Key result
Higher plasma endogenous ouabain levels independently predicted heart failure progression in idiopathic dilated cardiomyopathy (OR 5.417; 95% CI 2.044-14.355; p<0.001).
Why the study?
Do higher plasma endogenous ouabain levels predict heart failure progression in patients with idiopathic dilated cardiomyopathy?
Cohort (n=140)
Do higher plasma endogenous ouabain levels predict heart failure progression in patients with idiopathic dilated cardiomyopathy?
Circulating endogenous ouabain is an independent prognostic marker for heart failure progression in patients with idiopathic dilated cardiomyopathy.
Answers are grounded in this paper and cite their sources.
Endogenous ouabain may aid risk stratification in idiopathic dilated cardiomyopathy; leaves open whether targeting it improves outcomes.
Increased circulating levels of endogenous ouabain (EO) have been observed in some heart failure patients, but their long term clinical significance is unknown. This study investigated the prognostic value of EO for worsening heart failure among 140 optimally treated patients (age 50+/-14 years; 104 male; NYHA class 1.9+/-0.7) with idiopathic dilated cardiomyopathy. Plasma EO was determined by RIA and by liquid chromatography mass spectrometry, values were linearly correlated (r = 0.89) in regression analysis. During follow-up (13+/-5 months), heart failure progression was defined as worsening clinical condition leading to one or more of the following: sustained increase in conventional therapies, hospitalization, cardiac transplant, or death. NYHA functional class, age, LVEF, peak VO2 and plasma levels of EO were predictive for heart failure progression. Heart failure worsened 1.5 fold (HR: 1.005; 95% CI: 1.001-1.007; p<0.01) for each 100 pmol/L increase in plasma EO. Moreover, those patients with higher plasma EO values had an odds ratio of 5.417 (95% CI: 2.044-14.355; p<0.001) for heart failure progression. Following multivariate analysis, LVEF, NYHA class and plasma EO remained significantly linked with clinical events. This study provides the first evidence that circulating EO is a novel, independent and incremental marker that predicts the progression of heart failure.
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Pitzalis et al. (2005) conducted a cohort in Idiopathic dilated cardiomyopathy (n=140). Plasma endogenous ouabain (EO) vs. Lower plasma EO values was evaluated on Heart failure progression (worsening clinical condition leading to sustained increase in conventional therapies, hospitalization, cardiac transplant, or death) (OR 5.417, 95% CI 2.044-14.355, p=<0.001). Higher plasma endogenous ouabain levels independently predicted heart failure progression in idiopathic dilated cardiomyopathy (OR 5.417; 95% CI 2.044-14.355; p<0.001).
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