Key result
Elderly Chinese subjects carrying the ACE D-allele experienced significantly greater prolongation of QT dispersion over 4 years compared to non-carriers.
Why the study?
Does the ACE D-allele polymorphism increase the magnitude of QT dispersion prolongation in healthy elderly Chinese subjects?
Cohort (n=106)
No
Does the ACE D-allele polymorphism increase the magnitude of QT dispersion prolongation in healthy elderly Chinese subjects?
p-value: p=0.001
The ACE D-allele is associated with a greater magnitude of age-related QT and QTc dispersion prolongation in healthy elderly Chinese subjects, suggesting a genetic predisposition to repolarization abnormalities.
May flag higher-risk elderly Chinese for QT monitoring; leaves open arrhythmia outcome studies before any practice change.
BACKGROUND: There has not been a longitudinal investigation of the influence of angiotensin-converting enzyme (ACE) insertion/deletion and angiotensinogen (AGT) M235T gene polymorphisms on repolarization parameters, such as QT dispersion (QTd) and the peak and the end of the T-wave interval (Tpe). METHODS AND RESULTS: Electrocardiographys were recorded from 106 elderly Chinese at baseline, and 2nd and 4th year follow-up. The corrected QT (QTc), QTd, QTc dispersion (QTcd) and Tpe were manually calculated. Average age was 72.7+/-4.1 years (range 62-81). QTd, QTcd and Tpe were significantly prolonged (all p<0.001 at the 2nd and 4th year). At the 4th year the magnitude of the QTd prolongation, but not Tpe, was significantly higher in subjects carrying the ACE D allele than non-D-allele carriers (p=0.001), as was QTcd (p=0.002). This association was still significant in the multivariate analyses (p<0.001 and p=0.001 for QTc and QTcd, respectively). No significant correlation was found between repolarization parameters and AGT genotype. CONCLUSIONS: This longitudinal study shows that the ageing process is associated with prolongation of QTd, QTcd and Tpe after 4 years follow-up. The elderly Chinese subjects with the ACE D-allele had greater prolongation QTd and QTcd.
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Lin et al. (2006) conducted a cohort in Healthy aging (n=106). ACE I/D polymorphism (D-allele) vs. Non-D-allele carriers (II genotype) was evaluated on Magnitude of QT dispersion (QTd) prolongation at 4 years (p=0.001). Elderly Chinese subjects carrying the ACE D-allele experienced significantly greater prolongation of QT dispersion over 4 years compared to non-carriers.
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