Cardiac remodelling as a result of pre-term birth: implications for future cardiovascular disease

被引:140
作者
Bensley, Jonathan G. [1 ]
Stacy, Victoria K. [1 ]
De Matteo, Robert [1 ]
Harding, Richard [1 ]
Black, M. Jane [1 ]
机构
[1] Monash Univ, Dept Anat & Dev Biol, Sch Biomed Sci, Clayton, Vic 3168, Australia
基金
英国医学研究理事会;
关键词
Cardiomyocyte; Pre-term birth; Developmental programming; Paediatrics; Risk factors; NEONATAL DEXAMETHASONE TREATMENT; FETAL SHEEP; GROWTH RESTRICTION; MYOCARDIAL DNA; PLOIDY LEVEL; NUMBER; RISK; CORTISOL; HEARTS; RATS;
D O I
10.1093/eurheartj/ehq104
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Aims Pre-term birth affects 10-12% of live births and occurs when the myocardium is still developing; therefore, the final structure of the myocardium could be altered. We hypothesized that, in response to pre-term birth, structural remodelling occurs within the myocardium which enables the immature heart muscle to adapt to the haemodynamic transition at birth but results in persistent alterations in its structure. Our objective was to determine how pre-term birth alters the final structure of the myocardium. Methods and results Using sheep, pre-term birth was induced at 0.9 of term; hearts were examined at 9 weeks after term-equivalent age, when cardiomyocyte proliferation and maturation have ceased. In pre-term lambs, we found that cardiomyocytes of both ventricles and the interventricular septum were hypertrophied. Cardiomyocyte maturation in pre-term lambs was altered in that there was a greater proportion of mononucleated, polyploid (4n) cardiomyocytes in both ventricles compared with controls; importantly, induction of polyploidy is associated with irreversible stress-related changes in DNA. We also found a six- to seven-fold increase in collagen deposition, usually accompanied by lymphocytic infiltration. Conclusion We conclude that pre-term birth leads to remodelling of the myocardium that alters its final structure. This may programme for long-term cardiac vulnerability.
引用
收藏
页码:2058 / 2066
页数:9
相关论文
共 46 条
[1]   MYOCARDIAL DNA CONTENT, PLOIDY LEVEL AND CELL NUMBER IN GERIATRIC HEARTS - POSTMORTEM EXAMINATIONS OF HUMAN MYOCARDIUM IN OLD-AGE [J].
ADLER, CP ;
FRIEDBURG, H .
JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY, 1986, 18 (01) :39-53
[2]  
Adler CP, 1996, VIRCHOWS ARCH, V429, P159
[3]   Role of mast cells and their mediators in failing myocardium under mechanical ventricular support [J].
Akgul, A ;
Skrabal, CA ;
Thompson, LO ;
Loebe, M ;
Lafuente, JA ;
Noon, GP ;
Youker, KA .
JOURNAL OF HEART AND LUNG TRANSPLANTATION, 2004, 23 (06) :709-715
[4]   Neonatal cardiomyocyte ploidy reveals critical windows of heart development [J].
Anatskaya, Olga V. ;
Sidorenko, Nina V. ;
Beyer, Tamara V. ;
Vinogradov, Alexander E. .
INTERNATIONAL JOURNAL OF CARDIOLOGY, 2010, 141 (01) :81-91
[5]   Histopathological Changes of the Heart After Neonatal Dexamethasone Treatment: Studies in 4-, 8-, and 50-Week-Old Rats [J].
Bal, Miriam P. ;
de Vries, Willem B. ;
Steendijk, Paul ;
Homoet-van der Kraak, Petra ;
van der Leij, Feike R. ;
Baan, Jan ;
van Oosterhout, Matthijs F. M. ;
van Bel, Frank .
PEDIATRIC RESEARCH, 2009, 66 (01) :74-79
[6]   Developmental antecedents of cardiovascular disease: A historical perspective [J].
Barker, DJP ;
Bagby, SP .
JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY, 2005, 16 (09) :2537-2544
[7]   Antenatal corticosteroid therapy: benefits and risks [J].
Baud, O .
ACTA PAEDIATRICA, 2004, 93 :6-10
[8]  
BRODSKY VY, 1993, EUR J HISTOCHEM, V37, P199
[9]  
BRODSKY VY, 1994, VIRCHOWS ARCH, V424, P429
[10]   The relationship between myocardial extracellular matrix remodeling and ventricular function [J].
Brower, Gregory L. ;
Gardner, Jason D. ;
Forman, Mary F. ;
Murray, David B. ;
Voloshenyuk, Tetyana ;
Levick, Scott P. ;
Janicki, Joseph S. .
EUROPEAN JOURNAL OF CARDIO-THORACIC SURGERY, 2006, 30 (04) :604-610