(Circulation. 1999;100:e149.)
© 1999 American Heart Association, Inc.
Circulation Electronic Pages |
Department of Geriatrics and Metabolic Diseases and Institute of Pharmacology, Second University of Naples, Piazza Miraglia, Naples, Italy
| Introduction |
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QTc dispersion is an important predictor of cardiac mortality. In the Rotterdam Study,1 persons in the highest tertile (>60 ms) relative to the lowest tertile (<39 ms) of QTc dispersion had a 2-fold risk of cardiac death. The Rotterdam Study also confirms that QTc dispersion is larger in diabetic than in nondiabetic persons. QTc duration and QTc dispersion are associated with plasma glucose and insulin levels,2 but their relative contributions to each are still unclear. We evaluated the effect of acute hyperglycemia, with or without the accompanying hyperinsulinemia, on QTc duration and QTc dispersion in normal subjects.
We studied 27 healthy volunteers (17 men and 15 women) aged 49±6 years
(mean±SD). All subjects were given a hyperglycemic glucose clamp in
which plasma glucose concentrations were acutely raised with a bolus
injection of 0.33 g/kg glucose (50% solution) followed by a 30%
glucose infusion to achieve steady-state plasma glucose levels of
15 mmol/L for 120 minutes. On another occasion, which was
separated from the first by at least a 3-day interval and in random
order, the subjects underwent the same hyperglycemic clamp plus
octreotide administration (25 µg as IV bolus followed by a 0.5
µg/min infusion) to block the release of endogenous
insulin. All tests were made with the aid of an artificial pancreas
(Biostator). Electrocardiograms were recorded with
a standard resting 12-lead ECG at 50 mm/s. QT interval
analysis was done by a cardiologist who was blinded regarding
other information. QT intervals were corrected with Bazetts formula
Julius Centre for Patient-Oriented Research Utrecht, The Netherlands
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