Subclinical cardiac involvement in patients with facioscapulohumeral muscular dystrophy

被引:19
作者
Galetta, F
Franzoni, F
Sposito, R
Plantinga, Y
Femia, FR
Gauzzi, F
Rocchi, A
Santoro, G
Siciliano, G
机构
[1] Univ Pisa, Sch Med, Dept Internal Med, I-56126 Pisa, Italy
[2] Univ Pisa, Dept Neurosci, I-56126 Pisa, Italy
关键词
facio-scapulo-humeral muscular dystrophy; integrated backscatter; ventricular late potentials; QT dispersion;
D O I
10.1016/j.nmd.2005.02.006
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Myocardial involvement is a common finding in certain myopathics, while it has not been extensively investigated in facioscapulohumeral muscular dystrophy (FSHD1A). Aim of this study was to assess in FSHD1A patients the electrical and functional properties of the myocardium. Twenty-four patients with FSHD1A (mean age 41.2 +/- 14.5 years) and 24 matched healthy subjects were studied. Standard- and signal-averaged electrocardiography were recorded to determine QT dispersion and the presence of ventricular late potentials (VLPs). Standard echocardiography with systo-diastolic variations of integrated backscatter signal (CV-IBS) were performed to assess functional properties of the myocardium. Compared with control subjects, patients with FSHD1A had significantly lower CV-IBS and higher QT dispersion. Nine patients had positive VLPs. QT and QTc dispersion were inversely related to CV-IBS at both septum and posterior wall levels. Moreover, septal CV-IBS was inversely related to the Kpnl-BinI4q fragment size. These results suggest a subclinical cardiac involvement in FSHD1A patients, which can represent a substrate for ventricular arrhythmias and heart failure. (c) 2005 Elsevier B.V. All rights reserved.
引用
收藏
页码:403 / 408
页数:6
相关论文
共 23 条
[1]   QT DISPERSION AND SUDDEN UNEXPECTED DEATH IN CHRONIC HEART-FAILURE [J].
BARR, CS ;
NAAS, A ;
FREEMAN, M ;
LANG, CC ;
STRUTHERS, AD .
LANCET, 1994, 343 (8893) :327-329
[2]   STANDARDS FOR ANALYSIS OF VENTRICULAR LATE POTENTIALS USING HIGH-RESOLUTION OR SIGNAL-AVERAGED ELECTROCARDIOGRAPHY - A STATEMENT BY A TASK-FORCE-COMMITTEE OF THE EUROPEAN-SOCIETY-OF-CARDIOLOGY, THE AMERICAN-HEART-ASSOCIATION, AND THE AMERICAN-COLLEGE-OF-CARDIOLOGY [J].
BREITHARDT, G ;
CAIN, ME ;
ELSHERIF, N ;
FLOWERS, NC ;
HOMBACH, V ;
JANSE, M ;
SIMSON, MB ;
STEINBECK, G .
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 1991, 17 (05) :999-1006
[3]   CHROMOSOME 4Q35 HAPLOTYPES AND DNA REARRANGEMENTS SEGREGATING IN AFFECTED SUBJECTS OF 19 ITALIAN FAMILIES WITH FACIOSCAPULOHUMERAL MUSCULAR-DYSTROPHY (FSHD) [J].
CACURRI, S ;
DEIDDA, G ;
PIAZZO, N ;
NOVELLETTO, A ;
LACESA, I ;
SERVIDEI, S ;
GALLUZZI, G ;
WIJMENGA, C ;
FRANTS, RR ;
FELICETTI, L .
HUMAN GENETICS, 1994, 94 (04) :367-374
[4]   Sequence homology between 4qter and 10qter loci facilitates the instability of subtelomeric KpnI repeat units implicated in facioscapulohumeral muscular dystrophy [J].
Cacurri, S ;
Piazzo, N ;
Deidda, G ;
Vigneti, E ;
Galluzzi, G ;
Colantoni, L ;
Merico, B ;
Ricci, E ;
Felicetti, L .
AMERICAN JOURNAL OF HUMAN GENETICS, 1998, 63 (01) :181-190
[5]   Echocardiographic patterns of myocardial fibrosis in hypertensive patients: Endomyocardial biopsy versus ultrasonic tissue characterization [J].
Ciulla, M ;
Paliotti, R ;
Hess, DB ;
Tjahja, E ;
Campbell, SE ;
Magrini, F ;
Weber, KT .
JOURNAL OF THE AMERICAN SOCIETY OF ECHOCARDIOGRAPHY, 1997, 10 (06) :657-664
[6]  
FISHMAN MA, 1988, SCI PRACTICE PEDIAT, P2263
[7]   PATHOLOGY OF HEART IN PROGRESSIVE MUSCULAR-DYSTROPHY - EPIMYOCARDIAL FIBROSIS [J].
FRANKEL, KA ;
ROSSER, RJ .
HUMAN PATHOLOGY, 1976, 7 (04) :375-386
[8]  
Franzoni F, 2003, ACTA PAEDIATR, V92, P297, DOI 10.1080/08035250310009202
[9]   REPORT OF THE AMERICAN-SOCIETY-OF-ECHOCARDIOGRAPHY COMMITTEE-ON-NOMENCLATURE-AND-STANDARDS-IN-2-DIMENSIONAL-ECHOCARDIOGRAPHY [J].
HENRY, WL ;
DEMARIA, A ;
GRAMIAK, R ;
KING, DL ;
KISSLO, JA ;
POPP, RL ;
SAHN, DJ ;
SCHILLER, NB ;
TAJIK, A ;
TEICHHOLZ, LE ;
WEYMAN, AE .
CIRCULATION, 1980, 62 (02) :212-217
[10]  
HIGHAM P, 1994, BRIT HEART J, V71, P508