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Coronary Progenitor Cells and Soluble Biomarkers in Cardiovascular Prognosis after Coronary Angioplasty
Published on: January 28, 2020
Plasma markers of endothelial damage/dysfunction, inflammation and thrombogenesis in relation to TIMI risk
Kaeng W Lee1, Andrew D Blann, Gregory Y H Lip
1Haemostasis Thrombosis and Vascular Biology Unit, University Department of Medicine, City Hospital, Birmingham, UK.
Insights
The TIMI risk score effectively identifies acute coronary syndrome patients with higher risks of cardiac events. Elevated markers of vascular damage and inflammation predict short-term outcomes, refining risk stratification.
Area of Science:
- Cardiology
- Vascular Biology
- Biomarkers
Background:
- Acute coronary syndromes (ACS) require accurate risk stratification for optimal treatment.
- The TIMI risk score is used for unstable angina and NSTEMI, identifying high-risk patients.
- Endothelial damage, inflammation, and thrombogenicity are implicated in ACS pathophysiology.
Purpose of the Study:
- To investigate if a high TIMI risk score correlates with increased endothelial damage/dysfunction, inflammation, and thrombogenicity.
- To determine if these biological markers predict recurrent cardiac events in ACS patients.
- To assess if these markers can refine risk stratification beyond the TIMI score.
Main Methods:
- 88 ACS patients (UAP/NSTEMI) had TIMI risk scores assessed at admission and 48 hours.
- Levels of circulating endothelial cells (CECs), von Willebrand factor (vWf), interleukin-6 (IL-6), and plasma tissue factor (TF) were measured.
- Patients were stratified into high (TIMI score ≥4) and low (TIMI score <4) risk groups.
- Composite endpoints of death, myocardial infarction, or refractory angina were assessed at 14 and 30 days.
Main Results:
- Patients with high TIMI risk scores showed significantly higher baseline and 48-hour levels of CECs, vWf, IL-6, and TF compared to low-risk patients.
- Higher baseline CECs and delta vWf levels were independent predictors of cardiac events at 14 and 30 days.
- The TIMI risk score identified patients with greater vascular insult, inflammation, and thrombogenicity, predicting short-term outcomes.
Conclusions:
- The TIMI risk score for UAP/NSTEMI identifies patients with significant vascular damage, inflammation, and thrombogenicity.
- Baseline CECs and delta vWf are sensitive predictors of short-term adverse cardiac events in ACS patients.
- These biomarkers may enhance global risk stratification for short-term adverse cardiac events in ACS patients.
Abstract:
Risk stratification at presentation with acute coronary syndromes (ACS) on the basis of the TIMI risk score for unstable angina and non-ST-elevation myocardial infarction (UAP/NSTEMI) identifies patients at high risk of recurrent cardiac events and those who benefit from more aggressive treatment strategy. We hypothesised the following: (a) that a high TIMI risk score brings a greater degree of acute changes in endothelial damage/dysfunction (circulating endothelial cells [CECs], von Willebrand factor [vWf]), inflammation (interleukin-6, IL-6) and blood thrombogenicity (plasma tissue factor, TF); and (b) that these indices are higher in those with high TIMI risk score who experienced recurrent cardiac event at day 14 and day 30. TIMI risk scores were determined at admission and 48 hours later in 88 ACS patients (60 male, age 67+/-12 yrs) with UAP or NSTEMI. CECs, IL-6 and TF levels were measured at both time points and the acute change (delta) calculated. Patients were split into high (score > or =4) or low (<4) TIMI score groups. The composite end point of death, myocardial infarction, and refractory angina requiring revascularisation following 14 and 30 days' follow-up was ascertained. Fifty-eight patients with high TIMI risk score (mean 4.7) had significantly higher baseline and 48 h CEC, vWf, IL-6,TF and deltaTF levels, compared to low TIMI risk score (mean 2.4) patients (all p<0.05). Multivariate Cox regression analysis adjusted for clinical variables and TIMI risk score expressed as either continuous or categorical variable identified baseline CECs and deltavWf levels (both p< or =0.01) as independent predictors of subsequent cardiac events at both 14 days and 30 days. TIMI risk score for UA/NSTEMI identifies those patients with more profound vascular insult, inflammation and thrombogenicity that, in the 'high risk' patient group, predicts short-term outcomes, although vascular damage was the more sensitive predictor. These indices may further refine global risk stratification for short-term adverse cardiac events in these patients.
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