When stimulated by stress or stretch, ventricular myocytes activate transcription of the relevant gene and produce a 108 amino acid peptide (Pro BNP). Before excretion by the myocyte this peptide is cleaved to produce an inactive 76 amino acid N-terminal fragment and the C-terminal 32 amino acid with hormonal activity (BNP).2 Plasma half-life of BNP in vivo is 18 to 22 minutes so concentration promptly reflects changes in cardiac status.
Available assays measure either the inactive N-terminal fragment or the active 32 amino acid peptide. There are currently several assays available that do not give directly comparable results. Individual laboratory reference ranges should therefore be used.
Of all the neurohormones, BNP is the best candidate for use as a diagnostic test. When BNP rises it tends to go very high, which gives it good discriminatory power in separating ventricular causes of dyspnoea from other causes. In one series of patients presenting to an emergency ward with shortness of breath, those without heart failure had a mean BNP concentration of 38 pg/mL while in those with heart failure it averaged 1076 pg/mL. 3
Four studies (totalling1994 patients) have compared the test performance of BNP with the diagnosis of congestive heart failure made by echocardiography and consideration of all clinical details.1,3,4,5 The results show BNP has a sensitivity of 90-97% and a specificity of 76-92%.There have also been four studies(totalling 6109 people) which investigated using BNP to screen for pre-clinical heart disease in the community.6,7,8,9 Three of these studies showed good test performance with sensitivities ranging from77% to 100% and specificities from 70% to 96%. Recent results9 contradict these findings and show sensitivity in detecting any left ventricular systolic dysfunction of only 53% in men and 26% in women. For moderate to severe left ventricular systolic dysfunction these values are 65% and 80%, well below those found in the other studies. This suggests that although BNP shows good test performance in acutely sick hospital patients it is less accurate in the detection of ventricular dysfunction in asymptomatic individuals.
Only two of the studies (involving 232 patients) investigated the use of BNP as a diagnostic tool for suspected congestive heart failure in general practice. Further research is needed to validate the test in the milder spectrum of disease seen in general practice. One such study is currently under way in Newcastle, New South Wales.
Congestive heart failure can be due to either systolic or diastolic ventricular dysfunction. While there are guidelines10 and a wealth of good evidence from randomised controlled trials on the management of systolic dysfunction, there is scant evidence on how to manage diastolic failure. BNP is increased in both systolic and diastolic dysfunction so many patients will still need echocardiography in order to plan therapy. The value of the test may eventually be in its capacity to rule out heart failure as a cause of a patient's illness.
BNP has been shown to be a powerful predictor of prognosis in patients with heart failure. A high concentration is associated with a poor prognosis. Some centres are therefore using BNP concentrations to guide therapy, however this usage is still experimental.
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