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The relationship between angiotensin converting enzyme gene I/D polymorphism and QT dispersion in patients with
Cansin Tulunay Kaya1, Adalet Gurlek, Timucin Altin
1Departments of Cardiology, Ankara University School of Medicine, Ankara, Turkey.
Insights
Hypertrophic cardiomyopathy (HCM) is linked to increased QT dispersion (QTd). Patients with the angiotensin-converting enzyme (ACE) DD genotype show even greater QTd, suggesting a genetic link to cardiac repolarization abnormalities in HCM.
Area of Science:
- Cardiology
- Genetics
- Molecular Biology
Background:
- Hypertrophic cardiomyopathy (HCM) involves disorganized myocardial architecture, potentially leading to ventricular arrhythmias and sudden cardiac death.
- The angiotensin-converting enzyme (ACE) DD genotype is hypothesized to correlate with increased myocardial collagen.
- QT dispersion (QTd) assesses regional ventricular repolarization differences.
Purpose of the Study:
- To investigate QT dispersion (QTd) in hypertrophic cardiomyopathy (HCM) patients and controls.
- To examine the association between ACE genotypes and QTd in HCM and control groups.
Main Methods:
- Sixty-three HCM patients and 20 healthy controls were enrolled.
- QT parameters were measured using 12-lead electrocardiograms.
- ACE genotypes were determined via polymerase chain reaction (PCR) from DNA.
Main Results:
- QTd and corrected QTd (QTcd) were significantly elevated in HCM patients compared to controls.
- While QTd did not vary by genotype in controls, HCM patients with the ACE DD genotype exhibited significantly greater QTd and QTcd than other genotypes.
- Genotype frequencies were comparable between HCM and control groups.
Conclusions:
- QTd and QTcd are elevated in hypertrophic cardiomyopathy (HCM) patients.
- The ACE DD genotype is specifically associated with increased QTd and QTcd in HCM patients, highlighting a potential genetic influence on cardiac repolarization.
Introduction:
Hypertrophic cardiomyopathy (HCM) is characterized by disorganized myocardial architecture, and may cause ventricular arrhythmias and sudden death. The angiotensin-converting enzyme (ACE) with two deletion alleles (DD genotype) has been proposed to be associated with increased myocardial collagen content. We evaluated QT dispersion (QTd), which reflects regional differences in ventricular repolarization, in HCM patient and controls among the three different ACE genotypes.
Materials And Methods:
Sixty-three patients with HCM and 20 healthy subjects were included in the study. QT parameters were measured from 12 lead electrocardiograms. ACE genotypes were determined from the DNA extracted from peripheral blood by a polymerase chain reaction (PCR) method. QT parameters were compared among the three ACE genotypes both in HCM patients and controls.
Results:
Median ages were similar in HCM and control groups. QTd and corrected QTd (QTcd) were significantly greater in the HCM group compared with the controls. The frequencies of each genotype were similar in both groups. Although QTd and QTcd did not differ among the three genotypes in the control subjects, they were significantly greater in patients with DD genotype compared with other genotypes in the HCM group.
Conclusion:
QTd and QTcd are increased in patients with HCM, especially in those with the DD genotype.
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