Key result
Graves' disease was associated with a significantly prolonged Tpeak-Tend interval compared to euthyroid controls (88 ms vs 77 ms, p<0.001), suggesting its utility as an arrhythmogenicity index.
Why the study?
Cardiac problems are the leading cause of death and arrhythmia is the most common cardiac complication in hyperthyroidism, prompting evaluation of electrocardiographic markers to predict arrhythmia risk in Graves' disease.
Are the Tp-e interval, QTc interval, and Tp-e/QTc ratio prolonged in patients with Graves' disease compared to euthyroid controls?
Case-Control (n=121)
No
Are the Tp-e interval, QTc interval, and Tp-e/QTc ratio prolonged in patients with Graves' disease compared to euthyroid controls?
The Tp-e interval is significantly prolonged in patients with Graves' disease and may serve as a useful non-invasive ECG marker for assessing arrhythmia risk in this population.
Answers are grounded in this paper and cite their sources.
Tp-e prolongation may signal arrhythmia risk in Graves' disease; hypothesis-generating and requires prospective validation before clinical adoption.
Introduction.Graves’ disease is the most common cause of hyperthyroidism. The mortality rate increases by 20% in hyperthyroid patients; cardiac problems are the leading cause of death and arrhythmia is the most common cardiac complication. Our study aimed to evaluate the corrected QT interval (QTc), the Tpeak-Tend interval (Tp-e), and the Tp-e/QTc ratio to predict arrhythmia risk in patients with Graves’ disease. Methods. The study included 64 patients with Graves’ disease and 57 euthyroid controls. The 12-lead electrocardiograms of the individuals under study were evaluated. The QTc interval, the Tp-e interval, and the Tp-e/QTc ratio of all participants were determined and statistically evaluated with thyroid stimulating hormone (TSH), free triiodothyronine (fT3) and free thyroxine (fT4) values. Results. Tp-e (p < 0.001) and QTc (p < 0.05) were significantly prolonged in the group of patients with Graves’ disease as compared to the control group. Heart rate was higher in patients with Graves’ disease as well (p < 0.05). Correlation analysis in patients with hyperthyroidism demonstrated that Tp-e (r=0.372, p=0.002), QTc (r=0.291, p=0.020), and fT3 levels were significantly and positively correlated. Similarly, Tp-e (r=0.271, p=0.030), QTc (r=0.259, p=0.039), and fT4 levels were significantly and positively correlated. Conclusions. We observed a significant prolongation of the Tp-e and QTc intervals with the increase in fT3 and fT4 levels. On the other hand, our study demonstrated that the sensitivity and specificity of Tp-e in the prediction of hyperthyroidism were 70.3% and 70.1%, respectively (AUC=0.724 (CI: 0.629-0.818)), the optimal cut-off value=83.5 ms). The Tp-e interval, which has recently been used as one of the arrhythmogenicity indices, may be an indicator of arrhythmia risk in patients with Graves’ disease.
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Kıraç et al. (2023) conducted a case-control in Graves' disease (n=121). Graves' disease vs. Euthyroid healthy controls was evaluated on Tpeak-Tend interval (ms) (p=<0.001). Graves' disease was associated with a significantly prolonged Tpeak-Tend interval compared to euthyroid controls (88 ms vs 77 ms, p<0.001), suggesting its utility as an arrhythmogenicity index.
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