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BMI is not independently associated with coronary artery calcification in a large single‐center CT cohort
OBJECTIVE: Obesity is associated with cardiovascular disease (CVD) and CVD mortality. However, previous reports showed a paradoxical protective effect in patients with known CVD referred as “obesity paradox”. Therefore, the aim of the present study was to investigate the association of body mass ind...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10073817/ https://www.ncbi.nlm.nih.gov/pubmed/37034565 http://dx.doi.org/10.1002/osp4.636 |
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author | Altintas, Sibel van Workum, Samanta Kok, Madeleine Joosen, Ivo A. P. G. Versteylen, Mathijs O. Nelemans, Patricia J. Wildberger, Joachim E. Crijns, Harry J. G. M. Das, Marco Kietselaer, Bas L. J. H. |
author_facet | Altintas, Sibel van Workum, Samanta Kok, Madeleine Joosen, Ivo A. P. G. Versteylen, Mathijs O. Nelemans, Patricia J. Wildberger, Joachim E. Crijns, Harry J. G. M. Das, Marco Kietselaer, Bas L. J. H. |
author_sort | Altintas, Sibel |
collection | PubMed |
description | OBJECTIVE: Obesity is associated with cardiovascular disease (CVD) and CVD mortality. However, previous reports showed a paradoxical protective effect in patients with known CVD referred as “obesity paradox”. Therefore, the aim of the present study was to investigate the association of body mass index (BMI) with coronary artery calcification (CAC) in a large outpatient cardiac CT cohort. METHODS: 4.079 patients who underwent cardiac CT between December 2007–May 2014 were analyzed. BMI and clinical risk factors (current smoking, diabetes mellitus type 2, family history, systolic blood pressure, lipid spectrum) were assessed. Missing values were imputed using multiple imputation. CAC extent was categorized as absent (0), mild (>0–100), moderate (>100–400) and severe (>400). RESULTS: Multivariable multinomial logistic regression analysis, including all risk factors as independent variables, showed no association between BMI and CAC. Using absence of calcification as reference category, the odds ratios per unit increase in BMI were 1.01 for mild; 1.02 for moderate; and 1.00 for severe CAC (p‐values ≥0.103). CONCLUSIONS: No statistically significant association was observed between BMI and CAC after adjustment for other risk factors. |
format | Online Article Text |
id | pubmed-10073817 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-100738172023-04-06 BMI is not independently associated with coronary artery calcification in a large single‐center CT cohort Altintas, Sibel van Workum, Samanta Kok, Madeleine Joosen, Ivo A. P. G. Versteylen, Mathijs O. Nelemans, Patricia J. Wildberger, Joachim E. Crijns, Harry J. G. M. Das, Marco Kietselaer, Bas L. J. H. Obes Sci Pract Original Articles OBJECTIVE: Obesity is associated with cardiovascular disease (CVD) and CVD mortality. However, previous reports showed a paradoxical protective effect in patients with known CVD referred as “obesity paradox”. Therefore, the aim of the present study was to investigate the association of body mass index (BMI) with coronary artery calcification (CAC) in a large outpatient cardiac CT cohort. METHODS: 4.079 patients who underwent cardiac CT between December 2007–May 2014 were analyzed. BMI and clinical risk factors (current smoking, diabetes mellitus type 2, family history, systolic blood pressure, lipid spectrum) were assessed. Missing values were imputed using multiple imputation. CAC extent was categorized as absent (0), mild (>0–100), moderate (>100–400) and severe (>400). RESULTS: Multivariable multinomial logistic regression analysis, including all risk factors as independent variables, showed no association between BMI and CAC. Using absence of calcification as reference category, the odds ratios per unit increase in BMI were 1.01 for mild; 1.02 for moderate; and 1.00 for severe CAC (p‐values ≥0.103). CONCLUSIONS: No statistically significant association was observed between BMI and CAC after adjustment for other risk factors. John Wiley and Sons Inc. 2022-09-07 /pmc/articles/PMC10073817/ /pubmed/37034565 http://dx.doi.org/10.1002/osp4.636 Text en © 2022 The Authors. Obesity Science & Practice published by World Obesity and The Obesity Society and John Wiley & Sons Ltd. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Original Articles Altintas, Sibel van Workum, Samanta Kok, Madeleine Joosen, Ivo A. P. G. Versteylen, Mathijs O. Nelemans, Patricia J. Wildberger, Joachim E. Crijns, Harry J. G. M. Das, Marco Kietselaer, Bas L. J. H. BMI is not independently associated with coronary artery calcification in a large single‐center CT cohort |
title | BMI is not independently associated with coronary artery calcification in a large single‐center CT cohort |
title_full | BMI is not independently associated with coronary artery calcification in a large single‐center CT cohort |
title_fullStr | BMI is not independently associated with coronary artery calcification in a large single‐center CT cohort |
title_full_unstemmed | BMI is not independently associated with coronary artery calcification in a large single‐center CT cohort |
title_short | BMI is not independently associated with coronary artery calcification in a large single‐center CT cohort |
title_sort | bmi is not independently associated with coronary artery calcification in a large single‐center ct cohort |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10073817/ https://www.ncbi.nlm.nih.gov/pubmed/37034565 http://dx.doi.org/10.1002/osp4.636 |
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