN - NLM STAT- MEDLINE DCOM- 20180716 LR - 20181113 IS - 2047-9980 (Electronic) IS - 2047-9980 (Linking) VI - 6 IP - 12 DP - 2017 Nov 27 TI - Antihypertensive Treatment With beta-Blockade in Patients With Asymptomatic Aortic Stenosis and Association With Cardiovascular Events. LID - 10.1161/JAHA.117.006709 [doi] LID - e006709 AB - BACKGROUND: Patients with aortic stenosis (AS) often have concomitant hypertension. Antihypertensive treatment with a beta-blocker (Bbl) is frequently avoided because of fear of depression of left ventricular function. However, it remains unclear whether antihypertensive treatment with a Bbl is associated with increased risk of cardiovascular events in patients with asymptomatic mild to moderate AS. METHODS AND RESULTS: We did a post hoc analysis of 1873 asymptomatic patients with mild to moderate AS and preserved left ventricular ejection fraction in the SEAS (Simvastatin and Ezetimibe in Aortic Stenosis) study. Propensity-matched Cox regression and competing risk analyses were used to assess risk ratios for all-cause mortality, sudden cardiac death, and cardiovascular death. A total of 932 (50%) patients received Bbl at baseline. During a median follow-up of 4.3+/-0.9 years, 545 underwent aortic valve replacement, and 205 died; of those, 101 were cardiovascular deaths, including 40 sudden cardiovascular deaths. In adjusted analyses, Bbl use was associated with lower risk of all-cause mortality (hazard ratio 0.5, 95% confidence interval 0.3-0.7, P<0.001), cardiovascular death (hazard ratio 0.4, 95% confidence interval 0.2-0.7, P<0.001), and sudden cardiac death (hazard ratio 0.2, 95% confidence interval 0.1-0.6, P=0.004). This was confirmed in competing risk analyses (all P<0.004). No interaction was detected with AS severity (all P>0.1). CONCLUSIONS: In post hoc analyses Bbl therapy did not increase the risk of all-cause mortality, sudden cardiac death, or cardiovascular death in patients with asymptomatic mild to moderate AS. A prospective study may be warranted to determine if Bbl therapy is in fact beneficial. CLINICAL TRIAL REGISTRATION: URL: http://www.clinicaltrials.gov. Unique identifier: NCT00092677. CI - (c) 2017 The Authors. Published on behalf of the American Heart Association, Inc., by Wiley. FAU - Bang, Casper N AU - Bang CN AD - Department of Cardiology, Zealand University Hospital Roskilde, Roskilde, Denmark casperbang@hotmail.com. AD - Department of Medicine, Weill Cornell Medicine, New York, NY. FAU - Greve, Anders M AU - Greve AM AD - Department of Clinical Biochemistry, Rigshospitalet, Copenhagen, Denmark. FAU - Rossebo, Anne B AU - Rossebo AB AD - Department of Cardiology, Oslo University Hospital Ulleval, Oslo, Norway. FAU - Ray, Simon AU - Ray S AD - Department of Cardiology, Manchester Academic Health Sciences Centre, Manchester, United Kingdom. FAU - Egstrup, Kenneth AU - Egstrup K AD - Department of Cardiology, Odense University Hospital, Svendborg, Denmark. FAU - Boman, Kurt AU - Boman K AD - Institution of Public Health and Clinical Medicine, Medicine Skelleftea, Umea University, Skelleftea, Sweden. FAU - Nienaber, Christoph AU - Nienaber C AD - Department of Cardiology, University Hospital, Rostock, Germany. FAU - Okin, Peter M AU - Okin PM AD - Department of Medicine, Weill Cornell Medicine, New York, NY. FAU - Devereux, Richard B AU - Devereux RB AD - Department of Medicine, Weill Cornell Medicine, New York, NY. FAU - Wachtell, Kristian AU - Wachtell K AD - Department of Medicine, Weill Cornell Medicine, New York, NY. AD - Department of Cardiology, Oslo University Hospital, Oslo, Norway. LA - eng SI - ClinicalTrials.gov/NCT00092677 PT - Journal Article PT - Multicenter Study PT - Randomized Controlled Trial DEP - 20171127 PL - England TA - J Am Heart Assoc JT - Journal of the American Heart Association JID - 101580524 RN - 0 (Adrenergic beta-1 Receptor Antagonists) RN - 0 (Anticholesteremic Agents) RN - 0 (Hydroxymethylglutaryl-CoA Reductase Inhibitors) RN - AGG2FN16EV (Simvastatin) RN - EOR26LQQ24 (Ezetimibe) SB - IM MH - Adrenergic beta-1 Receptor Antagonists/*administration & dosage MH - Aged MH - Aged, 80 and over MH - Anticholesteremic Agents/administration & dosage MH - Aortic Valve Stenosis/*complications/mortality/physiopathology MH - Asymptomatic Diseases MH - Blood Pressure/drug effects/*physiology MH - Cause of Death/trends MH - Dose-Response Relationship, Drug MH - Double-Blind Method MH - Drug Therapy, Combination MH - Echocardiography, Doppler/methods MH - Ezetimibe/*administration & dosage MH - Female MH - Heart Ventricles/diagnostic imaging/*physiopathology MH - Humans MH - Hydroxymethylglutaryl-CoA Reductase Inhibitors/administration & dosage MH - Hypertension/*drug therapy/epidemiology/etiology MH - Male MH - Middle Aged MH - Morbidity/trends MH - Propensity Score MH - Simvastatin/*administration & dosage MH - Survival Rate/trends MH - United States/epidemiology PMC - PMC5779004 OTO - NOTNLM OT - aortic valve stenosis OT - arrhythmia (heart rhythm disorders) OT - atrial fibrillation OT - high blood pressure OT - hypertension OT - beta-blocker EDAT- 2017/11/29 06:00 MHDA- 2018/07/17 06:00 PMCR- 2017/12/01 CRDT- 2017/11/29 06:00 PHST- 2017/11/29 06:00 [entrez] PHST- 2017/11/29 06:00 [pubmed] PHST- 2018/07/17 06:00 [medline] PHST- 2017/12/01 00:00 [pmc-release] AID - JAHA.117.006709 [pii] AID - JAH32668 [pii] AID - 10.1161/JAHA.117.006709 [doi] PST - epublish SO - J Am Heart Assoc. 2017 Nov 27;6(12):e006709. doi: 10.1161/JAHA.117.006709.