Key result
Nocturnal hypoglycemia in pediatric T1D is linked to ~0.8 ms QTc prolongation per mmol/L glucose drop.
Why the study?
An association between QTc prolongation and nocturnal hypoglycemia had been observed in children with type 1 diabetes, but this relationship and other sources of QTc variability needed quantitative characterization.
Is nocturnal hypoglycemia associated with QTc prolongation in children with type 1 diabetes?
Observational (n=25)
Is nocturnal hypoglycemia associated with QTc prolongation in children with type 1 diabetes?
Mean Difference: 0.76 (95% CI 0.67–0.85)
Nocturnal hypoglycemia in children with type 1 diabetes is associated with a mild, delayed prolongation of the QTc interval, highlighting a potential mechanism for hypoglycemia-associated cardiac arrhythmias.
Nocturnal hypoglycemia may prolong QTc in pediatric T1D; hypothesis-generating and should not yet change practice.
An association between QT prolongation (Bazett's corrected QT interval, QTcB) of 7 milliseconds and nocturnal hypoglycemia, compared with euglycemia, has been observed in children with type 1 diabetes (T1D). The objective of this pharmacometric analysis was to understand this association and other sources of QTc variability quantitatively. Data originate from a prospective observational study (25 cardiac healthy children with T1D, aged 8.1‐17.6 years) with continuous subcutaneous glucose and electrocardiogram measurements for 5 consecutive nights. Mixed‐effect modeling was used to compare QTcB with individual heart‐rate correction (QTcI). Covariate models accounting for circadian variation, age, and sex were evaluated, followed by an investigation of glucose–QTc relationships (with univariable and combined adjusted analysis). Factors potentially modifying sensitivity to QTc lengthening were explored. Random inter‐individual variability was reduced in the QTcI versus QTcB model (±12.6 vs 14.1 milliseconds), and was further reduced in the adjusted covariate model (±9.7 milliseconds), accounting for the significantly (P < .01) shortened QTc in adolescent boys (–14.6 milliseconds), circadian variation (amplitude, 19.2 milliseconds; shift, 2.9 hours), and linear glucose–QTc relationship (delay rate, 0.56−h; slope, 0.76 milliseconds [95%CI 0.67‐ 0.85 milliseconds] per 1 mmol/L decrease in glucose). Differing sensitivity was suggested to depend upon hemoglobin A1c (HbA1c), T1D duration, and time spent in nocturnal hypoglycemia. In conclusion, a clinically mild association of QTc prolongation with nocturnal hypoglycemia was confirmed and quantified in this pharmacometric analysis, and the longest QTc interval was around 03:00 a.m. The characterized delayed association with glucose highlights the relevance of both the extent and the duration of hypoglycemia. Further clinical studies are warranted to investigate whether these factors contribute to increased risk of hypoglycemia‐associated cardiac arrhythmia in children with T1D.
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Gotta et al. (2023) conducted an observational in Type 1 diabetes (n=25). Nocturnal hypoglycemia (decrease in glucose) vs. Euglycemia was evaluated on QTc interval prolongation (linear glucose-QTc relationship) (slope 0.76 milliseconds per 1 mmol/L decrease, 95% CI 0.67-0.85). Nocturnal hypoglycemia in children with type 1 diabetes was associated with QTc prolongation, increasing by 0.76 milliseconds (95% CI 0.67-0.85) per 1 mmol/L decrease in glucose.
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