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Joint Effects of Smoking and Silicosis on Diseases to the Lungs

Smokers are subject to being more susceptible to the long-term effects of silica dust, whilst it remains unclear whether the joint effect of smoking and silicosis differs amongst diseases to the lungs; this study aims to address this knowledge gap. This was a historical cohort study comprised of 320...

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Autores principales: Tse, Lap Ah, Yu, Ignatius T. S., Qiu, Hong, Leung, Chi Chiu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4126694/
https://www.ncbi.nlm.nih.gov/pubmed/25105409
http://dx.doi.org/10.1371/journal.pone.0104494
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author Tse, Lap Ah
Yu, Ignatius T. S.
Qiu, Hong
Leung, Chi Chiu
author_facet Tse, Lap Ah
Yu, Ignatius T. S.
Qiu, Hong
Leung, Chi Chiu
author_sort Tse, Lap Ah
collection PubMed
description Smokers are subject to being more susceptible to the long-term effects of silica dust, whilst it remains unclear whether the joint effect of smoking and silicosis differs amongst diseases to the lungs; this study aims to address this knowledge gap. This was a historical cohort study comprised of 3202 silicotics in Hong Kong during 1981–2005 who were followed up till 31/12/2006. We estimated the standardized mortality ratio (SMR) in the smoking and never smoking silicotics using the mortality rates of male general population indiscriminately by smoking status, but these SMRs were regarded as biased. We adjusted these biased SMRs using “smoking adjustment factors (SAF)”. We assessed the multiplicative interaction between smoking and silicosis using ‘relative silicosis effect (RSE)’ that was the ratio of SAF-corrected SMR of smoking silicotics to the never smokers. A RSE differs significantly from one implies the presence of multiplicative interaction. A significant excess SMR was observed for respiratory diseases (lung cancer, chronic obstructive pulmonary diseases [COPD], silicosis) and other diseases to the lungs (pulmonary heart disease, tuberculosis). All the ‘biased-SMRs’ in smokers were higher than those in never smokers, but the SAF-corrected SMRs became higher in never smokers. The RSE was 0.95 (95%CI: 0.37–3.55), 0.94 (95%CI: 0.42–2.60), and 0.81 (95%CI: 0.60–1.19) for lung cancer, COPD, and silicosis; whilst it was 1.21 (95%CI: 0.32–10.26) for tuberculosis and 1.02 (95%CI: 0.16–42.90) for pulmonary heart disease. This study firstly demonstrated the joint effect of smoking and silicosis may differ amongst diseases to the lungs, but power is limited.
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spelling pubmed-41266942014-08-12 Joint Effects of Smoking and Silicosis on Diseases to the Lungs Tse, Lap Ah Yu, Ignatius T. S. Qiu, Hong Leung, Chi Chiu PLoS One Research Article Smokers are subject to being more susceptible to the long-term effects of silica dust, whilst it remains unclear whether the joint effect of smoking and silicosis differs amongst diseases to the lungs; this study aims to address this knowledge gap. This was a historical cohort study comprised of 3202 silicotics in Hong Kong during 1981–2005 who were followed up till 31/12/2006. We estimated the standardized mortality ratio (SMR) in the smoking and never smoking silicotics using the mortality rates of male general population indiscriminately by smoking status, but these SMRs were regarded as biased. We adjusted these biased SMRs using “smoking adjustment factors (SAF)”. We assessed the multiplicative interaction between smoking and silicosis using ‘relative silicosis effect (RSE)’ that was the ratio of SAF-corrected SMR of smoking silicotics to the never smokers. A RSE differs significantly from one implies the presence of multiplicative interaction. A significant excess SMR was observed for respiratory diseases (lung cancer, chronic obstructive pulmonary diseases [COPD], silicosis) and other diseases to the lungs (pulmonary heart disease, tuberculosis). All the ‘biased-SMRs’ in smokers were higher than those in never smokers, but the SAF-corrected SMRs became higher in never smokers. The RSE was 0.95 (95%CI: 0.37–3.55), 0.94 (95%CI: 0.42–2.60), and 0.81 (95%CI: 0.60–1.19) for lung cancer, COPD, and silicosis; whilst it was 1.21 (95%CI: 0.32–10.26) for tuberculosis and 1.02 (95%CI: 0.16–42.90) for pulmonary heart disease. This study firstly demonstrated the joint effect of smoking and silicosis may differ amongst diseases to the lungs, but power is limited. Public Library of Science 2014-08-08 /pmc/articles/PMC4126694/ /pubmed/25105409 http://dx.doi.org/10.1371/journal.pone.0104494 Text en © 2014 Tse et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Tse, Lap Ah
Yu, Ignatius T. S.
Qiu, Hong
Leung, Chi Chiu
Joint Effects of Smoking and Silicosis on Diseases to the Lungs
title Joint Effects of Smoking and Silicosis on Diseases to the Lungs
title_full Joint Effects of Smoking and Silicosis on Diseases to the Lungs
title_fullStr Joint Effects of Smoking and Silicosis on Diseases to the Lungs
title_full_unstemmed Joint Effects of Smoking and Silicosis on Diseases to the Lungs
title_short Joint Effects of Smoking and Silicosis on Diseases to the Lungs
title_sort joint effects of smoking and silicosis on diseases to the lungs
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4126694/
https://www.ncbi.nlm.nih.gov/pubmed/25105409
http://dx.doi.org/10.1371/journal.pone.0104494
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