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Leptin, but not ghrelin, is associated with food addiction scores in a population-based subject sample

BACKGROUND: Ghrelin and leptin are both peptide hormones and act as opposing players in the regulation of hunger, satiety and energy expenditure. Leptin reduces appetite and feelings of hunger and is secreted mainly by adipocytes, while ghrelin increases appetite and food intake and reduces metaboli...

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Autores principales: Wittekind, Dirk Alexander, Kratzsch, Jürgen, Mergl, Roland, Baber, Ronny, Wirkner, Kerstin, Schroeter, Matthias L., Witte, A. Veronica, Villringer, Arno, Kluge, Michael
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10407557/
https://www.ncbi.nlm.nih.gov/pubmed/37559914
http://dx.doi.org/10.3389/fpsyt.2023.1200021
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author Wittekind, Dirk Alexander
Kratzsch, Jürgen
Mergl, Roland
Baber, Ronny
Wirkner, Kerstin
Schroeter, Matthias L.
Witte, A. Veronica
Villringer, Arno
Kluge, Michael
author_facet Wittekind, Dirk Alexander
Kratzsch, Jürgen
Mergl, Roland
Baber, Ronny
Wirkner, Kerstin
Schroeter, Matthias L.
Witte, A. Veronica
Villringer, Arno
Kluge, Michael
author_sort Wittekind, Dirk Alexander
collection PubMed
description BACKGROUND: Ghrelin and leptin are both peptide hormones and act as opposing players in the regulation of hunger, satiety and energy expenditure. Leptin reduces appetite and feelings of hunger and is secreted mainly by adipocytes, while ghrelin increases appetite and food intake and reduces metabolic rate. Both hormones have been implicated in addictive disorders. Ghrelin was shown to have pro-addictive effects while leptin’s role in addiction yields more conflicting results. Their involvement in the regulation of both food intake and addictive behaviors make them interesting candidates when investigating the regulation of food addiction. However, only few human studies have been performed and large-scale studies are lacking to date. We aimed to investigate the association between total ghrelin and leptin serum levels with scores in the Yale Food Addiction Scale (YFAS). METHODS: Subjects were recruited in the LIFE Adult cohort. 909 subjects were included in the analysis and we performed univariate multiple linear regression models, adjusted for age, sex (in total group analyses only), alcohol consumption, smoking status, BMI scores, cortisol concentrations, Center for Epidemiological Studies Depression Scale (CES-D) and the 7-item Generalized Anxiety Disorder Scale (GAD-7) sum scores. The dependent variable was the YFAS score. RESULTS: In men, leptin serum levels showed a significant positive association (standardized β = 0.146; p = 0.012) with the YFAS score. This finding was confirmed in an extreme-group comparison: men in the highest quartile of leptin levels had significantly higher YFAS sum scores than men in the lowest quartile (1.55 vs. 1.18; p = 0.00014). There was no association with YFAS sum score in the total group (standardized β = −0.002; p = 0.974) or in women (standardized β = −0.034; p = 0.674). Total serum ghrelin showed no association with YFAS sum score neither in the total group (standardized β = −0.043; p = 0.196) nor in men (n = 530; standardized β = −0.063; p = 0.135) or women (n = 379; standardized β = −0.035; p = 0.494). CONCLUSION: Our findings are in line with previous literature and suggest that total ghrelin serum levels are not associated with food addiction scores. Leptin had been previously shown to be associated with food addiction and we confirmed this finding for men in a large, population-based approach.
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spelling pubmed-104075572023-08-09 Leptin, but not ghrelin, is associated with food addiction scores in a population-based subject sample Wittekind, Dirk Alexander Kratzsch, Jürgen Mergl, Roland Baber, Ronny Wirkner, Kerstin Schroeter, Matthias L. Witte, A. Veronica Villringer, Arno Kluge, Michael Front Psychiatry Psychiatry BACKGROUND: Ghrelin and leptin are both peptide hormones and act as opposing players in the regulation of hunger, satiety and energy expenditure. Leptin reduces appetite and feelings of hunger and is secreted mainly by adipocytes, while ghrelin increases appetite and food intake and reduces metabolic rate. Both hormones have been implicated in addictive disorders. Ghrelin was shown to have pro-addictive effects while leptin’s role in addiction yields more conflicting results. Their involvement in the regulation of both food intake and addictive behaviors make them interesting candidates when investigating the regulation of food addiction. However, only few human studies have been performed and large-scale studies are lacking to date. We aimed to investigate the association between total ghrelin and leptin serum levels with scores in the Yale Food Addiction Scale (YFAS). METHODS: Subjects were recruited in the LIFE Adult cohort. 909 subjects were included in the analysis and we performed univariate multiple linear regression models, adjusted for age, sex (in total group analyses only), alcohol consumption, smoking status, BMI scores, cortisol concentrations, Center for Epidemiological Studies Depression Scale (CES-D) and the 7-item Generalized Anxiety Disorder Scale (GAD-7) sum scores. The dependent variable was the YFAS score. RESULTS: In men, leptin serum levels showed a significant positive association (standardized β = 0.146; p = 0.012) with the YFAS score. This finding was confirmed in an extreme-group comparison: men in the highest quartile of leptin levels had significantly higher YFAS sum scores than men in the lowest quartile (1.55 vs. 1.18; p = 0.00014). There was no association with YFAS sum score in the total group (standardized β = −0.002; p = 0.974) or in women (standardized β = −0.034; p = 0.674). Total serum ghrelin showed no association with YFAS sum score neither in the total group (standardized β = −0.043; p = 0.196) nor in men (n = 530; standardized β = −0.063; p = 0.135) or women (n = 379; standardized β = −0.035; p = 0.494). CONCLUSION: Our findings are in line with previous literature and suggest that total ghrelin serum levels are not associated with food addiction scores. Leptin had been previously shown to be associated with food addiction and we confirmed this finding for men in a large, population-based approach. Frontiers Media S.A. 2023-07-25 /pmc/articles/PMC10407557/ /pubmed/37559914 http://dx.doi.org/10.3389/fpsyt.2023.1200021 Text en Copyright © 2023 Wittekind, Kratzsch, Mergl, Baber, Wirkner, Schroeter, Witte, Villringer and Kluge. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Psychiatry
Wittekind, Dirk Alexander
Kratzsch, Jürgen
Mergl, Roland
Baber, Ronny
Wirkner, Kerstin
Schroeter, Matthias L.
Witte, A. Veronica
Villringer, Arno
Kluge, Michael
Leptin, but not ghrelin, is associated with food addiction scores in a population-based subject sample
title Leptin, but not ghrelin, is associated with food addiction scores in a population-based subject sample
title_full Leptin, but not ghrelin, is associated with food addiction scores in a population-based subject sample
title_fullStr Leptin, but not ghrelin, is associated with food addiction scores in a population-based subject sample
title_full_unstemmed Leptin, but not ghrelin, is associated with food addiction scores in a population-based subject sample
title_short Leptin, but not ghrelin, is associated with food addiction scores in a population-based subject sample
title_sort leptin, but not ghrelin, is associated with food addiction scores in a population-based subject sample
topic Psychiatry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10407557/
https://www.ncbi.nlm.nih.gov/pubmed/37559914
http://dx.doi.org/10.3389/fpsyt.2023.1200021
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