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Sex differences between serum uric acid levels and cardiovascular outcomes in patients with coronary artery disease after stent implantation
被引:4
|作者:
Yuan, Song Lin
[1
]
Kim, Moo Hyun
[1
]
Lee, Kwang Min
[1
]
Jin, Xuan
[1
]
Song, Zhao Yan
[1
]
Park, Jong-Sung
[1
]
Cho, Young-Rak
[1
]
Lim, Kyunghee
[1
]
Yun, Sung-Cheol
[2
]
机构:
[1] Dong A Univ Hosp, Dept Cardiol, Pusan, South Korea
[2] Univ Ulsan, Asan Med Ctr, Dept Clin Epidemiol & Biostat, Coll Med, Seoul, South Korea
来源:
FRONTIERS IN CARDIOVASCULAR MEDICINE
|
2023年
/
10卷
基金:
新加坡国家研究基金会;
关键词:
sex;
serum uric acid;
cardiovascular outcomes (CV outcomes);
coronary artery disease;
stent implantation;
MYOCARDIAL-INFARCTION;
ALL-CAUSE;
MORTALITY;
EVENTS;
RISK;
D O I:
10.3389/fcvm.2023.1021277
中图分类号:
R5 [内科学];
学科分类号:
1002 ;
100201 ;
摘要:
BackgroundThe relationship between elevated serum uric acid (SUA) levels and cardiovascular outcomes after stent implantation remains uncertain. This study sought to evaluate the impact of SUA on 12-month cardiovascular outcomes after stent implantation. MethodsWe performed a retrospective study of patients who successfully underwent stent implantation and enrolled 3,222 patients with coronary artery disease (CAD) from a single center. SUA levels were measured before stent implantation. The patients were divided into six groups (<4, 4-4.9, 5-5.9, 6-6.9, 7-7.9 and >= 8 mg/dL) at SUA intervals of 1.0 mg/dL. The incidence of cardiovascular outcomes in the six groups was monitored for 1 year after stent implantation and the hazard ratios were estimated. Hazard ratios (HRs) and 95% confidence intervals (95% CIs) for cardiovascular outcomes were estimated using a Cox proportional hazard regression analysis. The primary endpoint was all-cause death. The secondary endpoint was a composite of all-cause death, myocardial infarction, target vessel revascularization, stent thrombosis and stroke. The follow-up duration was 12 months. ResultsOver the 12-month follow-up period, there were 101 all-cause deaths and 218 MACCE. After adjustment for several parameters, the group with SUA levels of more than or equal to 8 mg/dL had significantly higher hazard ratios in the incidence of all-cause death or MACCE. The group with <4.0 mg/dL had significantly higher hazard ratios in all-cause death only in male patients. In contrast, there were no significant differences observed for cardiovascular outcomes in female patients. ConclusionsOur study identified a U-shaped association between SUA levels and cardiovascular outcomes during 12-month follow-up for males, but not for females. Further studies are warranted to clarify the sex differences between SUA levels and clinical outcomes.
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