Document Detail


Left ventricular remodeling in hearts with tricuspid atresia: morphologic observations and possible basis for ventricular dysfunction after surgery.
MedLine Citation:
PMID:  14566242     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
OBJECTIVES: This study was undertaken to assess the pattern of left ventricular hypertrophy, the myocardial capillary network, and the extracellular matrix in hearts with tricuspid atresia. METHODS: We examined 32 hearts with tricuspid atresia and 27 normal hearts from control subjects with similar age and sex distribution. Wall thickness, inlet length, and outlet length were obtained from the left ventricle. Immunohistochemical staining for von Willebrand factor was used to label myocardial capillaries. By means of computer-assisted morphometry, the following data were obtained from the inlet, apex, and outlet of the left ventricle: transverse myocyte diameter, myocyte nuclear volume fraction, capillary volume fraction, interstitial fibrous volume fraction, and endocardial thickness. RESULTS: The wall thickness in affected hearts was not different from that in control hearts. The left ventricular outlet length was significantly greater in the malformed hearts (P =.005). The myocyte diameter did not differ from that in control hearts. The capillary volume fraction was decreased in the malformed hearts (P <.001). The interstitial fibrous deposition was greater in the malformed hearts at all sites analyzed (P <.001). Fibrosis was greater in the inlet and apex (P =.004) and also in the subendocardial half of the ventricular wall than in the subepicardial half. According to a logistic regression model, age was the only variable associated with the probability of occurrence of fibrosis. CONCLUSIONS: Our findings in hearts with tricuspid atresia possibly represent chronically induced volume overload in the presence of ischemia, rather than a typical model of volume overload. A decreased capillary volume fraction may indicate a greater susceptibility to ischemia. Fibrous deposition probably occurs early in life.
Authors:
Maria Angelica Binotto; Maria de Lourdes Higuchi; Vera Demarchi Aiello
Publication Detail:
Type:  Journal Article; Research Support, Non-U.S. Gov't    
Journal Detail:
Title:  The Journal of thoracic and cardiovascular surgery     Volume:  126     ISSN:  0022-5223     ISO Abbreviation:  J. Thorac. Cardiovasc. Surg.     Publication Date:  2003 Oct 
Date Detail:
Created Date:  2003-10-20     Completed Date:  2003-12-02     Revised Date:  2006-11-15    
Medline Journal Info:
Nlm Unique ID:  0376343     Medline TA:  J Thorac Cardiovasc Surg     Country:  United States    
Other Details:
Languages:  eng     Pagination:  1026-32     Citation Subset:  AIM; IM    
Affiliation:
Heart Institute (InCor), University of São Paulo Medical School, Pediatric Cardiology, Av. Higienopolis, 1048/86, São Paulo 01238-000, Brazil. conangelica@incor.usp.br
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MeSH Terms
Descriptor/Qualifier:
Age Factors
Capillaries / pathology
Female
Fibrosis / pathology
Humans
Hypertrophy, Left Ventricular / pathology
Immunohistochemistry
Infant
Male
Myocytes, Cardiac / pathology
Tricuspid Atresia / pathology*
Ventricular Remodeling / physiology*
von Willebrand Factor / analysis
Chemical
Reg. No./Substance:
0/von Willebrand Factor

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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