Key result
Higher serum PIIINP correlates strongly with reduced heart rate variability in heart failure patients.
Why the study?
Cardiac extracellular matrix fibrosis contributes to arrhythmogenicity and sudden cardiac death in heart failure, but serum markers to evaluate cardiac autonomic control are needed.
Observational (n=21)
Effect estimate: r=-0.722
p-value: p=<0.001
In patients with heart failure, serum PIIINP levels correlate significantly with reduced heart rate variability, suggesting its potential as a biomarker for cardiac autonomic control and sudden cardiac death risk.
Serum PIIINP correlated with HRV indices in small HF cohort; hypothesis-generating for SCD risk stratification, needs prospective validation.
BACKGROUND: Cardiac extra-cellular matrix (ECM) fibrosis plays an important role in the pathophysiology of heart failure (HF). It may provide electrical heterogeneity and a substrate for arrhythmogenicity, which may cause sudden cardiac death (SCD). METHODS: Twenty-one patients with manifestations of HF and a left ventricular ejection fraction (LVEF) ≤50% were enrolled. The median age was 62 years and median LVEF was 33%. Time- and frequency-domain analysis of heart rate variability (HRV) on 24 h ambulatory electrocardiography recording was assessed. Serum markers of ECM turnover including type I and III aminoterminal propeptide of procollagen (PINP and PIIINP), matrix metalloproteinase-2 and -9 (MMP-2 and MMP-9), and tissue inhibitor of metalloproteinase-1 (TIMP-1) were analyzed. RESULTS: The serum PIIINP concentration was correlated significantly with standard deviation of all normal to normal R-R intervals (SDNN) (r=-0.722, p=<0.001), percentage of adjacent NN interval differences >50 ms (pNN50) (r=-0.528, p=0.014), percentage of adjacent NN interval differences >20 ms (pNN20) (r=-0.545, p=0.002), very low frequency (VLF) (r=-0.490, p=0.024), low frequency (LF) (r=-0.491, p=0.024), and high frequency (HF) (r=-0.513, p=0.018). PINP, MMP-2, -9, TIMP-1 were not correlated with time- and frequency-domain analysis of HRV. CONCLUSIONS: PIIINP was significantly correlated with time- and frequency-domain analysis of HRV in HF patients. PIIINP is a potential serological marker to evaluate cardiac autonomic control and risk of SCD in HF patients.
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Lin et al. (2010) conducted an observational in Heart failure (n=21). Serum PIIINP concentration was evaluated on Correlation with standard deviation of all normal to normal R-R intervals (SDNN) (r=-0.722, p=<0.001). Serum PIIINP concentration was significantly inversely correlated with the standard deviation of all normal to normal R-R intervals (r=-0.722, p<0.001) in patients with heart failure.
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