Please use this identifier to cite or link to this item: https://hdl.handle.net/2445/216143
Full metadata record
DC FieldValueLanguage
dc.contributor.authorVellvé, Kilian-
dc.contributor.authorSepúlveda Martínez, Álvaro-
dc.contributor.authorRodríguez López, Mérida-
dc.contributor.authorCrovetto, Francesca-
dc.contributor.authorBernardino, Gabriel-
dc.contributor.authorBurgos, Felip-
dc.contributor.authorFaner, Rosa-
dc.contributor.authorAgustí García-Navarro, Àlvar-
dc.contributor.authorBijnens, Bart-
dc.contributor.authorGratacós Solsona, Eduard-
dc.contributor.authorCrispi Brillas, Fàtima-
dc.contributor.authorBlanco Vich, Isabel-
dc.date.accessioned2024-10-30T17:45:22Z-
dc.date.available2024-10-30T17:45:22Z-
dc.date.issued2023-02-
dc.identifier.issn1323-7799-
dc.identifier.urihttps://hdl.handle.net/2445/216143-
dc.description.abstractModerate to extreme prematurity is associated with lower lung function in adults1 while evidence is poorer and controversial for late prematurity.2 Likewise, the potential longterm impact on adult lung function of being born small for gestational age (SGA) at term is not well established since most previous studies in this field have been done in groups with participants enrolled by birthweight and not by SGA per se. This may be important because not all infants born SGA have experienced intrauterine growth restriction (IUGR) and the other way round, early IUGR does not necessarily bring fetal growth down below the 10th percentile (the definition of SGA). We recently showed that young adults born SGA at term had markedly reduced exercise capacity, mostly of cardiovascular origin.3 In particular, they showed lower maximal workload, peak oxygen consumption and oxygen pulse, as well as higher minute ventilation/carbon dioxide production equivalent at the anaerobic threshold, than age-matched controls. Here, we extend and complement these previously published observations with the analysis of pulmonary physiology (spirometry and carbon monoxide diffusing capacity [DLCO]) and the measurement of circulatory markers of abnormal lung development, including surfactant protein A and D (SP-A and SP-D) and club cell protein 16 (CC16).-
dc.format.extent4 p.-
dc.format.mimetypeapplication/pdf-
dc.language.isoeng-
dc.publisherBlackwell-
dc.relation.isformatofReproducció del document publicat a: https://doi.org/10.1111/resp.14361-
dc.relation.ispartofRespirology, 2023, vol. 28, num.2, p. 183-186-
dc.relation.urihttps://doi.org/10.1111/resp.14361-
dc.rightscc-by (c) Vellvé, Kilian et al., 2023-
dc.rights.urihttp://creativecommons.org/licenses/by/4.0*
dc.sourceArticles publicats en revistes (Biomedicina)-
dc.subject.classificationJoves-
dc.subject.classificationPulmó-
dc.subject.classificationRespiració-
dc.subject.classificationRetard del creixement intrauterí-
dc.subject.classificationInfants prematurs-
dc.subject.otherYouth-
dc.subject.otherLung-
dc.subject.otherRespiration-
dc.subject.otherFetal growth retardation-
dc.subject.otherPremature infants-
dc.titleLung function in young adults born small for gestational age at term-
dc.typeinfo:eu-repo/semantics/article-
dc.typeinfo:eu-repo/semantics/publishedVersion-
dc.identifier.idgrec729909-
dc.date.updated2024-10-30T17:45:22Z-
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess-
dc.identifier.pmid36172944-
Appears in Collections:Articles publicats en revistes (Biomedicina)

Files in This Item:
File Description SizeFormat 
256919.pdf383.71 kBAdobe PDFView/Open


This item is licensed under a Creative Commons License Creative Commons