首页> 外文期刊>JPC Bulletin on Iron & Steel >The Ratio of Eicosapentaenoic Acid (EPA) to Arachidonic Acid may be a Residual Risk Marker in Stable Coronary Artery Disease Patients Receiving Treatment with Statin Following EPA Therapy
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The Ratio of Eicosapentaenoic Acid (EPA) to Arachidonic Acid may be a Residual Risk Marker in Stable Coronary Artery Disease Patients Receiving Treatment with Statin Following EPA Therapy

机译:赤膦苯乙烯苯甲酸(EPA)与花生酸的比例可以是稳定冠状动脉疾病患者的残留风险标志物,其在EPA治疗后用他汀类药物接受治疗

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AbstractBackgroundWe investigated the relationship between the eicosapentaenoic acid (EPA)/arachidonic acid (AA) ratio and non-high-density lipoprotein cholesterol (non-HDL-C) level, a major residual risk of coronary artery disease (CAD), in statin-treated CAD patients following EPA therapy.MethodsWe conducted a 6-month, prospective, randomized clinical trial to investigate the effect of the additional administration of EPA on the EPA/AA ratio and the serum non-HDL-C level in stable CAD patients receiving statin treatment. We assigned CAD patients already receiving statin therapy to an EPA group (1800?mg/day;n?=?50) or a control group (n?=?50).ResultsA significant reduction in the serum non-HDL-C level was observed in the EPA group, compared with the control group (?9.7 vs. ?1.2%,p?=?0.01). A multiple-regression analysis with adjustments for coronary risk factors revealed that achieved EPA/AA ratio was more reliable as an independent and significant predictor of a reduction in the non-HDL-C level at a 6-month follow-up examination (β?=??0.324,p?=?0.033) than the absolute change in the EPA/AA ratio. Interestingly, significant negative correlations were found between the baseline levels and the absolute change values of both non-HDL-C and triglyceride-rich lipoproteins, both markers of residual risk of CAD, indicating that patients with a higher baseline residual risk achieved a greater reduction.ConclusionThe present results suggest that the achieved EPA/AA ratio, but not the absolute change in EPA/AA ratio, following EPA therapy might be a useful marker for the risk stratification of CAD among statin-treated patients with a high non-HDL-C level.Clinical Trial RegistrationUMIN (http://www.umin.ac.jp/) Study ID: UMIN000010452.]]>
机译:<![cdata [<标题>抽象 <标题>背景 ara id =“par1”>我们调查了eicosapentaeno酸(EPA)/ arachidonic之间的关系酸(AA)比和非高密度脂蛋白胆固醇(非HDL-C)水平,冠状动脉疾病(CAD)的主要残余风险,在EPA治疗后的毒素治疗的CAD患者中。 <标题>方法 我们进行了6个月,前瞻性,随机的临床试验,以调查额外的EPA给予的效果EPA / AA比率和血清非HDL-C水平在接受他汀类药物治疗的稳定CAD患者。我们分配了已经将他汀类药物治疗的CAD患者(1800?MG /天; <重点型=“斜体”> N ?=?50)或对照组(<重点键入=“斜体”> n ?=?50)。 <标题>结果 ara id =“par3”>血清的显着减少与对照组相比,在EPA组中观察到-HDL-C水平(?9.7与β1.2%,<重点型=“斜体”> P ?=?0.01)。具有冠状动脉危险因素的调整的多元回归分析显示,达到EPA / AA比例更可靠,因为在6个月的随访检查中的非HDL-C水平降低的独立和显着预测因子(<重点键入=“斜体”>β?= ?? 0.324,<重点型=“斜体”> P ?=?0.033)比EPA / AA比例的绝对变化。有趣的是,基线水平与富含Hdl-C和富甘膦的脂蛋白的绝对变化值之间发现了显着的负相关性,所述CAD的残余风险标记,表明患有较高基线残余风险的患者达到了更大的减少。 <标题>结论 ara id =“par4”>当前结果表明,实现了EPA / AA的比率,但不是绝对变化在EPA / AA的比例中,在EPA治疗中可能是调节蛋白处理的患者的CAD风险分层的有用标志物,其高HDL-C水平。 <标题>临床试验登记 ara id =“par5”> umin( http://www.um.ac.jp/ )研究ID:UMIN000010452。 ]]>

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