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Sparse System Identification of Leptin Dynamics in Women With Obesity

The prevalence of obesity is increasing around the world at an alarming rate. The interplay of the hormone leptin with the hypothalamus-pituitary-adrenal axis plays an important role in regulating energy balance, thereby contributing to obesity. This study presents a mathematical model, which descri...

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Autores principales: Amin, Md. Rafiul, Pednekar, Divesh Deepak, Azgomi, Hamid Fekri, van Wietmarschen, Herman, Aschbacher, Kirstin, Faghih, Rose T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9037068/
https://www.ncbi.nlm.nih.gov/pubmed/35480480
http://dx.doi.org/10.3389/fendo.2022.769951
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author Amin, Md. Rafiul
Pednekar, Divesh Deepak
Azgomi, Hamid Fekri
van Wietmarschen, Herman
Aschbacher, Kirstin
Faghih, Rose T.
author_facet Amin, Md. Rafiul
Pednekar, Divesh Deepak
Azgomi, Hamid Fekri
van Wietmarschen, Herman
Aschbacher, Kirstin
Faghih, Rose T.
author_sort Amin, Md. Rafiul
collection PubMed
description The prevalence of obesity is increasing around the world at an alarming rate. The interplay of the hormone leptin with the hypothalamus-pituitary-adrenal axis plays an important role in regulating energy balance, thereby contributing to obesity. This study presents a mathematical model, which describes hormonal behavior leading to an energy abnormal equilibrium that contributes to obesity. To this end, we analyze the behavior of two neuroendocrine hormones, leptin and cortisol, in a cohort of women with obesity, with simplified minimal state-space modeling. Using a system theoretic approach, coordinate descent method, and sparse recovery, we deconvolved the serum leptin-cortisol levels. Accordingly, we estimate the secretion patterns, timings, amplitudes, number of underlying pulses, infusion, and clearance rates of hormones in eighteen premenopausal women with obesity. Our results show that minimal state-space model was able to successfully capture the leptin and cortisol sparse dynamics with the multiple correlation coefficients greater than 0.83 and 0.87, respectively. Furthermore, the Granger causality test demonstrated a negative prospective predictive relationship between leptin and cortisol, 14 of 18 women. These results indicate that increases in cortisol are prospectively associated with reductions in leptin and vice versa, suggesting a bidirectional negative inhibitory relationship. As dysregulation of leptin may result in an abnormality in satiety and thereby associated to obesity, the investigation of leptin-cortisol sparse dynamics may offer a better diagnostic methodology to improve better treatments plans for individuals with obesity.
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spelling pubmed-90370682022-04-26 Sparse System Identification of Leptin Dynamics in Women With Obesity Amin, Md. Rafiul Pednekar, Divesh Deepak Azgomi, Hamid Fekri van Wietmarschen, Herman Aschbacher, Kirstin Faghih, Rose T. Front Endocrinol (Lausanne) Endocrinology The prevalence of obesity is increasing around the world at an alarming rate. The interplay of the hormone leptin with the hypothalamus-pituitary-adrenal axis plays an important role in regulating energy balance, thereby contributing to obesity. This study presents a mathematical model, which describes hormonal behavior leading to an energy abnormal equilibrium that contributes to obesity. To this end, we analyze the behavior of two neuroendocrine hormones, leptin and cortisol, in a cohort of women with obesity, with simplified minimal state-space modeling. Using a system theoretic approach, coordinate descent method, and sparse recovery, we deconvolved the serum leptin-cortisol levels. Accordingly, we estimate the secretion patterns, timings, amplitudes, number of underlying pulses, infusion, and clearance rates of hormones in eighteen premenopausal women with obesity. Our results show that minimal state-space model was able to successfully capture the leptin and cortisol sparse dynamics with the multiple correlation coefficients greater than 0.83 and 0.87, respectively. Furthermore, the Granger causality test demonstrated a negative prospective predictive relationship between leptin and cortisol, 14 of 18 women. These results indicate that increases in cortisol are prospectively associated with reductions in leptin and vice versa, suggesting a bidirectional negative inhibitory relationship. As dysregulation of leptin may result in an abnormality in satiety and thereby associated to obesity, the investigation of leptin-cortisol sparse dynamics may offer a better diagnostic methodology to improve better treatments plans for individuals with obesity. Frontiers Media S.A. 2022-04-05 /pmc/articles/PMC9037068/ /pubmed/35480480 http://dx.doi.org/10.3389/fendo.2022.769951 Text en Copyright © 2022 Amin, Pednekar, Azgomi, van Wietmarschen, Aschbacher and Faghih 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 Endocrinology
Amin, Md. Rafiul
Pednekar, Divesh Deepak
Azgomi, Hamid Fekri
van Wietmarschen, Herman
Aschbacher, Kirstin
Faghih, Rose T.
Sparse System Identification of Leptin Dynamics in Women With Obesity
title Sparse System Identification of Leptin Dynamics in Women With Obesity
title_full Sparse System Identification of Leptin Dynamics in Women With Obesity
title_fullStr Sparse System Identification of Leptin Dynamics in Women With Obesity
title_full_unstemmed Sparse System Identification of Leptin Dynamics in Women With Obesity
title_short Sparse System Identification of Leptin Dynamics in Women With Obesity
title_sort sparse system identification of leptin dynamics in women with obesity
topic Endocrinology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9037068/
https://www.ncbi.nlm.nih.gov/pubmed/35480480
http://dx.doi.org/10.3389/fendo.2022.769951
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