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本文引用的文献

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Copper futures: ceruloplasmin and heart failure.铜期货:铜蓝蛋白与心力衰竭
Circ Res. 2014 May 23;114(11):1678-80. doi: 10.1161/CIRCRESAHA.114.304091.
2
Low serum ferroxidase I activity is associated with mortality in heart failure and related to both peroxynitrite-induced cysteine oxidation and tyrosine nitration of ceruloplasmin.血清铁氧化酶 I 活性降低与心力衰竭患者的死亡率相关,并且与过氧亚硝酸盐诱导的半胱氨酸氧化和铜蓝蛋白的酪氨酸硝化有关。
Circ Res. 2014 May 23;114(11):1723-32. doi: 10.1161/CIRCRESAHA.114.302849. Epub 2014 Mar 31.
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Ceruloplasmin and atrial fibrillation: evidence of causality from a population-based Mendelian randomization study.血清铜蓝蛋白与心房颤动:基于人群的孟德尔随机化研究的因果关系证据。
J Intern Med. 2014 Feb;275(2):164-71. doi: 10.1111/joim.12144. Epub 2013 Oct 23.
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Serum ceruloplasmin levels in acute decompensated heart failure.急性失代偿性心力衰竭患者的血清铜蓝蛋白水平
Clin Ter. 2013 May-Jun;164(3):e187-91. doi: 10.7417/CT.2013.1558.
5
Ceruloplasmin and heart failure in the Atherosclerosis Risk in Communities study.载脂蛋白和社区动脉粥样硬化风险研究中的心力衰竭。
Circ Heart Fail. 2013 Sep 1;6(5):936-43. doi: 10.1161/CIRCHEARTFAILURE.113.000270. Epub 2013 Jul 16.
6
Ceruloplasmin and the extent of heart failure in ischemic and nonischemic cardiomyopathy patients.血清铜蓝蛋白与缺血性和非缺血性心肌病患者心力衰竭程度的关系。
Mediators Inflamm. 2013;2013:348145. doi: 10.1155/2013/348145. Epub 2013 May 28.
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Ceruloplasmin dysfunction and therapeutic potential for Parkinson disease.铜蓝蛋白功能障碍与帕金森病的治疗潜力。
Ann Neurol. 2013 Apr;73(4):554-9. doi: 10.1002/ana.23817. Epub 2013 Feb 19.
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Ceruloplasmin is an endogenous inhibitor of myeloperoxidase.铜蓝蛋白是髓过氧化物酶的内源性抑制剂。
J Biol Chem. 2013 Mar 1;288(9):6465-77. doi: 10.1074/jbc.M112.418970. Epub 2013 Jan 10.
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Clinical and genetic association of serum ceruloplasmin with cardiovascular risk.血清铜蓝蛋白与心血管风险的临床和遗传关联。
Arterioscler Thromb Vasc Biol. 2012 Feb;32(2):516-22. doi: 10.1161/ATVBAHA.111.237040. Epub 2011 Nov 10.
10
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血清铜蓝蛋白水平升高在心力衰竭患者中的预后价值。

Prognostic value of elevated serum ceruloplasmin levels in patients with heart failure.

作者信息

Hammadah Muhammad, Fan Yiying, Wu Yuping, Hazen Stanley L, Tang W H Wilson

机构信息

Department of Cardiovascular Medicine, Heart and Vascular Institute, Cleveland Clinic, Cleveland, Ohio.

Department of Mathematics, Cleveland State University, Cleveland, Ohio.

出版信息

J Card Fail. 2014 Dec;20(12):946-52. doi: 10.1016/j.cardfail.2014.08.001. Epub 2014 Aug 13.

DOI:10.1016/j.cardfail.2014.08.001
PMID:25128745
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4250410/
Abstract

BACKGROUND

Ceruloplasmin (Cp) is a copper-binding acute-phase protein that is increased in inflammatory states and deficient in Wilson's disease. Recent studies demonstrate that increased levels of Cp are associated with increased risk of developing heart failure. Our objective was to test the hypothesis that serum Cp provides incremental and independent prediction of survival in stable patients with heart failure.

METHODS AND RESULTS

We measured serum Cp levels in 890 patients with stable heart failure undergoing elective cardiac evaluation that included coronary angiography. We examined the role of Cp levels in predicting survival over 5 years of follow-up. Mean Cp level was 26.6 ± 6.9 mg/dL and demonstrated relatively weak correlation with B-type natriuretic peptide (BNP; r = 0.187; P < .001). Increased Cp levels were associated with increased 5-year all-cause mortality (quartile [Q] 4 vs Q1 hazard ratio [HR] 1.9, 95% confidence interval [CI] 1.4-2.8; P < .001). When controlled for coronary disease traditional risk factors, creatinine clearance, dialysis, body mass index, medications, history of myocardial infarction, BNP, left ventricular ejection fraction (LVEF), heart rate, QRS duration, left bundle branch blockage, and implantable cardioverter-defibrillator placement, higher Cp remained an independent predictor of increased mortality (Q4 vs Q1 HR 1.7, 95% CI 1.1-2.6; P < .05). Model quality was improved with addition of Cp to the aforementioned covariables (net reclassification improvement of 9.3%; P < .001).

CONCLUSIONS

Ceruloplasmin is an independent predictor of all-cause mortality in patients with heart failure. Measurement of Cp may help to identify patients at heightened mortality risk.

摘要

背景

铜蓝蛋白(Cp)是一种结合铜的急性期蛋白,在炎症状态下升高,在威尔逊病中缺乏。最近的研究表明,Cp水平升高与发生心力衰竭的风险增加有关。我们的目的是检验血清Cp能对稳定期心力衰竭患者的生存提供额外且独立预测的假设。

方法与结果

我们测量了890例接受包括冠状动脉造影在内的择期心脏评估的稳定期心力衰竭患者的血清Cp水平。我们研究了Cp水平在预测5年随访期生存中的作用。平均Cp水平为26.6±6.9mg/dL,与B型利钠肽(BNP)的相关性相对较弱(r = 0.187;P <.001)。Cp水平升高与5年全因死亡率增加相关(四分位数[Q]4与Q1的风险比[HR]为1.9,95%置信区间[CI]为1.4 - 2.8;P <.001)。当对冠心病传统危险因素、肌酐清除率、透析、体重指数、药物治疗、心肌梗死病史、BNP、左心室射血分数(LVEF)、心率、QRS时限、左束支传导阻滞和植入式心脏复律除颤器植入情况进行控制后,较高的Cp仍然是死亡率增加的独立预测因素(Q4与Q1的HR为1.7,95%CI为1.1 - 2.6;P <.05)。将Cp添加到上述协变量中可改善模型质量(净重新分类改善率为9.3%;P <.001)。

结论

铜蓝蛋白是心力衰竭患者全因死亡率的独立预测因素。测量Cp可能有助于识别死亡风险较高的患者。