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The corrected QT (QTc) prolongation in hyperthyroidism and the association of thyroid hormone with the QTc interval
Ye Seung Lee1, Joong Wan Choi1, Eun Ju Bae1
1Department of Pediatrics, Hallym University College of Medicine, Chuncheon, Korea.
Insights
Hyperthyroidism prolongs the corrected QT (QTc) interval, increasing arrhythmia risk. Higher free thyroxine (fT4) levels correlate with QTc prolongation, suggesting a link between thyroid status and cardiac mortality risk.
Area of Science:
- Cardiology
- Endocrinology
- Electrophysiology
Background:
- Ventricular repolarization, assessed by the corrected QT (QTc) interval, is crucial for cardiac health.
- Prolonged QTc is a known risk factor for potentially fatal arrhythmias and sudden cardiac death.
- Limited research exists on the impact of hyperthyroidism on ventricular repolarization and QTc duration.
Purpose of the Study:
- To investigate the association between thyroid hormone levels and QTc interval in hyperthyroid patients.
- To compare QTc intervals in hyperthyroid patients versus age-matched controls.
- To determine if serum free thyroxine (fT4) and thyroid-stimulating hormone (TSH) levels correlate with QTc prolongation in hyperthyroidism.
Main Methods:
- Retrospective analysis of electrocardiograms (ECGs) and clinical records from 38 hyperthyroid patients (<30 years old).
- Inclusion of 72 age-matched control subjects without hyperthyroidism for comparison.
- Evaluation of serum fT4 and TSH levels in relation to QTc interval measurements.
Main Results:
- Hyperthyroid patients exhibited significantly prolonged QTc intervals compared to controls (P<0.001).
- A higher prevalence of abnormally prolonged QTc was observed in the hyperthyroid group (P<0.001).
- Positive correlation found between elevated fT4 levels and QTc interval duration in hyperthyroid patients (P<0.05); no correlation with TSH levels.
Conclusions:
- Hyperthyroidism is significantly associated with QTc interval prolongation.
- Elevated fT4 levels in hyperthyroidism correlate with QTc prolongation, highlighting thyroid status's impact on cardiac repolarization.
- Findings suggest a potential link between thyroid dysfunction, QTc duration, and cardiac mortality risk.
Purpose:
Ventricular repolarization is assessed using the QT interval corrected by the heart rate (QTc) via an electrocardiogram (ECG). Prolonged QTc is associated with an increased risk of arrhythmias and cardiac mortality. As there have been few reports regarding the effects of hyperthyroidism on ventricular repolarization, we studied the association between serum free thyroxine (free T4 [fT4]) and thyroid stimulating hormone (TSH) levels and the QTc interval.
Methods:
Thirty-eight patients with hyperthyroidism (<30 years old) were included, and we used their clinical records and available ECGs (between August 2003 and August 2011) to evaluate the association between their fT4 and TSH levels and their QTc interval. In addition, we studied the ECGs of 72 age-matched patients with no hyperthyroidism (control group) and compared their data with that from the patients group.
Results:
The QTc duration in patients with hyperthyroidism was significantly prolonged compared to that in the control subjects (P<0.001). In addition, the number of hyperthyroid patients with abnormal prolonged QTc was significantly higher than that in the control group (P<0.001). Among the patients with hyperthyroidism, patients with prolonged QTc and borderline QTc had higher fT4 levels and there was positive correlation between their fT4 levels and their QTc interval (P<0.05). However, no correlation was observed between their TSH levels and their QTc interval.
Conclusion:
We report that hyperthyroidism is associated with QTc prolongation. The correlation between the fT4 levels and the QTc interval suggests that thyroid status is associated with QTc values and the risk of cardiac mortality.
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