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Interplay between adipose tissue secreted proteins, eating behavior and obesity

PURPOSE: Adipokines may play an important role in the complex etiology of human obesity and its metabolic complications. Here, we analyzed the relationship between 15 adipokines, eating behavior and body-mass index (BMI). METHODS: The study included 557 participants of the Sorbs (62.1% women, 37.9%...

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Autores principales: Würfel, Marleen, Breitfeld, Jana, Gebhard, Claudia, Scholz, Markus, Baber, Ronny, Riedel-Heller, Steffi G., Blüher, Matthias, Stumvoll, Michael, Kovacs, Peter, Tönjes, Anke
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8854280/
https://www.ncbi.nlm.nih.gov/pubmed/34636987
http://dx.doi.org/10.1007/s00394-021-02687-w
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author Würfel, Marleen
Breitfeld, Jana
Gebhard, Claudia
Scholz, Markus
Baber, Ronny
Riedel-Heller, Steffi G.
Blüher, Matthias
Stumvoll, Michael
Kovacs, Peter
Tönjes, Anke
author_facet Würfel, Marleen
Breitfeld, Jana
Gebhard, Claudia
Scholz, Markus
Baber, Ronny
Riedel-Heller, Steffi G.
Blüher, Matthias
Stumvoll, Michael
Kovacs, Peter
Tönjes, Anke
author_sort Würfel, Marleen
collection PubMed
description PURPOSE: Adipokines may play an important role in the complex etiology of human obesity and its metabolic complications. Here, we analyzed the relationship between 15 adipokines, eating behavior and body-mass index (BMI). METHODS: The study included 557 participants of the Sorbs (62.1% women, 37.9% men) and 3101 participants of the population-based LIFE-Adult cohorts (53.4% women, 46.4% men) who completed the German version of the Three-Factor-Eating Questionnaire to assess the eating behavior types cognitive restraint, disinhibition and hunger. Serum levels of 15 adipokines, including adiponectin, adipocyte fatty acid-binding protein (AFABP), angiopoietin-related growth factor (AGF), chemerin, fibroblast growth factor (FGF)-19, FGF-21, FGF-23, insulin-like growth factor (IGF)-1, interleukin (IL) 10, irisin, progranulin, vaspin, pro-neurotensin (pro-NT), pro-enkephalin (PENK) and leptin were measured. Based on significant correlations between several adipokines with different eating behavior items and BMI, we conducted mediation analyses, considering the eating behavior items as potential mediation variable towards BMI. RESULTS: Here, we found that the positive association between chemerin, AFABP or leptin and BMI in Sorbian women was mediated by higher restraint or disinhibited eating, respectively. Additionally, in Sorbian women, the negative relation between IGF-1 and BMI was mediated by higher disinhibition and the positive link between AGF and BMI by lower disinhibition. In Sorbian men, the negative relationship between PENK and BMI was mediated by lower disinhibition and hunger, whereas the negative relation between IGF-1 and BMI was mediated by higher hunger. In the LIFE-Adult women´s cohort, associations between chemerin and BMI were mediated by decreased hunger or disinhibition, respectively, whereas relations between PENK and BMI were fully mediated by decreased disinhibition. CONCLUSION: Our study suggests that adipokines such as PENK, IGF-1, chemerin, AGF, AFABP and leptin might affect the development of obesity by directly modifying individual eating behavior. Given the observational nature of the study, future experimental or mechanistic work is warranted. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00394-021-02687-w.
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spelling pubmed-88542802022-02-23 Interplay between adipose tissue secreted proteins, eating behavior and obesity Würfel, Marleen Breitfeld, Jana Gebhard, Claudia Scholz, Markus Baber, Ronny Riedel-Heller, Steffi G. Blüher, Matthias Stumvoll, Michael Kovacs, Peter Tönjes, Anke Eur J Nutr Original Contribution PURPOSE: Adipokines may play an important role in the complex etiology of human obesity and its metabolic complications. Here, we analyzed the relationship between 15 adipokines, eating behavior and body-mass index (BMI). METHODS: The study included 557 participants of the Sorbs (62.1% women, 37.9% men) and 3101 participants of the population-based LIFE-Adult cohorts (53.4% women, 46.4% men) who completed the German version of the Three-Factor-Eating Questionnaire to assess the eating behavior types cognitive restraint, disinhibition and hunger. Serum levels of 15 adipokines, including adiponectin, adipocyte fatty acid-binding protein (AFABP), angiopoietin-related growth factor (AGF), chemerin, fibroblast growth factor (FGF)-19, FGF-21, FGF-23, insulin-like growth factor (IGF)-1, interleukin (IL) 10, irisin, progranulin, vaspin, pro-neurotensin (pro-NT), pro-enkephalin (PENK) and leptin were measured. Based on significant correlations between several adipokines with different eating behavior items and BMI, we conducted mediation analyses, considering the eating behavior items as potential mediation variable towards BMI. RESULTS: Here, we found that the positive association between chemerin, AFABP or leptin and BMI in Sorbian women was mediated by higher restraint or disinhibited eating, respectively. Additionally, in Sorbian women, the negative relation between IGF-1 and BMI was mediated by higher disinhibition and the positive link between AGF and BMI by lower disinhibition. In Sorbian men, the negative relationship between PENK and BMI was mediated by lower disinhibition and hunger, whereas the negative relation between IGF-1 and BMI was mediated by higher hunger. In the LIFE-Adult women´s cohort, associations between chemerin and BMI were mediated by decreased hunger or disinhibition, respectively, whereas relations between PENK and BMI were fully mediated by decreased disinhibition. CONCLUSION: Our study suggests that adipokines such as PENK, IGF-1, chemerin, AGF, AFABP and leptin might affect the development of obesity by directly modifying individual eating behavior. Given the observational nature of the study, future experimental or mechanistic work is warranted. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00394-021-02687-w. Springer Berlin Heidelberg 2021-10-12 2022 /pmc/articles/PMC8854280/ /pubmed/34636987 http://dx.doi.org/10.1007/s00394-021-02687-w Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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 Original Contribution
Würfel, Marleen
Breitfeld, Jana
Gebhard, Claudia
Scholz, Markus
Baber, Ronny
Riedel-Heller, Steffi G.
Blüher, Matthias
Stumvoll, Michael
Kovacs, Peter
Tönjes, Anke
Interplay between adipose tissue secreted proteins, eating behavior and obesity
title Interplay between adipose tissue secreted proteins, eating behavior and obesity
title_full Interplay between adipose tissue secreted proteins, eating behavior and obesity
title_fullStr Interplay between adipose tissue secreted proteins, eating behavior and obesity
title_full_unstemmed Interplay between adipose tissue secreted proteins, eating behavior and obesity
title_short Interplay between adipose tissue secreted proteins, eating behavior and obesity
title_sort interplay between adipose tissue secreted proteins, eating behavior and obesity
topic Original Contribution
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8854280/
https://www.ncbi.nlm.nih.gov/pubmed/34636987
http://dx.doi.org/10.1007/s00394-021-02687-w
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