Advances in Clinical and Experimental Medicine

Title abbreviation: Adv Clin Exp Med
JCR Impact Factor (IF) – 2.1 (5-Year IF – 2.0)
Journal Citation Indicator (JCI) (2023) – 0.4
Scopus CiteScore – 3.7 (CiteScore Tracker 3.8)
Index Copernicus  – 171.00; MNiSW – 70 pts

ISSN 1899–5276 (print)
ISSN 2451-2680 (online)
Periodicity – monthly

Download original text (EN)

Advances in Clinical and Experimental Medicine

2018, vol. 27, nr 4, April, p. 501–507

doi: 10.17219/acem/68441

Publication type: original article

Language: English

Download citation:

  • BIBTEX (JabRef, Mendeley)
  • RIS (Papers, Reference Manager, RefWorks, Zotero)

Electrocardiographic T-wave parameters in families with long QT syndrome

Grażyna Markiewicz-Łoskot1,A,B,C,D,F, Ewa Moric-Janiszewska2,B,C,F, Bogusław Mazurek3,B,C, Marianna Łoskot4,B,C,D,E,F, Mariola Bartusek1,F, Agnieszka Skierska3,B, Lesław Szydłowski3,C,E,F

1 Department of Nursing and Social Medical Problems, School of Health Sciences in Katowice, Medical University of Silesia in Katowice, Poland

2 Department of Biochemistry, School of Pharmacy with the Division of Laboratory Medicine in Sosnowiec, Medical University of Silesia in Katowice, Poland

3 Department of Pediatric Cardiology, School of Medicine in Katowice, Medical University of Silesia in Katowice, Poland

4 Department of Nursing and Social Medical Problems, Students’ Research Group, School of Health Sciences in Katowice, Medical University of Silesia in Katowice, Poland

Abstract

Background. T-wave parameters, especially the Tpeak-Tend interval (TpTe), reflect the total dispersion of repolarization, whose amplification may lead to the development of life-threatening ventricular arrhythmias observed in the long QT syndrome (LQTS).
Objectives. The study attempted to evaluate QT, QTp (Q-Tpeak) and TpTe (Tpeak-Tend) intervals in unaffected and affected blood relatives of children with clinically confirmed LQTS as well as to determine whether the values of these repolarization parameters may be used in clinical practice.
Material and Methods. The study group included 47 affected blood relatives (27 LQTS1 and 20 LQTS2) and 68 unaffected family members without clinically confirmed LQTS symptoms. The TpTe, QT and QTp intervals were measured manually in the lead V5 of standard ECGs and corrected using Bazett’s and Fridericia’s formulas.
Results. The RR, QT, QTp and TpTe intervals with their corrected values were significantly longer (p < 0.0001) in the affected subjects than in the unaffected subjects and, similarly, in LQTS1 and LQTS2 patients compared with the unaffected family members. The TpTe interval in LQTS2 showed only a tendency to be longer compared to LQTS1, but did not reach statistical significance (p = 0.0933). For affected blood relatives, only the TpTe interval (p < 0.0409) and QT interval, corrected with Bazett’s (p < 0.0393) and Fridericia’s (p < 0.0495) formulas, enabled differentiation between LQTS1 (mean TpTe = 103 ±15) and LQTS2 women (mean TpTe = 106 ±17). Moreover, there were statistically significant differences (p < 0.05) in the TpTe interval between the 6 sex subgroups: unaffected women and men as well as women and men with LQTS1 and LQTS2.
Conclusion. The electrocardiographic Tpeak-Tend parameter, in addition to the QT interval, is helpful in identifying affected blood relatives of children with LQTS, particularly for the group of LQTS1 and LQTS2 women. Further studies are required to assess the clinical importance of the TpTe interval in families with long QT syndrome.

Key words

repolarization, long QT syndrome, QT, Q-Tpeak, Tpeak-Tend intervals

References (27)

  1. Schwartz PJ, Moss AJ, Vincent GM, Crampton RS. Diagnostic criteria for the long QT syndrome: An update. Circulation. 1993;88:782–784.
  2. Tester DJ, Ackerman MJ. Genetics of long QT syndrome. Methodist Debakey Cardiovasc J. 2014;10(1):29–33.
  3. Schwartz PJ, Priori SG, Spazzolini C, et al. Genotype-phenotype correlation in the long QT syndrome gene-specific triggers for life-threatening arrhythmias. Circulation. 2001;103:89–95.
  4. Van Langen IM, Birnie E, Alders M, Jongbloed RJ, Marec HLE, Wilde AAM. The use of genotype-phenotype correlations in mutations analysis for the long QT syndrome. J Med Genet. 2003;40:141–145.
  5. Zhang L, Timothy KW, Vincent GM, et al. Spectrum of ST-T-wave patterns and repolarization parameters in congenital longQT syndrome: ECG findings identify genotype. Circulation. 2000;102:2849–2855.
  6. Schwartz PJ, Ackerman MJ. The long QT syndrome: Transatlantic clinical approach to diagnosis and therapy. Eur Heart J. 2013;34:3109–3116.
  7. Markiewicz-Łoskot G. Electrocardiographic characteristics of a total of repolarization (QT), early repolarization phase (QTP) and late phase repolarization (TpTe) in healthy children and children with long QT syndrome. Habilitation Dissertation. Medical University of Silesia in Katowice. 2009;8:59–76.
  8. Viitasalo M, Oikarinen L, Swan H, et al. Ambulatory electrocardiographic evidence of transmural dispersion of repolarization in patients with long QT syndrome type 1 and 2. Circulation.2002;06:2473–2478.
  9. Takenaka K, Tomohiko A, Shimizu W, et al. Exercise stress test amplifies genotype-phenotype correlation in the LQT1 and LQT2 forms of the long-QT syndrome. Circulation. 2003;107:838–844.
  10. Swan H, Viitasalo M, Piippo K, Laitinen P, Kontula K, Toivonen L. Sinus node function and ventricular repolarization during exercise stress test in long QT syndrome patients with KvLQT1 and HERG potassium channel defects. J Am Coll Cardiol. 1999;34:823–824.
  11. Shimizu W, Tanabe Y, Aiba T, et al. Differential effects of betablockade on dispersion of repolarization in the absence and presence of sympathetic stimulation between the LQT1 and LQT2 forms of congenital long QT syndrome. J Am Coll Cardiol. 2002;39:1894–1896.
  12. Extramiana F, Denjoy I, Badilini F, et al. Heart rate influences on repolarization duration and morphology in symptomatic versus asymptomatic KCNQ1 mutation carriers. Am J Cardiol. 2005;95:406–409.
  13. Yamaguchi M, Shimizu M, Ino H, et al. T-wave peak-to-end interval and QT dispersion in acquired long QT syndrome: A new index for arrythmogenicity. Clin Sci. 2003;105:671–676.
  14. Antzelevitch C. Ionic, molecular and cellular bases of QT-interval prolongation and torsade de pointes. Europace 2007;9(4):4-15.
  15. Opthof T, Coronel R, Wilms-Schopman FJG, et al. Dispersion of repolarization in canine ventricle and the electrocardiographic T-wave:Tp-e interval does not reflect transmural dispersion. Heart Rhythm. 2007;4:341–348.
  16. Meijborg VMF, Conrath CE, Opthof T, Belterman CNW, Bakker JMT,Coronel R. Electrocardiographic T-wave and its relation with ventricular repolarization along major anatomical axes. Circ Arrhythm Electrophysiol. 2014;7:524–531.
  17. Moric-Janiszewska E, Głogowska-Ligus J, Paul-Samojedny M, et al. Expression of genes KCNQ1 and HERG encoding potassium ion channels lkr, lks in long QT syndrome. Kardiol Pol. 2011;5:423–429.
  18. Moric-Janiszewska E, Głogowska-Ligus J, Paul-Samojedny M, Węglarz L, Markiewicz-Łoskot G, Szydłowski L. Age- and sex dependent mRNA expression of KCNQ1 and HERG in patients with long QT syndrome type 1 and 2. Arch Med Sci. 2011;6:941–947.
  19. Rautaharju PM, Surawicz B, Gettes LS. AHA/ACCF/HRS recommendations for the standardization and interpretation of the electrocardiogram. Part IV: The ST segment, T- and U-waves, and the QT interval. A scientific statement from the American Heart Association Electrocardiography and Arrhythmias Committee, Council on Clinical Cardiology, the American College of Cardiology Foundation, and the Heart Rhythm Society, endorsed by the International Society for Computerized Electrocardiology. Circulation. 2009;119:241–250.
  20. Lubiński A, Lewicka-Nowak E, Kempa M, Baczyńska AM, Romanowska I, Świątecka G. New insight into repolarization abnormalities in patients with congenital long QT syndrome: The increased transmural dispersion of repolarization. Pacing Clin Electrophysiol.1998;21:172–175.
  21. Swan H, Toivonen L, Viitasalo M. Rate adaptation of QT intervals during and after exercise in children with congenital long QT syndrome. Eur Heart J. 1998;19:508–513.
  22. Haapalahti P, Viitasalo M, Perhonen M, et al. Electrocardiographic interventricular dispersion of repolarization during autonomic adaptation in LQTS1 subtype of long QT syndrome. Scand Cardiovasc J. 2008;42:130–136.
  23. Topilski I, Rogowski O, Rosso R, et al. The morphology of the QT interval predicts torsade de pointes during acquired bradyarrhythmias. J Am Coll Cardiol. 2007;49(3):320–328.
  24. Yan GX, Antzelevitch C. Cellular basis for the normal T-wave and the electrocardiographic manifestation of the long QT syndrome. Circulation. 1998;98:1928–1936.
  25. Kanters JK, Haarmark C, Vedel-Larsen E, et al. Tpeak-Tend interval in long QT syndrome. J Electrocardiol. 2008;41:603–608
  26. Van Camp G, Pasquet A, Sinnaeve P, Mairesse GH, De Pauw M, Claeys MJ. Summary 2015 ESC guidelines. Acta Cardiol. 2016;71(1):7–13.
  27. Markiewicz-Łoskot G, Moric-Janiszewska E, Mazurek U. The risk of cardiac events and management of LQTS patients on the basis of genotype. Ann Noninvasive Electrocardiol. 2009;14(1):86–92.