T‐peak to T‐end interval may be a better predictor of high‐risk patients with hypertrophic cardiomyopathy associated with a cardiac troponin i mutation than qt dispersion
Open Access
- 1 July 2002
- journal article
- research article
- Published by Wiley in Clinical Cardiology
- Vol. 25 (7) , 335-339
- https://doi.org/10.1002/clc.4950250706
Abstract
Background: Patients with hypertrophic cardiomyopathy (HCM) associated with a deletion of lysine 183 (K183del) in the cardiac troponin I (cTnI) gene suffer sudden cardiac death at all ages. However, the correlation between QT variables and sudden cardiac death in these patients remains uncertain. Hypothesis: We evaluated the correlation between QT variables and sudden cardiac death and/or ventricular tach‐yarrhythmia (SCD/VT) in patients with HCM associated with the cTnI mutation. Methods: We analyzed 10 probands with HCM associated with the cTnI gene K183del and their family members. The subjects were divided into three groups: Group A (n = 7), mutation carriers with SCD/VT; Group B (n = 16), mutation carriers without SCD/VT; Group C (n = 24), no mutation carriers. QT intervals were corrected using Bazett's formula. Results: Maximum QTc and corrected QT dispersion were significantly longer in Groups A and B than in Group C. However, there were no differences in either parameter between Groups A and B. On the contrary, the peak‐to‐end interval of T wave/QT interval in V5 (Tpe) in Group A was significantly longer than that in Groups B and C. Logistic regression analysis revealed that Tpe was a good clinical predictor for SCD/VT in patients with HCM in this study. Conclusions: These results suggest that Tpe rather than QT dispersion may be one of the best predictors for SCD/VT in patients with HCM associated with the K183del mutation in the cTnI gene.Keywords
This publication has 19 references indexed in Scilit:
- Epidemiology of Hypertrophic Cardiomyopathy–Related DeathCirculation, 2000
- Clinical Features of Hypertrophic Cardiomyopathy Caused by a Lys183 Deletion Mutation in the Cardiac Troponin I GeneCirculation, 2000
- Properties of mutant contractile proteins that cause hypertrophic cardiomyopathyCardiovascular Research, 1999
- Long-term outcome and prognostic determinants in children with hypertrophic cardiomyopathyJournal of the American College of Cardiology, 1998
- QT dispersion and risk factors for sudden cardiac death in patients with hypertrophic cardiomyopathyThe American Journal of Cardiology, 1998
- Cellular Basis for the Normal T Wave and the Electrocardiographic Manifestations of the Long-QT SyndromeCirculation, 1998
- Mutations in the cardiac troponin I gene associated with hypertrophic cardiomyopathyNature Genetics, 1997
- Comparison of QT dispersion in hypertrophic cardiomyopathy between patients with and without ventricular arrhythmias and sudden deathThe American Journal of Cardiology, 1993
- Rapid and sensitive detection of point mutations and DNA polymorphisms using the polymerase chain reactionGenomics, 1989
- Sudden death in patients with hypertrophic cardiomyopathy: Characterization of 26 patients without functional limitationThe American Journal of Cardiology, 1978