Key result
Well-developed coronary collaterals were associated with significantly lower overall Troponin I (2.25 vs 4.83 ng/ml) and CPK-MB levels compared to poor collaterals in patients with AMI.
Why the study?
The extent of benefit from coronary collateral circulation in protecting myocardium during acute myocardial infarction needed validation.
Does well-developed coronary collateral circulation reduce myocardial injury biomarkers in patients with acute myocardial infarction?
Cohort (n=3,616)
No
Does well-developed coronary collateral circulation reduce myocardial injury biomarkers in patients with acute myocardial infarction?
Well-developed coronary collaterals are associated with a blunted rise in myocardial injury biomarkers during acute myocardial infarction, suggesting a cardioprotective effect.
Answers are grounded in this paper and cite their sources.
Hypothesis-generating for cardioprotective effects of collaterals in AMI; prospective trials needed before clinical adoption.
Introduction: Quantitative analysis of cardiac biomarkers, troponin I and CPK-MB, estimates the extent of myocardial injury while extent of benefit from coronary collateral circulation (CCC) to protect myocardium during acute myocardial infarction (AMI) needs validation. We analysed if the extent of collaterals had impact on baseline biomarkers at the time of coronary angiogram. Methods: We analysed 3616 consecutive patients who presented with AMI and underwent invasive coronary angiography (CAG) with intent to revascularisation with biomarkers assessment at the time of CAG. CCC to Infarct related artery (IRA) were graded as per Rentrop grading viz. poorly-developed CCC (Grade 0/1 as Group A) and well-developed CCC (Grade 2/3 as Group B). Results: Both groups (A and B) were matched for demographics, traditional risk factors, SYNTAX 1 Score, time to CAG from onset of angina and eGFR. 36.59% of patients had Non-ST segment elevation myocardial infarction (NSTEMI) as compared to 63.41% ST -segment elevation infarction (STEMI). Overall Troponin I (P=0.01, P=0.01) and CPK MB (P=0.00, P=0.002) values were lower in group B in both NSTEMI and STEMI groups respectively. Troponin I and CPK-MB were significantly lower in group B [with NSTEMI for SVD (Single vessel disease) (P=0.05) and DVD (Double vessel disease) (P=0.04),but not for TVD (Triple vessel disease) and with STEMI in SVD (P=0.01), DVD (P=0.01) and TVD (P=0.001)]. Conclusion: Patients with well-developed coronary collaterals had a lower rise in biomarkers in AMI as compared to those with poor collaterals amongst both NSTEMI and STEMI groups.
No takes yet. Share an insight, caveat, or question.
Dubey et al. (2021) conducted a cohort in Acute Myocardial Infarction (n=3,616). Well-developed coronary collateral circulation (Rentrop Grade 2/3) vs. Poorly-developed coronary collateral circulation (Rentrop Grade 0/1) was evaluated on Overall Troponin I levels (ng/ml) (p=0.00). Well-developed coronary collaterals were associated with significantly lower overall Troponin I (2.25 vs 4.83 ng/ml) and CPK-MB levels compared to poor collaterals in patients with AMI.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: