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Low-density lipoprotein cholesterol and risk of COPD: Copenhagen General Population Study

BACKGROUND: Randomised controlled trials found that low-density lipoprotein (LDL) cholesterol-lowering statins increase lung function and possibly decrease rate of exacerbations in individuals with COPD. However, it is unknown whether high levels of LDL cholesterol are associated with increased susc...

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Autores principales: Freyberg, Josefine, Landt, Eskild M., Afzal, Shoaib, Nordestgaard, Børge G., Dahl, Morten
Formato: Online Artículo Texto
Lenguaje:English
Publicado: European Respiratory Society 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9986766/
https://www.ncbi.nlm.nih.gov/pubmed/36891075
http://dx.doi.org/10.1183/23120541.00496-2022
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author Freyberg, Josefine
Landt, Eskild M.
Afzal, Shoaib
Nordestgaard, Børge G.
Dahl, Morten
author_facet Freyberg, Josefine
Landt, Eskild M.
Afzal, Shoaib
Nordestgaard, Børge G.
Dahl, Morten
author_sort Freyberg, Josefine
collection PubMed
description BACKGROUND: Randomised controlled trials found that low-density lipoprotein (LDL) cholesterol-lowering statins increase lung function and possibly decrease rate of exacerbations in individuals with COPD. However, it is unknown whether high levels of LDL cholesterol are associated with increased susceptibility to COPD. METHODS: We tested the hypothesis that high LDL cholesterol is associated with increased risk of COPD, severe COPD exacerbation and COPD-specific mortality. We examined 107 301 adults from the Copenhagen General Population Study. COPD outcomes were ascertained at baseline and prospectively through nationwide registries. RESULTS: In cross-sectional analysis, low LDL cholesterol was associated with increased risk of COPD (odds ratio for 1st versus 4th quartile: 1.07 (95% CI 1.01–1.14)). Prospectively, low LDL cholesterol was associated with increased risk of COPD exacerbations with hazard ratios of 1.43 (1.21–1.70) for 1st versus 4th quartile, 1.21 (1.03–1.43) for 2nd versus 4th quartile, and 1.01 (0.85–1.20) for 3rd versus 4th quartile of LDL cholesterol (p-value for trend=6×10(−6)). Finally, low LDL cholesterol was likewise associated with increased risk of COPD-specific mortality (log-rank test: p=0.0009). Sensitivity analyses with death as competing risk provided similar results. CONCLUSION: Low LDL cholesterol was associated with increased risks of severe COPD exacerbation and COPD-specific mortality in the Danish general population. As this is opposite of that observed in randomised controlled trials with statins, our findings might be a result of reverse causation indicating that individuals with severe phenotypes of COPD have lower plasma levels of LDL cholesterol due to wasting.
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spelling pubmed-99867662023-03-07 Low-density lipoprotein cholesterol and risk of COPD: Copenhagen General Population Study Freyberg, Josefine Landt, Eskild M. Afzal, Shoaib Nordestgaard, Børge G. Dahl, Morten ERJ Open Res Original Research Articles BACKGROUND: Randomised controlled trials found that low-density lipoprotein (LDL) cholesterol-lowering statins increase lung function and possibly decrease rate of exacerbations in individuals with COPD. However, it is unknown whether high levels of LDL cholesterol are associated with increased susceptibility to COPD. METHODS: We tested the hypothesis that high LDL cholesterol is associated with increased risk of COPD, severe COPD exacerbation and COPD-specific mortality. We examined 107 301 adults from the Copenhagen General Population Study. COPD outcomes were ascertained at baseline and prospectively through nationwide registries. RESULTS: In cross-sectional analysis, low LDL cholesterol was associated with increased risk of COPD (odds ratio for 1st versus 4th quartile: 1.07 (95% CI 1.01–1.14)). Prospectively, low LDL cholesterol was associated with increased risk of COPD exacerbations with hazard ratios of 1.43 (1.21–1.70) for 1st versus 4th quartile, 1.21 (1.03–1.43) for 2nd versus 4th quartile, and 1.01 (0.85–1.20) for 3rd versus 4th quartile of LDL cholesterol (p-value for trend=6×10(−6)). Finally, low LDL cholesterol was likewise associated with increased risk of COPD-specific mortality (log-rank test: p=0.0009). Sensitivity analyses with death as competing risk provided similar results. CONCLUSION: Low LDL cholesterol was associated with increased risks of severe COPD exacerbation and COPD-specific mortality in the Danish general population. As this is opposite of that observed in randomised controlled trials with statins, our findings might be a result of reverse causation indicating that individuals with severe phenotypes of COPD have lower plasma levels of LDL cholesterol due to wasting. European Respiratory Society 2023-03-06 /pmc/articles/PMC9986766/ /pubmed/36891075 http://dx.doi.org/10.1183/23120541.00496-2022 Text en Copyright ©The authors 2023 https://creativecommons.org/licenses/by-nc/4.0/This version is distributed under the terms of the Creative Commons Attribution Non-Commercial Licence 4.0. For commercial reproduction rights and permissions contact permissions@ersnet.org (mailto:permissions@ersnet.org)
spellingShingle Original Research Articles
Freyberg, Josefine
Landt, Eskild M.
Afzal, Shoaib
Nordestgaard, Børge G.
Dahl, Morten
Low-density lipoprotein cholesterol and risk of COPD: Copenhagen General Population Study
title Low-density lipoprotein cholesterol and risk of COPD: Copenhagen General Population Study
title_full Low-density lipoprotein cholesterol and risk of COPD: Copenhagen General Population Study
title_fullStr Low-density lipoprotein cholesterol and risk of COPD: Copenhagen General Population Study
title_full_unstemmed Low-density lipoprotein cholesterol and risk of COPD: Copenhagen General Population Study
title_short Low-density lipoprotein cholesterol and risk of COPD: Copenhagen General Population Study
title_sort low-density lipoprotein cholesterol and risk of copd: copenhagen general population study
topic Original Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9986766/
https://www.ncbi.nlm.nih.gov/pubmed/36891075
http://dx.doi.org/10.1183/23120541.00496-2022
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