Key result
Spironolactone-induced serum PICP reduction links to improved diastolic dysfunction and decreased E/e'.
Why the study?
Understanding how collagen synthesis markers associate with cardiac structure and function abnormalities is important to screen for myocardial fibrosis and monitor antifibrotic medication effects, given non-cardiac comorbidity influences.
Is a reduction in serum PICP with spironolactone associated with improved echocardiographic markers of diastolic dysfunction in patients at risk of heart failure?
RCT (n=527)
Is a reduction in serum PICP with spironolactone associated with improved echocardiographic markers of diastolic dysfunction in patients at risk of heart failure?
Effect estimate: adjusted-beta 0.93 (95% CI 0.14-1.73)
p-value: p=0.022
In patients at risk of heart failure, a reduction in the collagen synthesis marker PICP with spironolactone correlates with improved diastolic function.
Does not support PICP-guided spironolactone use; leaves open its value as diastolic biomarker in at-risk patients.
Aims Procollagen type I C‐terminal propeptide (PICP) and procollagen type III N‐terminal propeptide (PIIINP) are markers reflecting collagen synthesis in cardiac fibrosis. However, they may be influenced by the presence of non‐cardiac comorbidities (e.g. ageing, obesity, renal impairment). Understanding the associations between markers of collagen synthesis and abnormalities of cardiac structure and function is important to screen for myocardial fibrosis and monitor the antifibrotic effect of medications. Methods and results The HOMAGE (Heart ‘OMics’ in AGEing) trial showed that spironolactone decreased serum PICP concentrations and improved cardiac remodelling over 9 months in a population at risk of developing heart failure (HF). We evaluated the associations between echocardiographic variables, PICP, PIIINP and galectin‐3 at baseline and during the course of the trial. Among 527 individuals (74 ± 7 years, 26% women), median serum concentrations of PICP, PIIINP and galectin‐3 were 80.6 μg/L (65.1–97.0), 3.9 μg/L (3.1–5.0), and 16.1 μg/L (13.5–19.7), respectively. After adjustment for potential confounders, higher serum PICP was significantly associated with left ventricular hypertrophy, left atrial enlargement, and greater ventricular stiffness (all p < 0.05), whereas serum PIIINP and galectin‐3 were not (all p > 0.05). In patients treated with spironolactone, a reduction in serum PICP during the trial was associated with a decrease in E/e′ (adjusted‐beta = 0.93, 95% confidence interval 0.14–1.73; p = 0.022). Conclusions In individuals at high risk of developing HF, serum PICP was associated with cardiac structural and functional abnormalities, and a decrease in PICP with spironolactone was correlated with improved diastolic dysfunction as assessed by E/e′. In contrast, no such associations were present for serum PIIINP and galectin‐3.
No takes yet. Share an insight, caveat, or question.
Kobayashi et al. (2022) conducted an RCT in At risk of developing heart failure (n=527). Spironolactone was evaluated on Decrease in E/e' associated with a reduction in serum PICP (adjusted-beta 0.93, 95% CI 0.14-1.73, p=0.022). A reduction in serum PICP during spironolactone treatment was associated with improved diastolic dysfunction as assessed by a decrease in E/e' (adjusted-beta 0.93; 95% CI 0.14-1.73; p=0.022).
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: