Key result
Hyperuricaemia was associated with increased all-cause mortality (HR 1.44; 95% CI 1.12-1.85; P=0.005) in systolic heart failure, driven by patients without chronic kidney disease.
Why the study?
Does hyperuricaemia increase the risk of all-cause mortality and heart failure hospitalization in patients with systolic heart failure, and does this risk vary by the presence of chronic kidney disease?
Cohort (n=1,260)
Does hyperuricaemia increase the risk of all-cause mortality and heart failure hospitalization in patients with systolic heart failure, and does this risk vary by the presence of chronic kidney disease?
Answers are grounded in this paper and cite their sources.
Hyperuricaemia predicts poor outcomes in systolic heart failure patients without chronic kidney disease, but not in those with CKD, suggesting its prognostic value depends on whether it reflects increased xanthine oxidase activity versus impaired renal excretion.
AIM: To determine if the association between hyperuricaemia and poor outcomes in heart failure (HF) varies by chronic kidney disease (CKD). METHODS AND RESULTS: Of the 2645 systolic HF patients in the Beta-Blocker Evaluation of Survival Trial with data on baseline serum uric acid, 1422 had hyperuricaemia (uric acid ≥6 mg/dL for women and ≥8 mg/dL for men). Propensity scores for hyperuricaemia, estimated for each patient, were used to assemble a matched cohort of 630 pairs of patients with and without hyperuricaemia who were balanced on 75 baseline characteristics. Associations of hyperuricaemia with outcomes during 25 months of median follow-up were examined in all patients and in those with and without CKD (estimated glomerular filtration rate of <60 mL/min/1.73 m(2)). Hyperuricaemia-associated hazard ratios (HRs) and 95% confidence intervals (CI) for all-cause mortality and HF hospitalization were 1.44 (1.12-1.85, P = 0.005) and 1.27 (1.02-1.58, P = 0.031), respectively. Hazard ratios (95% CIs) for all-cause mortality among those with and without CKD were 0.96 (0.70-1.31, P = 0.792) and 1.40 (1.08-1.82, P = 0.011), respectively (P for interaction, 0.071), and those for HF hospitalization among those with and without CKD were 0.99 (0.74-1.33, P = 0.942) and 1.49 (1.19-1.86, P = 0.001), respectively (P for interaction, 0.033). CONCLUSION: Hyperuricaemia has a significant association with poor outcomes in HF patients without CKD but not in those with CKD, suggesting that hyperuricaemia may predict poor outcomes when it is primarily a marker of increased xanthine oxidase activity, but not when it is primarily due to impaired renal excretion of uric acid.
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Filippatos et al. (2011) conducted a cohort in Systolic heart failure (n=1,260). Hyperuricaemia vs. Without hyperuricaemia was evaluated on All-cause mortality (HR 1.44, 95% CI 1.12-1.85, p=0.005). Hyperuricaemia was associated with increased all-cause mortality (HR 1.44; 95% CI 1.12-1.85; P=0.005) in systolic heart failure, driven by patients without chronic kidney disease.
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