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  • Declines in serum uric acid...
    Aoyama, Daisetsu; Uzui, Hiroyasu; Sekihara, Takayuki; Eguchi, Tomoya; Hasegawa, Kanae; Tsuji, Toshihiko; Kataoka, Tatsuhiro; Nagao, Moeko; Kakehashi, Shota; Mukai, Moe; Aiki, Takayoshi; Yamaguchi, Junya; Shiomi, Yuichiro; Tama, Naoto; Fukuoka, Yoshitomo; Ishida, Kentaro; Tada, Hiroshi

    Heart and vessels, 12/2022, Letnik: 37, Številka: 12
    Journal Article

    Background Few studies have examined whether catheter ablation for AF patients improves biomarkers other than serum levels of brain natriuretic peptide (BNP) and renal function. This study was to explore whether catheter ablation for atrial fibrillation (AF) patients affects uric acid (UA), glucose and lipid metabolism. Methods and results A total of 206 patients (66.6 ± 10.4 years; 132 men) who underwent initial AF ablation without changes to oral medications were included. Baseline BNP and UA levels significantly decreased at 1 year after ablation ( p  < 0.05 each). Changes in UA level correlated significantly with pre-procedural UA level ( r  = 0.57). In multivariable logistic regression modeling, pre-procedural UA level, persistent AF, and hemoglobin A1c ( p  < 0.05 each) were independent predictors of post-procedural UA level decline. Significant improvements in both persistent and paroxysmal AF patients were identified, and the magnitude of post-procedural serum UA level decline after ablation (ΔUA) was significantly greater in patients with persistent AF (0.8 ± 1.0 mg/dl) than in those with paroxysmal AF (0.2 ± 0.8 mg/dl, p  < 0.001). Of the 48 patients with high UA level before procedure, 28 patients showed improvement in UA level to normal range. Conclusions Catheter ablation for AF patients significantly improved serum UA levels without obvious influences of heart failure, renal function, or inflammation, suggesting that AF ablation may be effective for AF patients with hyperuricemia. Trial registration The study was approved by the Research Ethics Committee of University of Fukui (no. 20210132) and clinical trial registration (UMIN000044669).