Key result
Leukocyte telomere length does not differ between young AMI patients and controls or predict MACE.
Why the study?
Leukocyte telomere length is a potential marker of biological age related to endothelial dysfunction and atherosclerosis, but its relationship with premature acute myocardial infarction and predictive value for major cardiovascular events is unclear.
Does leukocyte telomere length predict the risk of premature acute myocardial infarction or major cardiovascular events in young adults?
Case-Control (n=389)
No
Does leukocyte telomere length predict the risk of premature acute myocardial infarction or major cardiovascular events in young adults?
Absolute Event Rate: 0.77% vs 0.76%
p-value: p=0.20
Leukocyte telomere length is not a reliable biomarker for predicting premature acute myocardial infarction or subsequent major cardiovascular events in young Italian patients.
LTL does not support risk prediction in young AMI patients; leaves open its value in other populations or as a research biomarker.
Leukocyte telomere length (LTL) provides a potential marker of biological age, closely related to the endothelial dysfunction and consequently to the atherosclerotic process. To investigate the relationship between the LTL and the risk of premature acute myocardial infarction and to evaluate the predictive value of LTL on the onset of major cardiovascular events, 199 patients from 18 to 48 years old with first diagnosis of acute myocardial infarction were enrolled and were matched with 190 controls for sex and age (± 1 year). Clinical data and coronary artery disease were evaluated at enrollment and at follow up. LTL was measured at enrollment using a quantitative PCR-based method. No significant differences were observed in LTL between cases and controls (p = 0.20) and with the presence of coronary artery disease in patients (p = 0.47). Hypercholesterolemic cases presented LTL significantly longer than cases without hypercholesterolemia (t/s: 0.82 ± 0.16 p = 0.79 and t/s norm: 0.79 ± 0.19 p = 0.01), as confirmed in multivariate regression analysis (p = 0.005, β = 0.09). Furthermore, multivariate regression analysis showed LTL significantly shorter in hypertensive cases than in normotensive cases (p = 0.04, β = -0.07). One hundred seventy-one cases (86%) ended the average follow up of 9 ± 5 years, 92 (54%) presented a major cardiovascular event. At multivariate regression analysis the LTL detected at enrollment did not represent a predictive factor of major cardiovascular events nor it significantly impacted with cumulative events. Based on present cohort of young Italian patients, the LTL did not represent a marker of acute myocardial infarction nor had a predictive role at medium term follow up.
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Russo et al. (2012) conducted a case-control in Juvenile Acute Myocardial Infarction (n=389). Leukocyte telomere length vs. Healthy matched controls was evaluated on Difference in leukocyte telomere length (t/s norm) between cases and controls (p=0.20). Leukocyte telomere length did not significantly differ between young patients with acute myocardial infarction and matched controls (0.77 vs 0.76, p=0.20) and did not predict major cardiovascular events.
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