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      Pulmonary function in patients with transfusion-dependent thalassemia and its associations with iron overload

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          Abstract

          In patients with transfusion-dependent thalassemia (TDT), pulmonary function impairment has been reported but data are conflicting. Moreover, it remains unclear whether pulmonary dysfunction is associated with iron overload. This study aimed to evaluate the pulmonary function in patients with TDT and to investigate the associations between pulmonary dysfunction and iron overload. It was a retrospective observational study. 101 patients with TDT were recruited for lung function tests. The most recent ferritin levels (pmol/L) and the magnetic resonance imaging (MRI) measurements of the myocardial and liver iron status, as measured by heart and liver T2* relaxation time (millisecond, ms) respectively, were retrieved from the computerized medical records. Only data within 12 months from the lung function measurement were included in the analysis. The serum ferritin, and the cardiac and liver T2* relaxation time were the surrogate indexes of body iron content. The threshold of abnormality in lung function was defined as under 80% of the predicted value. 101 subjects were recruited with a mean age of 25.1 years (standard deviation (SD) 7.9 years). Thirty-eight (38%) and five (5%) demonstrated restrictive and obstructive lung function deficits, respectively. A weak correlation of FVC %Predicted and TLC %Predicted with MRI myocardial T2* relaxation time (rho = 0.32, p = 0.03 and rho = 0.33, p = 0.03 respectively) was observed. By logistic regression, MRI cardiac T2* relaxation time was negatively associated with restrictive lung function deficit (B − 0.06; SE 0.03; Odds ratio 0.94; 95% confidence interval (CI) 0.89–0.99; p = 0.023) after adjusting for age, sex and body mass index. Restrictive pulmonary function deficit was commonly observed in patients with TDT, and the severity potentially correlates with myocardial iron content. Monitoring of lung function in this group of patients, particularly for those with iron overload, is important.

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          Standardisation of spirometry.

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            Standardisation of the measurement of lung volumes.

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              Lung function and mortality in the United States: data from the First National Health and Nutrition Examination Survey follow up study.

              D Mannino (2003)
              A study was undertaken to define the risk of death among a national cohort of US adults both with and without lung disease. Participants in the first National Health and Nutrition Examination Survey (NHANES I) followed for up to 22 years were studied. Subjects were classified using a modification of the Global Initiative for Chronic Obstructive Lung Disease criteria for chronic obstructive pulmonary disease (COPD) into the following mutually exclusive categories using the forced expiratory volume in 1 second (FEV(1)), forced vital capacity (FVC), FEV(1)/FVC ratio, and the presence of respiratory symptoms: severe COPD, moderate COPD, mild COPD, respiratory symptoms only, restrictive lung disease, and no lung disease. Proportional hazard models were developed that controlled for age, race, sex, education, smoking status, pack years of smoking, years since quitting smoking, and body mass index. A total of 1301 deaths occurred in the 5542 adults in the cohort. In the adjusted proportional hazards model the presence of severe or moderate COPD was associated with a higher risk of death (hazard ratios (HR) 2.7 and 1.6, 95% confidence intervals (CI) 2.1 to 3.5 and 1.4 to 2.0), as was restrictive lung disease (HR 1.7, 95% CI 1.4 to 2.0). The presence of both obstructive and restrictive lung disease is a significant predictor of earlier death in long term follow up.
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                Author and article information

                Contributors
                katechan@cuhk.edu.hk
                Journal
                Sci Rep
                Sci Rep
                Scientific Reports
                Nature Publishing Group UK (London )
                2045-2322
                4 March 2023
                4 March 2023
                2023
                : 13
                : 3674
                Affiliations
                [1 ]GRID grid.10784.3a, ISNI 0000 0004 1937 0482, Department of Paediatrics, Faculty of Medicine, , The Chinese University of Hong Kong, ; 6/F, Lui Che Woo Clinical Sciences Building, Prince of Wales Hospital, Shatin, N.T., Hong Kong SAR China
                [2 ]GRID grid.10784.3a, ISNI 0000 0004 1937 0482, Laboratory for Paediatric Respiratory Research, Faculty of Medicine, Li Ka Shing Institute of Health Sciences, , The Chinese University of Hong Kong, ; Shatin, Hong Kong SAR China
                [3 ]GRID grid.10784.3a, ISNI 0000 0004 1937 0482, Hong Kong Hub of Paediatric Excellence, , The Chinese University of Hong Kong, ; Shatin, Hong Kong SAR China
                [4 ]GRID grid.415229.9, ISNI 0000 0004 1799 7070, Department of Paediatrics and Adolescent Medicine, , Princess Margaret Hospital, ; Kowloon, Hong Kong SAR China
                [5 ]GRID grid.417336.4, ISNI 0000 0004 1771 3971, Department of Paediatrics and Adolescent Medicine, , Tuen Mun Hospital, ; Tuen Mun, Hong Kong SAR China
                [6 ]GRID grid.415550.0, ISNI 0000 0004 1764 4144, Department of Paediatrics and Adolescent Medicine, , Queen Mary Hospital, ; Pok Fu Lam, Hong Kong SAR China
                Article
                30784
                10.1038/s41598-023-30784-9
                9985598
                36871083
                0f1dc989-facd-49b8-9568-ec0a1ea23a8e
                © The Author(s) 2023

                Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.

                History
                : 25 August 2022
                : 1 March 2023
                Categories
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                Custom metadata
                © The Author(s) 2023

                Uncategorized
                haematological diseases,respiratory tract diseases
                Uncategorized
                haematological diseases, respiratory tract diseases

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