» Articles » PMID: 25006006

Leucocyte Telomere Length and Risk of Cardiovascular Disease: Systematic Review and Meta-analysis

Overview
Journal BMJ
Specialty General Medicine
Date 2014 Jul 10
PMID 25006006
Citations 450
Authors
Affiliations
Soon will be listed here.
Abstract

Objective: To assess the association between leucocyte telomere length and risk of cardiovascular disease.

Design: Systematic review and meta-analysis.

Data Sources: Studies published up to March 2014 identified through searches of Medline, Web of Science, and Embase.

Eligibility Criteria: Prospective and retrospective studies that reported on associations between leucocyte telomere length and coronary heart disease (defined as non-fatal myocardial infarction, coronary heart disease death, or coronary revascularisation) or cerebrovascular disease (defined as non-fatal stroke or death from cerebrovascular disease) and were broadly representative of general populations--that is, they did not select cohort or control participants on the basis of pre-existing cardiovascular disease or diabetes.

Results: Twenty four studies involving 43,725 participants and 8400 patients with cardiovascular disease (5566 with coronary heart disease and 2834 with cerebrovascular disease) were found to be eligible. In a comparison of the shortest versus longest third of leucocyte telomere length, the pooled relative risk for coronary heart disease was 1.54 (95% confidence interval 1.30 to 1.83) in all studies, 1.40 (1.15 to 1.70) in prospective studies, and 1.80 (1.32 to 2.44) in retrospective studies. Heterogeneity between studies was moderate (I(2) = 64%, 41% to 77%, Phet<0.001) and was not significantly explained by mean age of participants (P = 0.23), the proportion of male participants (P = 0.45), or distinction between retrospective versus prospective studies (P = 0.32). Findings for coronary heart disease were similar in meta-analyses restricted to studies that adjusted for conventional vascular risk factors (relative risk 1.42, 95% confidence interval 1.17 to 1.73); studies with ≥ 200 cases (1.44, 1.20 to 1.74); studies with a high quality score (1.53, 1.22 to 1.92); and in analyses that corrected for publication bias (1.34, 1.12 to 1.60). The pooled relative risk for cerebrovascular disease was 1.42 (1.11 to 1.81), with no significant heterogeneity between studies (I(2) = 41%, 0% to 72%, Phet = 0.08). Shorter telomeres were not significantly associated with cerebrovascular disease risk in prospective studies (1.14, 0.85 to 1.54) or in studies with a high quality score (1.21, 0.83 to 1.76).

Conclusion: Available observational data show an inverse association between leucocyte telomere length and risk of coronary heart disease independent of conventional vascular risk factors. The association with cerebrovascular disease is less certain.

Citing Articles

Telomere Length, Oxidative Stress, and Kidney Damage Biomarkers in Fabry Nephropathy.

Levstek T, Bahcic E, Vujkovac B, Cokan Vujkovac A, Tesovnik T, Remec Z Cells. 2025; 14(3).

PMID: 39937009 PMC: 11817696. DOI: 10.3390/cells14030218.


A Review of Telomere Attrition in Cancer and Aging: Current Molecular Insights and Future Therapeutic Approaches.

Iskandar M, Xiao Barbero M, Jaber M, Chen R, Gomez-Guevara R, Cruz E Cancers (Basel). 2025; 17(2).

PMID: 39858038 PMC: 11764024. DOI: 10.3390/cancers17020257.


Causal associations between telomere length and pulmonary arterial hypertension: A two-sample Mendelian randomization study.

Lyu T, Wang J, Tan J, Yang Y, Wang Y, Zhao J Medicine (Baltimore). 2025; 103(47):e40407.

PMID: 39809206 PMC: 11596709. DOI: 10.1097/MD.0000000000040407.


Marital and living status and biological ageing trajectories: a longitudinal cohort study with a 20-year follow-up.

Yin W, Li X, Chen R, Zhan Y, Jylhava J, Fang F Biogerontology. 2025; 26(1):34.

PMID: 39775304 PMC: 11711563. DOI: 10.1007/s10522-024-10171-1.


Association between telomere length and idiopathic normal pressure hydrocephalus: a Mendelian randomization study.

Yang F, Cai H, Ren Y, Huang K, Gao H, Qin L Front Neurol. 2025; 15:1393825.

PMID: 39741705 PMC: 11686450. DOI: 10.3389/fneur.2024.1393825.


References
1.
Higgins J, Thompson S . Quantifying heterogeneity in a meta-analysis. Stat Med. 2002; 21(11):1539-58. DOI: 10.1002/sim.1186. View

2.
Gorenne I, Kavurma M, Scott S, Bennett M . Vascular smooth muscle cell senescence in atherosclerosis. Cardiovasc Res. 2006; 72(1):9-17. DOI: 10.1016/j.cardiores.2006.06.004. View

3.
Nordfjall K, Osterman P, Melander O, Nilsson P, Roos G . hTERT (-1327)T/C polymorphism is not associated with age-related telomere attrition in peripheral blood. Biochem Biophys Res Commun. 2007; 358(1):215-8. DOI: 10.1016/j.bbrc.2007.04.099. View

4.
Zee R, Castonguay A, Barton N, Ridker P . Relative leukocyte telomere length and risk of incident ischemic stroke in men: a prospective, nested case-control approach. Rejuvenation Res. 2010; 13(4):411-4. PMC: 2914796. DOI: 10.1089/rej.2009.0975. View

5.
Panayiotou A, Nicolaides A, Griffin M, Tyllis T, Georgiou N, Bond D . Leukocyte telomere length is associated with measures of subclinical atherosclerosis. Atherosclerosis. 2010; 211(1):176-81. DOI: 10.1016/j.atherosclerosis.2010.01.037. View