期刊
DIABETES OBESITY & METABOLISM
卷 25, 期 6, 页码 1566-1575出版社
WILEY
DOI: 10.1111/dom.15005
关键词
cardiac arrhythmias; hyperglycaemia; hypoglycaemia; type 1 diabetes
The study investigated the effect of insulin-induced hypoglycemia and subsequent recovery to hyperglycemia or euglycemia on cardiac repolarization in people with type 1 diabetes. The results showed that hypoglycemia prolonged the QTc interval, indicating increased risk of serious cardiac arrhythmias and sudden cardiac death. This prolonged repolarization was sustained during the recovery period, regardless of the blood sugar level.
AimTo investigate changes in cardiac repolarization abnormalities (heart rate-corrected QT [QT(c)] [primary endpoint], T-wave abnormalities) and heart-rate variability measures in people with type 1 diabetes during insulin-induced hypoglycaemia followed by recovery hyperglycaemia versus euglycaemia.Methods: In a randomized crossover study, 24 individuals with type 1 diabetes underwent two experimental clamps with three steady-state phases during electrocardiographic monitoring: (1) a 45-minute euglycaemic phase (5-8 mmol/L), (2) a 60-minute insulin-induced hypoglycaemic phase (2.5 mmol/L), and (3) 60-minute recovery in either hyperglycaemia (20 mmol/L) or euglycaemia (5-8 mmol/L).Results: All measured markers of arrhythmic risk indicated increased risk during hypoglycaemia. These findings were accompanied by a decrease in vagal tone during both hyperglycaemia and euglycaemia clamps. Compared with baseline, the QT(c) interval increased during hypoglycaemia, and 63% of the participants exhibited a peak QT(c) of more than 500 ms. The prolonged QT(c) interval was sustained during both recovery phases with no difference between recovery hyperglycaemia versus euglycaemia. During recovery, no change from baseline was observed in heart-rate variability measures.Conclusions: In people with type 1 diabetes, insulin-induced hypoglycaemia prolongs cardiac repolarization, which is sustained during a 60-minute recovery period independently of recovery to hyperglycaemia or euglycaemia. Thus, vulnerability to serious cardiac arrhythmias and sudden cardiac death may extend beyond a hypoglycaemic event, regardless of hyperglycaemic or euglycaemic recovery.
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