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Low sCD163/TWEAK Ratio at First Day After Acute Myocardial Infarction Associated with Adverse Cardiac Remodeling in
Mehmet Sait Altintas1, Nilnur Eyerci2, Orhan Karayigit3
1Istanbul Research and Training Hospital.
Insights
A lower soluble CD163 (sCD163) to TWEAK ratio after myocardial infarction (MI) predicts adverse cardiac remodeling. This ratio shows higher diagnostic performance than individual markers for predicting left ventricular volume increase post-MI.
Area of Science:
- Cardiovascular Research
- Biomarker Discovery
- Myocardial Infarction Pathogenesis
Background:
- Cardiac remodeling is a significant complication following acute myocardial infarction (MI).
- Identifying early predictors of adverse remodeling (AR) is crucial for patient management.
- The role of the sCD163/TWEAK ratio in post-MI cardiac remodeling remains to be fully elucidated.
Purpose of the Study:
- To investigate the predictive role of the sCD163/TWEAK ratio in cardiac remodeling after first acute MI in non-elderly patients.
- To assess the diagnostic performance of the sCD163/TWEAK ratio compared to individual markers.
Main Methods:
- Forty-four non-elderly patients (40-64 years) with first ST-elevation MI were enrolled.
- Cardiac magnetic resonance (CMR) imaging was used to assess adverse remodeling (AR) at 6 months post-MI.
- Serum levels of sCD163 and TWEAK were measured at baseline, 2 weeks, and 6 weeks post-MI.
Main Results:
- Patients who developed AR had significantly higher baseline sCD163 and TWEAK levels but a lower sCD163/TWEAK ratio compared to those without AR.
- A lower sCD163/TWEAK ratio on day 1 post-MI was associated with increased left ventricular end-diastolic volume at 6 months.
- The sCD163/TWEAK ratio demonstrated superior diagnostic performance for predicting AR compared to sCD163 or TWEAK alone.
Conclusions:
- The sCD163/TWEAK ratio plays a significant role in the early pathogenesis of adverse cardiac remodeling post-MI.
- A diminished sCD163/TWEAK ratio in the acute phase following MI serves as a valuable early indicator of subsequent adverse cardiac remodeling.
Abstract:
Aim In this study, we aimed to investigate the role of sCD163 / tumor necrosis factor-like weak apoptosis-inducing (TWEAK) ratio in cardiac remodeling in non-elderly patients diagnosed with first acute myocardial infarction (MI).Material and Methods Forty-four patients (age ranges: 40-64 years) diagnosed with first-time acute ST-elevation MI in the emergency department were evaluated with cardiac magnetic resonance (CMR) imaging. Adverse remodeling (AR) was defined the increases of left ventricular end-diastolic volume by ≥12 % by CMR at 6‑month post-MI TWEAK and sCD163 were measured at the first day (baseline), 2 weeks and 6 weeks post-MI.Results The average age of patients included in the study was 53.6±5.1 years. AR was detected in 18 patients at the 6 months post-MI. At the first day post-MI, median sCD163 concentration (116 069 vs 86 394 pg / mL, p=0.040) and median TWEAK concentration (759.4 vs 220.1 pg / mL, p<0.001) were higher in AR group compared to group without AR (the non-AR group), median sCD163 / TWEAK ratio (101.4 vs. 406.8; p<0.001) was lower. At the first day post-MI, concentrations of TWEAK and sCD163 showed a positive correlation in AR group and group without AR s. At 2 weeks post-MI, positive correlation continued in the non-AR group, but no significant correlation was found in the AR group. At the first day post-MI, sCD163 / TWEAK ratio was higher diagnostic performance compared to TWEAK and sCD163.Conclusion In the early phase post-MI, the relationship between sCD163 - TWEAK may have an important role in AR pathogenesis. A lower sCD163 / TWEAK ratio on the first day after MI was associated with an increase in left ventricular end-diastolic volume after 6 months of follow-up.
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