Mutation and gender-specific risk in type 2 long QT syndrome

Implications for risk stratification for life-threatening cardiac events in patients with long QT syndrome

Dimitry Migdalovich, Arthur J. Moss, Coeli M. Lopes, Jason Costa, Gregory Ouellet, Alon Barsheshet, Scott McNitt, Slava Polonsky, Jennifer L. Robinson, Wojciech Zareba, Michael J. Ackerman, Jesaia Benhorin, Elizabeth S. Kaufman, Pyotr G. Platonov, Wataru Shimizu, Jeffrey Towbin, G. Michael Vincent, Arthur A.M. Wilde, Ilan Goldenberg

Research output: Contribution to journalArticle

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Abstract

Background: Men and women with type 2 long QT syndrome (LQT2) exhibit time-dependent differences in the risk for cardiac events. We hypothesized that data regarding the location of the disease-causing mutation in the KCNH2 channel may affect gender-specific risk in LQT2. Objective: This study sought to risk-stratify LQT2 patients for life-threatening cardiac events based on clinical and genetic information. Methods: The risk for life-threatening cardiac events from birth through age 40 years (comprising aborted cardiac arrest [ACA] or sudden cardiac death [SCD]) was assessed among 1,166 LQT2 male (n = 490) and female (n = 676) patients by the location of the LQTS-causing mutation in the KCNH2 channel (prespecified in the primary analysis as pore-loop vs. nonpore-loop). Results: During follow-up, the cumulative probability of life-threatening cardiac events years was significantly higher among LQT2 women (26%) as compared with men (14%; P <.001). Multivariate analysis showed that the risk for life-threatening cardiac events was not significantly different between women with and without pore-loop mutations (hazard ratio 1.20; P =.33). In contrast, men with pore-loop mutations displayed a significant >2-fold higher risk of a first ACA or SCD as compared with those with nonpore-loop mutations (hazard ratio 2.18; P =.01). Consistently, women experienced a high rate of life-threatening events regardless of mutation location (pore-loop: 35%, nonpore-loop: 23%), whereas in men the rate of ACA or SCD was high among those with pore-loop mutations (28%) and relatively low among those with nonpore-loop mutations (8%). Conclusion: Combined assessment of clinical and mutation-specific data can be used for improved risk stratification for life-threatening cardiac events in LQT2.

Original languageEnglish (US)
Pages (from-to)1537-1543
Number of pages7
JournalHeart Rhythm
Volume8
Issue number10
DOIs
StatePublished - Jan 1 2011
Externally publishedYes

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Long QT Syndrome
Mutation
Sudden Cardiac Death
Heart Arrest
Parturition

All Science Journal Classification (ASJC) codes

  • Cardiology and Cardiovascular Medicine
  • Physiology (medical)

Cite this

Mutation and gender-specific risk in type 2 long QT syndrome : Implications for risk stratification for life-threatening cardiac events in patients with long QT syndrome. / Migdalovich, Dimitry; Moss, Arthur J.; Lopes, Coeli M.; Costa, Jason; Ouellet, Gregory; Barsheshet, Alon; McNitt, Scott; Polonsky, Slava; Robinson, Jennifer L.; Zareba, Wojciech; Ackerman, Michael J.; Benhorin, Jesaia; Kaufman, Elizabeth S.; Platonov, Pyotr G.; Shimizu, Wataru; Towbin, Jeffrey; Vincent, G. Michael; Wilde, Arthur A.M.; Goldenberg, Ilan.

In: Heart Rhythm, Vol. 8, No. 10, 01.01.2011, p. 1537-1543.

Research output: Contribution to journalArticle

Migdalovich, D, Moss, AJ, Lopes, CM, Costa, J, Ouellet, G, Barsheshet, A, McNitt, S, Polonsky, S, Robinson, JL, Zareba, W, Ackerman, MJ, Benhorin, J, Kaufman, ES, Platonov, PG, Shimizu, W, Towbin, J, Vincent, GM, Wilde, AAM & Goldenberg, I 2011, 'Mutation and gender-specific risk in type 2 long QT syndrome: Implications for risk stratification for life-threatening cardiac events in patients with long QT syndrome', Heart Rhythm, vol. 8, no. 10, pp. 1537-1543. https://doi.org/10.1016/j.hrthm.2011.03.049
Migdalovich, Dimitry ; Moss, Arthur J. ; Lopes, Coeli M. ; Costa, Jason ; Ouellet, Gregory ; Barsheshet, Alon ; McNitt, Scott ; Polonsky, Slava ; Robinson, Jennifer L. ; Zareba, Wojciech ; Ackerman, Michael J. ; Benhorin, Jesaia ; Kaufman, Elizabeth S. ; Platonov, Pyotr G. ; Shimizu, Wataru ; Towbin, Jeffrey ; Vincent, G. Michael ; Wilde, Arthur A.M. ; Goldenberg, Ilan. / Mutation and gender-specific risk in type 2 long QT syndrome : Implications for risk stratification for life-threatening cardiac events in patients with long QT syndrome. In: Heart Rhythm. 2011 ; Vol. 8, No. 10. pp. 1537-1543.
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abstract = "Background: Men and women with type 2 long QT syndrome (LQT2) exhibit time-dependent differences in the risk for cardiac events. We hypothesized that data regarding the location of the disease-causing mutation in the KCNH2 channel may affect gender-specific risk in LQT2. Objective: This study sought to risk-stratify LQT2 patients for life-threatening cardiac events based on clinical and genetic information. Methods: The risk for life-threatening cardiac events from birth through age 40 years (comprising aborted cardiac arrest [ACA] or sudden cardiac death [SCD]) was assessed among 1,166 LQT2 male (n = 490) and female (n = 676) patients by the location of the LQTS-causing mutation in the KCNH2 channel (prespecified in the primary analysis as pore-loop vs. nonpore-loop). Results: During follow-up, the cumulative probability of life-threatening cardiac events years was significantly higher among LQT2 women (26{\%}) as compared with men (14{\%}; P <.001). Multivariate analysis showed that the risk for life-threatening cardiac events was not significantly different between women with and without pore-loop mutations (hazard ratio 1.20; P =.33). In contrast, men with pore-loop mutations displayed a significant >2-fold higher risk of a first ACA or SCD as compared with those with nonpore-loop mutations (hazard ratio 2.18; P =.01). Consistently, women experienced a high rate of life-threatening events regardless of mutation location (pore-loop: 35{\%}, nonpore-loop: 23{\%}), whereas in men the rate of ACA or SCD was high among those with pore-loop mutations (28{\%}) and relatively low among those with nonpore-loop mutations (8{\%}). Conclusion: Combined assessment of clinical and mutation-specific data can be used for improved risk stratification for life-threatening cardiac events in LQT2.",
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T2 - Implications for risk stratification for life-threatening cardiac events in patients with long QT syndrome

AU - Migdalovich, Dimitry

AU - Moss, Arthur J.

AU - Lopes, Coeli M.

AU - Costa, Jason

AU - Ouellet, Gregory

AU - Barsheshet, Alon

AU - McNitt, Scott

AU - Polonsky, Slava

AU - Robinson, Jennifer L.

AU - Zareba, Wojciech

AU - Ackerman, Michael J.

AU - Benhorin, Jesaia

AU - Kaufman, Elizabeth S.

AU - Platonov, Pyotr G.

AU - Shimizu, Wataru

AU - Towbin, Jeffrey

AU - Vincent, G. Michael

AU - Wilde, Arthur A.M.

AU - Goldenberg, Ilan

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N2 - Background: Men and women with type 2 long QT syndrome (LQT2) exhibit time-dependent differences in the risk for cardiac events. We hypothesized that data regarding the location of the disease-causing mutation in the KCNH2 channel may affect gender-specific risk in LQT2. Objective: This study sought to risk-stratify LQT2 patients for life-threatening cardiac events based on clinical and genetic information. Methods: The risk for life-threatening cardiac events from birth through age 40 years (comprising aborted cardiac arrest [ACA] or sudden cardiac death [SCD]) was assessed among 1,166 LQT2 male (n = 490) and female (n = 676) patients by the location of the LQTS-causing mutation in the KCNH2 channel (prespecified in the primary analysis as pore-loop vs. nonpore-loop). Results: During follow-up, the cumulative probability of life-threatening cardiac events years was significantly higher among LQT2 women (26%) as compared with men (14%; P <.001). Multivariate analysis showed that the risk for life-threatening cardiac events was not significantly different between women with and without pore-loop mutations (hazard ratio 1.20; P =.33). In contrast, men with pore-loop mutations displayed a significant >2-fold higher risk of a first ACA or SCD as compared with those with nonpore-loop mutations (hazard ratio 2.18; P =.01). Consistently, women experienced a high rate of life-threatening events regardless of mutation location (pore-loop: 35%, nonpore-loop: 23%), whereas in men the rate of ACA or SCD was high among those with pore-loop mutations (28%) and relatively low among those with nonpore-loop mutations (8%). Conclusion: Combined assessment of clinical and mutation-specific data can be used for improved risk stratification for life-threatening cardiac events in LQT2.

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