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Chromogranin A in heart failure; a novel neurohumoral factor and a predictor for mortality
C Ceconi1, R Ferrari, T Bachetti
1Cardiovascular Pathophysiology Research Centre, Salvatore Maugeri Foundation, IRCCS, Gussago, Italy.
Insights
Serum Chromogranin-A (CgA) levels are elevated in chronic heart failure patients and correlate with disease severity. Elevated CgA is an independent predictor of mortality in heart failure.
Area of Science:
- Cardiology
- Endocrinology
- Biomarkers
Background:
- Chronic heart failure (CHF) involves activation of multiple hormonal systems.
- Serum Chromogranin-A (CgA), a neuroendocrine cell secretory granule protein, is investigated for its role in CHF.
Purpose of the Study:
- To determine if serum CgA levels are increased in CHF patients.
- To assess if CgA levels predict mortality in CHF.
Main Methods:
- Serum CgA and other neuroendocrine hormones were measured in 160 CHF patients.
- Patients were classified by New York Heart Association (NYHA) functional class.
- Prognostic significance was evaluated using univariate and Cox proportional-hazard multivariate analyses.
Main Results:
- Serum CgA levels were significantly elevated in CHF patients and correlated with NYHA class severity (Class I < II < III < IV).
- Univariate analysis identified CgA, ejection fraction, noradrenaline, atrial natriuretic peptide, and NYHA class as prognosticators.
- Multivariate analysis revealed CgA and NYHA class as independent predictors of mortality.
Conclusions:
- Serum CgA levels are increased in chronic heart failure.
- CgA is a significant independent predictor of mortality in patients with chronic heart failure.
Background:
In chronic heart failure, several hormonal systems are activated with diagnostic and prognostic implications. We tested the hypotheses that serum Chromogranin-A (CgA) -- a 49 kDa acid protein present in the secretor granules of neuroendocrine cells -- is increased in chronic heart failure and that CgA levels are a predictive factor for mortality.
Method And Results:
In 160 patients with chronic heart failure, we measured serum CgA and other neuroendocrine hormones. The results showed that CgA is increased in chronic heart failure and the increase is related to the clinical severity of the syndrome: CgA levels in New York Heart Failure (NYHA) class II (median 146.9 ng x ml(-1), inter-quartiles 108.3-265.5) were significantly higher (P<0.05) than in class I (median 109.7 ng x ml(-1), inter-quartiles 96.7-137.6), and significantly lower (P<0.05) than in class III (median 279.0 ng x ml(-1), inter-quartiles 203.6-516.1). Class IV patients showed the highest serum levels of CgA (median 545.0 ng. ml(-1), inter-quartiles 231.8-1068.3), being statistically significantly different from class III patients (P<0.001). The association between survival and some recognized variables of prognostic significance, including CgA was also studied. The results showed that ejection fraction, noradrenaline, atrial natriuretic peptide, NYHA class and CgA were significant univariate prognosticators; however, in the multivariate analysis by the Cox proportional-hazard model, CgA and NYHA class were the only independent predictive factors for mortality (P<0.005, RR=1.22, 95% CI=1.06-1.41 and P=0.04, RR=1.58, 95% CI=1.02-2.46, respectively).
Conclusions:
CgA is a pro-hormone, precursor of several active fragments likely to exert biological effects in chronic heart failure. CgA serum levels are increased in patients with chronic heart failure and are a predictive factor for mortality.
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