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Development of lung diffusion to adulthood following extremely preterm birth

BACKGROUND: Gas exchange in extremely preterm (EP) infants must take place in fetal lungs. Childhood lung diffusing capacity of the lung for carbon monoxide (D(LCO)) is reduced; however, longitudinal development has not been investigated. We describe the growth of D(LCO) and its subcomponents to adu...

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Autores principales: Satrell, Emma, Clemm, Hege, Røksund, Ola Drange, Hufthammer, Karl Ove, Thorsen, Einar, Halvorsen, Thomas, Vollsæter, Maria
Formato: Online Artículo Texto
Lenguaje:English
Publicado: European Respiratory Society 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9117733/
https://www.ncbi.nlm.nih.gov/pubmed/34625479
http://dx.doi.org/10.1183/13993003.04103-2020
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author Satrell, Emma
Clemm, Hege
Røksund, Ola Drange
Hufthammer, Karl Ove
Thorsen, Einar
Halvorsen, Thomas
Vollsæter, Maria
author_facet Satrell, Emma
Clemm, Hege
Røksund, Ola Drange
Hufthammer, Karl Ove
Thorsen, Einar
Halvorsen, Thomas
Vollsæter, Maria
author_sort Satrell, Emma
collection PubMed
description BACKGROUND: Gas exchange in extremely preterm (EP) infants must take place in fetal lungs. Childhood lung diffusing capacity of the lung for carbon monoxide (D(LCO)) is reduced; however, longitudinal development has not been investigated. We describe the growth of D(LCO) and its subcomponents to adulthood in EP compared with term-born subjects. METHODS: Two area-based cohorts born at gestational age ≤28 weeks or birthweight ≤1000 g in 1982–1985 (n=48) and 1991–1992 (n=35) were examined twice, at ages 18 and 25 years and 10 and 18 years, respectively, and compared with matched term-born controls. Single-breath D(LCO) was measured at two oxygen pressures, with subcomponents (membrane diffusion (D(M)) and pulmonary capillary blood volume (V(C))) calculated using the Roughton–Forster equation. RESULTS: Age-, sex- and height-standardised transfer coefficients for carbon monoxide (K(CO)) and D(LCO) were reduced in EP compared with term-born subjects, and remained so during puberty and early adulthood (p-values for all time-points and both cohorts ≤0.04), whereas alveolar volume (V(A)) was similar. Development occurred in parallel to term-born controls, with no signs of pubertal catch-up growth nor decline at age 25 years (p-values for lack of parallelism within cohorts 0.99, 0.65, 0.71, 0.94 and 0.44 for z-D(LCO), z-V(A), z-K(CO), D(M) and V(C), respectively). Split by membrane and blood volume components, findings were less clear; however, membrane diffusion seemed most affected. CONCLUSIONS: Pulmonary diffusing capacity was reduced in EP compared with term-born subjects, and development from childhood to adulthood tracked in parallel to term-born subjects, with no signs of catch-up growth nor decline at age 25 years.
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spelling pubmed-91177332022-05-20 Development of lung diffusion to adulthood following extremely preterm birth Satrell, Emma Clemm, Hege Røksund, Ola Drange Hufthammer, Karl Ove Thorsen, Einar Halvorsen, Thomas Vollsæter, Maria Eur Respir J Original Research Articles BACKGROUND: Gas exchange in extremely preterm (EP) infants must take place in fetal lungs. Childhood lung diffusing capacity of the lung for carbon monoxide (D(LCO)) is reduced; however, longitudinal development has not been investigated. We describe the growth of D(LCO) and its subcomponents to adulthood in EP compared with term-born subjects. METHODS: Two area-based cohorts born at gestational age ≤28 weeks or birthweight ≤1000 g in 1982–1985 (n=48) and 1991–1992 (n=35) were examined twice, at ages 18 and 25 years and 10 and 18 years, respectively, and compared with matched term-born controls. Single-breath D(LCO) was measured at two oxygen pressures, with subcomponents (membrane diffusion (D(M)) and pulmonary capillary blood volume (V(C))) calculated using the Roughton–Forster equation. RESULTS: Age-, sex- and height-standardised transfer coefficients for carbon monoxide (K(CO)) and D(LCO) were reduced in EP compared with term-born subjects, and remained so during puberty and early adulthood (p-values for all time-points and both cohorts ≤0.04), whereas alveolar volume (V(A)) was similar. Development occurred in parallel to term-born controls, with no signs of pubertal catch-up growth nor decline at age 25 years (p-values for lack of parallelism within cohorts 0.99, 0.65, 0.71, 0.94 and 0.44 for z-D(LCO), z-V(A), z-K(CO), D(M) and V(C), respectively). Split by membrane and blood volume components, findings were less clear; however, membrane diffusion seemed most affected. CONCLUSIONS: Pulmonary diffusing capacity was reduced in EP compared with term-born subjects, and development from childhood to adulthood tracked in parallel to term-born subjects, with no signs of catch-up growth nor decline at age 25 years. European Respiratory Society 2022-05-19 /pmc/articles/PMC9117733/ /pubmed/34625479 http://dx.doi.org/10.1183/13993003.04103-2020 Text en Copyright ©The authors 2022. https://creativecommons.org/licenses/by-nc/4.0/This version is distributed under the terms of the Creative Commons Attribution Non-Commercial Licence 4.0. For commercial reproduction rights and permissions contact permissions@ersnet.org (mailto:permissions@ersnet.org)
spellingShingle Original Research Articles
Satrell, Emma
Clemm, Hege
Røksund, Ola Drange
Hufthammer, Karl Ove
Thorsen, Einar
Halvorsen, Thomas
Vollsæter, Maria
Development of lung diffusion to adulthood following extremely preterm birth
title Development of lung diffusion to adulthood following extremely preterm birth
title_full Development of lung diffusion to adulthood following extremely preterm birth
title_fullStr Development of lung diffusion to adulthood following extremely preterm birth
title_full_unstemmed Development of lung diffusion to adulthood following extremely preterm birth
title_short Development of lung diffusion to adulthood following extremely preterm birth
title_sort development of lung diffusion to adulthood following extremely preterm birth
topic Original Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9117733/
https://www.ncbi.nlm.nih.gov/pubmed/34625479
http://dx.doi.org/10.1183/13993003.04103-2020
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