Prognostic implications of mutation-specific QTc standard deviation in congenital long QT syndrome

Andrew Mathias, Arthur J. Moss, Coeli M. Lopes, Alon Barsheshet, Scott McNitt, Wojciech Zareba, Jennifer L. Robinson, Emanuela H. Locati, Michael John Ackerman, Jesaia Benhorin, Elizabeth S. Kaufman, Pyotr G. Platonov, Ming Qi, Wataru Shimizu, Jeffrey A. Towbin, G. Michael Vincent, Arthur A M Wilde, Li Zhang, Ilan Goldenberg

Research output: Contribution to journalArticle

14 Citations (Scopus)

Abstract

Background: Individual corrected QT interval (QTc) may vary widely among carriers of the same long QT syndrome (LQTS) mutation. Currently, neither the mechanism nor the implications of this variable penetrance are well understood. Objectives: To hypothesize that the assessment of QTc variance in patients with congenital LQTS who carry the same mutation provides incremental prognostic information on the patient-specific QTc. Methods: The study population comprised 1206 patients with LQTS with 95 different mutations and≥5 individuals who carry the same mutation. Multivariate Cox proportional hazards regression analysis was used to assess the effect of mutation-specific standard deviation of QTc (QTcSD) on the risk of cardiac events (comprising syncope, aborted cardiac arrest, and sudden cardiac death) from birth through age 40 years in the total population and by genotype. Results: Assessment of mutation-specific QTcSD showed large differences among carriers of the same mutations (median QTcSD 45 ms). Multivariate analysis showed that each 20 ms increment in QTcSD was associated with a significant 33% (P =.002) increase in the risk of cardiac events after adjustment for the patient-specific QTc duration and the family effect on QTc. The risk associated with QTcSD was pronounced among patients with long QT syndrome type 1 (hazard ratio 1.55 per 20 ms increment; P<.001), whereas among patients with long QT syndrome type 2, the risk associated with QTcSD was not statistically significant (hazard ratio 0.99; P =.95; P value for QTcSD-by-genotype interaction =.002). Conclusions: Our findings suggest that mutations with a wider variation in QTc duration are associated with increased risk of cardiac events. These findings appear to be genotype-specific, with a pronounced effect among patients with the long QT syndrome type 1 genotype.

Original languageEnglish (US)
Pages (from-to)720-725
Number of pages6
JournalHeart Rhythm
Volume10
Issue number5
DOIs
StatePublished - May 2013

Fingerprint

Long QT Syndrome
Mutation
Romano-Ward Syndrome
Genotype
Penetrance
Sudden Cardiac Death
Syncope
Heart Arrest
Population
Multivariate Analysis
Regression Analysis
Parturition

Keywords

  • Corrected QT interval
  • Long QT syndrome
  • Sudden cardiac death

ASJC Scopus subject areas

  • Cardiology and Cardiovascular Medicine
  • Physiology (medical)

Cite this

Mathias, A., Moss, A. J., Lopes, C. M., Barsheshet, A., McNitt, S., Zareba, W., ... Goldenberg, I. (2013). Prognostic implications of mutation-specific QTc standard deviation in congenital long QT syndrome. Heart Rhythm, 10(5), 720-725. https://doi.org/10.1016/j.hrthm.2013.01.032

Prognostic implications of mutation-specific QTc standard deviation in congenital long QT syndrome. / Mathias, Andrew; Moss, Arthur J.; Lopes, Coeli M.; Barsheshet, Alon; McNitt, Scott; Zareba, Wojciech; Robinson, Jennifer L.; Locati, Emanuela H.; Ackerman, Michael John; Benhorin, Jesaia; Kaufman, Elizabeth S.; Platonov, Pyotr G.; Qi, Ming; Shimizu, Wataru; Towbin, Jeffrey A.; Michael Vincent, G.; Wilde, Arthur A M; Zhang, Li; Goldenberg, Ilan.

In: Heart Rhythm, Vol. 10, No. 5, 05.2013, p. 720-725.

Research output: Contribution to journalArticle

Mathias, A, Moss, AJ, Lopes, CM, Barsheshet, A, McNitt, S, Zareba, W, Robinson, JL, Locati, EH, Ackerman, MJ, Benhorin, J, Kaufman, ES, Platonov, PG, Qi, M, Shimizu, W, Towbin, JA, Michael Vincent, G, Wilde, AAM, Zhang, L & Goldenberg, I 2013, 'Prognostic implications of mutation-specific QTc standard deviation in congenital long QT syndrome', Heart Rhythm, vol. 10, no. 5, pp. 720-725. https://doi.org/10.1016/j.hrthm.2013.01.032
Mathias, Andrew ; Moss, Arthur J. ; Lopes, Coeli M. ; Barsheshet, Alon ; McNitt, Scott ; Zareba, Wojciech ; Robinson, Jennifer L. ; Locati, Emanuela H. ; Ackerman, Michael John ; Benhorin, Jesaia ; Kaufman, Elizabeth S. ; Platonov, Pyotr G. ; Qi, Ming ; Shimizu, Wataru ; Towbin, Jeffrey A. ; Michael Vincent, G. ; Wilde, Arthur A M ; Zhang, Li ; Goldenberg, Ilan. / Prognostic implications of mutation-specific QTc standard deviation in congenital long QT syndrome. In: Heart Rhythm. 2013 ; Vol. 10, No. 5. pp. 720-725.
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abstract = "Background: Individual corrected QT interval (QTc) may vary widely among carriers of the same long QT syndrome (LQTS) mutation. Currently, neither the mechanism nor the implications of this variable penetrance are well understood. Objectives: To hypothesize that the assessment of QTc variance in patients with congenital LQTS who carry the same mutation provides incremental prognostic information on the patient-specific QTc. Methods: The study population comprised 1206 patients with LQTS with 95 different mutations and≥5 individuals who carry the same mutation. Multivariate Cox proportional hazards regression analysis was used to assess the effect of mutation-specific standard deviation of QTc (QTcSD) on the risk of cardiac events (comprising syncope, aborted cardiac arrest, and sudden cardiac death) from birth through age 40 years in the total population and by genotype. Results: Assessment of mutation-specific QTcSD showed large differences among carriers of the same mutations (median QTcSD 45 ms). Multivariate analysis showed that each 20 ms increment in QTcSD was associated with a significant 33{\%} (P =.002) increase in the risk of cardiac events after adjustment for the patient-specific QTc duration and the family effect on QTc. The risk associated with QTcSD was pronounced among patients with long QT syndrome type 1 (hazard ratio 1.55 per 20 ms increment; P<.001), whereas among patients with long QT syndrome type 2, the risk associated with QTcSD was not statistically significant (hazard ratio 0.99; P =.95; P value for QTcSD-by-genotype interaction =.002). Conclusions: Our findings suggest that mutations with a wider variation in QTc duration are associated with increased risk of cardiac events. These findings appear to be genotype-specific, with a pronounced effect among patients with the long QT syndrome type 1 genotype.",
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AU - Mathias, Andrew

AU - Moss, Arthur J.

AU - Lopes, Coeli M.

AU - Barsheshet, Alon

AU - McNitt, Scott

AU - Zareba, Wojciech

AU - Robinson, Jennifer L.

AU - Locati, Emanuela H.

AU - Ackerman, Michael John

AU - Benhorin, Jesaia

AU - Kaufman, Elizabeth S.

AU - Platonov, Pyotr G.

AU - Qi, Ming

AU - Shimizu, Wataru

AU - Towbin, Jeffrey A.

AU - Michael Vincent, G.

AU - Wilde, Arthur A M

AU - Zhang, Li

AU - Goldenberg, Ilan

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N2 - Background: Individual corrected QT interval (QTc) may vary widely among carriers of the same long QT syndrome (LQTS) mutation. Currently, neither the mechanism nor the implications of this variable penetrance are well understood. Objectives: To hypothesize that the assessment of QTc variance in patients with congenital LQTS who carry the same mutation provides incremental prognostic information on the patient-specific QTc. Methods: The study population comprised 1206 patients with LQTS with 95 different mutations and≥5 individuals who carry the same mutation. Multivariate Cox proportional hazards regression analysis was used to assess the effect of mutation-specific standard deviation of QTc (QTcSD) on the risk of cardiac events (comprising syncope, aborted cardiac arrest, and sudden cardiac death) from birth through age 40 years in the total population and by genotype. Results: Assessment of mutation-specific QTcSD showed large differences among carriers of the same mutations (median QTcSD 45 ms). Multivariate analysis showed that each 20 ms increment in QTcSD was associated with a significant 33% (P =.002) increase in the risk of cardiac events after adjustment for the patient-specific QTc duration and the family effect on QTc. The risk associated with QTcSD was pronounced among patients with long QT syndrome type 1 (hazard ratio 1.55 per 20 ms increment; P<.001), whereas among patients with long QT syndrome type 2, the risk associated with QTcSD was not statistically significant (hazard ratio 0.99; P =.95; P value for QTcSD-by-genotype interaction =.002). Conclusions: Our findings suggest that mutations with a wider variation in QTc duration are associated with increased risk of cardiac events. These findings appear to be genotype-specific, with a pronounced effect among patients with the long QT syndrome type 1 genotype.

AB - Background: Individual corrected QT interval (QTc) may vary widely among carriers of the same long QT syndrome (LQTS) mutation. Currently, neither the mechanism nor the implications of this variable penetrance are well understood. Objectives: To hypothesize that the assessment of QTc variance in patients with congenital LQTS who carry the same mutation provides incremental prognostic information on the patient-specific QTc. Methods: The study population comprised 1206 patients with LQTS with 95 different mutations and≥5 individuals who carry the same mutation. Multivariate Cox proportional hazards regression analysis was used to assess the effect of mutation-specific standard deviation of QTc (QTcSD) on the risk of cardiac events (comprising syncope, aborted cardiac arrest, and sudden cardiac death) from birth through age 40 years in the total population and by genotype. Results: Assessment of mutation-specific QTcSD showed large differences among carriers of the same mutations (median QTcSD 45 ms). Multivariate analysis showed that each 20 ms increment in QTcSD was associated with a significant 33% (P =.002) increase in the risk of cardiac events after adjustment for the patient-specific QTc duration and the family effect on QTc. The risk associated with QTcSD was pronounced among patients with long QT syndrome type 1 (hazard ratio 1.55 per 20 ms increment; P<.001), whereas among patients with long QT syndrome type 2, the risk associated with QTcSD was not statistically significant (hazard ratio 0.99; P =.95; P value for QTcSD-by-genotype interaction =.002). Conclusions: Our findings suggest that mutations with a wider variation in QTc duration are associated with increased risk of cardiac events. These findings appear to be genotype-specific, with a pronounced effect among patients with the long QT syndrome type 1 genotype.

KW - Corrected QT interval

KW - Long QT syndrome

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