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Body Fat Distribution and Systolic Blood Pressure in 10,000 Adults with Whole‐Body Imaging: UK Biobank and Oxford BioBank

OBJECTIVE: This study aimed to quantify the associations of regional fat mass and fat‐free mass with systolic blood pressure. METHODS: This analysis combined individual participant data from two large‐scale imaging studies: UK Biobank and Oxford BioBank. In both studies, participants were interviewe...

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Autores principales: Malden, Deborah, Lacey, Ben, Emberson, Jonathan, Karpe, Fredrik, Allen, Naomi, Bennett, Derrick, Lewington, Sarah
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6618903/
https://www.ncbi.nlm.nih.gov/pubmed/31081601
http://dx.doi.org/10.1002/oby.22509
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author Malden, Deborah
Lacey, Ben
Emberson, Jonathan
Karpe, Fredrik
Allen, Naomi
Bennett, Derrick
Lewington, Sarah
author_facet Malden, Deborah
Lacey, Ben
Emberson, Jonathan
Karpe, Fredrik
Allen, Naomi
Bennett, Derrick
Lewington, Sarah
author_sort Malden, Deborah
collection PubMed
description OBJECTIVE: This study aimed to quantify the associations of regional fat mass and fat‐free mass with systolic blood pressure. METHODS: This analysis combined individual participant data from two large‐scale imaging studies: UK Biobank and Oxford BioBank. In both studies, participants were interviewed and measured, and they underwent dual‐energy x‐ray absorptiometry imaging. Linear regression was used to relate systolic blood pressure to anthropometric measures of adiposity (BMI, waist circumference, and waist to hip ratio) and dual‐energy x‐ray absorptiometry–derived measures of body composition (visceral android fat, subcutaneous android fat, subcutaneous gynoid fat, and fat‐free mass). RESULTS: Among 10,260 participants (mean age 49; 96% white), systolic blood pressure was positively associated with visceral android fat (3.2 mmHg/SD in men; 2.8 mmHg/SD in women) and fat‐free mass (1.92 mmHg/SD in men; 1.64 mmHg/SD in women), but there was no evidence of an association with subcutaneous android or gynoid fat. Associations of systolic blood pressure with BMI were slightly steeper than those with waist circumference or waist to hip ratio; these associations remained unchanged following adjustment for fat‐free mass, but adjustment for visceral android fat eliminated associations with waist circumference and waist to hip ratio and more than halved associations with BMI. CONCLUSIONS: This analysis indicates that visceral fat is the primary etiological component of excess adiposity underlying the development of adiposity‐related hypertension.
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spelling pubmed-66189032019-07-22 Body Fat Distribution and Systolic Blood Pressure in 10,000 Adults with Whole‐Body Imaging: UK Biobank and Oxford BioBank Malden, Deborah Lacey, Ben Emberson, Jonathan Karpe, Fredrik Allen, Naomi Bennett, Derrick Lewington, Sarah Obesity (Silver Spring) Original Articles OBJECTIVE: This study aimed to quantify the associations of regional fat mass and fat‐free mass with systolic blood pressure. METHODS: This analysis combined individual participant data from two large‐scale imaging studies: UK Biobank and Oxford BioBank. In both studies, participants were interviewed and measured, and they underwent dual‐energy x‐ray absorptiometry imaging. Linear regression was used to relate systolic blood pressure to anthropometric measures of adiposity (BMI, waist circumference, and waist to hip ratio) and dual‐energy x‐ray absorptiometry–derived measures of body composition (visceral android fat, subcutaneous android fat, subcutaneous gynoid fat, and fat‐free mass). RESULTS: Among 10,260 participants (mean age 49; 96% white), systolic blood pressure was positively associated with visceral android fat (3.2 mmHg/SD in men; 2.8 mmHg/SD in women) and fat‐free mass (1.92 mmHg/SD in men; 1.64 mmHg/SD in women), but there was no evidence of an association with subcutaneous android or gynoid fat. Associations of systolic blood pressure with BMI were slightly steeper than those with waist circumference or waist to hip ratio; these associations remained unchanged following adjustment for fat‐free mass, but adjustment for visceral android fat eliminated associations with waist circumference and waist to hip ratio and more than halved associations with BMI. CONCLUSIONS: This analysis indicates that visceral fat is the primary etiological component of excess adiposity underlying the development of adiposity‐related hypertension. John Wiley and Sons Inc. 2019-05-13 2019-07 /pmc/articles/PMC6618903/ /pubmed/31081601 http://dx.doi.org/10.1002/oby.22509 Text en © 2019 The Authors. Obesity published by Wiley Periodicals, Inc. on behalf of The Obesity Society (TOS) This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Malden, Deborah
Lacey, Ben
Emberson, Jonathan
Karpe, Fredrik
Allen, Naomi
Bennett, Derrick
Lewington, Sarah
Body Fat Distribution and Systolic Blood Pressure in 10,000 Adults with Whole‐Body Imaging: UK Biobank and Oxford BioBank
title Body Fat Distribution and Systolic Blood Pressure in 10,000 Adults with Whole‐Body Imaging: UK Biobank and Oxford BioBank
title_full Body Fat Distribution and Systolic Blood Pressure in 10,000 Adults with Whole‐Body Imaging: UK Biobank and Oxford BioBank
title_fullStr Body Fat Distribution and Systolic Blood Pressure in 10,000 Adults with Whole‐Body Imaging: UK Biobank and Oxford BioBank
title_full_unstemmed Body Fat Distribution and Systolic Blood Pressure in 10,000 Adults with Whole‐Body Imaging: UK Biobank and Oxford BioBank
title_short Body Fat Distribution and Systolic Blood Pressure in 10,000 Adults with Whole‐Body Imaging: UK Biobank and Oxford BioBank
title_sort body fat distribution and systolic blood pressure in 10,000 adults with whole‐body imaging: uk biobank and oxford biobank
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6618903/
https://www.ncbi.nlm.nih.gov/pubmed/31081601
http://dx.doi.org/10.1002/oby.22509
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