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Published on: March 22, 2024
The Association between Leucocyte Telomere Length and Survival Outcomes in Patients with Cardiovascular Disease
Jin-Yu Sun1,2, Qian Xu2, Hui Shen2
1Department of Cardiology, Gusu School, Nanjing Medical University, 215008 Suzhou, Jiangsu, China.
Insights
Shorter leucocyte telomere length (LTL) is linked to increased all-cause mortality in cardiovascular disease (CVD) patients, particularly women. This finding highlights LTL as a potential marker for CVD tertiary prevention.
Area of Science:
- Biomedical research
- Cardiovascular epidemiology
- Gerontology
Background:
- Investigating the relationship between leucocyte telomere length (LTL) and mortality risk in patients with cardiovascular disease (CVD).
- Understanding the role of cellular aging markers in predicting adverse outcomes in CVD populations.
Purpose of the Study:
- To explore the association between LTL and all-cause mortality.
- To assess the impact of LTL on cardiovascular disease (CVD)-specific death.
Main Methods:
- Utilized data from 1599 CVD patients from a US population survey.
- Employed Kaplan-Meier curves, weighted Cox regression, and restricted cubic splines for all-cause mortality analysis.
- Applied competing risk regression to evaluate CVD-specific mortality, with non-CVD death as a competing event.
Main Results:
- Shorter LTL was associated with a higher risk of all-cause death (adjusted HR: 1.25).
- A linear dose-response relationship was observed between LTL and all-cause mortality.
- Female patients with shorter LTL showed a significantly higher risk of death (weighted HR: 1.79), unlike males.
- No significant association was found between LTL and CVD-specific mortality, but a significant link to non-CVD death (adjusted HR: 1.24).
Conclusions:
- Leucocyte telomere length (LTL) is inversely associated with all-cause mortality in female CVD patients.
- Reduced LTL may serve as a prognostic indicator for increased all-cause mortality in CVD patients.
- LTL emerges as a potential biomarker for tertiary prevention strategies in cardiovascular disease.
Background:
We explore the association between leucocyte telomere length (LTL) and all-cause and cardiovascular disease (CVD)-specific death in CVD patients.
Methods:
We acquired 1599 CVD patients from a nationally representative US population survey for this study. We applied Kaplan-Meier curves, adjusted weighted Cox regression models, and restricted cubic spline to investigate the association between LTL and all-cause death. Additionally, we employed competing risk regression to assess the impact of LTL on cardiovascular-specific death, setting non-cardiovascular death as a competing event.
Results:
The overall mortality rate was 31.0% after a median follow-up of 13.9 years. Patients with shorter LTL exhibited a higher risk of all-cause death, with an adjusted hazard ratio (HR) of 1.25 (95% confidence interval (CI): 1.05-1.48). Restricted cubic spline illustrated a linear dose-response relationship. In gender-specific analyses, female patients with shorter LTL showed a higher risk of death (weighted HR, 1.79; 95% CI, 1.29-2.48), whereas this association was not observed in males (weighted HR, 0.90; 95% CI, 0.61-1.32). The Fine-Gray competing risk model revealed no significant relationship between LTL and cardiovascular-specific mortality but a significant association with non-cardiovascular death (adjusted HR, 1.24; 95% CI, 1.02-1.51).
Conclusions:
LTL is inversely associated with all-cause death in female CVD patients. The significant correlation between reduced LTL and increased all-cause mortality emphasizes LTL as a potential marker for tertiary prevention against cardiovascular disease.
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