Key result
Serum fetuin-A levels were significantly decreased in patients with systolic heart failure compared to healthy controls (P < 0.01).
Why the study?
Are serum fetuin-A levels decreased in patients with systolic heart failure compared to healthy controls?
Case-Control (n=97)
Are serum fetuin-A levels decreased in patients with systolic heart failure compared to healthy controls?
p-value: p=<0.01
Serum fetuin-A is significantly decreased in patients with systolic heart failure and may serve as a diagnostic biomarker with high sensitivity and specificity.
May support fetuin-A as HF biomarker candidate; hypothesis-generating from case-control data, needs prospective validation.
OBJECTIVE: Inflammation and dystrophic calcification have been associated with cardiovascular disease (CVD) and chronic heart failure (CHF). The aim of the present study was to investigate the potential usefulness of fetuin-A as a biomarker in CHF. METHODS: Serum fetuin-A was measured in 66 CHF patients with left ventricular function < 50% and in 31 healthy controls at baseline. Fetuin-A was evaluated as a diagnostic marker for systolic heart failure and compared with C-reactive protein (CRP) and pro-brain natriuretic peptide (pro-BNP). RESULTS: The levels of serum fetuin-A were significantly decreased in the CHF patients compared to the control group (P < 0.01). Although there were significant correlations between fetuin-A and certain parameters in patients and controls, none of these were present consistently in either group. It was found that serum fetuin-A levels could identify patients with systolic heart failure with a high degree of sensitivity and specificity. CONCLUSIONS: Serum fetuin-A is decreased in CHF patients, indicating that anti-inflammatory activity is downregulated in CHF and that calcification may be associated with CHF.
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Keçebaş et al. (2014) conducted a case-control in Systolic heart failure (n=97). Serum fetuin-A levels vs. Healthy controls was evaluated on Serum fetuin-A levels (p=<0.01). Serum fetuin-A levels were significantly decreased in patients with systolic heart failure compared to healthy controls (P < 0.01).
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