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Cytokine-Based Validation of the Inflammation-Based Risk Score in Patients with ST-Segment Elevation Myocardial
Brianda Amezcua-Guerra1, Luis M Amezcua-Castillo2, Jazmín A Guerra-López3
1School of Medicine, Universidad Nacional Autónoma de México, Mexico City, Mexico.
Insights
An inflammation risk score effectively predicts cytokine profiles, including elevated interleukin-6 and reduced interferon-γ-induced protein-10, in ST-segment elevation myocardial infarction (STEMI) patients. Higher scores correlate with adverse cardiovascular events.
Area of Science:
- Cardiology
- Immunology
- Biomarkers
Background:
- Systemic inflammation plays a critical role in ST-segment elevation myocardial infarction (STEMI) pathogenesis.
- Accurate assessment of inflammation is crucial for predicting patient outcomes.
- Existing risk scores may not fully capture the inflammatory state in STEMI.
Purpose of the Study:
- To validate an inflammation-based risk score using cytokine profiles in STEMI patients.
- To investigate the association between the risk score and specific inflammatory biomarkers.
- To determine if the risk score predicts major adverse cardiovascular events (MACE).
Main Methods:
- Developed an inflammation risk score based on leukocyte count, high-sensitivity C-reactive protein (hsCRP), and serum albumin levels.
- Categorized STEMI patients into no, mild, and severe inflammation groups.
- Measured serum levels of 16 key cytokines, including IL-6 and IP-10, and analyzed their correlation with the risk score and clinical outcomes.
Main Results:
- Higher inflammation risk scores were significantly associated with elevated Interleukin-6 (IL-6) and decreased Interferon-γ-induced protein-10 (IP-10) levels.
- IL-6 showed positive correlation with hsCRP and negative correlation with albumin.
- IP-10 demonstrated a negative correlation with leukocyte count.
- The inflammation score was linked to an increased incidence of MACE, particularly acute heart failure.
Conclusions:
- The inflammation-based risk score is a valid tool for assessing systemic inflammation in STEMI.
- The score correlates with specific cytokine profiles (IL-6, IP-10) and predicts adverse cardiovascular events.
- This score can aid in risk stratification and management of STEMI patients.
Abstract:
This study aimed to validate an inflammation-based risk score in patients with ST-segment elevation myocardial infarction (STEMI) by examining their cytokine profiles. Upon admission, patients were evaluated for systemic inflammation using a risk score that assigned points based on specific biomarkers: 1 point for leukocyte count ≥9.3 × 10³ cells/μL, 2 points for high-sensitivity C-reactive protein (hsCRP) ≥13.0 mg/L, and 3 points for serum albumin ≤3.6 g/dL. Patients were categorized into three groups: no inflammation (0 points, n = 13), mild inflammation (1-2 points, n = 35), and severe inflammation (3-6 points, n = 26). Serum levels of 16 key cytokines were measured. Patients with higher risk scores showed elevated interleukin (IL)-6 levels (19.6 vs. 8.5 vs. 6.8 pg/mL; P = 0.021) and decreased interferon-γ-induced protein-10 (IP-10) levels (73.4 vs. 68.8 vs. 112.2 pg/mL; P = 0.011). IL-6 was positively correlated with hsCRP (ρ 0.307) and negatively correlated with albumin (ρ -0.298), while IP-10 was negatively correlated with leukocyte count (ρ -0.301). No other cytokines showed significant association with the risk score. Higher inflammation scores were also associated with an increased incidence of major adverse cardiovascular events, particularly acute heart failure. This study underscores the association between the inflammation-based risk score and cytokine levels, specifically IL-6 and IP-10, in patients with STEMI.
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