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The association of vitamin K status with lung function and disease in a general population
INTRODUCTION: Matrix Gla protein (MGP) is an inhibitor of lung tissue calcification. The plasma level of dephosphorylated-uncarboxylated MGP (dp-ucMGP) is a biomarker of vitamin K status. The present study assessed whether lower vitamin K status (reflected by higher dp-ucMGP) was associated with lun...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
European Respiratory Society
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10423920/ https://www.ncbi.nlm.nih.gov/pubmed/37588689 http://dx.doi.org/10.1183/23120541.00208-2023 |
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author | Jespersen, Torkil Kampmann, Freja Bach Dantoft, Thomas Meinertz Jørgensen, Niklas Rye Kårhus, Line Lund Madsen, Flemming Linneberg, Allan Thysen, Sanne Marie |
author_facet | Jespersen, Torkil Kampmann, Freja Bach Dantoft, Thomas Meinertz Jørgensen, Niklas Rye Kårhus, Line Lund Madsen, Flemming Linneberg, Allan Thysen, Sanne Marie |
author_sort | Jespersen, Torkil |
collection | PubMed |
description | INTRODUCTION: Matrix Gla protein (MGP) is an inhibitor of lung tissue calcification. The plasma level of dephosphorylated-uncarboxylated MGP (dp-ucMGP) is a biomarker of vitamin K status. The present study assessed whether lower vitamin K status (reflected by higher dp-ucMGP) was associated with lung function and lung disease/symptoms. METHODS: A general population sample of 4092 individuals, aged 24 to 77 years, underwent a health examination including questionnaires, spirometry and measurements of plasma dp-ucMGP. Associations of dp-ucMGP with lung function and self-reported disease/symptoms were estimated using regression models adjusted for age, sex and height. Associations were expressed as β-estimates or odds ratios (ORs) per doubling in dp-ucMGP. RESULTS: Lower vitamin K status (higher dp-ucMGP) was associated with lower forced expiratory volume in 1 s (FEV(1)) (98 mL; 95% CI: 54–141 mL) and lower forced vital capacity (FVC) (136 mL; 95% CI: 85–187 mL). Dp-ucMGP was not associated with the FEV(1)/FVC ratio (0.0 percentage points higher than the expected value; 95% CI: −1.0–1.0). Furthermore, lower vitamin K status was associated with COPD (OR 2.24, 95% CI: 1.53–3.27), wheezing (OR 1.81, 95% CI: 1.44–2.28) and asthma (OR 1.44, 95% CI: 1.12–1.83). CONCLUSION: Lower vitamin K status was associated with lower ventilatory capacity (lower FEV(1) and FVC), and with higher risk of self-reported asthma, COPD and wheezing. Vitamin K status was not associated with airflow obstruction (FEV(1)/FVC ratio). |
format | Online Article Text |
id | pubmed-10423920 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | European Respiratory Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-104239202023-08-15 The association of vitamin K status with lung function and disease in a general population Jespersen, Torkil Kampmann, Freja Bach Dantoft, Thomas Meinertz Jørgensen, Niklas Rye Kårhus, Line Lund Madsen, Flemming Linneberg, Allan Thysen, Sanne Marie ERJ Open Res Original Research Articles INTRODUCTION: Matrix Gla protein (MGP) is an inhibitor of lung tissue calcification. The plasma level of dephosphorylated-uncarboxylated MGP (dp-ucMGP) is a biomarker of vitamin K status. The present study assessed whether lower vitamin K status (reflected by higher dp-ucMGP) was associated with lung function and lung disease/symptoms. METHODS: A general population sample of 4092 individuals, aged 24 to 77 years, underwent a health examination including questionnaires, spirometry and measurements of plasma dp-ucMGP. Associations of dp-ucMGP with lung function and self-reported disease/symptoms were estimated using regression models adjusted for age, sex and height. Associations were expressed as β-estimates or odds ratios (ORs) per doubling in dp-ucMGP. RESULTS: Lower vitamin K status (higher dp-ucMGP) was associated with lower forced expiratory volume in 1 s (FEV(1)) (98 mL; 95% CI: 54–141 mL) and lower forced vital capacity (FVC) (136 mL; 95% CI: 85–187 mL). Dp-ucMGP was not associated with the FEV(1)/FVC ratio (0.0 percentage points higher than the expected value; 95% CI: −1.0–1.0). Furthermore, lower vitamin K status was associated with COPD (OR 2.24, 95% CI: 1.53–3.27), wheezing (OR 1.81, 95% CI: 1.44–2.28) and asthma (OR 1.44, 95% CI: 1.12–1.83). CONCLUSION: Lower vitamin K status was associated with lower ventilatory capacity (lower FEV(1) and FVC), and with higher risk of self-reported asthma, COPD and wheezing. Vitamin K status was not associated with airflow obstruction (FEV(1)/FVC ratio). European Respiratory Society 2023-09-25 /pmc/articles/PMC10423920/ /pubmed/37588689 http://dx.doi.org/10.1183/23120541.00208-2023 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 Jespersen, Torkil Kampmann, Freja Bach Dantoft, Thomas Meinertz Jørgensen, Niklas Rye Kårhus, Line Lund Madsen, Flemming Linneberg, Allan Thysen, Sanne Marie The association of vitamin K status with lung function and disease in a general population |
title | The association of vitamin K status with lung function and disease in a general population |
title_full | The association of vitamin K status with lung function and disease in a general population |
title_fullStr | The association of vitamin K status with lung function and disease in a general population |
title_full_unstemmed | The association of vitamin K status with lung function and disease in a general population |
title_short | The association of vitamin K status with lung function and disease in a general population |
title_sort | association of vitamin k status with lung function and disease in a general population |
topic | Original Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10423920/ https://www.ncbi.nlm.nih.gov/pubmed/37588689 http://dx.doi.org/10.1183/23120541.00208-2023 |
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