Abstract

BackgroundTelomere shortening, an indicator of aging, is associated with age-related diseases. This study aims to investigate the association between leukocyte telomere length (LTL) and thin-capped fibroatheromata (TCFA) and the impact of using LTL cutoff to determine the incidence of major adverse cardiovascular events (MACEs) in patients with angiographically intermediate coronary lesions.MethodsThis was a signal-center retrospective study focusing on patients who underwent coronary angiography and optical coherence tomography (OCT). The degree of coronary stenosis was assessed by angiography. The presence of TCFA was determined by OCT imaging. A total of 156 patients with angiographically intermediate coronary lesions were enrolled.ResultsLeukocyte telomere lengths were significantly shorter in the TCFA group compared with non-TCFA group [11.95 (10.56, 15.21) kb vs. 13.81 (12.06, 16.11) kb, p = 0.003]. The short-LTL group and long-LTL group were divided according to the optimal cut-off value which was determined by the receiver operating characteristic (ROC) curve analysis. Logistic regression model revealed that short-LTL was independently associated with TCFA incidence (odds ratio [OR] 4.387, 95% CI: 1.902–10.120, p = 0.001) after adjusting for confounding factors. Over a 24-months follow-up, the MACE incidence among patients with short-LTL was significantly higher than those in the long-LTL group (12.5 vs. 2.0%, p = 0.006 by log-rank test). Multivariable cox regression analysis indicated that short-LTL (hazard ratio [HR] 9.716, 95% CI: 1.995–47.319, p = 0.005) was an independent prognostic factor of MACE incidence in angiographically intermediate coronary lesions patients.ConclusionsShort-LTL was independently associated with the incidence of TCFA and may serve as a prognostic factor for MACE risk on top of conventional risk factors.

Highlights

  • Telomere, hexamer repetitive sequence, together with shelterin proteins form the protective capping complex at the end of eukaryotic chromosomes

  • This study aims to investigate the association between leukocyte telomere length (LTL) and thin-capped fibroatheromata (TCFA) and the impact of using LTL cutoff to determine the incidence of major adverse cardiovascular events (MACEs) in patients with angiographically intermediate coronary lesions

  • Logistic regression model revealed that short-LTL was independently associated with thincapped fibroatheromata (TCFA) incidence after adjusting for confounding factors

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Summary

Introduction

Hexamer repetitive sequence, together with shelterin proteins form the protective capping complex at the end of eukaryotic chromosomes. Many epidemiological studies have suggested the association between leukocyte telomere length (LTL) and cardiovascular ischemic events [4,5,6]. Optical coherence tomography (OCT) is currently the best validated against histology with excellent intraobserver reproducibility to identify plaque composition and fine structural changes in coronary arterial walls, such as thincapped fibroatheromata (TCFA), macrophages, microvessels, and cholesterol crystals [9]. TCFAs are thin fibrous caps that separate a necrotic core from the vascular lumen, which along with macrophage accumulation, microvessels, and cholesterol crystals, are considered as the characteristic of unstable plaques [10]. This study aims to investigate the association between leukocyte telomere length (LTL) and thin-capped fibroatheromata (TCFA) and the impact of using LTL cutoff to determine the incidence of major adverse cardiovascular events (MACEs) in patients with angiographically intermediate coronary lesions

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