田飞飞, 魏子秀, 徐勤成, 孙晓斐. 瑞舒伐他汀联合贝那普利对阵发性心房颤动患者的治疗效果及其作用机制[J]. 心脏杂志, 2014, 26(3): 296-298.
    引用本文: 田飞飞, 魏子秀, 徐勤成, 孙晓斐. 瑞舒伐他汀联合贝那普利对阵发性心房颤动患者的治疗效果及其作用机制[J]. 心脏杂志, 2014, 26(3): 296-298.
    Therapeutic efficacy and mechanism of rosuvastatin combined with benazepril in patients with paroxysmal atrial fibrillation[J]. Chinese Heart Journal, 2014, 26(3): 296-298.
    Citation: Therapeutic efficacy and mechanism of rosuvastatin combined with benazepril in patients with paroxysmal atrial fibrillation[J]. Chinese Heart Journal, 2014, 26(3): 296-298.

    瑞舒伐他汀联合贝那普利对阵发性心房颤动患者的治疗效果及其作用机制

    Therapeutic efficacy and mechanism of rosuvastatin combined with benazepril in patients with paroxysmal atrial fibrillation

    • 摘要: 目的:观察瑞舒伐他汀与贝那普利联合应用对阵发性房颤的治疗效果及其作用机制。方法:入选70例阵发性房颤患者,随机分为试药组(口服胺碘酮+瑞舒伐他汀+贝那普利)及对照组(口服胺碘酮),比较两组患者房颤治疗效果、C反应蛋白(CRP)水平及左房内径(LAD)。结果:经过6个月的随访,与对照组比较,试药组房颤发作次数、房颤持续时间显著下降,总有效率提高,差异均具有显著性(P<005)。且CPR水平、LAD显著低于对照组(均P<0.05)。结论:瑞舒伐他汀联合贝那普利可以减少房颤发生,其机制可能与减少炎症反应,抑制心肌重构有关。

       

      Abstract: AIM:To observe the therapeutic efficacy and mechanism of rosuvastatin combined with benazepril on patients with paroxysmal atrial fibrillation (PAF). METHODS: Seventy patients with PAF were randomized to reagent group and control group. Patients in the reagent group were given amiodarone, rosuvastatin and benazepril, whereas patients in control group were given amiodarone alone. Therapeutic efficacy, serum level of C-reactive protein (CRP) and left atrial diameter (LAD) were observed. RESULTS: After 6 months’ follow-up, PAF times and AF duration were significantly decreased and the total effective rate was elevated in the reagent group compared with those in the control group (P<0.05). Serum level of CRP and the size of the LAD in the reagent group were significantly lower than those in the control group (P<0.05). CONCLUSION: Rosuvastatin combined with benazepril effectively inhibits the occurrence of PAF and the mechanism is probably associated with the effect of inflammatory reaction reduction and myocardium reconstitution inhibition.

       

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