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Serum Levels of Hormones Regulating Appetite in Patients with Fetal Alcohol Spectrum Disorders

Prenatal alcohol exposure is the cause of impaired growth and a wide range of developmental and behavioral disorders in the child. Improper eating patterns are commonly associated with fetal alcohol spectrum disorders (FASD) and may contribute to poor nutrition and growth restriction. To date, there...

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Autores principales: Podgórski, Rafał, Galiniak, Sabina, Mazur, Artur, Podgórska, Dominika, Domin, Agnieszka
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10574197/
https://www.ncbi.nlm.nih.gov/pubmed/37836499
http://dx.doi.org/10.3390/nu15194215
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author Podgórski, Rafał
Galiniak, Sabina
Mazur, Artur
Podgórska, Dominika
Domin, Agnieszka
author_facet Podgórski, Rafał
Galiniak, Sabina
Mazur, Artur
Podgórska, Dominika
Domin, Agnieszka
author_sort Podgórski, Rafał
collection PubMed
description Prenatal alcohol exposure is the cause of impaired growth and a wide range of developmental and behavioral disorders in the child. Improper eating patterns are commonly associated with fetal alcohol spectrum disorders (FASD) and may contribute to poor nutrition and growth restriction. To date, there have been only a few studies investigating the hormonal regulation of appetite in patients with FASD. We analyzed the levels of neuropeptide Y (NPY), Agouti signaling protein (ASP), alpha-melanocyte-stimulating hormone (α-MSH), and kisspeptin (KISS1) in 57 patients with FASD and 23 healthy controls. A comparison of the hormone levels studied was also performed in subgroups of fetal alcohol syndrome (FAS) and neurobehavioral disorder associated with prenatal alcohol exposure (ND PAE), as well as in males and females. We have found no differences in hormone levels tested between affected individuals and the controls and between FASD subgroups. In addition, sex had no effect on hormone levels. However, we identified some associations between hormone concentrations and parameters describing the clinical status of patients with FASD. Most of them concerned ASP, which has shown a positive correlation with age and hormones involved in appetite and metabolism, such as proopiomelanocortin (POMC) and adrenocorticotropic hormone (ACTH). We have also found a negative correlation of α-MSH with age, BMI percentile, and glycated hemoglobin (HbA1c). Furthermore, we found a weak negative correlation of NPY with HbA1c. Although FASD has been associated with impaired child growth and development, including nutrition and puberty onset, we did not identify differences in the levels of the hormones studied, which may suggest that prenatal alcohol exposure does not affect the levels of these metabolites.
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spelling pubmed-105741972023-10-14 Serum Levels of Hormones Regulating Appetite in Patients with Fetal Alcohol Spectrum Disorders Podgórski, Rafał Galiniak, Sabina Mazur, Artur Podgórska, Dominika Domin, Agnieszka Nutrients Article Prenatal alcohol exposure is the cause of impaired growth and a wide range of developmental and behavioral disorders in the child. Improper eating patterns are commonly associated with fetal alcohol spectrum disorders (FASD) and may contribute to poor nutrition and growth restriction. To date, there have been only a few studies investigating the hormonal regulation of appetite in patients with FASD. We analyzed the levels of neuropeptide Y (NPY), Agouti signaling protein (ASP), alpha-melanocyte-stimulating hormone (α-MSH), and kisspeptin (KISS1) in 57 patients with FASD and 23 healthy controls. A comparison of the hormone levels studied was also performed in subgroups of fetal alcohol syndrome (FAS) and neurobehavioral disorder associated with prenatal alcohol exposure (ND PAE), as well as in males and females. We have found no differences in hormone levels tested between affected individuals and the controls and between FASD subgroups. In addition, sex had no effect on hormone levels. However, we identified some associations between hormone concentrations and parameters describing the clinical status of patients with FASD. Most of them concerned ASP, which has shown a positive correlation with age and hormones involved in appetite and metabolism, such as proopiomelanocortin (POMC) and adrenocorticotropic hormone (ACTH). We have also found a negative correlation of α-MSH with age, BMI percentile, and glycated hemoglobin (HbA1c). Furthermore, we found a weak negative correlation of NPY with HbA1c. Although FASD has been associated with impaired child growth and development, including nutrition and puberty onset, we did not identify differences in the levels of the hormones studied, which may suggest that prenatal alcohol exposure does not affect the levels of these metabolites. MDPI 2023-09-29 /pmc/articles/PMC10574197/ /pubmed/37836499 http://dx.doi.org/10.3390/nu15194215 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Podgórski, Rafał
Galiniak, Sabina
Mazur, Artur
Podgórska, Dominika
Domin, Agnieszka
Serum Levels of Hormones Regulating Appetite in Patients with Fetal Alcohol Spectrum Disorders
title Serum Levels of Hormones Regulating Appetite in Patients with Fetal Alcohol Spectrum Disorders
title_full Serum Levels of Hormones Regulating Appetite in Patients with Fetal Alcohol Spectrum Disorders
title_fullStr Serum Levels of Hormones Regulating Appetite in Patients with Fetal Alcohol Spectrum Disorders
title_full_unstemmed Serum Levels of Hormones Regulating Appetite in Patients with Fetal Alcohol Spectrum Disorders
title_short Serum Levels of Hormones Regulating Appetite in Patients with Fetal Alcohol Spectrum Disorders
title_sort serum levels of hormones regulating appetite in patients with fetal alcohol spectrum disorders
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10574197/
https://www.ncbi.nlm.nih.gov/pubmed/37836499
http://dx.doi.org/10.3390/nu15194215
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