Cargando…

Statin use and lung cancer risk in chronic obstructive pulmonary disease patients: a population-based cohort study

BACKGROUND: Patients living with chronic obstructive pulmonary disease (COPD) are at an increased risk of lung cancer. A common comorbidity of COPD is cardiovascular disease; as such, COPD patients often receive statins. This study sought to understand the association between statin exposure and lun...

Descripción completa

Detalles Bibliográficos
Autores principales: Raymakers, AJN, Sin, D. D., Sadatsafavi, M., FitzGerald, JM, Marra, C. A., Lynd, L. D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7236956/
https://www.ncbi.nlm.nih.gov/pubmed/32429927
http://dx.doi.org/10.1186/s12931-020-01344-w
_version_ 1783536239321808896
author Raymakers, AJN
Sin, D. D.
Sadatsafavi, M.
FitzGerald, JM
Marra, C. A.
Lynd, L. D.
author_facet Raymakers, AJN
Sin, D. D.
Sadatsafavi, M.
FitzGerald, JM
Marra, C. A.
Lynd, L. D.
author_sort Raymakers, AJN
collection PubMed
description BACKGROUND: Patients living with chronic obstructive pulmonary disease (COPD) are at an increased risk of lung cancer. A common comorbidity of COPD is cardiovascular disease; as such, COPD patients often receive statins. This study sought to understand the association between statin exposure and lung cancer risk in a population-based cohort of COPD patients. METHODS: We identified a population-based cohort of COPD patients based on having filled at least three prescriptions for an anticholinergic or short-acting beta-agonist (SABA). We used an array of methods of defining medication exposure including three conventional methods (ever statin exposure, cumulative duration of use, and cumulative dose) and two novel methods (recency-weighted cumulative duration of use and recency-weighted cumulative dose). To assess residual confounding, a negative control exposure was used to test the validity of our results. All exposure variables were time-dependent. RESULTS: The population-based cohort of COPD had 39,879 patients with mean age of 70.6 (SD: 11.2) years and, of which, 53.5% were female. There were 12,469 patients who received at least one statin prescription. Results from the reference case multivariable analysis indicated a reduced risk from statin exposure (HR: 0.85 (95% CI: 0.73–1.00) in COPD patients, but this result not statistically significant. Using the two recency-weighted modelling approaches, statin exposure was associated with a statistically significant reduction in lung cancer risk (recency-weighted cumulative dose, HR: 0.85 (95% CI: 0.77–0.93) and recency-weighted cumulative duration of use, HR: 0.97 (95% CI: 0.96–0.99). Multivariable analysis incorporating the negative control exposure was not statistically significant (HR: 0.89 (95% CI: 0.75–1.10). CONCLUSIONS: The results of this population-based analysis indicate that statin use in COPD patients may reduce the risk of lung cancer. While the effect was not statistically significantly across all exposure definitions, the overall results support the hypothesis that COPD patients might benefit from statin therapy.
format Online
Article
Text
id pubmed-7236956
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-72369562020-05-27 Statin use and lung cancer risk in chronic obstructive pulmonary disease patients: a population-based cohort study Raymakers, AJN Sin, D. D. Sadatsafavi, M. FitzGerald, JM Marra, C. A. Lynd, L. D. Respir Res Research BACKGROUND: Patients living with chronic obstructive pulmonary disease (COPD) are at an increased risk of lung cancer. A common comorbidity of COPD is cardiovascular disease; as such, COPD patients often receive statins. This study sought to understand the association between statin exposure and lung cancer risk in a population-based cohort of COPD patients. METHODS: We identified a population-based cohort of COPD patients based on having filled at least three prescriptions for an anticholinergic or short-acting beta-agonist (SABA). We used an array of methods of defining medication exposure including three conventional methods (ever statin exposure, cumulative duration of use, and cumulative dose) and two novel methods (recency-weighted cumulative duration of use and recency-weighted cumulative dose). To assess residual confounding, a negative control exposure was used to test the validity of our results. All exposure variables were time-dependent. RESULTS: The population-based cohort of COPD had 39,879 patients with mean age of 70.6 (SD: 11.2) years and, of which, 53.5% were female. There were 12,469 patients who received at least one statin prescription. Results from the reference case multivariable analysis indicated a reduced risk from statin exposure (HR: 0.85 (95% CI: 0.73–1.00) in COPD patients, but this result not statistically significant. Using the two recency-weighted modelling approaches, statin exposure was associated with a statistically significant reduction in lung cancer risk (recency-weighted cumulative dose, HR: 0.85 (95% CI: 0.77–0.93) and recency-weighted cumulative duration of use, HR: 0.97 (95% CI: 0.96–0.99). Multivariable analysis incorporating the negative control exposure was not statistically significant (HR: 0.89 (95% CI: 0.75–1.10). CONCLUSIONS: The results of this population-based analysis indicate that statin use in COPD patients may reduce the risk of lung cancer. While the effect was not statistically significantly across all exposure definitions, the overall results support the hypothesis that COPD patients might benefit from statin therapy. BioMed Central 2020-05-19 2020 /pmc/articles/PMC7236956/ /pubmed/32429927 http://dx.doi.org/10.1186/s12931-020-01344-w Text en © The Author(s) 2020 Open AccessThis 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/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Raymakers, AJN
Sin, D. D.
Sadatsafavi, M.
FitzGerald, JM
Marra, C. A.
Lynd, L. D.
Statin use and lung cancer risk in chronic obstructive pulmonary disease patients: a population-based cohort study
title Statin use and lung cancer risk in chronic obstructive pulmonary disease patients: a population-based cohort study
title_full Statin use and lung cancer risk in chronic obstructive pulmonary disease patients: a population-based cohort study
title_fullStr Statin use and lung cancer risk in chronic obstructive pulmonary disease patients: a population-based cohort study
title_full_unstemmed Statin use and lung cancer risk in chronic obstructive pulmonary disease patients: a population-based cohort study
title_short Statin use and lung cancer risk in chronic obstructive pulmonary disease patients: a population-based cohort study
title_sort statin use and lung cancer risk in chronic obstructive pulmonary disease patients: a population-based cohort study
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7236956/
https://www.ncbi.nlm.nih.gov/pubmed/32429927
http://dx.doi.org/10.1186/s12931-020-01344-w
work_keys_str_mv AT raymakersajn statinuseandlungcancerriskinchronicobstructivepulmonarydiseasepatientsapopulationbasedcohortstudy
AT sindd statinuseandlungcancerriskinchronicobstructivepulmonarydiseasepatientsapopulationbasedcohortstudy
AT sadatsafavim statinuseandlungcancerriskinchronicobstructivepulmonarydiseasepatientsapopulationbasedcohortstudy
AT fitzgeraldjm statinuseandlungcancerriskinchronicobstructivepulmonarydiseasepatientsapopulationbasedcohortstudy
AT marraca statinuseandlungcancerriskinchronicobstructivepulmonarydiseasepatientsapopulationbasedcohortstudy
AT lyndld statinuseandlungcancerriskinchronicobstructivepulmonarydiseasepatientsapopulationbasedcohortstudy