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Placing Ureaplasma within the Context of Bronchopulmonary Dysplasia Endotypes and Phenotypes

Bibliographic Data

ID15717455
AuthorsKaren Van Mechelen (0000-0003-2853-2079, Maastricht University), Elke van Westering-Kroon (Maastricht University), Matthi as C Hütten (0000-0003-4870-5782, Maastricht University), Matthias Hütten (Department of Pediatrics, Maastricht University Medical Center, School for Oncology and Reproduction (GROW), Maastricht University, 6229 HX Maastricht, The Netherlands), Ludo Mahieu (0000-0001-7863-6357, Antwerp University Hospital), Eduardo Villamor (0000-0003-3937-5574, Maastricht University, corresponding author)
Year2023
Volume10
Issue2
Pages256-256
Publication date2023-01-31
Peer ReviewedYes
Open AccessYes
TypeARTICLE
VenueChildren (JOURNAL)
Journal identifiersISSN: 2227-9067 • E-ISSN: 2227-9067
PublisherMultidisciplinary Digital Publishing Institute (PUBLISHER • CH)
DOI10.3390/children10020256
PMID36832386
OpenAlexW4318613399
LanguageEN
References cited114

Different pathophysiological pathways (endotypes), leading to very preterm birth may result in distinct clinical phenotypes of bronchopulmonary dysplasia (BPD). Ureaplasma is a unique player in the pathogenesis of BPD. The interaction between factors inherent to Ureaplasma (virulence, bacterial load, duration of exposure), and to the host (immune response, infection clearance, degree of prematurity, respiratory support, concomitant infections) may contribute to BPD development in a variable manner. The data reviewed herein support the hypothesis that Ureaplasma , as a representative of the infectious/inflammatory endotype, may produce pulmonary damage predominantly in parenchyma, interstitium, and small airways. In contrast, Ureaplasma may have a very limited role in the pathogenesis of the vascular phenotype of BPD. In addition, if Ureaplasma is a key factor in BPD pathogenesis, its eradication by macrolides should prevent BPD. However, various meta-analyses do not show consistent evidence that this is the case. The limitations of current definitions and classifications of BPD, based on respiratory support needs instead of pathophysiology and phenotypes, may explain this and other failures in strategies aimed to prevent BPD. The precise mechanisms through which Ureaplasma infection leads to altered lung development and how these pathways can result in different BPD phenotypes warrant further investigation

Biology · Bronchopulmonary dysplasia · Context (archaeology · Gene · Gestational age · Mycoplasma · Pathogenesis · Pathology · Pathophysiology · Phenotype · Pregnancy · Ureaplasma · Ureaplasma urealyticum · Congenital Diaphragmatic Hernia Studies · Medicine · Neonatal Respiratory Health Research · Respiratory viral infections research · Genetics · Immunology · Microbiology

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