Impaired fasting glucose, diabetes mellitus, and cardiovascular disease risk factors are associated with prolonged QTc duration. Results from the Third National Health and Nutrition Examination Survey

J Cardiovasc Risk. 2001 Aug;8(4):227-33. doi: 10.1177/174182670100800407.

Abstract

Background: Impaired glucose tolerance and diabetes mellitus have been associated with a prolonged QT interval among select populations. However, these associations remain unclear among the general population.

Methods: We examined these relationships using data from 5833 adults aged 40-90 years from NHANES III (1988-1994). Univariate differences in cardiovascular disease (CVD) risk factors were examined across tertiles of heart rate corrected QT (QTc). The association between glucose intolerance, CVD risk factors and a prolonged QTc (> or = 0.440 s) was also assessed with logistic regression adjusting for age, race, gender, education, and heart rate.

Results: Prolonged QTc was observed among 22.0% of persons with normal glucose tolerance (NGT), 29.9% of those with impaired fasting glucose (IFG), and among 42.2% of persons with diabetes. Hypertension, serum cholesterol, obesity, heart rate, and fasting C-peptide and serum insulin levels were associated with prolonged QTc (all: P < or = 0.05). After multivariate adjustment, persons with IFG were 1.2 times (95% CI=0.7-2.0) as likely and persons with diabetes 1.6 times (95% CI=1.1-2.3) as likely to have a prolonged QTc as persons with NGT. In addition, persons with diabetes and two or more additional CVD risk factors were 2.3 times (95% CI=1.3-4.0) as likely to have a prolonged QTc as persons with NGT and no CVD risk factors after multivariate adjustment.

Conclusion: Diabetes was associated with an increased likelihood of prolonged QTc independent of age, race, gender, education, and heart rate. In addition, persons with diabetes and multiple CVD risk factors were more likely to have a prolonged QTc than those with NGT and no additional risk factors, suggesting that these persons may be at increased risk for cardiac arrhythmia and sudden death.

MeSH terms

  • Blood Glucose / metabolism
  • C-Peptide / blood
  • Diabetes Mellitus / blood
  • Diabetes Mellitus / physiopathology*
  • Electrocardiography*
  • Female
  • Glucose Intolerance / blood
  • Glucose Intolerance / physiopathology*
  • Health Surveys
  • Heart Diseases / blood
  • Heart Diseases / physiopathology*
  • Humans
  • Insulin / blood
  • Male
  • Middle Aged
  • Multivariate Analysis
  • Risk Factors

Substances

  • Blood Glucose
  • C-Peptide
  • Insulin