益生菌联合沙库巴曲缬沙坦及胺碘酮对心房颤动射频消融术后近期与远期疗效的影响

Effects of probiotics combined with sacubitril valsartan and amiodarone on short-term and long-term efficacy of patients with atrial fibrillation after radiofrequency ablation

  • 摘要:
    目的 探讨益生菌联合沙库巴曲缬沙坦及胺碘酮对心房颤动(简称房颤)射频消融术后近期及远期疗效的影响。
    方法 将2021年6月-2022年6月张家口市第一医院收治的90例房颤射频消融术后患者随机分为3组, 每组30例。对照组采用胺碘酮治疗, 沙库巴曲缬沙坦组采用胺碘酮及沙库巴曲缬沙坦治疗, 益生菌组采用益生菌联合胺碘酮及沙库巴曲缬沙坦治疗。比较3组复发情况、心房结构指标左心房内径(LAD)、左心室射血分数(LVEF)、左室收缩末期容积指数(LVESVI)、左心房容积(LAV)、左室舒张末期容积指数(LVEDVI)、心肌纤维化指标半乳凝素-3(Gal-3)、可溶性生长刺激表达基因2蛋白(sST2)、炎症反应指标细胞间黏附分子-1(ICAM-1)、C反应蛋白(CRP)、白细胞介素-6(IL-6)、神经内分泌激素指标醛固酮、去甲肾上腺素(NE)、血管紧张素Ⅱ(AngⅡ)、肠道菌群代谢产物总胆汁酸、氧化三甲胺(TMAO)及不良事件发生率。
    结果 治疗后12个月, 益生菌组复发率低于沙库巴曲缬沙坦组、对照组, 差异有统计学意义(P < 0.05); 治疗3、6、12个月后, 益生菌组LAD、LAV、LVESVI、LVEDVI、sST2、Gal-3低于沙库巴曲缬沙坦组、对照组, 沙库巴曲缬沙坦组上述指标低于对照组, 差异均有统计学意义(P < 0.05); 治疗3、6、12个月后, 益生菌组LVEF高于沙库巴曲缬沙坦组、对照组, 沙库巴曲缬沙坦组LVEF高于对照组, 差异有统计学意义(P < 0.05); 治疗3、6、12个月后, 益生菌组CRP、IL-6、ICAM-1、NE、醛固酮、AngⅡ低于沙库巴曲缬沙坦组、对照组, 沙库巴曲缬沙坦组上述指标低于对照组, 差异有统计学意义(P < 0.05); 治疗3、6、12个月后, 益生菌组TMAO、总胆汁酸低于对照组、沙库巴曲缬沙坦组, 差异有统计学意义(P < 0.05); 3组不良事件发生率比较, 差异无统计学意义(P>0.05)。
    结论 益生菌联合沙库巴曲缬沙坦、胺碘酮可改善房颤射频消融术后心房结构, 抑制心肌纤维化, 减轻炎症反应, 调节神经内分泌激素、肠道菌群代谢产物, 预防房颤远期复发, 且安全性高。

     

    Abstract:
    Objective To investigate the effects of probiotics combined with sacubitril valsartan and amiodarone on short-term and long-term efficacy of patients with atrial fibrillation after radiofrequency ablation.
    Methods A total of 90 patients with atrial fibrillation after radiofrequency ablation in the First Hospital of Zhangjiakou City from June 2021 to June 2022 were selected and randomly divided into three groups, with 30 cases in each group. Control group was treated with amiodarone, sacubitril valsartan group was treated with amiodarone and sacubitril valsartan, and probiotics group was treated with probiotics, amiodarone and sacubitril valsartan. The recurrence situation, atrial structure indexesleft atrial diameter (LAD), left ventricular ejection fraction (LVEF), left ventricular end systolic volume index (LVESVI), left atrial volume (LAV), left ventricular end diastolic volume index (LVEDVI), myocardial fibrosis indexesgalactin-3 (Gal-3), soluble growth stimulation expression gene 2 protein (sST2), inflammatory response indexesintercellular adhesion molecule-1 (ICAM-1), C reactive protein (CRP), interleukin-6 (IL-6), neuroendocrine hormone indexesaldosterone, norepinephrine (NE), angiotensin Ⅱ (AngⅡ), metabolites of gut microbiotatotal bile acids, trimethylamine oxide (TMAO) and incidence of adverse events were compared among the three groups.
    Results At 12 months after treatment, the recurrence rate of the probiotics group was significantly lower than that of the sacubitril valsartan group and the control group (P < 0.05); after 3, 6 and 12 months of treatment, the LAD, LAV, LVESVI, LVEDVI, sST2 and Gal-3 in the probiotics group were significantly lower than those in the sacubitril valsartan group and the control group (P < 0.05), and these indexes in the sacubitril valsartan group were also significantly lower than those in the control group (P < 0.05); after 3, 6 and 12 months of treatment, the LVEF of the probiotics group was significantly higher than that of the sacubitril valsartan group and the control group (P < 0.05), and the LVEF of the sacubitril valsartan group was also significantly higher than that of the control group (P < 0.05); after 3, 6 and 12 months of treatment, the CRP, IL-6, ICAM-1, NE, aldosterone and AngⅡ in the probiotics group were significantly lower than those in the sacubitril valsartan group and the control group, and these indexes in the sacubitril valsartan group were also significantly lower than those in the control group (P < 0.05); after 3, 6 and 12 months of treatment, the TMAO and total bile acids in the probiotics group were significantly lower than those in the control group and the sacubitril valsartan group (P < 0.05); there was no significant difference in the incidence of adverse events among the three groups (P>0.05).
    Conclusion Probiotics combined with sacubitril valsartan and amiodarone can improve atrial structure after radiofrequency ablation of atrial fibrillation, inhibit myocardial fibrosis, reduce inflammatory response, regulate neuroendocrine hormones and metabolites of gut microbiota, prevent long-term recurrence of atrial fibrillation, and have a high safety.

     

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