Effect of lipid lowering on new-onset atrial fibrillation in patients with asymptomatic aortic stenosis: The Simvastatin and Ezetimibe in Aortic Stenosis (SEAS) study

被引:14
作者
Bang, Casper N. [1 ,2 ]
Greve, Anders M. [1 ,2 ]
Boman, Kurt [3 ]
Egstrup, Kenneth [4 ]
Gohlke-Baerwolf, Christa [5 ]
Kober, Lars [1 ]
Nienaber, Christoph A. [6 ]
Ray, Simon [7 ]
Rossebo, Anne B. [8 ]
Wachtell, Kristian [1 ,2 ]
机构
[1] Rigshosp, Dept Cardiol, Ctr Heart, DK-2100 Copenhagen, Denmark
[2] Gentofte Univ Hosp, Dept Cardiol, Hellerup, Denmark
[3] Umea Univ, Inst Publ Hlth & Clin Med, Umea, Sweden
[4] Svendborg Hosp, Dept Med, Svendborg, Denmark
[5] Herz Zentrum Bad Krozingen, Dept Cardiol, Bad Krozingen, Germany
[6] Univ Klinikum Rostock, Dept Cardiol, Rostock, Germany
[7] Manchester Acad Hlth Sci Ctr, Dept Cardiol, Manchester, Lancs, England
[8] Oslo Univ Hosp, Dept Cardiol, Oslo, Norway
关键词
ENDOTHELIAL FUNCTION; VALVE STENOSIS; STATIN THERAPY; MYOCARDIAL-INFARCTION; RISK-FACTORS; IMPACT; RECOMMENDATIONS; INFLAMMATION; METAANALYSIS; DISEASE;
D O I
10.1016/j.ahj.2012.01.026
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background Lipid-lowering drugs, particularly statins, have anti-inflammatory and antioxidant properties that may prevent atrial fibrillation (AF). This effect has not been investigated on new-onset AF in asymptomatic patients with aortic stenosis (AS). Methods Asymptomatic patients with mild-to-moderate AS (n = 1,421) were randomized (1: 1) to double-blind simvastatin 40 mg and ezetimibe 10 mg combination or placebo and followed up for a mean of 4.3 years. The primary end point was the time to new-onset AF adjudicated by 12-lead electrocardiogram at a core laboratory reading center. Secondary outcomes were the correlates of new-onset AF with nonfatal nonhemorrhagic stroke and a combined end point of AS-related events. Results During the course of the study, new-onset AF was detected in 85 (6%) patients (14.2/1,000 person-years of follow-up). At baseline, patients who developed AF were, compared with those remaining in sinus rhythm, older and had a higher left ventricular mass index a smaller aortic valve area index. Treatment with simvastatin and ezetimibe was not associated with less new-onset AF (odds ratio 0.89 [95% CI 0.57-1.97], P = .717). In contrast, age (hazard ratio [HR] 1.07 [95% CI 1.05-1.10], P < .001) and left ventricular mass index (HR 1.01 [95% CI 1.01-1.02], P < .001) were independent predictors of new-onset AF. The occurrence of new-onset AF was independently associated with 2-fold higher risk of AS-related outcomes (HR 1.65 [95% CI 1.02-2.66], P = .04) and 4-fold higher risk of nonfatal nonhemorrhagic stroke (HR 4.04 [95% CI 1.18-13.82], P = .03). Conclusions Simvastatin and ezetimibe were not associated with less new-onset AF. Older age and greater left ventricular mass index were independent predictors of AF development. New-onset AF was associated with a worsening of prognosis. (Am Heart J 2012;163:690-6.)
引用
收藏
页码:690 / 696
页数:7
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