High serum uric acid trajectories are associated with risk of myocardial infarction and all-cause mortality in general Chinese population

被引:10
|
作者
Tian, Xue [1 ,2 ]
Zuo, Yingting [1 ,2 ]
Chen, Shuohua [3 ]
Wu, Shouling [3 ]
Wang, Anxin [4 ,5 ]
Luo, Yanxia [1 ,2 ]
机构
[1] Capital Med Univ, Sch Publ Hlth, Dept Epidemiol & Hlth Stat, 10 Xitoutiao, Beijing 100069, Peoples R China
[2] Beijing Municipal Key Lab Clin Epidemiol, Beijing, Peoples R China
[3] North China Univ Sci & Technol, Kailuan Hosp, Dept Cardiol, 57 Xinhua East Rd, Tangshan 063000, Peoples R China
[4] Capital Med Univ, Beijing Tiantan Hosp, China Natl Clin Res Ctr Neurol Dis, 119 South 4th Ring West Rd, Beijing 100070, Peoples R China
[5] Capital Med Univ, Beijing Tiantan Hosp, Dept Neurol, Beijing, Peoples R China
基金
中国国家自然科学基金;
关键词
Serum uric acid; Trajectories; Myocardial infarction; All-cause mortality; CHRONIC KIDNEY-DISEASE; INFLAMMATORY RESPONSES; ALCOHOL-CONSUMPTION; HYPERTENSION; HEALTH; LEVEL; CELLS;
D O I
10.1186/s13075-022-02812-y
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background Long-term patterns of serum uric acid (SUA) and their association with the risk of myocardial infarction (MI) and mortality are poorly characterized as prior studies measured SUA at a single time point. This study aimed to identify SUA trajectories and determine their associations with incident MI and all-cause mortality. Methods We included 85,503 participants who were free of MI in or prior 2012 from the Kailuan study. SUA trajectories during 2006-2012 were identified by group-based trajectory modeling. Cox proportional hazard models were used to assess the association of SUA trajectories with MI and all-cause mortality. Results We identified three SUA trajectories during 2006-2012: low-stable (n=44,124, mean SUA: 236-249 mu mol/L), moderate-stable (n=34,431, mean SUA: 324-354 mu mol/L) and high-stable (n=6,984, mean SUA: 425-463 mu mol/L). During a median follow-up of 6.8 years, we documented 817 (0.96%) incident MI and 6498 (7.60%) mortality. Compared with the low-stable group, high-stable group experienced a higher risk of MI (hazard ratio [HR], 1.35; 95% confidence [CI], 1.07-1.71) and all-cause mortality (HR, 1.22; 95% CI, 1.12-1.33). Multiple sensitivity analyses yielded similar results. Additionally, the association of SUA trajectory with MI and all-cause mortality was more pronounced in individuals without a history of hypertension (P-interaction=0.0359) and those aged <60 years (P-interaction<0.0001), respectively. Conclusions Higher SUA trajectories were associated with altered risk of MI and all-cause mortality, suggesting that monitoring SUA trajectory may assist in identifying subpopulations at higher risk of MI and all-cause mortality.
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收藏
页数:10
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