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Hsp-27 levels and thrombus burden relate to clinical outcomes in patients with ST-segment elevation myocardial
Maozhou Tian1, Lingmin Zhu2, Hongyang Lin3
1Department of Cardiac Surgery, The Affiliated Yantai Yuhuangding Hospital of Qingdao University, Yantai, Shangdong 264000, P.R. China.
Insights
High levels of Heat Shock Protein-27 (Hsp-27) in ST-segment elevation myocardial infarction (STEMI) patients correlate with increased thrombus burden and major adverse cardiovascular events (MACE). This finding may aid in predicting outcomes post-primary percutaneous coronary intervention (pPCI).
Area of Science:
- Cardiovascular Medicine
- Biomarkers
- Interventional Cardiology
Background:
- High thrombus burden in ST-segment elevation myocardial infarction (STEMI) complicates urgent revascularization, leading to poor outcomes.
- The role of Heat Shock Protein-27 (Hsp-27) in relation to thrombus burden and clinical outcomes in STEMI patients remains unclear.
- Understanding novel biomarkers is crucial for improving risk stratification in STEMI.
Purpose of the Study:
- To investigate the association between plasma Hsp-27 levels and thrombus burden in STEMI patients undergoing primary percutaneous coronary intervention (pPCI).
- To evaluate the predictive value of Hsp-27 for major adverse cardiovascular events (MACE) in this patient cohort.
Main Methods:
- Prospective study of 146 STEMI patients undergoing pPCI within 12 hours of symptom onset.
- Patients were categorized into low and high thrombus burden groups.
- Plasma Hsp-27 levels were measured; association with thrombus burden and MACE was analyzed using ROC curves and multivariate Cox regression.
Main Results:
- Patients with high thrombus burden exhibited significantly higher plasma Hsp-27 levels (58.0 ± 12.3 ng/mL) compared to those with low thrombus burden (32.0 ± 8.6 ng/mL).
- Plasma Hsp-27 levels demonstrated significant diagnostic value for high thrombus burden (AUC, 0.847).
- Hsp-27 levels > 45 ng/mL were positively correlated with a higher incidence of MACE (HR 2.801) and lower MACE-free survival at 180 days.
Conclusions:
- Plasma Hsp-27 is positively correlated with high thrombus burden in STEMI patients undergoing pPCI.
- Elevated plasma Hsp-27 levels serve as a significant predictor of MACE in STEMI patients.
- Hsp-27 may be a valuable biomarker for risk stratification and outcome prediction in STEMI.
Abstract:
High thrombus burden, subsequent distal embolization, and myocardial no-reflow remain a large obstacle that may negate the benefits of urgent coronary revascularization in patients with ST-segment elevation myocardial infarction (STEMI). However, the biological function and clinical association of Hsp-27 with thrombus burden and clinical outcomes in patients with STEMI is not clear. Consecutive patients (n = 146) having STEMI undergoing primary percutaneous coronary intervention (pPCI) within 12 hours from the onset of symptoms were enrolled in this prospective study in the Affiliated Yantai Yuhuangding Hospital of Qingdao University, Yantai, Shangdong, P.R. China. Patients were divided into low thrombus burden and high thrombus burden groups. The present study demonstrated that patients with high-thrombus burden had higher plasma Hsp-27 levels ([32.0 ± 8.6 vs. 58.0 ± 12.3] ng/mL, P < 0.001). The median value of Hsp-27 levels in all patients with STEMI was 45 ng/mL. Using the receiver operating characteristic (ROC) curve analysis, plasma Hsp-27 levels were of significant diagnostic value for high thrombus burden (AUC, 0.847; 95% CI, 0.775-0.918; P < 0.01). The multivariate cox regression analysis demonstrated that Hsp-27 > 45 ng/mL (HR 2.801, 95% CI 1.296-4.789, P = 0.001), were positively correlated with the incidence of major adverse cardiovascular events (MACE). Kaplan-Meier survival analysis demonstrated that MACE-free survival at 180-day follow-up was significantly lower in patients with Hsp-27 > 45 ng/mL (log rank = 10.28, P < 0.001). Our data demonstrate that plasma Hsp-27 was positively correlated with high thrombus burden and the incidence of MACE in patients with STEMI who underwent pPCI.
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