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Overweight/obesity in young adulthood interacts with aspects of EBV infection in MS etiology

OBJECTIVE: Because obesity affects the cellular immune response to infections, we aimed to investigate whether high body mass index (BMI) in young adulthood and high Epstein-Barr nuclear antigen 1 (EBNA-1) antibody levels interact with regard to MS risk. We also aimed at exploring potential 3-way in...

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Autores principales: Hedström, Anna Karin, Brenner, Nicole, Butt, Julia, Hillert, Jan, Waterboer, Tim, Olsson, Tomas, Alfredsson, Lars
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7803338/
https://www.ncbi.nlm.nih.gov/pubmed/33465039
http://dx.doi.org/10.1212/NXI.0000000000000912
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author Hedström, Anna Karin
Brenner, Nicole
Butt, Julia
Hillert, Jan
Waterboer, Tim
Olsson, Tomas
Alfredsson, Lars
author_facet Hedström, Anna Karin
Brenner, Nicole
Butt, Julia
Hillert, Jan
Waterboer, Tim
Olsson, Tomas
Alfredsson, Lars
author_sort Hedström, Anna Karin
collection PubMed
description OBJECTIVE: Because obesity affects the cellular immune response to infections, we aimed to investigate whether high body mass index (BMI) in young adulthood and high Epstein-Barr nuclear antigen 1 (EBNA-1) antibody levels interact with regard to MS risk. We also aimed at exploring potential 3-way interactions between BMI at age 20 years, aspects of Epstein-Barr virus (EBV) infection (high EBNA-1 antibody levels and infectious mononucleosis [IM] history, respectively) and the human leukocyte antigen (HLA)-DRB1*15:01 allele. METHODS: Using Swedish population-based case-control studies (5,460 cases and 7,275 controls), we assessed MS risk in relation to interactions between overweight/obesity at age 20 years, IM history, EBNA-1 levels, and HLA-DRB1*15:01 status by calculating ORs with 95% CIs using logistic regression. Potential interactions were evaluated on the additive scale. RESULTS: Overweight/obesity, compared with normal weight, interacted significantly with high (>50th percentile) EBNA-1 antibody levels (attributable proportion due to interaction 0.2, 95% CI 0.1–0.4). The strength of the interaction increased with higher category of EBNA-1 antibody levels. Furthermore, 3-way interactions were present between HLA-DRB1*15:01, overweight/obesity at age 20 years, and each aspect of EBV infection. CONCLUSIONS: With regard to MS risk, overweight/obesity in young adulthood acts synergistically with both aspects of EBV infection, predominantly among those with a genetic susceptibility to the disease. The obese state both induces a chronic immune-mediated inflammation and affects the cellular immune response to infections, which may contribute to explain our findings.
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spelling pubmed-78033382021-01-13 Overweight/obesity in young adulthood interacts with aspects of EBV infection in MS etiology Hedström, Anna Karin Brenner, Nicole Butt, Julia Hillert, Jan Waterboer, Tim Olsson, Tomas Alfredsson, Lars Neurol Neuroimmunol Neuroinflamm Article OBJECTIVE: Because obesity affects the cellular immune response to infections, we aimed to investigate whether high body mass index (BMI) in young adulthood and high Epstein-Barr nuclear antigen 1 (EBNA-1) antibody levels interact with regard to MS risk. We also aimed at exploring potential 3-way interactions between BMI at age 20 years, aspects of Epstein-Barr virus (EBV) infection (high EBNA-1 antibody levels and infectious mononucleosis [IM] history, respectively) and the human leukocyte antigen (HLA)-DRB1*15:01 allele. METHODS: Using Swedish population-based case-control studies (5,460 cases and 7,275 controls), we assessed MS risk in relation to interactions between overweight/obesity at age 20 years, IM history, EBNA-1 levels, and HLA-DRB1*15:01 status by calculating ORs with 95% CIs using logistic regression. Potential interactions were evaluated on the additive scale. RESULTS: Overweight/obesity, compared with normal weight, interacted significantly with high (>50th percentile) EBNA-1 antibody levels (attributable proportion due to interaction 0.2, 95% CI 0.1–0.4). The strength of the interaction increased with higher category of EBNA-1 antibody levels. Furthermore, 3-way interactions were present between HLA-DRB1*15:01, overweight/obesity at age 20 years, and each aspect of EBV infection. CONCLUSIONS: With regard to MS risk, overweight/obesity in young adulthood acts synergistically with both aspects of EBV infection, predominantly among those with a genetic susceptibility to the disease. The obese state both induces a chronic immune-mediated inflammation and affects the cellular immune response to infections, which may contribute to explain our findings. Lippincott Williams & Wilkins 2020-12-15 /pmc/articles/PMC7803338/ /pubmed/33465039 http://dx.doi.org/10.1212/NXI.0000000000000912 Text en Copyright © 2020 The Author(s). Published by Wolters Kluwer Health, Inc. on behalf of the American Academy of Neurology. This is an open access article distributed under the terms of the Creative Commons Attribution License 4.0 (CC BY) (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Article
Hedström, Anna Karin
Brenner, Nicole
Butt, Julia
Hillert, Jan
Waterboer, Tim
Olsson, Tomas
Alfredsson, Lars
Overweight/obesity in young adulthood interacts with aspects of EBV infection in MS etiology
title Overweight/obesity in young adulthood interacts with aspects of EBV infection in MS etiology
title_full Overweight/obesity in young adulthood interacts with aspects of EBV infection in MS etiology
title_fullStr Overweight/obesity in young adulthood interacts with aspects of EBV infection in MS etiology
title_full_unstemmed Overweight/obesity in young adulthood interacts with aspects of EBV infection in MS etiology
title_short Overweight/obesity in young adulthood interacts with aspects of EBV infection in MS etiology
title_sort overweight/obesity in young adulthood interacts with aspects of ebv infection in ms etiology
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7803338/
https://www.ncbi.nlm.nih.gov/pubmed/33465039
http://dx.doi.org/10.1212/NXI.0000000000000912
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