(Circulation. 2001;104:676.)
© 2001 American Heart Association, Inc.
Clinical Investigation and Reports |
From Departments of Medicine (S.J.S., A.P.-V., W.M., J.A.F., M.M.K., M.L.E., M.A.Q., G.T.-A.), Thoracic and Cardiovascular Surgery (G.P.N.), and Cardiac Pathology (D.G.W.), and Sections of Cardiology and Cardiovascular Sciences (S.J.S., A.P.-V., W.M., J.A.F., M.M.K., M.L.E., M.A.Q., G.T.-A.), The DeBakey Heart Center and The Gene and Judy Campbell Lab for Cardiac Transplant Research, The Winters Center for Heart Failure Research, Baylor College of Medicine and The Methodist Hospital, Houston, Tex.
Reprint requests to Guillermo Torre-Amione, MD, PhD, Baylor College of Medicine, 6550 Fannin, Suite 1901, Houston, TX 77030. E-mail gtorre{at}bcm.tmc.edu
Background The mechanisms that contribute to cardiac allograft hypertrophy are not known; however, the rapid progression and severity of hypertrophy suggest that nonhemodynamic factors may play a contributory role. Tumor necrosis factor-
(TNF-
) is a cytokine produced in cardiac allografts and capable of producing hypertrophy and fibrosis; therefore, we suggest that TNF-
may play a contributory role. Accordingly, the aims of our study were to define the role of systemic hypertension in the development of hypertrophy, characterize the histological determinants of hypertrophy, and characterize the expression of myocardial TNF-
after heart transplantation.
Methods and Results To separate the effect of hypertension from immune injury in the development of cardiac allograft hypertrophy, we measured the gain in left ventricular mass by 2D echocardiography in heart transplant recipients and lung transplant recipients who developed similar rates of systemic hypertension. The gain in left ventricular mass was 73% in heart transplant recipients and 7% in lung transplant recipients (P<0.0001). By comparing myocardial samples obtained during the first week after transplant and at 1 year, we found that there was a significant increase in total collagen content (P<0.0001), collagen I (P<0.0001), collagen III (P<0.0001), and myocyte size (P<0.0001). These changes were associated with persistent myocardial TNF-
expression.
Conclusions We suggest that the contribution of hypertension to cardiac allograft hypertrophy is minimal and that persistent intracardiac expression of TNF-
may contribute to the development of cardiac allograft hypertrophy.
Key Words: growth substances transplantation hypertrophy
This article has been cited by other articles:
![]() |
L. Lin, S. C. Kim, Y. Wang, S. Gupta, B. Davis, S. I. Simon, G. Torre-Amione, and A. A. Knowlton HSP60 in heart failure: abnormal distribution and role in cardiac myocyte apoptosis Am J Physiol Heart Circ Physiol, October 1, 2007; 293(4): H2238 - H2247. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. Wilhelmi, K. Pethig, M. Wilhelmi, H. Nguyen, M. Struber, and A. Haverich Heart transplantation: echocardiographic assessment of morphology and function after more than 10 years of follow-up Ann. Thorac. Surg., October 1, 2002; 74(4): 1075 - 1079. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. Amadou, A. Nawrocki, M. Best-Belpomme, C. Pavoine, and F. Pecker Arachidonic acid mediates dual effect of TNF-alpha on Ca2+ transients and contraction of adult rat cardiomyocytes Am J Physiol Cell Physiol, June 1, 2002; 282(6): C1339 - C1347. [Abstract] [Full Text] [PDF] |
||||
|
Circulation Home | Subscriptions | Archives | Feedback | Authors | Help | AHA Journals Home | Search Copyright © 2001 American Heart Association, Inc. All rights reserved. Unauthorized use prohibited. |