Association of hemoglobin glycation index with clinical outcomes in patients with coronary artery disease: a prospective cohort study

被引:0
作者
Wen, Zhi-Ying [1 ]
Li, Fa-Peng [2 ]
Wu, Ting-Ting [1 ]
Hou, Xian-Geng [1 ]
Pan, Ying [1 ]
Deng, Chang-Jiang [1 ]
Li, Yan-Xiao [3 ]
He, Xue-Chun [1 ]
Gao, Wei-Tong [1 ]
Chen, Hong-Xia [1 ]
Zheng, Ying-Ying [1 ]
Xie, Xiang [1 ]
机构
[1] Xinjiang Med Univ, Affiliated Hosp 1, Dept Cardiol, Urumqi 830054, Peoples R China
[2] Xinjiang Med Univ, Affiliated Hosp 5, Dept Cardiol, Urumqi 830011, Peoples R China
[3] Zhengzhou Univ, Affiliated Hosp 1, Dept Cardiol, Zhengzhou 450052, Peoples R China
关键词
Coronary artery disease; Hemoglobin glycosylation index; Major adverse cardiovascular events; Mortality; BIOLOGICAL VARIATION; A(1C); RISK;
D O I
10.1186/s13098-024-01475-w
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background To analyze the association between the hemoglobin glycation index (HGI) and the long-term prognosis of patients with coronary artery disease (CAD). Methods HGI represented the difference between laboratory measured Hemoglobin A1c (HbA1c) and predicted HbA1c based on a liner regression between Hb1Ac and fasting plasma glucose (FPG). A total of 10 598 patients who treated with percutaneous coronary intervention (PCI) were stratified into three groups (low HGI group: HGI<-0.506, medium HGI group: -0.506 <= HGI < 0.179, and high HGI group: HGI >= 0.179). The primary endpoints includes all-cause mortality (ACM) and cardiac mortality (CM). The secondary endpoints were major adverse cardiac events (MACEs) and major adverse cardiac and cerebrovascular events (MACCEs). Results A total of 321 ACMs, 243 CMs, 774 MACEs, and 854 MACCEs were recorded during a 60-month follow-up period. After adjusting for confounders using a multivariate Cox regression analysis, the patients in the low HGI group had a significantly increased risk of ACM (adjusted HR = 1.683, 95%CI:1.179-2.404, P = 0.004) and CM (HR = 1.604, 95%CI:1.064-2.417, P = 0.024) as compared with patients in the medium HGI group. Similarly, the patients in the high HGI group had an increased risk of MACEs (HR = 1.247, 95% CI: 1.023-1.521, P = 0.029) as compared with patients in the medium HGI group. For ACM, CM, and MACEs, a U-shaped relation were found among these three groups. However, we did not find significant differences in the incidence of MACCEs among these three groups. Conclusion The present study indicates that HGI could be an independent predictor for the risk of mortality and MACEs in patients with CAD.
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