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The added value of haemoglobin to height, age, and sex to predict DLCO in subjects with preserved exercise capacity

BACKGROUND: The single breath diffusion capacity for carbon monoxide (DLCO) captures several aspects of the role of the lung in meeting the metabolic demands of the body. The magnitude of the independent contributors to the DLCO is unknown. The aim of this study was to investigate the factors that i...

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Autores principales: Priel, Eldar, Diab, Nermin, Patel, Matthew, Wahab, Mustafaa, Freitag, Andreas, O’Byrne, Paul M., Killian, Kieran J., Satia, Imran
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10409289/
https://www.ncbi.nlm.nih.gov/pubmed/37552695
http://dx.doi.org/10.1371/journal.pone.0289540
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author Priel, Eldar
Diab, Nermin
Patel, Matthew
Wahab, Mustafaa
Freitag, Andreas
O’Byrne, Paul M.
Killian, Kieran J.
Satia, Imran
author_facet Priel, Eldar
Diab, Nermin
Patel, Matthew
Wahab, Mustafaa
Freitag, Andreas
O’Byrne, Paul M.
Killian, Kieran J.
Satia, Imran
author_sort Priel, Eldar
collection PubMed
description BACKGROUND: The single breath diffusion capacity for carbon monoxide (DLCO) captures several aspects of the role of the lung in meeting the metabolic demands of the body. The magnitude of the independent contributors to the DLCO is unknown. The aim of this study was to investigate the factors that independently contribute to the DLCO. OBJECTIVES: The objective was to investigate the impact of height, age, sex and haemoglobin on DLCO, alveolar volume (VA) and carbon monoxide transfer coefficient (KCO). METHODS: Study participants were pre-screened based on normal exercise capacity achieved during an incremental cardio-pulmonary exercise testing (CPET) using cycle ergometry at McMaster University Medical Center between 1988–2012. Participants who had an FEV1>80% predicted, with an FEV1/FVC ≥0.7 and who achieved a maximum power output ≥80% were selected for analysis. In total, 16,298 subjects [61% male, mean height 1.70m (range 1.26–2.07), age 49 yrs (10–94), weight 79 kg (23–190) had DLCO measured while demonstrating normal spirometry and exercise capacity. RESULTS: The DLCO increased exponentially with height, was 15% greater in males, increased with age yearly until 20, then decreased yearly after the age of 35, and was 6% higher per gram of haemoglobin (5.58*Height(m)(1.69)*1.15 in Males*(1–0.006*Age>35)*(1+0.01*Age<20) *(1+0.06*Hb gm/dl), (r = 0.76). CONCLUSION: Height, age, sex, and haemoglobin all have independent influence on the DLCO in subjects with normal spirometry and preserved exercise capacity.
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spelling pubmed-104092892023-08-09 The added value of haemoglobin to height, age, and sex to predict DLCO in subjects with preserved exercise capacity Priel, Eldar Diab, Nermin Patel, Matthew Wahab, Mustafaa Freitag, Andreas O’Byrne, Paul M. Killian, Kieran J. Satia, Imran PLoS One Research Article BACKGROUND: The single breath diffusion capacity for carbon monoxide (DLCO) captures several aspects of the role of the lung in meeting the metabolic demands of the body. The magnitude of the independent contributors to the DLCO is unknown. The aim of this study was to investigate the factors that independently contribute to the DLCO. OBJECTIVES: The objective was to investigate the impact of height, age, sex and haemoglobin on DLCO, alveolar volume (VA) and carbon monoxide transfer coefficient (KCO). METHODS: Study participants were pre-screened based on normal exercise capacity achieved during an incremental cardio-pulmonary exercise testing (CPET) using cycle ergometry at McMaster University Medical Center between 1988–2012. Participants who had an FEV1>80% predicted, with an FEV1/FVC ≥0.7 and who achieved a maximum power output ≥80% were selected for analysis. In total, 16,298 subjects [61% male, mean height 1.70m (range 1.26–2.07), age 49 yrs (10–94), weight 79 kg (23–190) had DLCO measured while demonstrating normal spirometry and exercise capacity. RESULTS: The DLCO increased exponentially with height, was 15% greater in males, increased with age yearly until 20, then decreased yearly after the age of 35, and was 6% higher per gram of haemoglobin (5.58*Height(m)(1.69)*1.15 in Males*(1–0.006*Age>35)*(1+0.01*Age<20) *(1+0.06*Hb gm/dl), (r = 0.76). CONCLUSION: Height, age, sex, and haemoglobin all have independent influence on the DLCO in subjects with normal spirometry and preserved exercise capacity. Public Library of Science 2023-08-08 /pmc/articles/PMC10409289/ /pubmed/37552695 http://dx.doi.org/10.1371/journal.pone.0289540 Text en © 2023 Priel et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Priel, Eldar
Diab, Nermin
Patel, Matthew
Wahab, Mustafaa
Freitag, Andreas
O’Byrne, Paul M.
Killian, Kieran J.
Satia, Imran
The added value of haemoglobin to height, age, and sex to predict DLCO in subjects with preserved exercise capacity
title The added value of haemoglobin to height, age, and sex to predict DLCO in subjects with preserved exercise capacity
title_full The added value of haemoglobin to height, age, and sex to predict DLCO in subjects with preserved exercise capacity
title_fullStr The added value of haemoglobin to height, age, and sex to predict DLCO in subjects with preserved exercise capacity
title_full_unstemmed The added value of haemoglobin to height, age, and sex to predict DLCO in subjects with preserved exercise capacity
title_short The added value of haemoglobin to height, age, and sex to predict DLCO in subjects with preserved exercise capacity
title_sort added value of haemoglobin to height, age, and sex to predict dlco in subjects with preserved exercise capacity
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10409289/
https://www.ncbi.nlm.nih.gov/pubmed/37552695
http://dx.doi.org/10.1371/journal.pone.0289540
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