Document Detail


Biomarker responses during and after treatment with nesiritide infusion in patients with decompensated chronic heart failure.
MedLine Citation:
PMID:  15615816     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
BACKGROUND: Objective methods to assess the adequacy of medication therapy for patients with advanced heart failure are lacking. Serial measurements of biomarkers might be beneficial. Therapy guided by N-terminal pro-B-type natriuretic peptide (NT-proBNP) might be helpful because NT-proBNP should be lowered by therapies that decrease endogenous BNP secretion. METHODS: NT-proBNP and BNP were measured in a nonconsecutive patient cohort receiving clinically indicated intravenous nesiritide. Blood samples were drawn before, at 6 and 24 h during, and at 6 h after infusion. A reduction in NT-proBNP was defined as a decrease from baseline during infusion ("infusion responders") of >3 SD of the variability of the assay measurement (approximately 20%). Patients with decreases >20% in both NT-pro BNP and BNP at 6 h post infusion were designated "biochemical responders". RESULTS: Forty patients [27 males; mean (SE) age, 68 (2) years; mean (SE) left ventricular ejection fraction, 25 (1.4)%] were studied. All patients improved clinically. Overall, the changes in NT-proBNP were a 18 (4.6)% [mean (SE)] and 19.8% (median) decrease from baseline at 24 h of infusion and a 22 (6.0)% and 17.8% decrease at 6 h post infusion (P <0.001 compared with baseline). In a large number of patients, decreases in NT-proBNP were, however, within the variability of the assay. Subgroup analysis showed that 22 of 40 patients were infusion responders with a >20% decrease from baseline in NT-proBNP during nesiritide infusion, whereas only 12 patients were biochemical responders with >20% decreases from baseline postinfusion for both NT-proBNP and BNP. CONCLUSIONS: In this study, many patients had decreased NT-proBNP and BNP values after therapy with nesiritide, but the majority of patients did not demonstrate biochemically significant decreases in analytes despite a clinical response. Until we know more about the responses of natriuretic peptides to therapies such as nesiritide, a strategy of monitoring NT-proBNP and BNP to guide therapy cannot be universally advocated.
Authors:
Wayne L Miller; Karen A Hartman; Mary F Burritt; Daniel D Borgeson; John C Burnett; Allan S Jaffe
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Publication Detail:
Type:  Journal Article; Research Support, Non-U.S. Gov't     Date:  2004-12-22
Journal Detail:
Title:  Clinical chemistry     Volume:  51     ISSN:  0009-9147     ISO Abbreviation:  Clin. Chem.     Publication Date:  2005 Mar 
Date Detail:
Created Date:  2005-03-01     Completed Date:  2005-04-11     Revised Date:  2007-11-15    
Medline Journal Info:
Nlm Unique ID:  9421549     Medline TA:  Clin Chem     Country:  United States    
Other Details:
Languages:  eng     Pagination:  569-77     Citation Subset:  IM    
Affiliation:
Division of Cardiovascular Diseases and Internal Medicine, Mayo Clinic Rochester, MN 55905, USA. miller.wayne@mayo.edu
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MeSH Terms
Descriptor/Qualifier:
Aged
Biological Markers / blood
Chemiluminescent Measurements
Chronic Disease
Cohort Studies
Drug Monitoring / methods
Female
Heart Failure / drug therapy*
Humans
Immunoassay
Infusions, Intravenous
Male
Natriuretic Peptide, Brain / administration & dosage,  blood*,  therapeutic use*
Nerve Tissue Proteins / blood*
Peptide Fragments / blood*
Protein Precursors / blood*
Recombinant Proteins / administration & dosage,  therapeutic use
Treatment Outcome
Chemical
Reg. No./Substance:
0/Biological Markers; 0/Nerve Tissue Proteins; 0/Peptide Fragments; 0/Protein Precursors; 0/Recombinant Proteins; 0/pro-brain natriuretic peptide (1-76); 114471-18-0/Natriuretic Peptide, Brain
Comments/Corrections
Erratum In:
Clin Chem. 2005 Apr;51(4):798

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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