Measurement of brain natriuretic peptide in plasma samples and cardiac tissue extracts by means of an immunoradiometric assay method

We evaluated the analytical characteristics and clinical usefulness of a co mmercial immunoradiometric assay (IRMA) kit for brain natriuretic peptide ( BNP). Mean (+/-SD) plasma BNP concentrations measured in 129 normal subject s were 2.9+/-2.7 pmol/l (median 2.2 pmol/l; range 0.1-12.4 pmol/l). The mea n (+/-SD) value observed in healthy men (2.1+/-2.0 pmol/l, n=49) was signif icantly (p=0.0009) different to that found in women (3.4+/-2.9 pmol/l, n=80 ). A positive relationship (R=0.214, p=0.0174) was found between BNP values and age; In 65 patients with cardiac diseases, BNP levels increased with t he progression of clinical severity of disease; patients with more severe d isease [NYHA functional class III-IV, mean (+/-SD) BNP=254+/-408 pmol/l, n= 22] showed significantly (p<0.0001) increased values compared to patients w ith mild symptoms of disease (NYHA functional class I-II, mean (+/-SD) BNP= 19.6+/-17.2 pmol/l, n=43). Furthermore, in 32 patients with chronic renal f ailure, greatly increased (p<0.0001) BNP Values were found both before (mea n+/-SD=88.1+/-111.1 pmol/l) and after haemodialysis (mean +/- SD=65.6+/-76. 7 pmol/l), with a significant reduction after haemodialysis (p=0.0004) comp ared to pre-haemodialysis. The mean (+/-SD) BNP value found in atrial extra cts collected during aorto-coronary bypass operations in 15 patients was 14 .5+/-51.9 pmol/g of cardiac tissue. Moreover, the mean (+/-SD) tissue level s of BNP in 7 heart transplant recipients were 128.4+/-117.2 pmol/g of card iac tissue in atrium, 68.4+/-76.7 pmol/g in ventricle, and 10.9+/-8.5 pmol/ g in interventricular septum. Finally, BNP values found in cardiac tissues of two subjects collected at autopsy were considerably lower (on average 1/ 1000) than those observed in cardiac tissues of patients with cardiac disea ses. The IRMA method for BNP determination evaluated in this study showed a good degree of sensitivity, precision and practicability. Therefore, this method should be a reliable tool for the measurement of plasma BNP levels f or both experimental studies and routine assay.