Donate Help Contact The AHA Sign In Home
American Heart Association
Circulation
Search: search_blue_button Advanced Search
Circulation. 1999;99:1041-1046

This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrowRequest Permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Lazarus, A.
Right arrow Articles by Duboc, D.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Lazarus, A.
Right arrow Articles by Duboc, D.
Related Collections
Right arrow Electrophysiology
Right arrow Arrhythmias, clinical electrophysiology, drugs

(Circulation. 1999;99:1041-1046.)
© 1999 American Heart Association, Inc.


Clinical Investigation and Reports

Relationships Among Electrophysiological Findings and Clinical Status, Heart Function, and Extent of DNA Mutation in Myotonic Dystrophy

A. Lazarus, MD; J. Varin, MD; Z. Ounnoughene, MD; H. Radvanyi, MD; C. Junien, PharmD, PhD; J. Coste, MD; P. Laforet, MD; B. Eymard, MD; H. M. Becane, MD; S. Weber, MD; D. Duboc, MD

From Services de Cardiologie et de Biostatistique, Hôpital Cochin, Paris, France (A.L., J.V., Z.O., J.C., S.W., D.D.); Association Cardiologie Val d'Or, St. Cloud, France (A.L.); Laboratoire de Biochimie Génétique, Hôpital Ambroise Paré, Boulogne-Billancourt, France (H.R., C.J.); and Institut de Myologie, Hôpital de la Salpétrière, Paris, France (P.L., B.E., H.M.B.).

Correspondence to Dr Denis Duboc, Service de Cardiologie, Hôpital Cochin 27, Rue du Faubourg St Jacques, 75014 Paris, France. E-mail Alazarus1{at}aol.com

Background—Impulse-conduction abnormalities and arrhythmias are common in myotonic dystrophy (MD). This study was performed to determine whether a correlation exists between electrophysiological (EP) testing data and clinical status, heart function, or size of the DNA abnormality (cytosine-thymine-guanine sequence repeat).

Methods and Results—Eighty-three MD patients underwent invasive EP studies prompted primarily by the presence of asymptomatic conduction abnormalities. AV conduction disturbances were common and mainly distal (HV interval, 66.2±14 ms). AV conduction observed from the surface ECG was generally concordant with endocardial measurements. However, 11 of 20 patients with normal surface ECGs had abnormal subhisian conduction. Atrial arrhythmias were inducible in 41% of cases and correlated with prolongation of the AH interval (P=0.02) and a shorter atrial refractory period (P=0.04). Induction of ventricular arrhythmias (18%) correlated strongly with age (P=0.0003). After adjustment for age, the extent of DNA mutation correlated with the Walton score (P=0.0018) but not with conduction abnormalities or induction of arrhythmias.

Conclusions—Prolongation of the HV interval is the most common conduction abnormality in MD and can be reliably recognized only by invasive EP testing. It raises the issue of prophylactic pacing to limit the incidence of sudden death in MD. Atrial and ventricular arrhythmias are often inducible, although their predictive value remains to be determined. Young age emerged as the most powerful predictor of inducible ventricular tachyarrhythmias. Conversely, we found no relationship between ECG or EP abnormalities recorded during invasive testing and the DNA mutation size or severity of peripheral muscle involvement.


Key Words: myotonic dystrophy • arrhythmia • heart block




This article has been cited by other articles:


Home page
Am. J. Physiol. Heart Circ. Physiol.Home page
N. D. Ullrich, M. Fanchaouy, K. Gusev, N. Shirokova, and E. Niggli
Hypersensitivity of excitation-contraction coupling in dystrophic cardiomyocytes
Am J Physiol Heart Circ Physiol, December 1, 2009; 297(6): H1992 - H2003.
[Abstract] [Full Text] [PDF]


Home page
J. Neurol. Neurosurg. PsychiatryHome page
P Cudia, P Bernasconi, R Chiodelli, F Mangiola, F Bellocci, A D. Russo, C Angelini, V Romeo, P Melacini, L Politano, et al.
Risk of arrhythmia in type I myotonic dystrophy: the role of clinical and genetic variables
J. Neurol. Neurosurg. Psychiatry, July 1, 2009; 80(7): 790 - 793.
[Abstract] [Full Text] [PDF]


Home page
NEJMHome page
A. D. Russo, M. Pace, F. Bellocci, M. C.E. Hermans, C. G. Faber, Y. M. Pinto, B. Vrtovec, F. Haddad, A. A. Sovari, S. C. Dudley Jr., et al.
Sudden Death in Myotonic Dystrophy
N. Engl. J. Med., October 9, 2008; 359(15): 1626 - 1629.
[Full Text] [PDF]


Home page
NEJMHome page
W. J. Groh, M. R. Groh, C. Saha, J. C. Kincaid, Z. Simmons, E. Ciafaloni, R. Pourmand, R. F. Otten, D. Bhakta, G. V. Nair, et al.
Electrocardiographic Abnormalities and Sudden Death in Myotonic Dystrophy Type 1
N. Engl. J. Med., June 19, 2008; 358(25): 2688 - 2697.
[Abstract] [Full Text] [PDF]


Home page
QJMHome page
R.P. Beynon and S.G. Ray
Cardiac involvement in muscular dystrophies
QJM, May 1, 2008; 101(5): 337 - 344.
[Abstract] [Full Text] [PDF]


Home page
NeurologyHome page
G. Bassez, A. Lazarus, I. Desguerre, J. Varin, P. Laforet, H. M. Becane, C. Meune, M. C. Arne-Bes, Z. Ounnoughene, H. Radvanyi, et al.
Severe cardiac arrhythmias in young patients with myotonic dystrophy type 1
Neurology, November 23, 2004; 63(10): 1939 - 1941.
[Abstract] [Full Text] [PDF]


Home page
J Child NeurolHome page
F. Muntoni
Cardiac Complications of Childhood Myopathies
J Child Neurol, March 1, 2003; 18(3): 191 - 202.
[Abstract] [PDF]


Home page
HeartHome page
G Pelargonio, A D. Russo, T Sanna, G De Martino, and F Bellocci
MYOTONIC DYSTROPHY AND THE HEART
Heart, December 1, 2002; 88(6): 665 - 670.
[Full Text] [PDF]


Home page
J Am Coll CardiolHome page
A. Lazarus, J. Varin, D. Babuty, F. Anselme, J. Coste, and D. Duboc
Long-term follow-up of arrhythmias in patients with myotonic dystrophy treated by pacing: A multicenter diagnostic pacemaker study
J. Am. Coll. Cardiol., November 6, 2002; 40(9): 1645 - 1652.
[Abstract] [Full Text] [PDF]


Home page
RadiologyHome page
O. Vignaux, A. Lazarus, J. Varin, J. Coste, P. Carlier, C. Argaud, P. Laforet, S. Weber, P. Legmann, and D. Duboc
Right Ventricular MR Abnormalities in Myotonic Dystrophy and Relationship with Intracardiac Electrophysiologic Test Findings: Initial Results
Radiology, July 1, 2002; 224(1): 231 - 235.
[Abstract] [Full Text]


Home page
HeartHome page
N R A Clarke, A D Kelion, J Nixon, D Hilton-Jones, and J C Forfar
Does cytosine-thymine-guanine (CTG) expansion size predict cardiac events and electrocardiographic progression in myotonic dystrophy?
Heart, October 1, 2001; 86(4): 411 - 416.
[Abstract] [Full Text] [PDF]


Home page
NeurologyHome page
G. Antonini, F. Giubilei, A. Mammarella, P. Amicucci, M. Fiorelli, F. Gragnani, S. Morino, V. Ceschin, P. V. Fragola, and M. Gennarelli
Natural history of cardiac involvement in myotonic dystrophy: Correlation with CTG repeats
Neurology, October 24, 2000; 55(8): 1207 - 1209.
[Abstract] [Full Text] [PDF]


Home page
CirculationHome page
J. L. Merino, R. Peinado, J. A. Sobrino, A. Lazarus, J. Varin, Z. Ounnoughene, H. Radvanyi, C. Junien, J. Coste, P. Laforet, et al.
Sudden Death in Myotonic Dystrophy: The Potential Role of Bundle-Branch Reentry • Response
Circulation, February 8, 2000; 101 (5): e73 - e73.
[Full Text] [PDF]