Key result
Hypoglycemia prolongs QTc by ~32 ms versus euglycemia, unaffected by mineralocorticoid receptor blockade.
Why the study?
The impact of repeated hypoglycemia episodes on QTc interval recovery and whether mineralocorticoid receptor blockade prevents these alterations remained unclear.
Does hypoglycemia prolong the QTc interval in healthy individuals and those with type 2 diabetes, and does mineralocorticoid receptor blockade prevent this?
RCT (n=43)
Double-blind
Crossover
Does hypoglycemia prolong the QTc interval in healthy individuals and those with type 2 diabetes, and does mineralocorticoid receptor blockade prevent this?
Absolute Event Rate: 439.06% vs 406.96%
p-value: p=< .0001
Hypoglycemia causes transient QTc prolongation in both healthy individuals and those with type 2 diabetes, which resolves quickly upon return to euglycemia and is not prevented by mineralocorticoid receptor blockade.
Hypoglycemia prolongs QTc independently of MR blockade; extends arrhythmia risk data to repeated episodes, warranting monitoring in glycemic trials.
BACKGROUND: Our goal was to determine in healthy individuals and individuals with type 2 diabetes the impact of repeated episodes of hypoglycemia on the corrected QT (QTc) interval and the time course for QTc recovery. Further, since hypoglycemia increases aldosterone and patients with primary aldosteronism have prolonged QTc, we also determined whether mineralocorticoid receptor blockade prevents hypoglycemia-induced QTc alterations. METHODS: Twenty-seven healthy participants completed a double-blinded crossover trial contrasting 3 experimental conditions: (1) euglycemia, (2) hypoglycemia, and (3) hypoglycemia with mineralocorticoid receptor blockade pretreatment. Sixteen participants with type 2 diabetes completed 1 condition, hypoglycemia. Hyperinsulinemic clamps were performed to induce the hypoglycemic and euglycemic conditions. Electrocardiograms were performed before, during, and after the clamps. RESULTS: Healthy participants had a significant (P < .0001) prolongation of QTc during both the morning and afternoon hypoglycemic clamps as compared with euglycemic clamps (morning hypoglycemia vs euglycemia: 439.06 ± 41.18 ms vs 406.96 ± 26.16 ms; afternoon hypoglycemia vs euglycemia: 441.50 ± 34.36 ms vs 407.78 ± 19.18 ms). Mineralocorticoid receptor (MR) blockade did not alter the response to hypoglycemia. Participants with diabetes achieved a significant prolongation of QTc during the afternoon hypoglycemia only (afternoon hypoglycemia vs morning baseline: 461.96 ± 49.14 vs 428.90 ± 28.54, P < .05). In both participant populations, QTc intervals were similar to baseline 90 minutes after return to euglycemia and the following day. CONCLUSION: Hypoglycemia prolonged QTc in healthy participants, and this was not altered by MR blockade. In individuals with type 2 diabetes, 2 hypoglycemic episodes were required to achieve prolongation. Reassuringly, in both study populations, hypoglycemia-induced QTc prolongation resolved quickly with no apparent residual effects the next day.
No takes yet. Share an insight, caveat, or question.
Haas et al. (2025) conducted an RCT in Type 2 diabetes and healthy individuals (n=43). Hypoglycemia vs. Euglycemia was evaluated on Corrected QT (QTc) interval (p=< .0001). Hypoglycemia significantly prolonged the QTc interval compared with euglycemia in healthy participants (439.06 vs 406.96 ms; P<0.0001), an effect not altered by mineralocorticoid receptor blockade.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: