Vanderbilt Charles, Free Marcia, Li Jie, Gebretsadik Tebeb, Bian Aihua, Shintani Ayumi, McBride Brian F, Solus Joseph, Milne Ginger, Crossley George H, Thompson David, Vidaillet Humberto, Okafor Henry, Darbar Dawood, Murray Katherine T, Stein C Michael
Division of Clinical Pharmacology, Department of Medicine, Vanderbilt University School of Medicine, Nashville, Tennessee; Department of Pharmacology, Vanderbilt University School of Medicine, Nashville, Tennessee.
Department of Biostatistics, Vanderbilt University School of Medicine, Nashville, Tennessee.
Am J Cardiol. 2015 Jan 15;115(2):196-201. doi: 10.1016/j.amjcard.2014.10.022. Epub 2014 Oct 29.
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, double-blind, 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 F2-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 F2-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. (Clinical trial registration number, NCT 00552084.).
ω-3多不饱和脂肪酸(n-3 PUFAs)预防心房颤动(AF)复发的疗效存在争议,其对该人群炎症和氧化应激的影响尚不清楚。本研究探讨了在传统治疗基础上加用高剂量海洋n-3 PUFAs对AF复发以及炎症和氧化应激标志物的影响。在一项前瞻性、双盲、安慰剂对照、平行组研究中,阵发性或持续性AF患者按2:1的比例随机分为n-3 PUFAs组(4 g/天;n = 126)或安慰剂组(n = 64)。主要结局是AF复发时间。次要结局是炎症生物标志物(血清白细胞介素[IL]-6、IL-8、IL-10、肿瘤坏死因子α、单核细胞趋化蛋白-1和血管内皮生长因子)、N末端脑钠肽前体以及氧化应激(尿F2-异前列腺素)的变化。随机分组至n-3 PUFAs组的74例患者(58.7%)和接受安慰剂治疗的30例患者(46.9%)出现AF复发;两组的AF复发时间无显著差异(风险比1.20;95%置信区间0.76至1.90,校正p = 0.438)。与安慰剂相比,n-3 PUFAs对炎症标志物、N末端脑钠肽前体或F2-异前列腺素的浓度未产生具有临床意义的变化。总之,对于阵发性或持续性AF患者,每天服用4 g n-3 PUFAs治疗并未降低AF复发率,也未对炎症和氧化应激标志物浓度产生具有临床重要意义的影响。(临床试验注册号,NCT 00552084。)