Pulmonary hypoplasia associated with congenital heart diseases: a fetal study.

<h4>Background</h4>Abnormalities of the fetal pulmonary vasculature may affect lung morphogenesis. Postnatal studies have suggested that pulmonary hypoplasia (PH) may be associated with congenital heart diseases (CHDs).<h4>Objective</h4>To determine the prevalence of PH assoc...

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Main Authors: Isabelle Ruchonnet-Metrailler, Bettina Bessieres, Damien Bonnet, Shamila Vibhushan, Christophe Delacourt
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2014-01-01
Series:PLoS ONE
Online Access:https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/24699523/?tool=EBI
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spelling doaj-701308db2f264f648e19dd35b05a2b9e2021-06-19T04:59:24ZengPublic Library of Science (PLoS)PLoS ONE1932-62032014-01-0194e9355710.1371/journal.pone.0093557Pulmonary hypoplasia associated with congenital heart diseases: a fetal study.Isabelle Ruchonnet-MetraillerBettina BessieresDamien BonnetShamila VibhushanChristophe Delacourt<h4>Background</h4>Abnormalities of the fetal pulmonary vasculature may affect lung morphogenesis. Postnatal studies have suggested that pulmonary hypoplasia (PH) may be associated with congenital heart diseases (CHDs).<h4>Objective</h4>To determine the prevalence of PH associated with CHDs, and to evaluate whether CHDs with right outflow obstruction were associated with the highest risk of lung growth impairment.<h4>Methods</h4>Between January 2006 and December 2010, fetuses with CHD obtained following the termination of pregnancies due to fetal abnormalities were examined in a prospective manner for the detection of heart and lung defects. CHDs were classified into five pathophysiological groups. Lung weight (LW), body weight (BW), and LW/BW ratio were analyzed for each case. The expression of CD31 and VEGF in the lung was evaluated by immunohistochemistry.<h4>Results</h4>Fetuses with CHDs and right outflow obstruction had significantly lower LW for a given BW, and significantly lower LW/BW ratios for a given gestational age. When defining PH as a fetal LW/BW ratio <0.015 before 28 weeks, and <0.012 after 28 weeks, PH was detected in 15 of the 119 fetuses analyzed (13%). It was significantly associated with CHD with right outflow obstruction, independently of chromosomal abnormalities and associated extracardiac abnormalities (p<0.03). Right outflow obstruction was detected in 60% of the fetuses with CHD and PH, but in only 32% of those with CHD but no PH. In fetuses with right outflow obstruction, no difference was observed between those with PH and those without PH, in terms of the ratio of pulmonary artery diameter to aortic diameter, lung CD31 expression, or lung VEGF expression.<h4>Conclusion</h4>CHDs with right outflow obstruction are a significant risk factor for prenatally acquired PH. The occurrence of fetal PH is not correlated with abnormalities of the pulmonary vasculature, suggesting the involvement of perfusion-independent mechanisms.https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/24699523/?tool=EBI
collection DOAJ
language English
format Article
sources DOAJ
author Isabelle Ruchonnet-Metrailler
Bettina Bessieres
Damien Bonnet
Shamila Vibhushan
Christophe Delacourt
spellingShingle Isabelle Ruchonnet-Metrailler
Bettina Bessieres
Damien Bonnet
Shamila Vibhushan
Christophe Delacourt
Pulmonary hypoplasia associated with congenital heart diseases: a fetal study.
PLoS ONE
author_facet Isabelle Ruchonnet-Metrailler
Bettina Bessieres
Damien Bonnet
Shamila Vibhushan
Christophe Delacourt
author_sort Isabelle Ruchonnet-Metrailler
title Pulmonary hypoplasia associated with congenital heart diseases: a fetal study.
title_short Pulmonary hypoplasia associated with congenital heart diseases: a fetal study.
title_full Pulmonary hypoplasia associated with congenital heart diseases: a fetal study.
title_fullStr Pulmonary hypoplasia associated with congenital heart diseases: a fetal study.
title_full_unstemmed Pulmonary hypoplasia associated with congenital heart diseases: a fetal study.
title_sort pulmonary hypoplasia associated with congenital heart diseases: a fetal study.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2014-01-01
description <h4>Background</h4>Abnormalities of the fetal pulmonary vasculature may affect lung morphogenesis. Postnatal studies have suggested that pulmonary hypoplasia (PH) may be associated with congenital heart diseases (CHDs).<h4>Objective</h4>To determine the prevalence of PH associated with CHDs, and to evaluate whether CHDs with right outflow obstruction were associated with the highest risk of lung growth impairment.<h4>Methods</h4>Between January 2006 and December 2010, fetuses with CHD obtained following the termination of pregnancies due to fetal abnormalities were examined in a prospective manner for the detection of heart and lung defects. CHDs were classified into five pathophysiological groups. Lung weight (LW), body weight (BW), and LW/BW ratio were analyzed for each case. The expression of CD31 and VEGF in the lung was evaluated by immunohistochemistry.<h4>Results</h4>Fetuses with CHDs and right outflow obstruction had significantly lower LW for a given BW, and significantly lower LW/BW ratios for a given gestational age. When defining PH as a fetal LW/BW ratio <0.015 before 28 weeks, and <0.012 after 28 weeks, PH was detected in 15 of the 119 fetuses analyzed (13%). It was significantly associated with CHD with right outflow obstruction, independently of chromosomal abnormalities and associated extracardiac abnormalities (p<0.03). Right outflow obstruction was detected in 60% of the fetuses with CHD and PH, but in only 32% of those with CHD but no PH. In fetuses with right outflow obstruction, no difference was observed between those with PH and those without PH, in terms of the ratio of pulmonary artery diameter to aortic diameter, lung CD31 expression, or lung VEGF expression.<h4>Conclusion</h4>CHDs with right outflow obstruction are a significant risk factor for prenatally acquired PH. The occurrence of fetal PH is not correlated with abnormalities of the pulmonary vasculature, suggesting the involvement of perfusion-independent mechanisms.
url https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/24699523/?tool=EBI
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