Abstract

Non-ST elevation acute coronary syndrome (NSTEACS) occurs more frequently in older patients with an increased occurrence of recurrent cardiac events following the index presentation. Telomeres are structures consisting of repeated DNA sequences as associated shelterin proteins at the ends of chromosomes. We aim to determine whether telomere length (TL) and telomerase activity (TA) predicted poor outcomes in older patients presenting with NSTEACS undergoing invasive care. Older patients undergoing invasive management for NSTEACS were recruited to the ICON-1 biomarker study (NCT01933581). Peripheral blood mononuclear cells (PBMC) were recovered on 153 patients. DNA was isolated and mean TL was measured by quantitative PCR expressed as relative T (telomere repeat copy number) to S (single copy gene number) ratio (T/S ratio), and a telomere repeat amplification assay was used to assess TA during index presentation with NSTEACS. Primary clinical outcomes consisted of death, myocardial infarction (MI), unplanned revascularisation, stroke and significant bleeding recorded at 1 year. TL and TA were divided into tertile groups for analysis. Cox proportional hazards regression was performed. Ordinal regression was performed to evaluate the relationship between TL and TA and traditional cardiovascular risk factors at baseline. 298 patients were recruited in the ICON-1 study of which 153 had PBMC recovered. The mean age was 81.0 ± 4.0 years (64% male). Mean telomere length T/S ratio was 0.47 ± 0.25 and mean TA was 1.52 ± 0.61 units. The primary composite outcome occurred in 44 (28.8%) patients. There was no association between short TL or low TA and incidence of the primary composite outcome (Hazard Ratio [HR] 1.50, 95% Confidence Interval [CI] 0.68-3.34, p = 0.32 and HR 1.33, 95% CI 0.52-3.36, p = 0.51 respectively). TL and TA are not found to be associated with the incidence of adverse outcomes in older patients presenting with NSTEACS undergoing invasive care. URL: https://www.clinicaltrials.gov Unique identifier: NCT01933581.

Highlights

  • Older age is a well-known cardiovascular disease (CVD) risk factor, especially for coronary artery disease (CAD)[1,2,3]

  • telomere length (TL) and telomerase activity (TA) are not found to be associated with the incidence of adverse outcomes in older patients presenting with Non-ST elevation acute coronary syndrome (NSTEACS) undergoing invasive care

  • Non ST-elevation acute coronary syndromes (NSTEACS) are more common within the older population, with the UK’s Myocardial Ischaemia National Audit Project (MINAP) data showing that 46% of all non ST elevation myocardial infarction (NSTEMIs) suffered between 2006 and 2010 occurred in patients aged 75 years old[4]

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Summary

Introduction

Older age is a well-known cardiovascular disease (CVD) risk factor, especially for coronary artery disease (CAD)[1,2,3]. Telomeres are structures of tandemly repeated hexanucleotide TTAGGG sequences associated with specific shelterin proteins at the end of eukaryotic chromosomes. They protect internal chromosomal regions of DNA from degradation during cell division and gradually shorten with each cycle due to the end replication problem as well as the sensitivity to oxidative stress[5]. Shorter TL has been linked to an increased risk of adverse events in patients with pre-existing CAD[6]. These studies have mostly been restricted to younger patients, resulting in a paucity of research investigating this relationship in older patients. We aim to determine whether telomere length (TL) and telomerase activity (TA) predicted poor outcomes in older patients presenting with NSTEACS undergoing invasive care

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