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How the metabolic phenotype in adulthood is affected by long-lasting immunological trajectories since adolescence

A close relationship between immune and metabolic systems has been perceived in the recent past. We aimed to assess whether the immunological trajectories of circulating white blood cells (WBC) started in adolescence, affects the metabolic phenotype in adulthood. We used data from 1183 participants...

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Autores principales: Barroso, Isaac, Guimarães, João Tiago, Craveiro, Vanda, Severo, Milton, Ramos, Elisabete
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9156771/
https://www.ncbi.nlm.nih.gov/pubmed/35641590
http://dx.doi.org/10.1038/s41598-022-13126-z
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author Barroso, Isaac
Guimarães, João Tiago
Craveiro, Vanda
Severo, Milton
Ramos, Elisabete
author_facet Barroso, Isaac
Guimarães, João Tiago
Craveiro, Vanda
Severo, Milton
Ramos, Elisabete
author_sort Barroso, Isaac
collection PubMed
description A close relationship between immune and metabolic systems has been perceived in the recent past. We aimed to assess whether the immunological trajectories of circulating white blood cells (WBC) started in adolescence, affects the metabolic phenotype in adulthood. We used data from 1183 participants of the population-based EPITeen cohort, evaluated at 13, 17, 21, 24 and 27 years of age. The Immunological trajectories from 13 to 27 years old were identified by mixed-effects models, being their association with metabolic features at 27 years old measured by logistic regression. The Higher Inflammatory Activation trajectory (HIA trajectory) had the highest percentage of individuals with metabolic syndrome, while Lowest Levels of WBC trajectory (LLWBC trajectory) showed the lowest percentage. Participants with HIA trajectory had significantly higher triglycerides, waist circumference, serum uric acid and BMI. After adjustment for sex and sports practice and hs-CRP, the odds of having one or more metabolic features in adulthood was significantly lower in LLWBC trajectory. Individuals with immunological trajectories of WBC linked with a pattern of higher immune activation showed a less favorable metabolic profile, while those with the lowest levels of WBC were less likely to have metabolic risk factors in adulthood.
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spelling pubmed-91567712022-06-02 How the metabolic phenotype in adulthood is affected by long-lasting immunological trajectories since adolescence Barroso, Isaac Guimarães, João Tiago Craveiro, Vanda Severo, Milton Ramos, Elisabete Sci Rep Article A close relationship between immune and metabolic systems has been perceived in the recent past. We aimed to assess whether the immunological trajectories of circulating white blood cells (WBC) started in adolescence, affects the metabolic phenotype in adulthood. We used data from 1183 participants of the population-based EPITeen cohort, evaluated at 13, 17, 21, 24 and 27 years of age. The Immunological trajectories from 13 to 27 years old were identified by mixed-effects models, being their association with metabolic features at 27 years old measured by logistic regression. The Higher Inflammatory Activation trajectory (HIA trajectory) had the highest percentage of individuals with metabolic syndrome, while Lowest Levels of WBC trajectory (LLWBC trajectory) showed the lowest percentage. Participants with HIA trajectory had significantly higher triglycerides, waist circumference, serum uric acid and BMI. After adjustment for sex and sports practice and hs-CRP, the odds of having one or more metabolic features in adulthood was significantly lower in LLWBC trajectory. Individuals with immunological trajectories of WBC linked with a pattern of higher immune activation showed a less favorable metabolic profile, while those with the lowest levels of WBC were less likely to have metabolic risk factors in adulthood. Nature Publishing Group UK 2022-05-31 /pmc/articles/PMC9156771/ /pubmed/35641590 http://dx.doi.org/10.1038/s41598-022-13126-z Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Barroso, Isaac
Guimarães, João Tiago
Craveiro, Vanda
Severo, Milton
Ramos, Elisabete
How the metabolic phenotype in adulthood is affected by long-lasting immunological trajectories since adolescence
title How the metabolic phenotype in adulthood is affected by long-lasting immunological trajectories since adolescence
title_full How the metabolic phenotype in adulthood is affected by long-lasting immunological trajectories since adolescence
title_fullStr How the metabolic phenotype in adulthood is affected by long-lasting immunological trajectories since adolescence
title_full_unstemmed How the metabolic phenotype in adulthood is affected by long-lasting immunological trajectories since adolescence
title_short How the metabolic phenotype in adulthood is affected by long-lasting immunological trajectories since adolescence
title_sort how the metabolic phenotype in adulthood is affected by long-lasting immunological trajectories since adolescence
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9156771/
https://www.ncbi.nlm.nih.gov/pubmed/35641590
http://dx.doi.org/10.1038/s41598-022-13126-z
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