Does subclinical cardiac and noncardiac organ dysfunction increase the risk of incident heart failure in a community-based cohort?
1038 participants of the Framingham Heart Study original cohort, mean age 76±5 years, 39% men.
Presence of subclinical cardiac dysfunction (left ventricular systolic and diastolic) and noncardiac organ dysfunction (renal, pulmonary, hematologic).
Absence of subclinical cardiac and noncardiac organ dysfunction.
Incident heart failure events.hard clinical
Antecedent subclinical cardiac and noncardiac organ dysfunction independently predict the development of incident heart failure, highlighting HF as a progressive, multiorgan syndrome.
BACKGROUND: Heart failure (HF) is a clinical syndrome characterized by signs and symptoms involving multiple organ systems. Longitudinal data demonstrating that asymptomatic cardiac dysfunction precedes overt HF are scarce, and the contribution of noncardiac dysfunction to HF progression is unclear. We hypothesized that subclinical cardiac and noncardiac organ dysfunction would accelerate the manifestation of HF. METHODS AND RESULTS: We studied 1038 participants of the Framingham Heart Study original cohort (mean age, 76±5 years; 39% men) with routine assessment of left ventricular systolic and diastolic function. Major noncardiac organ systems were assessed with the use of serum creatinine (renal), serum albumin (hepatic), ratio of forced expiratory volume in 1 second to forced vital capacity (FEV(1):FVC ratio; pulmonary), hemoglobin concentration (hematologic/oxygen-carrying capacity), and white blood cell count (systemic inflammation). On follow-up (mean, 11 years), there were 248 incident HF events (146 in women). After adjustment for established HF risk factors, antecedent left ventricular systolic dysfunction (hazard ratio, 2.33; 95% confidence interval, 1.43 to 3.78) and diastolic dysfunction (hazard ratio, 1.32; 95% confidence interval, 1.01 to 1.71) were associated with increased HF risk. After adjustment for cardiac dysfunction, higher serum creatinine, lower FEV1:FVC ratios, and lower hemoglobin concentrations were associated with increased HF risk (all P<0.05); serum albumin and white blood cell count were not. Subclinical dysfunction in each noncardiac organ system was associated with a 30% increased risk of HF (P=0.013). CONCLUSIONS: Antecedent cardiac dysfunction and noncardiac organ dysfunction are associated with increased incidence of HF, supporting the notion that HF is a progressive syndrome and underscoring the importance of noncardiac factors in its occurrence.
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Carolyn S.P. Lam
Asya Lyass
Elisabeth Kraigher‐Krainer
Circulation
University of Toronto
Boston University
Mayo Clinic in Arizona
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Lam et al. (Tue,) studied this question.
www.synapsesocial.com/papers/69f14aa22811130d0cde1e73 — DOI: https://doi.org/10.1161/circulationaha.110.979203