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Alterations by Air Pollution in Inflammation and Metals in Pleural Effusion of Pneumonia Patients
Air pollution is known to increase the risk of pneumonia. However, the effects of air pollution on the pleural effusion of patients with pneumonia are unclear. The objective of this study was to investigate alterations in inflammatory–immune biomarkers by air pollution in patients with pneumonia by...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6427250/ https://www.ncbi.nlm.nih.gov/pubmed/30818785 http://dx.doi.org/10.3390/ijerph16050705 |
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author | Bai, Kuan-Jen Chuang, Kai-Jen Chen, Jen-Kun Tsai, Cheng-Yu Yang, You-Lan Chang, Chih-Cheng Chen, Tzu-Tao Lee, Chun-Nin Feng, Po-Hao Chen, Kuan-Yuan Lee, Kang-Yun Su, Chein-Ling Ho, Shu-Chuan Wu, Sheng-Ming Chuang, Hsiao-Chi |
author_facet | Bai, Kuan-Jen Chuang, Kai-Jen Chen, Jen-Kun Tsai, Cheng-Yu Yang, You-Lan Chang, Chih-Cheng Chen, Tzu-Tao Lee, Chun-Nin Feng, Po-Hao Chen, Kuan-Yuan Lee, Kang-Yun Su, Chein-Ling Ho, Shu-Chuan Wu, Sheng-Ming Chuang, Hsiao-Chi |
author_sort | Bai, Kuan-Jen |
collection | PubMed |
description | Air pollution is known to increase the risk of pneumonia. However, the effects of air pollution on the pleural effusion of patients with pneumonia are unclear. The objective of this study was to investigate alterations in inflammatory–immune biomarkers by air pollution in patients with pneumonia by analyzing their pleural effusion. Patients who had undergone thoracentesis to drain their pleural effusion in a hospital were recruited for this study. Patients with pneumonia and those with congestive heart failure respectively served as the case and control groups. We observed that an increase of 1 ppb in one-year NO(2) was associated with a decrease of 0.105 ng/mL in cluster of differentiation 62 (CD62) (95% confidence interval (CI) = −0.085, −0.004, p < 0.05) in the pleural effusion. Furthermore, we observed that an increase in one−year 1 ppb of NO(2) was associated with a decrease of 0.026 ng/mL in molybdenum (Mo) (95% CI = −0.138, −0.020, p < 0.05). An increase in one-year 1 ppb of SO(2) was associated with a decrease of 0.531 ng/mL in zinc (95% CI = −0.164, −0.006, p < 0.05). Also, an increase in one-year 1 ppb of O(3) was associated with a decrease of 0.025 ng/mL in Mo (95% CI = −0.372, −0.053, p < 0.05). In conclusion, air pollution exposure, especially gaseous pollution, may be associated with the regulation of immune responses and changes in metal levels in the pleural effusion of pneumonia patients. |
format | Online Article Text |
id | pubmed-6427250 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-64272502019-04-10 Alterations by Air Pollution in Inflammation and Metals in Pleural Effusion of Pneumonia Patients Bai, Kuan-Jen Chuang, Kai-Jen Chen, Jen-Kun Tsai, Cheng-Yu Yang, You-Lan Chang, Chih-Cheng Chen, Tzu-Tao Lee, Chun-Nin Feng, Po-Hao Chen, Kuan-Yuan Lee, Kang-Yun Su, Chein-Ling Ho, Shu-Chuan Wu, Sheng-Ming Chuang, Hsiao-Chi Int J Environ Res Public Health Article Air pollution is known to increase the risk of pneumonia. However, the effects of air pollution on the pleural effusion of patients with pneumonia are unclear. The objective of this study was to investigate alterations in inflammatory–immune biomarkers by air pollution in patients with pneumonia by analyzing their pleural effusion. Patients who had undergone thoracentesis to drain their pleural effusion in a hospital were recruited for this study. Patients with pneumonia and those with congestive heart failure respectively served as the case and control groups. We observed that an increase of 1 ppb in one-year NO(2) was associated with a decrease of 0.105 ng/mL in cluster of differentiation 62 (CD62) (95% confidence interval (CI) = −0.085, −0.004, p < 0.05) in the pleural effusion. Furthermore, we observed that an increase in one−year 1 ppb of NO(2) was associated with a decrease of 0.026 ng/mL in molybdenum (Mo) (95% CI = −0.138, −0.020, p < 0.05). An increase in one-year 1 ppb of SO(2) was associated with a decrease of 0.531 ng/mL in zinc (95% CI = −0.164, −0.006, p < 0.05). Also, an increase in one-year 1 ppb of O(3) was associated with a decrease of 0.025 ng/mL in Mo (95% CI = −0.372, −0.053, p < 0.05). In conclusion, air pollution exposure, especially gaseous pollution, may be associated with the regulation of immune responses and changes in metal levels in the pleural effusion of pneumonia patients. MDPI 2019-02-27 2019-03 /pmc/articles/PMC6427250/ /pubmed/30818785 http://dx.doi.org/10.3390/ijerph16050705 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Bai, Kuan-Jen Chuang, Kai-Jen Chen, Jen-Kun Tsai, Cheng-Yu Yang, You-Lan Chang, Chih-Cheng Chen, Tzu-Tao Lee, Chun-Nin Feng, Po-Hao Chen, Kuan-Yuan Lee, Kang-Yun Su, Chein-Ling Ho, Shu-Chuan Wu, Sheng-Ming Chuang, Hsiao-Chi Alterations by Air Pollution in Inflammation and Metals in Pleural Effusion of Pneumonia Patients |
title | Alterations by Air Pollution in Inflammation and Metals in Pleural Effusion of Pneumonia Patients |
title_full | Alterations by Air Pollution in Inflammation and Metals in Pleural Effusion of Pneumonia Patients |
title_fullStr | Alterations by Air Pollution in Inflammation and Metals in Pleural Effusion of Pneumonia Patients |
title_full_unstemmed | Alterations by Air Pollution in Inflammation and Metals in Pleural Effusion of Pneumonia Patients |
title_short | Alterations by Air Pollution in Inflammation and Metals in Pleural Effusion of Pneumonia Patients |
title_sort | alterations by air pollution in inflammation and metals in pleural effusion of pneumonia patients |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6427250/ https://www.ncbi.nlm.nih.gov/pubmed/30818785 http://dx.doi.org/10.3390/ijerph16050705 |
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