Clinical and genetic variables associated with acute arousal and nonarousal-related cardiac events among subjects with the long QT syndrome

被引:52
作者
Ali, RHH
Zareba, W
Moss, AJ
Schwartz, PJ
Benhorin, J
Vincent, GM
Locati, EH
Priori, S
Napolitano, C
Towbin, JA
Hall, WJ
Robinson, JL
Andrews, ML
Zhang, L
Timothy, K
Medina, A
机构
[1] Univ Rochester, Sch Med & Dent, Med Ctr, Cardiol Unit,Heart Res Follow Program, Rochester, NY 14642 USA
[2] Univ Rochester, Sch Med & Dent, Dept Med, Rochester, NY 14642 USA
[3] Univ Rochester, Sch Med & Dent, Dept Biostat, Rochester, NY 14642 USA
[4] Univ Rochester, Sch Med & Dent, Dept Community & Prevent Med, Rochester, NY 14642 USA
[5] Long Isl Jewish Hosp N Shore Hlth Syst, Cardiol Unit, Manhasset, NY USA
[6] Univ Pavia, Dept Cardiol, I-27100 Pavia, Italy
[7] Policlin San Matteo, IRCCS, I-27100 Pavia, Italy
[8] Hebrew Univ Jerusalem, Bikur Cholim Hosp, Dept Cardiol, Jerusalem, Israel
[9] LDS Hosp, Salt Lake City, UT USA
[10] Univ Perugia, Dept Clin Med Pathol & Pharmacol, Cardiol Sect, I-06100 Perugia, Italy
[11] Fdn Maugeri, Pavia, Italy
[12] Texas Childrens Hosp, Baylor Coll Med, Dept Pediat, Houston, TX 77030 USA
关键词
D O I
10.1016/S0002-9149(99)90772-5
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
In patients with the long QT syndrome (LQTS), the occurrence of cardiac events (syncope or cardiac arrest) is frequently associated with acute arousal caused by exercise, swimming, emotion, or noise. However, cardiac events may also occur during sleep or with ordinary daily activities. The purpose of this study was to determine whether there are differential clinical, electrocardiographic, and genetic features among LQTS patients who experienced cardiac events with and without acute arousal. We identified 1,325 patients with cardiac events from the International LQTS Registry. Based on the precipitating conditions of the first event, 427 patients were classified as arousal, 345 as nonarousal, and the remaining 553 were unknown (not classifiable). Gene linkage was known in 78 of the 772 patients with classifiable first events. The age at first cardiac event was significantly younger in the arousal than the non-arousal group (11.7 vs 15.5 years, respectively; p <0.001). The arousal-type patients had a higher rate of subsequent cardiac events during follow-up after the index event than the nonarousal-type patients (p = 0.02). Arousal-related cardiac events occurred in 85% of LQT1, 67% of LQT2, and 33% of LQT3 patients (p = 0.008). This study provides evidence that the genotype is on important determinant of the LQTS phenotype in terms of arousal and nonarousal-related cardiac events. (C) 2000 by Excerpta Medico, Inc.
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收藏
页码:457 / 461
页数:5
相关论文
共 26 条
  • [1] A MOLECULAR-BASIS FOR CARDIAC-ARRHYTHMIA - HERG MUTATIONS CAUSE LONG QT SYNDROME
    CURRAN, ME
    SPLAWSKI, I
    TIMOTHY, KW
    VINCENT, GM
    GREEN, ED
    KEATING, MT
    [J]. CELL, 1995, 80 (05) : 795 - 803
  • [2] THE LONG QT SYNDROME IN CHILDREN - AN INTERNATIONAL STUDY OF 287 PATIENTS
    GARSON, A
    DICK, M
    FOURNIER, A
    GILLETTE, PC
    HAMILTON, R
    KUGLER, JD
    VANHARE, GF
    VETTER, V
    VICK, GW
    [J]. CIRCULATION, 1993, 87 (06) : 1866 - 1872
  • [3] 2 LONG QT SYNDROME LOCI MAP TO CHROMOSOME-3 AND CHROMOSOME-7 WITH EVIDENCE FOR FURTHER HETEROGENEITY
    JIANG, CA
    ATKINSON, D
    TOWBIN, JA
    SPLAWSKI, I
    LEHMANN, MH
    LI, H
    TIMOTHY, K
    TAGGART, RT
    SCHWARTZ, PJ
    VINCENT, GM
    MOSS, AJ
    KEATING, MT
    [J]. NATURE GENETICS, 1994, 8 (02) : 141 - 147
  • [4] LINKAGE OF A CARDIAC-ARRHYTHMIA, THE LONG QT SYNDROME, AND THE HARVEY RAS-1 GENE
    KEATING, M
    ATKINSON, D
    DUNN, C
    TIMOTHY, K
    VINCENT, GM
    LEPPERT, M
    [J]. SCIENCE, 1991, 252 (5006) : 704 - 706
  • [5] Age- and sex-related differences in clinical manifestations in patients with congenital long-QT syndrome - Findings from the international LQTS registry
    Locati, EH
    Zareba, W
    Moss, AJ
    Schwartz, PJ
    Vincent, GM
    Lehmann, MH
    Towbin, JA
    Priori, SG
    Napolitano, C
    Robinson, JL
    Andrews, M
    Timothy, K
    Hall, WJ
    [J]. CIRCULATION, 1998, 97 (22) : 2237 - 2244
  • [6] MOSS AJ, 1986, JAMA-J AM MED ASSOC, V256, P2985
  • [7] Comparison of clinical and genetic variables of cardiac events associated with loud noise versus swimming among subjects with the long QT syndrome
    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
    [J]. AMERICAN JOURNAL OF CARDIOLOGY, 1999, 84 (08) : 876 - 879
  • [8] THE LONG QT SYNDROME - PROSPECTIVE LONGITUDINAL-STUDY OF 328 FAMILIES
    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
    [J]. CIRCULATION, 1991, 84 (03) : 1136 - 1144
  • [9] THE LONG QT SYNDROME - A PROSPECTIVE INTERNATIONAL STUDY
    MOSS, AJ
    SCHWARTZ, PJ
    CRAMPTON, RS
    LOCATI, E
    CARLEEN, E
    [J]. CIRCULATION, 1985, 71 (01) : 17 - 21
  • [10] MOSS AJ, 1970, NEW ENGL J MED, V285, P903