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Evaluation of lung function in a German single center cohort of young patients with sickle cell disease using EIT and standard techniques
BACKGROUND AND OBJECTIVE: Sickle cell disease (SCD) is a very common autosomal recessive hemoglobinopathy leading to multiple pulmonary complications that are closely associated with mortality. The pathophysiology of chronic pulmonary involvement is not yet fully understood and no specific therapies...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10040809/ https://www.ncbi.nlm.nih.gov/pubmed/36993804 http://dx.doi.org/10.3389/fmed.2023.1100180 |
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author | Rein, Alina Ngo, Chuong van den Berg, Maike Böll, Svenja Lassay, Lisa Kontny, Udo Wagner, Norbert Leonhardt, Steffen Tenbrock, Klaus Verjans, Eva |
author_facet | Rein, Alina Ngo, Chuong van den Berg, Maike Böll, Svenja Lassay, Lisa Kontny, Udo Wagner, Norbert Leonhardt, Steffen Tenbrock, Klaus Verjans, Eva |
author_sort | Rein, Alina |
collection | PubMed |
description | BACKGROUND AND OBJECTIVE: Sickle cell disease (SCD) is a very common autosomal recessive hemoglobinopathy leading to multiple pulmonary complications that are closely associated with mortality. The pathophysiology of chronic pulmonary involvement is not yet fully understood and no specific therapies are available. METHODS: The aim of this cross-sectional study was to characterize the lung function of children and young adolescents with SCD in a German single-center cohort and to extend conventional lung function testing by the use of a new imaging method. We performed spirometry and body plethysmography in 35 children and young adults with hemoglobin SS, SC, S/β-thalassemia as well as 50 controls. These data were compared with clinical characteristics and typical laboratory parameters of hemolysis and disease activity in SCD. To identify lung inhomogeneities, for example due to atelectasis, hyperinflation, air trapping or vascular occlusions, we used the promising new method of electrical impedance tomography (EIT) and calculated global inhomogeneity indices. RESULTS: Lung function of patients with SCD was significantly reduced compared to that of healthy controls. When the result was found to be pathological, the most commonly observed type of breathing disorder was classified as restrictive. Laboratory parameters showed typical features of SCD including decreased levels of hemoglobin and hematocrit and elevated levels of leucocytes, platelets, lactate dehydrogenase and total bilirubin. However, there was no correlation between blood values and reduced lung function. Electrical impedance tomography (EIT) revealed no abnormalities in SCD patients compared to healthy controls. In particular, we were unable to demonstrate any regional inhomogeneities in lung ventilation. CONCLUSION: In our study, SCD patients showed impaired lung function, with a relevant percentage of patients suffering from restrictive breathing disorder. Signs of obstruction could not be detected. Electrical impedance tomography (EIT) measurements revealed no unevenness that would suggest air entrapment, blockage of blood vessels, excessive inflation, obstruction, or other forms of lung disease. Additionally, the reduction in lung function observed in SCD patients was not related to the disease severity or laboratory test results. |
format | Online Article Text |
id | pubmed-10040809 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-100408092023-03-28 Evaluation of lung function in a German single center cohort of young patients with sickle cell disease using EIT and standard techniques Rein, Alina Ngo, Chuong van den Berg, Maike Böll, Svenja Lassay, Lisa Kontny, Udo Wagner, Norbert Leonhardt, Steffen Tenbrock, Klaus Verjans, Eva Front Med (Lausanne) Medicine BACKGROUND AND OBJECTIVE: Sickle cell disease (SCD) is a very common autosomal recessive hemoglobinopathy leading to multiple pulmonary complications that are closely associated with mortality. The pathophysiology of chronic pulmonary involvement is not yet fully understood and no specific therapies are available. METHODS: The aim of this cross-sectional study was to characterize the lung function of children and young adolescents with SCD in a German single-center cohort and to extend conventional lung function testing by the use of a new imaging method. We performed spirometry and body plethysmography in 35 children and young adults with hemoglobin SS, SC, S/β-thalassemia as well as 50 controls. These data were compared with clinical characteristics and typical laboratory parameters of hemolysis and disease activity in SCD. To identify lung inhomogeneities, for example due to atelectasis, hyperinflation, air trapping or vascular occlusions, we used the promising new method of electrical impedance tomography (EIT) and calculated global inhomogeneity indices. RESULTS: Lung function of patients with SCD was significantly reduced compared to that of healthy controls. When the result was found to be pathological, the most commonly observed type of breathing disorder was classified as restrictive. Laboratory parameters showed typical features of SCD including decreased levels of hemoglobin and hematocrit and elevated levels of leucocytes, platelets, lactate dehydrogenase and total bilirubin. However, there was no correlation between blood values and reduced lung function. Electrical impedance tomography (EIT) revealed no abnormalities in SCD patients compared to healthy controls. In particular, we were unable to demonstrate any regional inhomogeneities in lung ventilation. CONCLUSION: In our study, SCD patients showed impaired lung function, with a relevant percentage of patients suffering from restrictive breathing disorder. Signs of obstruction could not be detected. Electrical impedance tomography (EIT) measurements revealed no unevenness that would suggest air entrapment, blockage of blood vessels, excessive inflation, obstruction, or other forms of lung disease. Additionally, the reduction in lung function observed in SCD patients was not related to the disease severity or laboratory test results. Frontiers Media S.A. 2023-03-13 /pmc/articles/PMC10040809/ /pubmed/36993804 http://dx.doi.org/10.3389/fmed.2023.1100180 Text en Copyright © 2023 Rein, Ngo, Van den Berg, Böll, Lassay, Kontny, Wagner, Leonhardt, Tenbrock and Verjans. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Medicine Rein, Alina Ngo, Chuong van den Berg, Maike Böll, Svenja Lassay, Lisa Kontny, Udo Wagner, Norbert Leonhardt, Steffen Tenbrock, Klaus Verjans, Eva Evaluation of lung function in a German single center cohort of young patients with sickle cell disease using EIT and standard techniques |
title | Evaluation of lung function in a German single center cohort of young patients with sickle cell disease using EIT and standard techniques |
title_full | Evaluation of lung function in a German single center cohort of young patients with sickle cell disease using EIT and standard techniques |
title_fullStr | Evaluation of lung function in a German single center cohort of young patients with sickle cell disease using EIT and standard techniques |
title_full_unstemmed | Evaluation of lung function in a German single center cohort of young patients with sickle cell disease using EIT and standard techniques |
title_short | Evaluation of lung function in a German single center cohort of young patients with sickle cell disease using EIT and standard techniques |
title_sort | evaluation of lung function in a german single center cohort of young patients with sickle cell disease using eit and standard techniques |
topic | Medicine |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10040809/ https://www.ncbi.nlm.nih.gov/pubmed/36993804 http://dx.doi.org/10.3389/fmed.2023.1100180 |
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