Could vitamin D reduce obesity-associated inflammation?:observational and Mendelian randomization study

Abstract Background: Obesity is associated with inflammation but the role of vitamin D in this process is not clear. Objectives: We aimed to assess the associations between serum 25-hydroxyvitamin D [25(OH)D], BMI, and 16 inflammatory biomarkers, and to assess the role of vitamin D as a potential me...

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Main Authors: Palaniswamy, S. (Saranya), Gill, D. (Dipender), De Silva, N. M. (N. Maneka), Lowry, E. (Estelle), Jokelainen, J. (Jari), Karhu, T. (Toni), Mutt, S. J. (Shivaprakash J.), Dehghan, A. (Abbas), Sliz, E. (Eeva), Chasman, D. I. (Daniel I.), Timonen, M. (Markku), Viinamäki, H. (Heimo), Keinänen-Kiukaanniemi, S. (Sirkka), Hyppönen, E. (Elina), Herzig, K.-H. (Karl-Heinz), Sebert, S. (Sylvain), Järvelin, M.-R. (Marjo-Riitta)
Format: Article in Journal/Newspaper
Language:English
Published: Oxford University Press 2020
Subjects:
BMI
Online Access:http://urn.fi/urn:nbn:fi-fe2020070646938
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spelling ftunivoulu:oai:oulu.fi:nbnfi-fe2020070646938 2023-07-30T04:05:50+02:00 Could vitamin D reduce obesity-associated inflammation?:observational and Mendelian randomization study Palaniswamy, S. (Saranya) Gill, D. (Dipender) De Silva, N. M. (N. Maneka) Lowry, E. (Estelle) Jokelainen, J. (Jari) Karhu, T. (Toni) Mutt, S. J. (Shivaprakash J.) Dehghan, A. (Abbas) Sliz, E. (Eeva) Chasman, D. I. (Daniel I.) Timonen, M. (Markku) Viinamäki, H. (Heimo) Keinänen-Kiukaanniemi, S. (Sirkka) Hyppönen, E. (Elina) Herzig, K.-H. (Karl-Heinz) Sebert, S. (Sylvain) Järvelin, M.-R. (Marjo-Riitta) 2020 application/pdf http://urn.fi/urn:nbn:fi-fe2020070646938 eng eng Oxford University Press info:eu-repo/grantAgreement/EC/H2020/633595/EU/Understanding the dynamic determinants of glucose homeostasis and social capability to promote Healthy and active aging/DYNAHEALTH info:eu-repo/grantAgreement/EC/H2020/733206/EU/Early-life stressors and LifeCycle health/LIFECYCLE info:eu-repo/grantAgreement/EC/H2020/643774/EU/Family-based intervention to improve healthy lifestyle and prevent Type 2 Diabetes amongst South Asians with central obesity and prediabetes/iHealth-T2D info:eu-repo/semantics/openAccess © The Author(s) 2020. This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com https://creativecommons.org/licenses/by-nc/4.0/ 25(OH)D BMI Mendelian randomization inflammation mediation obesity vitamin D info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion 2020 ftunivoulu 2023-07-08T19:56:58Z Abstract Background: Obesity is associated with inflammation but the role of vitamin D in this process is not clear. Objectives: We aimed to assess the associations between serum 25-hydroxyvitamin D [25(OH)D], BMI, and 16 inflammatory biomarkers, and to assess the role of vitamin D as a potential mediator in the association between higher BMI and inflammation. Methods: Northern Finland Birth Cohort 1966 (NFBC1966) 31-y data on 3586 individuals were analyzed to examine the observational associations between BMI, 25(OH)D, and 16 inflammatory biomarkers. Multivariable regression analyses and 2-sample regression-based Mendelian randomization (MR) mediation analysis were performed to assess any role of vitamin D in mediating a causal effect of BMI on inflammatory biomarkers [soluble intercellular adhesion molecule 1 (sICAM-1), high sensitivity C-reactive protein (hs-CRP), and α1-acid glycoprotein (AGP)] for which observational associations were detected. For MR, genome-wide association study summary results ranging from 5163 to 806,834 individuals were used for biomarkers, 25(OH)D, and BMI. Findings were triangulated with a literature review of vitamin D supplementation trials. Results: In NFBC1966, mean BMI (kg/m²) was 24.8 (95% CI: 24.7, 25.0) and mean 25(OH)D was 50.3 nmol/L (95% CI: 49.8, 50.7 nmol/L). Inflammatory biomarkers correlated as 4 independent clusters: interleukins, adhesion molecules, acute-phase proteins, and chemokines. BMI was positively associated with 9 inflammatory biomarkers and inversely with 25(OH)D (false discovery rate < 0.05). 25(OH)D was inversely associated with sICAM-1, hs-CRP, and AGP, which were positively associated with BMI. The MR analyses showed causal association of BMI on these 3 inflammatory biomarkers. There was no observational or MR evidence that circulating 25(OH)D concentrations mediated the association between BMI and these 3 inflammatory markers. Review of randomized controlled trials (RCTs) supported our findings showing no impact of vitamin D supplementation on ... Article in Journal/Newspaper Northern Finland Jultika - University of Oulu repository
institution Open Polar
collection Jultika - University of Oulu repository
op_collection_id ftunivoulu
language English
topic 25(OH)D
BMI
Mendelian randomization
inflammation
mediation
obesity
vitamin D
spellingShingle 25(OH)D
BMI
Mendelian randomization
inflammation
mediation
obesity
vitamin D
Palaniswamy, S. (Saranya)
Gill, D. (Dipender)
De Silva, N. M. (N. Maneka)
Lowry, E. (Estelle)
Jokelainen, J. (Jari)
Karhu, T. (Toni)
Mutt, S. J. (Shivaprakash J.)
Dehghan, A. (Abbas)
Sliz, E. (Eeva)
Chasman, D. I. (Daniel I.)
Timonen, M. (Markku)
Viinamäki, H. (Heimo)
Keinänen-Kiukaanniemi, S. (Sirkka)
Hyppönen, E. (Elina)
Herzig, K.-H. (Karl-Heinz)
Sebert, S. (Sylvain)
Järvelin, M.-R. (Marjo-Riitta)
Could vitamin D reduce obesity-associated inflammation?:observational and Mendelian randomization study
topic_facet 25(OH)D
BMI
Mendelian randomization
inflammation
mediation
obesity
vitamin D
description Abstract Background: Obesity is associated with inflammation but the role of vitamin D in this process is not clear. Objectives: We aimed to assess the associations between serum 25-hydroxyvitamin D [25(OH)D], BMI, and 16 inflammatory biomarkers, and to assess the role of vitamin D as a potential mediator in the association between higher BMI and inflammation. Methods: Northern Finland Birth Cohort 1966 (NFBC1966) 31-y data on 3586 individuals were analyzed to examine the observational associations between BMI, 25(OH)D, and 16 inflammatory biomarkers. Multivariable regression analyses and 2-sample regression-based Mendelian randomization (MR) mediation analysis were performed to assess any role of vitamin D in mediating a causal effect of BMI on inflammatory biomarkers [soluble intercellular adhesion molecule 1 (sICAM-1), high sensitivity C-reactive protein (hs-CRP), and α1-acid glycoprotein (AGP)] for which observational associations were detected. For MR, genome-wide association study summary results ranging from 5163 to 806,834 individuals were used for biomarkers, 25(OH)D, and BMI. Findings were triangulated with a literature review of vitamin D supplementation trials. Results: In NFBC1966, mean BMI (kg/m²) was 24.8 (95% CI: 24.7, 25.0) and mean 25(OH)D was 50.3 nmol/L (95% CI: 49.8, 50.7 nmol/L). Inflammatory biomarkers correlated as 4 independent clusters: interleukins, adhesion molecules, acute-phase proteins, and chemokines. BMI was positively associated with 9 inflammatory biomarkers and inversely with 25(OH)D (false discovery rate < 0.05). 25(OH)D was inversely associated with sICAM-1, hs-CRP, and AGP, which were positively associated with BMI. The MR analyses showed causal association of BMI on these 3 inflammatory biomarkers. There was no observational or MR evidence that circulating 25(OH)D concentrations mediated the association between BMI and these 3 inflammatory markers. Review of randomized controlled trials (RCTs) supported our findings showing no impact of vitamin D supplementation on ...
format Article in Journal/Newspaper
author Palaniswamy, S. (Saranya)
Gill, D. (Dipender)
De Silva, N. M. (N. Maneka)
Lowry, E. (Estelle)
Jokelainen, J. (Jari)
Karhu, T. (Toni)
Mutt, S. J. (Shivaprakash J.)
Dehghan, A. (Abbas)
Sliz, E. (Eeva)
Chasman, D. I. (Daniel I.)
Timonen, M. (Markku)
Viinamäki, H. (Heimo)
Keinänen-Kiukaanniemi, S. (Sirkka)
Hyppönen, E. (Elina)
Herzig, K.-H. (Karl-Heinz)
Sebert, S. (Sylvain)
Järvelin, M.-R. (Marjo-Riitta)
author_facet Palaniswamy, S. (Saranya)
Gill, D. (Dipender)
De Silva, N. M. (N. Maneka)
Lowry, E. (Estelle)
Jokelainen, J. (Jari)
Karhu, T. (Toni)
Mutt, S. J. (Shivaprakash J.)
Dehghan, A. (Abbas)
Sliz, E. (Eeva)
Chasman, D. I. (Daniel I.)
Timonen, M. (Markku)
Viinamäki, H. (Heimo)
Keinänen-Kiukaanniemi, S. (Sirkka)
Hyppönen, E. (Elina)
Herzig, K.-H. (Karl-Heinz)
Sebert, S. (Sylvain)
Järvelin, M.-R. (Marjo-Riitta)
author_sort Palaniswamy, S. (Saranya)
title Could vitamin D reduce obesity-associated inflammation?:observational and Mendelian randomization study
title_short Could vitamin D reduce obesity-associated inflammation?:observational and Mendelian randomization study
title_full Could vitamin D reduce obesity-associated inflammation?:observational and Mendelian randomization study
title_fullStr Could vitamin D reduce obesity-associated inflammation?:observational and Mendelian randomization study
title_full_unstemmed Could vitamin D reduce obesity-associated inflammation?:observational and Mendelian randomization study
title_sort could vitamin d reduce obesity-associated inflammation?:observational and mendelian randomization study
publisher Oxford University Press
publishDate 2020
url http://urn.fi/urn:nbn:fi-fe2020070646938
genre Northern Finland
genre_facet Northern Finland
op_relation info:eu-repo/grantAgreement/EC/H2020/633595/EU/Understanding the dynamic determinants of glucose homeostasis and social capability to promote Healthy and active aging/DYNAHEALTH
info:eu-repo/grantAgreement/EC/H2020/733206/EU/Early-life stressors and LifeCycle health/LIFECYCLE
info:eu-repo/grantAgreement/EC/H2020/643774/EU/Family-based intervention to improve healthy lifestyle and prevent Type 2 Diabetes amongst South Asians with central obesity and prediabetes/iHealth-T2D
op_rights info:eu-repo/semantics/openAccess
© The Author(s) 2020. This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
https://creativecommons.org/licenses/by-nc/4.0/
_version_ 1772818091401543680