Donate Help Contact The AHA Sign In Home
American Heart Association
Circulation
Search: search_blue_button Advanced Search
Circulation. 2004;109:2930-2932
doi: 10.1161/01.CIR.0000133180.77213.43
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 Schwartz, P. J.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Schwartz, P. J.
Related Collections
Right arrow Clinical genetics
Right arrow Electrocardiology
Right arrow Pediatric and congenital heart disease, including cardiovascular surgery
Right arrow Arrhythmias, clinical electrophysiology, drugs
Right arrow Cardiac development
Right arrow Genetics of cardiovascular disease
Right arrowRelated Article

(Circulation. 2004;109:2930-2932.)
© 2004 American Heart Association, Inc.


Focused Perspective

Stillbirths, Sudden Infant Deaths, and Long-QT Syndrome

Puzzle or Mosaic, the Pieces of the Jigsaw Are Being Fitted Together

Peter J. Schwartz, MD

From the Department of Cardiology, IRCCS Policlinico S. Matteo, Pavia, University of Pavia, Pavia, Italy.

Correspondence to Peter J. Schwartz, MD, Professor and Chairman, Department of Cardiology, Policlinico S. Matteo IRCCS, V.le Golgi, 19 27100 Pavia, Italy. E-mail PJQT@compuserve.com


Key Words: Focused Perspectives • long-QT syndrome • death, sudden • genetics • pediatrics


An extract of the first 250 words of the full text is provided, because this article has no abstract.
 

Stillbirths contribute substantially to perinatal mortality in developed countries.1 Their prevalence ranges between 4 and 6 per 1000 births.1–3 Despite careful investigation, at least 25%,4 and possibly 50%,1 remain unexplained. Another mysterious cause of early sudden death is represented by sudden infant death syndrome (SIDS),5,6 which is still the leading cause of mortality during the first year of life. Finally, a relatively large number of sudden deaths in the young (infants, children, and teenagers) is due to long-QT syndrome (LQTS).7–10 Are these entities completely unrelated or is there a link between them, such that the latter might be a contributor to the former? As a matter of fact, this specific hypothesis has already been proposed.11,12 Its interest lies in the fact that, beyond the scientific and conceptual implications, if proven correct it could offer an opportunity to prevent those fetal or infant deaths sharing the same genetic and arrhythmogenic mechanism.

See p 3029

The value of scientific hypotheses lies in the possibility of testing them to be either dismissed or confirmed, thus advancing knowledge. The relatively small number, in absolute terms, of stillbirths and SIDS makes prospective studies difficult, albeit not impossible.13 Thus, to a large extent, the scientific community still has to rest on the evidence provided by well-documented case reports which sometimes can offer unexpected insights and can represent proof of concept. One such example is represented by the article by Miller et al14 in this issue of Circulation.

Their study was prompted by what initially appeared . . . [Full Text of this Article]


Related Article:

Recurrent Third-Trimester Fetal Loss and Maternal Mosaicism for Long-QT Syndrome
Todd E. Miller, Elicia Estrella, Robert J. Myerburg, Jocelyn Garcia de Viera, Niberto Moreno, Paolo Rusconi, Mary Ellen Ahearn, Lisa Baumbach, Paul Kurlansky, Grace Wolff, and Nanette H. Bishopric
Circulation 2004 109: 3029-3034. [Abstract] [Full Text]



This article has been cited by other articles:


Home page
ESC Textbook of Cardiovascular MedicineHome page
L. Eckardt, G&#x.;n. Breithardt, and S. Hohnloser
CHAPTER 30 Ventricular Tachycardia and Sudden Cardiac Death
ESC Textbook of Cardiovascular Medicine, January 1, 2009; 2(1): med-9780199566990-chapter - med-9780199566990-chapter.
[Abstract] [Full Text] [PDF]


Home page
Circ Arrhythm ElectrophysiolHome page
D. W. Wang, L. Crotti, W. Shimizu, M. Pedrazzini, F. Cantu, P. De Filippo, K. Kishiki, A. Miyazaki, T. Ikeda, P. J. Schwartz, et al.
Malignant Perinatal Variant of Long-QT Syndrome Caused by a Profoundly Dysfunctional Cardiac Sodium Channel
Circ Arrhythm Electrophysiol, December 1, 2008; 1(5): 370 - 378.
[Abstract] [Full Text] [PDF]


Home page
J Am Coll CardiolHome page
M. J. Heradien, A. Goosen, L. Crotti, G. Durrheim, V. Corfield, P. A. Brink, and P. J. Schwartz
Does Pregnancy Increase Cardiac Risk for LQT1 Patients With the KCNQ1-A341V Mutation?
J. Am. Coll. Cardiol., October 3, 2006; 48(7): 1410 - 1415.
[Abstract] [Full Text] [PDF]


Home page
Cardiovasc ResHome page
D. J. Tester and M. J. Ackerman
Sudden infant death syndrome: How significant are the cardiac channelopathies?
Cardiovasc Res, August 15, 2005; 67(3): 388 - 396.
[Abstract] [Full Text] [PDF]