Growth differentiation factor-15 as a biomarker of coronary microvascular dysfunction in ST-segment elevation myocardial infarction

被引:0
|
作者
Tian, Rui [1 ,2 ,3 ,4 ,5 ]
Wang, Zerui [1 ,2 ,3 ,4 ,5 ]
Zhang, Shenglin [1 ,2 ,3 ,4 ,5 ]
Wang, Xiaojun [1 ,2 ,3 ,4 ,5 ]
Zhang, Yiwen [1 ,2 ,3 ,4 ,5 ]
Yuan, Jiaquan [1 ,2 ,3 ,4 ,5 ]
Zhang, Jiajun [1 ,2 ,3 ,4 ,5 ]
Xu, Feng [1 ,2 ,3 ,4 ,5 ]
Chen, Yuguo [1 ,2 ,3 ,4 ,5 ]
Li, Chuanbao [1 ,2 ,3 ,4 ,5 ]
机构
[1] Shandong Univ, Qilu Hosp, Dept Emergency Med, Jinan 250012, Peoples R China
[2] Shandong Univ, Qilu Hosp, Inst Emergency Crit Care Med, Shandong Prov Clin Res Ctr Emergency & Crit Care M, Jinan 250012, Peoples R China
[3] Shandong Univ, Qilu Hosp, Key Lab Cardiopulm Cerebral Resuscitat Res Shandon, Shandong Prov Engn Lab Emergency & Crit Care Med,, Jinan 250012, Peoples R China
[4] Shandong Univ, Qilu Hosp, Shandong Key Lab Magnet Field free Med & Funct Ima, Jinan 250012, Peoples R China
[5] Shandong Univ, Qilu Hosp, NMPA Key Lab Clin Res & Evaluat Innovat Drug, Jinan 250012, Peoples R China
基金
国家重点研发计划; 中国国家自然科学基金;
关键词
Growth differentiation factor-15; ST-Segment elevation myocardial infarction; Percutaneous coronary intervention; Coronary microvascular dysfunction; No-reflow phenomenon; Hemodynamics; FRACTIONAL FLOW RESERVE; ESC WORKING GROUP; RISK STRATIFICATION; PROGNOSTIC VALUE; MORTALITY; PATHOPHYSIOLOGY; ASSOCIATION; ANGIOGRAPHY; ACTIVATION; MARKER;
D O I
10.1016/j.heliyon.2024.e35476
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Background: The predictive value of growth differentiation factor-15 (GDF-15) in coronary microvascular dysfunction (CMD) following primary percutaneous coronary intervention (PPCI) in ST-segment elevation myocardial infarction (STEMI) patients is unclear. Methods: This study continuously recruited STEMI patients treated with PPCI at the Chest Pain Center of Qilu Hospital of Shandong University from April 2023 to December 2023. Blood samples were taken before PPCI and the level of circulating GDF-15 was measured by enzyme-linked immunosorbent assay (ELISA), and the patients were divided into CMD and Control group according to angiographic microvascular resistance (AMR) (cut-off value 2.50 mmHg*s/cm). The differences in GDF-15 expression levels between the two groups were compared, and the predictive value of GDF-15 for CMD was systematically evaluated. Results: A total of 134 patients, with an average age of 59.78 +/- 12.69 years and 75.37 % being male, were included in this study. Multivariable logistic regression revealed a significant association between GDF-15 and CMD (adjusted OR = 2.505, 95 % CI: 1.661-3.779, P < 0.001). The area under the curve (AUC) of GDF-15 for CMD was 0.782 (95 % CI: 0.704-0.861), with a sensitivity of 0.795 and specificity of 0.643 in predicting CMD in PPCI. The AUC of the GDF-15 model (Model With GDF-15) was 0.867 (95 % CI: 0.806-0.928), significantly outperforming the clinical baseline model (Model Without GDF-15) (Delta AUC = 0.079, 95 % CI: 0.020-0.138, P = 0.009). Furthermore, the net reclassification improvement (NRI) was 0.854 (95 % CI: 0.543-1.166, P < 0.001), and the integrated discrimination improvement (IDI) was 0.151 (95 % CI: 0.089-0.213, P < 0.001). Conclusions: GDF-15 can serve as a biomarker for predicting the development of CMD in STEMI patients undergoing PPCI.
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页数:14
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