Key result
Overt hyperthyroidism in Graves' disease linked to ~9° wider frontal QRS-T angle vs. euthyroidism.
Why the study?
Thyroid hormone excess may alter ventricular depolarization and repolarization, but data on the frontal QRS-T angle in overt hyperthyroidism remain limited.
Is overt hyperthyroidism due to Graves' disease associated with an increased frontal QRS-T angle compared with euthyroid controls?
Cross-Sectional (n=97)
No
Is overt hyperthyroidism due to Graves' disease associated with an increased frontal QRS-T angle compared with euthyroid controls?
Overt hyperthyroidism in Graves' disease is associated with a wider frontal QRS-T angle independently of heart rate, age, sex, and BMI, indicating increased ventricular depolarization-repolarization discordance not solely attributable to sinus tachycardia.
Answers are grounded in this paper and cite their sources.
May signal ventricular discordance in Graves' hyperthyroidism; hypothesis-generating for arrhythmia risk and requires prospective validation before clinical adoption.
Introduction Thyroid hormone excess may alter ventricular electrophysiology, affecting both depolarization and repolarization. The frontal QRS-T (fQRS-T) angle reflects the directional relationship between these processes and may provide information on ventricular electrical heterogeneity. However, data on the fQRS-T angle in overt hyperthyroidism (OHT) remain limited. We evaluated the fQRS-T angle in patients with Graves’ disease presenting with OHT compared with euthyroid controls. Materials and methods This retrospective single-center study included 55 patients with Graves’ disease and biochemically confirmed OHT and 42 euthyroid controls. Frontal QRS and T axes were calculated from ECG measurements in leads I and aVF. Between-group comparisons, multivariable regression adjusted for age, sex, body mass index, and heart rate, sensitivity analyses, ROC analysis, and correlations with thyroid function parameters were performed. Results: The median fQRS-T angle was greater in patients with OHT than in controls (21.89° [12.37–44.09] vs. 17.36° [9.02–27.29], p = 0.006), with a rank-biserial correlation of 0.328 (95% CI 0.106–0.535). An fQRS-T angle >45° occurred in 23.6% of patients with OHT and in none of the controls (p < 0.001), whereas the QRS and T axes did not differ significantly between groups. After adjustment for age, sex, body mass index, and heart rate, OHT remained associated with a greater fQRS-T angle (β = 9.00°, 95% CI 1.77–16.22; p = 0.015), with consistent findings in sensitivity analyses. Discriminatory performance was modest (AUC 0.664, 95% CI 0.552–0.768). No significant associations were observed between fQRS-T angle and FT3, FT4, TSH, or heart rate. Discussion Patients with Graves’ disease and OHT exhibited greater discordance between ventricular depolarization and repolarization despite similar individual QRS and T axes. This association persisted after adjustment for heart rate and other potential confounders, suggesting that fQRS-T widening may reflect electrophysiological alterations associated with OHT rather than tachycardia alone. Conclusion Overt hyperthyroidism due to Graves’ disease is associated with a wider fQRS-T angle independently of age, sex, body mass index, and heart rate. Larger prospective, multicenter studies with longitudinal ECG assessment are needed to determine the reversibility and prognostic significance of these alterations.
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Kłosowicz et al. (2026) conducted a cross-sectional in Graves' disease with overt hyperthyroidism (n=97). Overt hyperthyroidism due to Graves' disease vs. Euthyroid controls was evaluated on Frontal QRS-T (fQRS-T) angle (degrees) (adjusted β 9.00° (rank-biserial correlation 0.328), 95% CI 1.77-16.22, p=0.006 (unadjusted); 0.015 (adjusted)). Overt hyperthyroidism in Graves' disease was associated with a wider median frontal QRS-T angle than euthyroidism (21.89° vs 17.36°, p=0.006; adjusted β=9.00°, p=0.015).
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