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首页> 外文期刊>Clinical Chemistry >Only Large Reductions in Concentrations of Natriuretic Peptides (BNP and NT-proBNP) Are Associated with Improved Outcome in Ambulatory Patients with Chronic Heart Failure
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Only Large Reductions in Concentrations of Natriuretic Peptides (BNP and NT-proBNP) Are Associated with Improved Outcome in Ambulatory Patients with Chronic Heart Failure

机译:在慢性心力衰竭门诊患者中,钠尿肽(BNP和NT-proBNP)浓度的大幅降低仅与改善的结果相关

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Concentrations of B-type natriuretic peptides (BNPs), including N-terminal pro-B-type natriuretic peptide (NT-proBNP), can be used to estimate prognosis in chronic heart failure. Large biologic variability, however, limits the usefulness of serial measurements in individual patients. As a result, the magnitude of change in peptide concentrations that is clinically meaningful remains to be established. We studied 172 New York Heart Association class III-IV outpatients. Primary endpoints were death/transplantation or heart failure hospitalization. The magnitude of peptide changes was categorized as no change (80% increase or decrease. Changes were also assessed using cutpoints (500 ng/L for BNP and 1000 ng/L for NT-proBNP). Fifty-two patients died or received transplants during the course of the study. Risk reduction for heart failure hospitalization was demonstrated only for BNP decreases of >80% from enrollment [hazard ratio (HR) 0.318, P = 0.0315]. BNP increases from less than to more than the prespecified cutpoint of 500 ng/L were associated with increased mortality risk (HR 2.101, P = 0.0069), whereas decreases from more than to less than the cutpoint did not reduce risk. NT-proBNP decreases from more than to less than the cutpoint of 1000 ng/L were associated with reduced risk of death/transplantation (HR 0.119, P = 0.0354). BNP increases from less than to more than the cutpoint were associated with increased risk of events, whereas further increases did not add to risk. In contrast, only substantial natriuretic peptide decreases (>80%) reduced risk. These data suggest that only robust decreases in natriuretic peptide concentrations should be targeted to reduce mortality and heart failure- related hospitalizations.
机译:包括N端前B型利钠肽(NT-proBNP)在内的B型利钠肽(BNP)的浓度可用于评估慢性心力衰竭的预后。然而,较大的生物学变异性限制了单个患者进行连续测量的有效性。结果,具有临床意义的肽浓度变化幅度尚待确定。我们研究了172名纽约心脏协会III-IV级门诊患者。主要终点是死亡/移植或心力衰竭住院。肽段变化的程度归类为无变化(增加或减少80%。还使用切点(BNP为500 ng / L,NT-proBNP为1000 ng / L)评估了变化。在此期间有52例患者死亡或接受了移植研究表明,仅当入院时BNP下降> 80%才可降低心力衰竭住院风险[风险比(HR)0.318,P = 0.0315]。BNP上升幅度小于或等于预先设定的临界值500 ng / L与死亡风险增加相关(HR 2.101,P = 0.0069),而从大于或小于阈值的降低并未降低风险; NT-proBNP从大于或小于阈值1000 ng / L的降低与死亡/移植的风险降低相关(HR 0.119,P = 0.0354)。BNP从小于或高于临界值增加与事件风险增加相关,而进一步的增加并没有增加风险。利钠肽折痕(> 80%)降低了风险。这些数据表明,仅应将利钠肽浓度的大幅降低作为降低死亡率和与心力衰竭相关的住院治疗的目标。

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    《Clinical Chemistry》 |2009年第1期|p.78-84|共7页
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    Wayne L. Miller,1* Karen A. Hartman,1 Diane E. Grill,2 John C. Burnett, Jr.,1 and Allan S. Jaffe1,31 Cardiovascular Division, Mayo Medical Center, Rochester, MN, 2 Department of Biostatistics, Mayo Medical Center, Rochester, MN, 3 Department of Laboratory Medicine and Pathology, Mayo Medical Center, Rochester, MN.* Address correspondence to this author at: Mayo Clinic, 200 First St., SW, Rochester, MN 55905. Fax 507-266-9142, e-mail miller.wayne@mayo.edu.Received April 18, 2008, accepted October 29, 2008.Previously published online at DOI: 10.1373/clinchem.2008.108928Author Contributions: All authors confirmed they have contributed to the intellectual content of this paper and have met the following 3 requirements: (a) significant contributions to the conception and design, acquisition of data, or analysis and interpretation of data, (b) drafting or revising the article for intellectual content, and (c) final approval of the published article.Authors' Disclosures of Potential Conflicts of Interest: Upon manuscript submission, all authors completed the Disclosures of Potential Conflict of Interest form. Potential conflicts of interest:Employment or Leadership: None declared.Consultant or Advisory Role: A.S. Jaffe, Siemens, Beckman- Coulter, Critical Diagnostics, Singulex, Novartis, and Bayer.Stock Ownership: None declared.Honoraria: None declared.Research Funding: W.L. Miller, Dade Behring and Siemens, A.S. Jaffe, Siemens and Beckman-Coulter. The current research was supported in part by a grant from Siemens.Expert Testimony: None declared.Role of Sponsor: The funding organizations played no role in the design of study, choice of enrolled patients, review and interpretation of data, or preparation or approval of manuscript.,;

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