Key result
Leucocyte telomere length is linked to ~10% higher MACE risk but adds no prognostic value beyond age.
Why the study?
Leucocyte telomere length is suggested to be shorter in patients with CAD and heart failure and its association with clinical outcomes in ischaemic heart failure was unclear.
Cohort (n=3,275)
Yes
Shorter telomere length was associated with worse outcomes in ischaemic HF; confirms prognostic link but adds nothing beyond chronological age.
AIMS: Leucocyte telomere length is considered a marker of biological ageing and has been suggested to be shorter in patients with CAD and heart failure compared with healthy controls. The aim of this study was to determine whether telomere length is associated with clinical outcomes in patients with ischaemic heart failure and whether this association is superior to chronological age as defined by date of birth. METHODS AND RESULTS: We measured leucocyte telomere length in 3275 patients with chronic ischaemic systolic heart failure participating in the COntrolled ROsuvastatin multiNAtional Trial in Heart Failure (CORONA) study. The primary composite endpoint was cardiovascular death, non-fatal myocardial infarction, and non-fatal stroke, which occurred in 575 patients during follow-up. We observed a significant association of leucocyte telomere lengths with the primary endpoint (hazard ratio 1.10; 95% confidence interval 1.01-1.20; P=0.03). However, this observation was not superior to age as defined by date of birth. The neutral effect of rosuvastatin treatment on clinical outcomes was not modified by baseline telomere length. CONCLUSION: Biological age as defined by leucocyte telomere length was associated with clinical outcomes in patients with ischaemic heart failure, but this association did not add prognostic information above age as defined by date of birth.
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Haver et al. (2015) conducted a cohort in Chronic ischaemic systolic heart failure (n=3,275). Leucocyte telomere length vs. Chronological age was evaluated on Cardiovascular death, non-fatal myocardial infarction, and non-fatal stroke (HR 1.10, 95% CI 1.01-1.20, p=0.03). Leucocyte telomere length was significantly associated with the primary composite endpoint (HR 1.10; 95% CI 1.01-1.20; P=0.03), but did not add prognostic information above chronological age.
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