atrial-natriuretic-factor-(4-23)nh2--de-gln(18)-de-ser(19)-de-gly(20-22)-de-leu(21)- has been researched along with Heart-Failure* in 2 studies
1 trial(s) available for atrial-natriuretic-factor-(4-23)nh2--de-gln(18)-de-ser(19)-de-gly(20-22)-de-leu(21)- and Heart-Failure
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The potential of brain natriuretic peptide as a biomarker for New York Heart Association class during the outpatient treatment of heart failure.
Plasma C-terminal atrial natriuretic peptide (C-ANP), N-terminal ANP (N-ANP), and brain natriuretic peptide (BNP) have diagnostic utility in detecting left ventricular dysfunction. Their relative value in monitoring symptom status during the chronic treatment of congestive heart failure (CHF) remains undefined.. Ninety-eight subjects with CHF were evaluated. Baseline natriuretic peptides were measured by radioimmunoassay, left ventricular ejection fraction (LVEF) was estimated with echocardiography, and New York Heart Association (NYHA) class was determined independently by attending heart failure specialists. Forty-one subjects were restudied during a 6- to 12-month follow-up period after optimizing therapy. At baseline, all natriuretic peptides and LVEF correlated positively with NYHA class (P <.005). Plasma BNP, however, correlated best with NYHA class. At follow-up, only changes of BNP correlated to changes of NYHA class (P =.04). BNP decreased (-45% +/- 12%, N = 14, P =.002) in subjects whose NYHA class improved whereas BNP remained unchanged (-1% +/- 10%, N = 25, P =.95) in those whose NYHA class was stable.. This investigation demonstrates the superiority of plasma BNP as compared to ANP and LVEF in objectively assessing NYHA class during the chronic treatment of CHF. Given that clinical assessment of CHF is subjective, plasma BNP is a useful objective biomarker in monitoring human CHF in the outpatient setting. Topics: Adult; Aged; Aged, 80 and over; Ambulatory Care; Atrial Natriuretic Factor; Biomarkers; Female; Heart Failure; Humans; Male; Middle Aged; Natriuretic Peptide, Brain; Peptide Fragments; Protein Precursors; Radioimmunoassay; Single-Blind Method; Treatment Outcome; Ventricular Dysfunction, Left | 2002 |
1 other study(ies) available for atrial-natriuretic-factor-(4-23)nh2--de-gln(18)-de-ser(19)-de-gly(20-22)-de-leu(21)- and Heart-Failure
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Clearance receptors and endopeptidase: equal role in natriuretic peptide metabolism in heart failure.
The effects of separate and combined endopeptidase inhibition (by SCH-32615) and natriuretic peptide receptor C blockade [by C-ANP-(4-23)] on the clearance and bioactivity of atrial (ANP) and brain (BNP) natriuretic peptides was investigated in eight sheep with heart failure. SCH-32615 and C-ANP-(4-23) administered separately induced significant and proportionate dose-dependent rises in plasma ANP, BNP, and guanosine 3',5'-cyclic monophosphate (cGMP) levels. Associated with these changes were reductions in arterial pressure, left atrial pressure, and peripheral resistance and increases in cardiac output, urine volume, sodium excretion, and creatinine clearance. SCH-32615 induced greater diuresis and natriuresis than C-ANP-(4-23). Combined administration of SCH-32615 and C-ANP-(4-23) induced greater than additive rises in plasma ANP, BNP, and cGMP concentrations, with enhanced hemodynamic effects, diuresis, and natriuresis and reduced plasma aldosterone levels. In conclusion, we find that the enzymatic and receptor clearance pathways contribute equally to the metabolism of endogenous ANP and BNP in sheep with heart failure. Combined inhibition of both degradative pathways was associated with enhanced hormonal, hemodynamic, and renal effects and may have greater potential therapeutic value than either agent separately. Topics: Aldosterone; Animals; Atrial Function, Left; Atrial Natriuretic Factor; Blood Pressure; Cyclic GMP; Dipeptides; Diuresis; Endopeptidases; Female; Guanylate Cyclase; Heart Failure; Hemodynamics; Natriuresis; Natriuretic Peptide, Brain; Nerve Tissue Proteins; Peptide Fragments; Protease Inhibitors; Receptors, Atrial Natriuretic Factor; Sheep; Time Factors; Vascular Resistance | 1997 |