Neuropediatrics 2015; 46(01): 033-036
DOI: 10.1055/s-0034-1395348
Original Article
Georg Thieme Verlag KG Stuttgart · New York

Cardiac Function in Types II and III Spinal Muscular Atrophy: Should We Change Standards of Care?

Flaviana Bianco
1   Department of Paediatric Neurology, Catholic University, Rome, Italy
,
Marika Pane
1   Department of Paediatric Neurology, Catholic University, Rome, Italy
,
Adele D'Amico
2   Department of Laboratory Medicine, Unit of Molecular Medicine, Bambino Gesù Hospital, Rome, Italy
,
Sonia Messina
3   Department of Neurosciences, Psychiatry and Anaesthesiology, University of Messina, Messina, Italy
,
Angelica Bibiana Delogu
1   Department of Paediatric Neurology, Catholic University, Rome, Italy
,
Gianni Soraru
5   Department of Neurosciences and Psychiatry and Anaesthesiology, University of Padoa, Padoa, Italy
,
Maria Carmela Pera
1   Department of Paediatric Neurology, Catholic University, Rome, Italy
,
Tiziana Mongini
6   Neuromuscular Center, S.G. Battista Hospital, University of Turin, Turin, Italy
,
Luisa Politano
7   Department of Experimental Medicine, Cardiomiology and Medical Genetics, Second University of Naples, Naples, Italy
,
Giovanni Baranello
8   Developmental Neurology Unit, Neurological Institute C. Besta, Milan, Italy
,
Gianluca Vita
3   Department of Neurosciences, Psychiatry and Anaesthesiology, University of Messina, Messina, Italy
,
Francesco Danilo Tiziano
9   Medical Genetics Institute, Catholic University, Rome, Italy
,
Lucia Morandi
4   Department of Myopathology and Neuroimmunolgy, Pediatric Neurology and Neuroradiology Units, Neurological Institute C. Besta, Milan, Italy
,
Enrico Bertini
2   Department of Laboratory Medicine, Unit of Molecular Medicine, Bambino Gesù Hospital, Rome, Italy
,
Eugenio Mercuri
1   Department of Paediatric Neurology, Catholic University, Rome, Italy
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Publikationsverlauf

08. August 2014

20. September 2014

Publikationsdatum:
24. Dezember 2014 (online)

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Abstract

Objective In the last years, there has been increasing evidence of cardiac involvement in spinal muscular atrophy (SMA). Autonomic dysfunction has been reported in animal models and in several patients with types I and III SMA, these findings raising the question whether heart rate should be routinely investigated in all SMA patients. The aim of our study was to detect possible signs of autonomic dysfunction and, more generally, of cardiac involvement in types II and III SMA.

Patients and Methods We retrospectively reviewed 24-hour electrocardiography (ECG) in 157 types II and III SMA patients (age range, 2–74 years). Of them, 82 also had echocardiography.

Results None of the patients had signs of bradycardia, atrial fibrillation, or the other previously reported rhythm disturbances regardless of the age at examination or the type of SMA. Echocardiography was also normal. There were no signs of congenital cardiac defects with the exception of one patient with a history of ventricular septal defects.

Conclusions Our results suggest that cardiac abnormalities are not common in type II and type III SMA. These findings provide no evidence to support a more accurate cardiac surveillance or changes in the existing standards of care.