End-stage heart failure was associated with significantly increased left ventricular mRNA levels of both BNP and ANP compared to controls (p<0.01), which correlated negatively with Ca(2+)-ATPase mRNA.
Observational (n=39)
BNP and ANP gene expression is upregulated in end-stage human heart failure and inversely correlates with sarcoplasmic reticulum Ca(2+)-ATPase gene expression.
p-value: p=<0.01
Brain natriuretic peptide (BNP) and C-type natriuretic peptide (CNP) are novel natriuretic peptides, originally isolated from porcine brain. Similar to atrial natriuretic peptide (ANP), BNP is also synthesized in and secreted from cardiocytes, but CNP is not expressed at significant levels in normal adult myocardium. Previous studies have indicated that the serum level and ventricular expression of the ANP gene were augmented in patients with heart failure. Recently, the serum level of BNP was also reported to increase in human heart failure. To examine whether or not the expression of these natriuretic peptides is regulated in ventricular myocardium in a concordant manner, we performed Northern blot analysis using total cellular RNA isolated from the diseased left ventricles of 30 cardiac transplant recipients with end-stage heart failure, seven ventricles from organ donors (control group), and two ventricles of artificially aborted 17- and 19-week-old fetuses. The levels of mRNAs encoding both BNP and ANP increased significantly (p less than 0.01) in the left ventricular myocardium from the patients with end-stage heart failure as compared with the control group. The levels of BNP mRNA correlated positively with those of ANP mRNA (r = 0.73, p less than 0.01) and negatively with those of sarcoplasmic reticulum Ca(2+)-ATPase mRNA (r = -0.66, p less than 0.01) in the left ventricular myocardium from the patients with heart failure. There was also a negative correlation between the levels of ANP and the sarcoplasmic reticulum Ca(2+)-ATPase mRNAs (r = -0.65, p less than 0.01).(ABSTRACT TRUNCATED AT 250 WORDS)
Takahashi et al. (1992) conducted an observational in End-stage heart failure (n=39). End-stage heart failure vs. Normal adult myocardium (organ donors) was evaluated on Levels of mRNAs encoding BNP and ANP (p=<0.01). End-stage heart failure was associated with significantly increased left ventricular mRNA levels of both BNP and ANP compared to controls (p<0.01), which correlated negatively with Ca(2+)-ATPase mRNA.