The relationship between telomere length and putative markers of vascular ageing: A systematic review and meta-analysis

Mech Ageing Dev. 2022 Jan:201:111604. doi: 10.1016/j.mad.2021.111604. Epub 2021 Nov 11.

Abstract

Accelerated biological aging contributes to the evolution of cardiovascular disease. However, its influence on subclinical organ damage remains unclear. Leukocyte telomere length (LTL) is emerging as a marker of biological cardiovascular aging. We performed a systematic review and meta-analysis to assess the association between LTL and measures of end-organ damage. PubMed, Medline, Embase, Cinahl Plus, ClinicalTrials.gov, and grey literature databases were searched for studies that assessed the association of LTL with arterial pulse wave velocity (aPWV), carotid intima-media thickness (cIMT), left ventricular mass (LVM or LVMI), renal outcomes, coronary artery calcium (CAC) and presence of carotid plaques. In a sample of 7256 patients, we found that cIMT (pooled correlation coefficient (r) = -0.249; 95 %CI -0.37, -0.128) and aPWV (pooled r = -0.194; 95 % CI -0.290, -0.100) inversely correlate with LTL. Compared to aPWV, cIMT had a stronger correlation with LTL. Patients without carotid plaques had longer telomeres than patients with carotid plaques. Quantitative analyses documented LTL association with renal outcomes and CAC, but not with LVM/LVMI. Among measures of end-organ damage, cIMT and aPWV provide the most accurate information on the contribution of biological aging to the process of vascular remodeling/damage.

Keywords: Ageing; Carotid intima-media thickness; Carotid plaques; Coronary artery calcium; Left ventricular hypertrophy; Pulse wave velocity; Renal outcomes; Telomere.

Publication types

  • Meta-Analysis
  • Systematic Review

MeSH terms

  • Aging / physiology*
  • Blood Vessels* / pathology
  • Blood Vessels* / physiopathology
  • Cardiovascular Physiological Phenomena
  • Cellular Senescence / physiology*
  • Humans
  • Telomere Homeostasis / physiology*
  • Vascular Remodeling*