The separate and joint effects of prolonged QT interval and heart rate on mortality

Nan Hee Kim, Meda E. Pavkov, Robert G. Nelson, Robert L. Hanson, Peter H. Bennett, Jeffrey M. Curtis, Maurice L. Sievers, William C. Knowler

Research output: Contribution to journalArticle

2 Citations (Scopus)

Abstract

Objectives: Understanding why prolonged Bazett-corrected QT interval (QTc) is a risk factor for mortality is difficult, because QTc is positively correlated with heart rate. To optimally distinguish the effects of QT interval and heart rate on mortality, QT interval and heart rate were modeled separately and jointly in Pima Indians. Methods: The effects of QT and heart rate on all-cause and cause-specific mortality were assessed in the overall study population and according to the presence or absence of diabetes using multivariable time-dependent proportional hazards models. Results: Among 1488 nondiabetic and 990 diabetic subjects ≥25 years old, 81 nondiabetic and 149 diabetic subjects died during a median follow-up of 7.3 years. When included in the same regression model, QT and heart rate each predicted all-cause mortality [hazard ratios per standard deviation (SD) (95% confidence interval)=1.31 (1.10-1.57) and 1.57 (1.32-1.87) respectively]. In nondiabetic subjects, hazard ratios for all-cause mortality were 1.54 (1.19-1.99) for QT and 1.86 (1.46-2.37) for heart rate. In diabetic subjects, hazard ratios for all-cause mortality were lower, 1.27 (1.00-1.62) for QT and 1.41 (1.12-1.78) for heart rate. In the overall study population, neither QT nor heart rate significantly predicted cardiovascular disease (CVD) mortality [hazard ratios=1.13 (0.77-1.64) and 1.46 (0.98-2.19)] when adjusted for each other. Heart rate unadjusted for QT, however, predicted CVD mortality [hazard ratio=1.34 (1.00-1.79)] in a separate model. Conclusions: QT prolongation and high heart rate both predict all-cause mortality in Pima Indians, but heart rate was consistently the stronger predictor of the two.

Original languageEnglish
Pages (from-to)539-544
Number of pages6
JournalAtherosclerosis
Volume209
Issue number2
DOIs
Publication statusPublished - 2010 Apr 1

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Heart Rate
Mortality
Potassium Iodide
Cardiovascular Diseases
Proportional Hazards Models
Population
Confidence Intervals

Keywords

  • Cardiovascular disease
  • Heart rate
  • Mortality
  • QT interval

ASJC Scopus subject areas

  • Cardiology and Cardiovascular Medicine

Cite this

Kim, N. H., Pavkov, M. E., Nelson, R. G., Hanson, R. L., Bennett, P. H., Curtis, J. M., ... Knowler, W. C. (2010). The separate and joint effects of prolonged QT interval and heart rate on mortality. Atherosclerosis, 209(2), 539-544. https://doi.org/10.1016/j.atherosclerosis.2009.09.026

The separate and joint effects of prolonged QT interval and heart rate on mortality. / Kim, Nan Hee; Pavkov, Meda E.; Nelson, Robert G.; Hanson, Robert L.; Bennett, Peter H.; Curtis, Jeffrey M.; Sievers, Maurice L.; Knowler, William C.

In: Atherosclerosis, Vol. 209, No. 2, 01.04.2010, p. 539-544.

Research output: Contribution to journalArticle

Kim, NH, Pavkov, ME, Nelson, RG, Hanson, RL, Bennett, PH, Curtis, JM, Sievers, ML & Knowler, WC 2010, 'The separate and joint effects of prolonged QT interval and heart rate on mortality', Atherosclerosis, vol. 209, no. 2, pp. 539-544. https://doi.org/10.1016/j.atherosclerosis.2009.09.026
Kim, Nan Hee ; Pavkov, Meda E. ; Nelson, Robert G. ; Hanson, Robert L. ; Bennett, Peter H. ; Curtis, Jeffrey M. ; Sievers, Maurice L. ; Knowler, William C. / The separate and joint effects of prolonged QT interval and heart rate on mortality. In: Atherosclerosis. 2010 ; Vol. 209, No. 2. pp. 539-544.
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abstract = "Objectives: Understanding why prolonged Bazett-corrected QT interval (QTc) is a risk factor for mortality is difficult, because QTc is positively correlated with heart rate. To optimally distinguish the effects of QT interval and heart rate on mortality, QT interval and heart rate were modeled separately and jointly in Pima Indians. Methods: The effects of QT and heart rate on all-cause and cause-specific mortality were assessed in the overall study population and according to the presence or absence of diabetes using multivariable time-dependent proportional hazards models. Results: Among 1488 nondiabetic and 990 diabetic subjects ≥25 years old, 81 nondiabetic and 149 diabetic subjects died during a median follow-up of 7.3 years. When included in the same regression model, QT and heart rate each predicted all-cause mortality [hazard ratios per standard deviation (SD) (95{\%} confidence interval)=1.31 (1.10-1.57) and 1.57 (1.32-1.87) respectively]. In nondiabetic subjects, hazard ratios for all-cause mortality were 1.54 (1.19-1.99) for QT and 1.86 (1.46-2.37) for heart rate. In diabetic subjects, hazard ratios for all-cause mortality were lower, 1.27 (1.00-1.62) for QT and 1.41 (1.12-1.78) for heart rate. In the overall study population, neither QT nor heart rate significantly predicted cardiovascular disease (CVD) mortality [hazard ratios=1.13 (0.77-1.64) and 1.46 (0.98-2.19)] when adjusted for each other. Heart rate unadjusted for QT, however, predicted CVD mortality [hazard ratio=1.34 (1.00-1.79)] in a separate model. Conclusions: QT prolongation and high heart rate both predict all-cause mortality in Pima Indians, but heart rate was consistently the stronger predictor of the two.",
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AU - Curtis, Jeffrey M.

AU - Sievers, Maurice L.

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AB - Objectives: Understanding why prolonged Bazett-corrected QT interval (QTc) is a risk factor for mortality is difficult, because QTc is positively correlated with heart rate. To optimally distinguish the effects of QT interval and heart rate on mortality, QT interval and heart rate were modeled separately and jointly in Pima Indians. Methods: The effects of QT and heart rate on all-cause and cause-specific mortality were assessed in the overall study population and according to the presence or absence of diabetes using multivariable time-dependent proportional hazards models. Results: Among 1488 nondiabetic and 990 diabetic subjects ≥25 years old, 81 nondiabetic and 149 diabetic subjects died during a median follow-up of 7.3 years. When included in the same regression model, QT and heart rate each predicted all-cause mortality [hazard ratios per standard deviation (SD) (95% confidence interval)=1.31 (1.10-1.57) and 1.57 (1.32-1.87) respectively]. In nondiabetic subjects, hazard ratios for all-cause mortality were 1.54 (1.19-1.99) for QT and 1.86 (1.46-2.37) for heart rate. In diabetic subjects, hazard ratios for all-cause mortality were lower, 1.27 (1.00-1.62) for QT and 1.41 (1.12-1.78) for heart rate. In the overall study population, neither QT nor heart rate significantly predicted cardiovascular disease (CVD) mortality [hazard ratios=1.13 (0.77-1.64) and 1.46 (0.98-2.19)] when adjusted for each other. Heart rate unadjusted for QT, however, predicted CVD mortality [hazard ratio=1.34 (1.00-1.79)] in a separate model. Conclusions: QT prolongation and high heart rate both predict all-cause mortality in Pima Indians, but heart rate was consistently the stronger predictor of the two.

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