Associations of long-term mortality with serum uric acid at admission in acute decompensated heart failure with different phenotypes

BACKGROUND AND AIMS: It remains unclear whether the long-term prognostic value of serum uric acid (SUA) at admission differs in acute decompensated heart failure (HF) patients across the spectrum of left ventricular ejection fraction (EF). METHODS AND RESULTS: In 2375 patients (38.9% women; mean age...

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Veröffentlicht in:NUTRITION METABOLISM AND CARDIOVASCULAR DISEASES 2023-10, Vol.33 (10), p.1998-2005
Hauptverfasser: Wei, Fang-Fei, Chen, Xuwei, Cheng, Winglam, Chen, Shilan, Wu, Yuzhong, Yu, Zhongping, Huang, Jiale, Zhao, Jingjing, He, Jiangui, Cauwenberghs, Nicholas, Dong, Yugang, Liu, Chen
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container_end_page 2005
container_issue 10
container_start_page 1998
container_title NUTRITION METABOLISM AND CARDIOVASCULAR DISEASES
container_volume 33
creator Wei, Fang-Fei
Chen, Xuwei
Cheng, Winglam
Chen, Shilan
Wu, Yuzhong
Yu, Zhongping
Huang, Jiale
Zhao, Jingjing
He, Jiangui
Cauwenberghs, Nicholas
Dong, Yugang
Liu, Chen
description BACKGROUND AND AIMS: It remains unclear whether the long-term prognostic value of serum uric acid (SUA) at admission differs in acute decompensated heart failure (HF) patients across the spectrum of left ventricular ejection fraction (EF). METHODS AND RESULTS: In 2375 patients (38.9% women; mean age, 68.8 years), we assessed the risk of long-term (>1 year) all-cause mortality associated with per 1-SD increase in SUA at admission, using multivariable Cox regression in HF with preserved (HFpEF), mildly reduced (HFmrEF) and reduced (HFrEF) EF. During a median follow-up of 4.1 years, the long-term mortality rate was 39.9%. In all patients, the multivariable-adjusted hazard ratio (HR) expressing the risk of long-term mortality associated with SUA was 1.18 (95% CI, 1.11-1.26; P 
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METHODS AND RESULTS: In 2375 patients (38.9% women; mean age, 68.8 years), we assessed the risk of long-term (&gt;1 year) all-cause mortality associated with per 1-SD increase in SUA at admission, using multivariable Cox regression in HF with preserved (HFpEF), mildly reduced (HFmrEF) and reduced (HFrEF) EF. During a median follow-up of 4.1 years, the long-term mortality rate was 39.9%. In all patients, the multivariable-adjusted hazard ratio (HR) expressing the risk of long-term mortality associated with SUA was 1.18 (95% CI, 1.11-1.26; P &lt; 0.001). Compared with the low tertile of the SUA distribution, the sex- and age-adjusted cumulative incidence of long-term mortality was higher in the top tertile. In patients with HFpEF and HFrEF, SUA predicted the risk of long-term mortality with HRs amounting to 1.12 (95% CI, 1.02-1.21; P = 0.012) and 1.28 (95% CI, 1.12-1.47; P &lt; 0.001), respectively. However, there were no associations between the risk of mortality and SUA in HFmrEF. Furthermore, age, sex, NYHA class, and the prevalence of coronary heart disease interacted significantly with SUA for predicting long-term mortality. CONCLUSION: Higher levels of SUA at admission were associated with higher risk of long-term mortality in patients with different HF subtypes. The risk conferred by SUA was age and sex dependent. Our observations highlight that measuring SUA at admission may help to improve risk stratification.</description><identifier>ISSN: 0939-4753</identifier><language>eng</language><publisher>ELSEVIER SCI LTD</publisher><ispartof>NUTRITION METABOLISM AND CARDIOVASCULAR DISEASES, 2023-10, Vol.33 (10), p.1998-2005</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,315,780,784,27859</link.rule.ids></links><search><creatorcontrib>Wei, Fang-Fei</creatorcontrib><creatorcontrib>Chen, Xuwei</creatorcontrib><creatorcontrib>Cheng, Winglam</creatorcontrib><creatorcontrib>Chen, Shilan</creatorcontrib><creatorcontrib>Wu, Yuzhong</creatorcontrib><creatorcontrib>Yu, Zhongping</creatorcontrib><creatorcontrib>Huang, Jiale</creatorcontrib><creatorcontrib>Zhao, Jingjing</creatorcontrib><creatorcontrib>He, Jiangui</creatorcontrib><creatorcontrib>Cauwenberghs, Nicholas</creatorcontrib><creatorcontrib>Dong, Yugang</creatorcontrib><creatorcontrib>Liu, Chen</creatorcontrib><title>Associations of long-term mortality with serum uric acid at admission in acute decompensated heart failure with different phenotypes</title><title>NUTRITION METABOLISM AND CARDIOVASCULAR DISEASES</title><description>BACKGROUND AND AIMS: It remains unclear whether the long-term prognostic value of serum uric acid (SUA) at admission differs in acute decompensated heart failure (HF) patients across the spectrum of left ventricular ejection fraction (EF). METHODS AND RESULTS: In 2375 patients (38.9% women; mean age, 68.8 years), we assessed the risk of long-term (&gt;1 year) all-cause mortality associated with per 1-SD increase in SUA at admission, using multivariable Cox regression in HF with preserved (HFpEF), mildly reduced (HFmrEF) and reduced (HFrEF) EF. During a median follow-up of 4.1 years, the long-term mortality rate was 39.9%. In all patients, the multivariable-adjusted hazard ratio (HR) expressing the risk of long-term mortality associated with SUA was 1.18 (95% CI, 1.11-1.26; P &lt; 0.001). Compared with the low tertile of the SUA distribution, the sex- and age-adjusted cumulative incidence of long-term mortality was higher in the top tertile. In patients with HFpEF and HFrEF, SUA predicted the risk of long-term mortality with HRs amounting to 1.12 (95% CI, 1.02-1.21; P = 0.012) and 1.28 (95% CI, 1.12-1.47; P &lt; 0.001), respectively. However, there were no associations between the risk of mortality and SUA in HFmrEF. Furthermore, age, sex, NYHA class, and the prevalence of coronary heart disease interacted significantly with SUA for predicting long-term mortality. CONCLUSION: Higher levels of SUA at admission were associated with higher risk of long-term mortality in patients with different HF subtypes. The risk conferred by SUA was age and sex dependent. 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METHODS AND RESULTS: In 2375 patients (38.9% women; mean age, 68.8 years), we assessed the risk of long-term (&gt;1 year) all-cause mortality associated with per 1-SD increase in SUA at admission, using multivariable Cox regression in HF with preserved (HFpEF), mildly reduced (HFmrEF) and reduced (HFrEF) EF. During a median follow-up of 4.1 years, the long-term mortality rate was 39.9%. In all patients, the multivariable-adjusted hazard ratio (HR) expressing the risk of long-term mortality associated with SUA was 1.18 (95% CI, 1.11-1.26; P &lt; 0.001). Compared with the low tertile of the SUA distribution, the sex- and age-adjusted cumulative incidence of long-term mortality was higher in the top tertile. In patients with HFpEF and HFrEF, SUA predicted the risk of long-term mortality with HRs amounting to 1.12 (95% CI, 1.02-1.21; P = 0.012) and 1.28 (95% CI, 1.12-1.47; P &lt; 0.001), respectively. However, there were no associations between the risk of mortality and SUA in HFmrEF. Furthermore, age, sex, NYHA class, and the prevalence of coronary heart disease interacted significantly with SUA for predicting long-term mortality. CONCLUSION: Higher levels of SUA at admission were associated with higher risk of long-term mortality in patients with different HF subtypes. The risk conferred by SUA was age and sex dependent. Our observations highlight that measuring SUA at admission may help to improve risk stratification.</abstract><pub>ELSEVIER SCI LTD</pub></addata></record>
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title Associations of long-term mortality with serum uric acid at admission in acute decompensated heart failure with different phenotypes
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