Effect of Omega-Three Polyunsaturated Fatty Acids on Inflammation, Oxidative Stress, and Recurrence of Atrial Fibrillation

被引:53
作者
Vanderbilt, Charles [1 ,2 ]
Free, Marcia [1 ,2 ]
Li, Jie [1 ,2 ]
Gebretsadik, Tebeb [3 ]
Bian, Aihua [3 ]
Shintani, Ayumi [3 ]
McBride, Brian F. [1 ,2 ]
Solus, Joseph [1 ,2 ]
Milne, Ginger [1 ,2 ]
Crossley, George H. [4 ]
Thompson, David [5 ]
Vidaillet, Humberto [6 ]
Okafor, Henry [4 ,7 ]
Darbar, Dawood [1 ,2 ,4 ]
Murray, Katherine T. [1 ,2 ,4 ]
Stein, C. Michael [1 ,2 ]
机构
[1] Vanderbilt Univ, Sch Med, Dept Med, Div Clin Pharmacol, Nashville, TN 37212 USA
[2] Vanderbilt Univ, Sch Med, Dept Pharmacol, Nashville, TN 37212 USA
[3] Vanderbilt Univ, Sch Med, Dept Biostat, Nashville, TN 37212 USA
[4] Vanderbilt Univ, Sch Med, Dept Med, Div Cardiovasc Med, Nashville, TN 37212 USA
[5] St Thomas Res Inst, Nashville, TN USA
[6] Marshfield Clin Res Fdn, Marshfield, WI USA
[7] Meharry Med Coll, Nashville, TN 37208 USA
基金
美国国家卫生研究院;
关键词
FISH-OIL SUPPLEMENTATION; ELECTRICAL CARDIOVERSION; EICOSAPENTAENOIC ACID; IN-VIVO; PREVENTION; OMEGA-3-FATTY-ACIDS; F-3-ISOPROSTANES; PATHOGENESIS; METAANALYSIS; EFFICACY;
D O I
10.1016/j.amjcard.2014.10.022
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The efficacy of omega-3 polyunsaturated fatty acids (n-3 PUFAs) in preventing recurrence of atrial fibrillation (AF) is controversial and their effects on inflammation and oxidative stress in this population are not known. This study examined the effects of high-dose marine n-3 PUFAs added to conventional therapy on the recurrence of AF and on markers of inflammation and oxidative stress. Patients with paroxysmal or persistent AF were randomized to n-3 PUFAs (4 g/day; n = 126) or placebo (n = 64) in a 2:1 ratio in a prospective, doubleblind, placebo-controlled, parallel group study. The primary outcome was time to recurrence of AF. Secondary outcomes were changes in biomarkers of inflammation (serum interleukin [IL]-6, IL-8, IL-10, tissue necrosis factor alpha, monocyte chemoattractant protein-1, and vascular endothelial growth factor), N-terminal-pro-brain-type natriuretic peptide, and oxidative stress (urinary F-2-isoprostanes). AF recurred in 74 patients (58.7%) randomized to n-3 PUFAs and in 30 patients (46.9%) who received placebo; time to recurrence of AF did not differ significantly in the 2 groups (hazard ratio 1.20; 95% confidence interval 0.76 to 1.90, adjusted p = 0.438). Compared with placebo, n-3 PUFAs did not result in clinically meaningful changes in concentrations of inflammatory markers, N-terminal-pro-brain-type natriuretic peptide or F-2-isoprostanes. In conclusion, in patients with paroxysmal or persistent AF, treatment with n-3 PUFAs 4 g/day did not reduce the recurrence of AF, nor was it associated with clinically important effects on concentrations of markers of inflammation and oxidative stress. (C) 2015 Elsevier Inc. All rights reserved.
引用
收藏
页码:196 / 201
页数:6
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