Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Patel, Mehul S, McKie, Elizabeth, Steiner, Michael C, Pascoe, Steven J, Polkey, Michael I
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2019
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
_version_ 1783449962728652800
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
work_keys_str_mv AT patelmehuls anaemiaandirondysregulationuntappedtherapeutictargetsinchroniclungdisease
AT mckieelizabeth anaemiaandirondysregulationuntappedtherapeutictargetsinchroniclungdisease
AT steinermichaelc anaemiaandirondysregulationuntappedtherapeutictargetsinchroniclungdisease
AT pascoestevenj anaemiaandirondysregulationuntappedtherapeutictargetsinchroniclungdisease
AT polkeymichaeli anaemiaandirondysregulationuntappedtherapeutictargetsinchroniclungdisease