Gene-specific response of dynamic ventricular repolarization to sympathetic stimulation in LQT1, LQT2 and LQT3 forms of congenital long QT syndrome

被引:83
作者
Noda, T
Takaki, H
Kurita, T
Suyama, K
Nagaya, N
Taguchi, A
Aihara, N
Kamakura, S
Sunagawa, K
Nakamura, K
Ohe, T
Horie, M
Napolitano, C
Towbin, JA
Priori, SG
Shimizu, W
机构
[1] Natl Cardiovasc Ctr, Dept Internal Med, Div Cardiol, Suita, Osaka 5658565, Japan
[2] Natl Cardiovasc Ctr, Dept Cardiovasc Dynam, Suita, Osaka 5658565, Japan
[3] Okayama Univ, Grad Sch Med & Dent, Dept Cardiovasc Med, Okayama, Japan
[4] Kyoto Univ, Grad Sch Med, Dept Cardiovasc Med, Kyoto, Japan
[5] Salvatore Maugeri Fdn, Pavia, Italy
[6] Baylor Coll Med, Dept Pediat Cardiol Mol & Human Genet, Houston, TX 77030 USA
关键词
action potentials; catecholamines; genetics; long-QT syndrome; nervous system; sympathetic;
D O I
10.1053/euhj.2001.3079
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Aims Differences in the sensitivity of the genotype of the congenital long QT syndrome to sympathetic stimulation have been suggested. This study compared the influence of sympathetic stimulation on continuous corrected QT (QTc) intervals between LQT1, LQT2 and LQT3 forms of the congenital long QT syndrome. Methods and Results We recorded a 12-lead electrocardiogram continuously before and after bolus injection (0.1 mug. kg(-1)) of epinephrine followed by continuous infusion (0.1 mug. kg(-1) min(-1)) in 12 LQT1, 10 LQT2, 6 LQT3, and 13 control patients. The QT intervals and previous RR intervals of all beats were measured semi-automatically, and the QTc intervals of all beats were calculated by Bazett's method. The dynamic response of the RR interval to epinephrine was no different between the four groups. The QTc was prolonged remarkably (477 +/- 42 to 631 +/- 59 ms; P<0.0005, % delta prolongation = + 32%) as the RR was maximally decreased (at peak of epinephrine), and remained prolonged at steady state conditions of epinephrine (556 +/- 56 ms; P<0.0005 vs baseline, + 17%) in LQT1 patients. Epinephrine also prolonged the QTc dramatically (502 +/- 23 to 620 +/- 39 ms, P<0.0005, +24%) at peak of epinephrine in LQT2 patients, but this shortened to baseline levels at steady state (531 25 ms; P=ns vs baseline, +6%). The QTc was Much less prolonged at peak of epinephrine in LQT3 (478 +/- 44 to 532 +/- 41 ms; P<0.05, +11%) and controls (394 +/- 21 to 456 +/- 18 ms; P<0.0005, + 16%) than in LQT1 and LQT2 patients, and shortened to the baseline levels (LQT3; 466 +/- 49 ms, -3%, controls; 397 +/- 16 ms, +1%; P=ns vs baseline) at steady state. Conclusion Our data suggest that the dynamic response of ventricular repolarization to sympathetic stimulation differs between LQT1, LQT2 and LQT3 syndromes, and may explain why the trigger of cardiac events differs between the genotypes. (C) 2002 The European Society of Cardiology. Published by Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:975 / 983
页数:9
相关论文
共 22 条
[1]   MiRP1 forms IKr potassium channels with HERG and is associated with cardiac arrhythmia [J].
Abbott, GW ;
Sesti, F ;
Splawski, I ;
Buck, ME ;
Lehmann, WH ;
Timothy, KW ;
Keating, MT ;
Goldstein, SAN .
CELL, 1999, 97 (02) :175-187
[2]  
ANTZELEVITCH C, 1999, CARDIAC ELECTROPHYSI, P222
[3]   QUINIDINE-INDUCED ACTION-POTENTIAL PROLONGATION, EARLY AFTERDEPOLARIZATIONS, AND TRIGGERED ACTIVITY IN CANINE PURKINJE-FIBERS - EFFECTS OF STIMULATION RATE, POTASSIUM, AND MAGNESIUM [J].
DAVIDENKO, JM ;
COHEN, L ;
GOODROW, R ;
ANTZELEVITCH, C .
CIRCULATION, 1989, 79 (03) :674-686
[4]   Comparison of clinical and genetic variables of cardiac events associated with loud noise versus swimming among subjects with the long QT syndrome [J].
Moss, AJ ;
Robinson, JL ;
Gessman, L ;
Gillespie, R ;
Zareba, W ;
Schwartz, PJ ;
Vincent, GM ;
Benhorin, J ;
Heilbron, EL ;
Towbin, JA ;
Priori, SG ;
Napolitano, C ;
Zhang, L ;
Medina, A ;
Andrews, ML ;
Timothy, K .
AMERICAN JOURNAL OF CARDIOLOGY, 1999, 84 (08) :876-879
[5]   THE LONG QT SYNDROME - PROSPECTIVE LONGITUDINAL-STUDY OF 328 FAMILIES [J].
MOSS, AJ ;
SCHWARTZ, PJ ;
CRAMPTON, RS ;
TZIVONI, D ;
LOCATI, EH ;
MACCLUER, J ;
HALL, WJ ;
WEITKAMP, L ;
VINCENT, GM ;
GARSON, A ;
ROBINSON, JL ;
BENHORIN, J ;
CHOI, SS .
CIRCULATION, 1991, 84 (03) :1136-1144
[6]   THE LONG QT SYNDROME - A PROSPECTIVE INTERNATIONAL STUDY [J].
MOSS, AJ ;
SCHWARTZ, PJ ;
CRAMPTON, RS ;
LOCATI, E ;
CARLEEN, E .
CIRCULATION, 1985, 71 (01) :17-21
[7]   ECG T-WAVE PATTERNS IN GENETICALLY DISTINCT FORMS OF THE HEREDITARY LONG QT SYNDROME [J].
MOSS, AJ ;
ZAREBA, W ;
BENHORIN, J ;
LOCATI, EH ;
HALL, WJ ;
ROBINSON, JL ;
SCHWARTZ, PJ ;
TOWBIN, JA ;
VINCENT, GM ;
LEHMANN, MH ;
KEATING, MT ;
MACCLUER, JW ;
TIMOTHY, KW .
CIRCULATION, 1995, 92 (10) :2929-2934
[8]   Genetic and molecular basis of cardiac arrhythmias: Impact on clinical management parts I and II [J].
Priori, SG ;
Barhanin, J ;
Hauer, RNW ;
Haverkamp, W ;
Jongsma, HJ ;
Kleber, AG ;
McKenna, WJ ;
Roden, DM ;
Rudy, Y ;
Schwartz, K ;
Schwartz, PJ ;
Towbin, JA ;
Wilde, AM .
CIRCULATION, 1999, 99 (04) :518-528
[9]   Differential response to Na+ channel blockade, beta-adrenergic stimulation, and rapid pacing in a cellular model mimicking the SCN5A and HERG defects present in the long-QT syndrome [J].
Priori, SG ;
Napolitano, C ;
Cantu, F ;
Brown, AM ;
Schwartz, PJ .
CIRCULATION RESEARCH, 1996, 78 (06) :1009-1015
[10]   Multiple mechanisms in the long-QT syndrome - Current knowledge, gaps, and future directions [J].
Roden, DM ;
Lazzara, R ;
Rosen, M ;
Schwartz, PJ ;
Towbin, J ;
Vincent, GM .
CIRCULATION, 1996, 94 (08) :1996-2012