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Anaemia and iron dysregulation: untapped therapeutic targets in chronic lung disease?
Hypoxia is common in many chronic lung diseases. Beyond pulmonary considerations, delivery of oxygen (O(2)) to the tissues and subsequent O(2) utilisation is also determined by other factors including red blood cell mass and iron status; consequently, disruption to these mechanisms provides further...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BMJ Publishing Group
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6733331/ https://www.ncbi.nlm.nih.gov/pubmed/31548896 http://dx.doi.org/10.1136/bmjresp-2019-000454 |
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author | Patel, Mehul S McKie, Elizabeth Steiner, Michael C Pascoe, Steven J Polkey, Michael I |
author_facet | Patel, Mehul S McKie, Elizabeth Steiner, Michael C Pascoe, Steven J Polkey, Michael I |
author_sort | Patel, Mehul S |
collection | PubMed |
description | Hypoxia is common in many chronic lung diseases. Beyond pulmonary considerations, delivery of oxygen (O(2)) to the tissues and subsequent O(2) utilisation is also determined by other factors including red blood cell mass and iron status; consequently, disruption to these mechanisms provides further physiological strains on an already stressed system. O(2) availability influences ventilation, regulates pulmonary blood flow and impacts gene expression throughout the body. Deleterious effects of poor tissue oxygenation include decreased exercise tolerance, increased cardiac strain and pulmonary hypertension in addition to pathophysiological involvement of multiple other organs resulting in progressive frailty. Increasing inspired O(2) is expensive, disliked by patients and does not normalise tissue oxygenation; thus, other strategies that improve O(2) delivery and utilisation may provide novel therapeutic opportunities in patients with lung disease. In this review, we focus on the rationale and possibilities for doing this by increasing haemoglobin availability or improving iron regulation. |
format | Online Article Text |
id | pubmed-6733331 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BMJ Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-67333312019-09-23 Anaemia and iron dysregulation: untapped therapeutic targets in chronic lung disease? Patel, Mehul S McKie, Elizabeth Steiner, Michael C Pascoe, Steven J Polkey, Michael I BMJ Open Respir Res Respiratory Physiology Hypoxia is common in many chronic lung diseases. Beyond pulmonary considerations, delivery of oxygen (O(2)) to the tissues and subsequent O(2) utilisation is also determined by other factors including red blood cell mass and iron status; consequently, disruption to these mechanisms provides further physiological strains on an already stressed system. O(2) availability influences ventilation, regulates pulmonary blood flow and impacts gene expression throughout the body. Deleterious effects of poor tissue oxygenation include decreased exercise tolerance, increased cardiac strain and pulmonary hypertension in addition to pathophysiological involvement of multiple other organs resulting in progressive frailty. Increasing inspired O(2) is expensive, disliked by patients and does not normalise tissue oxygenation; thus, other strategies that improve O(2) delivery and utilisation may provide novel therapeutic opportunities in patients with lung disease. In this review, we focus on the rationale and possibilities for doing this by increasing haemoglobin availability or improving iron regulation. BMJ Publishing Group 2019-08-30 /pmc/articles/PMC6733331/ /pubmed/31548896 http://dx.doi.org/10.1136/bmjresp-2019-000454 Text en © Author(s) (or their employer(s)) 2019. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/. |
spellingShingle | Respiratory Physiology Patel, Mehul S McKie, Elizabeth Steiner, Michael C Pascoe, Steven J Polkey, Michael I Anaemia and iron dysregulation: untapped therapeutic targets in chronic lung disease? |
title | Anaemia and iron dysregulation: untapped therapeutic targets in chronic lung disease? |
title_full | Anaemia and iron dysregulation: untapped therapeutic targets in chronic lung disease? |
title_fullStr | Anaemia and iron dysregulation: untapped therapeutic targets in chronic lung disease? |
title_full_unstemmed | Anaemia and iron dysregulation: untapped therapeutic targets in chronic lung disease? |
title_short | Anaemia and iron dysregulation: untapped therapeutic targets in chronic lung disease? |
title_sort | anaemia and iron dysregulation: untapped therapeutic targets in chronic lung disease? |
topic | Respiratory Physiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6733331/ https://www.ncbi.nlm.nih.gov/pubmed/31548896 http://dx.doi.org/10.1136/bmjresp-2019-000454 |
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