Literature DB >> 15886026

Correction of QT values to allow for increases in heart rate in conscious Beagle dogs in toxicology assessment.

Marshall Leslie Tattersall1, Michael Dymond, Tim Hammond, Jean-Pierre Valentin.   

Abstract

INTRODUCTION: Estimation of a direct effect of drugs on the duration of the electrocardiogram (ECG) QT interval can be confused by drug-induced increases in heart rate (HR). The objective of this assessment was to identify a correction formula that adequately corrects QT over a wide range of HRs.
METHODS: Paired recordings of HR and QT interval measurements were obtained from 177 conscious Beagle dogs from both sexes in 9 toxicology studies. ECGs used for this evaluation were collected in either control vehicle-treated dogs, or from dogs prior to the first dose of a daily dosing regimen. Where more than one recording was available per dog, only one was used in the analyses. The assessments were made based on the lowest and highest pre-dose HR for each dog. Correction factors according to [Bazett, H.C. (1920). An analysis of the time relationships or time-relations of electrocardiograms. Heart 7:353-380], [Sagie, A., Larson, M.G., Goldberg, R.J., Bengtson, J.R., & Levy, D. (1992). An improved method for adjusting the QT interval for heart rate (the Framingham heart study). American Journal of Cardiology 70:797-801], [Fridericia, L.S. (1920). Die sytolendauer in elektrokardiogramm bei normalen menschen und bei herzkranken. Acta Medica Scandinavica 53:469-505.], [Todt, H., Krumpl, G., Krejcy, K. & Raberger, G. (1992). Mode of QT correction for heart rate: implications for the detection of inhomogeneous repolarization after myocardial infarction. American Heart Journal 124(3):602-609.] and [Van de Water, A., Verheyen, J., Xhonneux, R., & Reneman, R.S. (1989). An improved method to correct the QT interval of the electrocardiogram for changes in heart rate. Journal of Pharmacological Methods 22:207-217.] were applied to these QT intervals and plotted against HR. Linear regression statistical analyses using a single or multiple (i.e., baseline, sex and study) parameters model was then applied to trend lines.
RESULTS: Although two correction factors ([Todt, H., Krumpl, G., Krejcy, K. & Raberger, G. (1992). Mode of QT correction for heart rate: implications for the detection of inhomogeneous repolarization after myocardial infarction. American Heart Journal 124(3):602-609.] and [Van de Water, A., Verheyen, J., Xhonneux, R., & Reneman, R.S. (1989). An improved method to correct the QT interval of the electrocardiogram for changes in heart rate. Journal of Pharmacological Methods 22:207-217.]) adequately corrected QT for changes in HR [i.e., slope of QTc versus HR not statistically significantly different from zero (p>0.05)] that of Van de Water showed a statistically superior correction. Although the method of analyses accounted for baseline, sex and study it was independently demonstrated that sex did not influence the outcome of the evaluations. Furthermore, higher HRs (i.e., maximum HRs for each dog) were better corrected than the lower HRs. In addition, statistical power analysis applied to these data showed that group sizes of 4-8 could, with 80% chance, detect a 10-5% change, respectively, in appropriately corrected QT. DISCUSSION: Overall, the data suggest that an evaluation of the most appropriate correction factor should be applied to each laboratory using their own data collected by their own method in their particular strain of dog.

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Year:  2006        PMID: 15886026     DOI: 10.1016/j.vascn.2005.02.005

Source DB:  PubMed          Journal:  J Pharmacol Toxicol Methods        ISSN: 1056-8719            Impact factor:   1.950


  8 in total

Review 1.  An introduction to QT interval prolongation and non-clinical approaches to assessing and reducing risk.

Authors:  Chris E Pollard; N Abi Gerges; M H Bridgland-Taylor; A Easter; T G Hammond; J-P Valentin
Journal:  Br J Pharmacol       Date:  2010-01       Impact factor: 8.739

Review 2.  Strategies to reduce the risk of drug-induced QT interval prolongation: a pharmaceutical company perspective.

Authors:  C E Pollard; J-P Valentin; T G Hammond
Journal:  Br J Pharmacol       Date:  2008-05-26       Impact factor: 8.739

3.  Combined pharmacological block of I(Kr) and I(Ks) increases short-term QT interval variability and provokes torsades de pointes.

Authors:  C Lengyel; A Varró; K Tábori; J G Papp; I Baczkó
Journal:  Br J Pharmacol       Date:  2007-05-29       Impact factor: 8.739

Review 4.  Sex differences in the mechanisms underlying long QT syndrome.

Authors:  Guy Salama; Glenna C L Bett
Journal:  Am J Physiol Heart Circ Physiol       Date:  2014-06-27       Impact factor: 4.733

5.  Detection of QTc interval prolongation using jacket telemetry in conscious non-human primates: comparison with implanted telemetry.

Authors:  K Derakhchan; R W Chui; D Stevens; W Gu; H M Vargas
Journal:  Br J Pharmacol       Date:  2014-01       Impact factor: 8.739

6.  Sudden death associated with QT interval prolongation and KCNQ1 gene mutation in a family of English Springer Spaniels.

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Journal:  J Vet Intern Med       Date:  2015-03-16       Impact factor: 3.333

7.  Molecular remodeling of Cx43, but not structural remodeling, promotes arrhythmias in an arrhythmogenic canine model of nonischemic heart failure.

Authors:  Jiajie Yan; Cheryl Killingsworth; Greg Walcott; Yujie Zhu; Silvio Litovsky; Jian Huang; Xun Ai; Steven M Pogwizd
Journal:  J Mol Cell Cardiol       Date:  2021-05-31       Impact factor: 5.000

Review 8.  The history, hotspots, and trends of electrocardiogram.

Authors:  Xiang-Lin Yang; Guo-Zhen Liu; Yun-Hai Tong; Hong Yan; Zhi Xu; Qi Chen; Xiang Liu; Hong-Hao Zhang; Hong-Bo Wang; Shao-Hua Tan
Journal:  J Geriatr Cardiol       Date:  2015-07       Impact factor: 3.327

  8 in total

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