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Essential Fatty Acid Deficiency Associates with Growth Faltering and Environmental Enteric Dysfunction in Children

Environmental enteric dysfunction (EED) is characterized by intestinal inflammation, malabsorption and growth-faltering in children with heightened exposure to gut pathogens. The aim of this study was to characterize serum non-esterified fatty acids (NEFA), in association with childhood undernutriti...

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Autores principales: Narvaez-Rivas, Monica, Setchell, Kenneth D. R., Galandi, Stephanie L., Zhao, Xueheng, Iqbal, Najeeha Talat, Ahmed, Sheraz, Iqbal, Junaid, Syed, Sana, Ali, Syed Asad, Moore, Sean R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10142200/
https://www.ncbi.nlm.nih.gov/pubmed/37110148
http://dx.doi.org/10.3390/metabo13040489
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author Narvaez-Rivas, Monica
Setchell, Kenneth D. R.
Galandi, Stephanie L.
Zhao, Xueheng
Iqbal, Najeeha Talat
Ahmed, Sheraz
Iqbal, Junaid
Syed, Sana
Ali, Syed Asad
Moore, Sean R.
author_facet Narvaez-Rivas, Monica
Setchell, Kenneth D. R.
Galandi, Stephanie L.
Zhao, Xueheng
Iqbal, Najeeha Talat
Ahmed, Sheraz
Iqbal, Junaid
Syed, Sana
Ali, Syed Asad
Moore, Sean R.
author_sort Narvaez-Rivas, Monica
collection PubMed
description Environmental enteric dysfunction (EED) is characterized by intestinal inflammation, malabsorption and growth-faltering in children with heightened exposure to gut pathogens. The aim of this study was to characterize serum non-esterified fatty acids (NEFA), in association with childhood undernutrition and EED, as potential biomarkers to predict growth outcomes. The study comprised a cohort of undernourished rural Pakistani infants (n = 365) and age-matched controls followed prospectively up to 24 months of age. Serum NEFA were quantified at ages 3–6 and 9 months and correlated with growth outcomes, serum bile acids and EED histopathological biomarkers. Serum NEFA correlated with linear growth-faltering and systemic and gut biomarkers of EED. Undernourished children exhibited essential fatty acid deficiency (EFAD), with low levels of linoleic acid and total n-6 polyunsaturated fatty acids, compensated by increased levels of oleic acid and increased elongase and desaturase activities. EFAD correlated with reduced anthropometric Z scores at 3–6 and 9 months of age. Serum NEFA also correlated with elevated BA and liver dysfunction. Essential fatty acid depletion and altered NEFA metabolism were highly prevalent and associated with acute and chronic growth-faltering in EED. The finding suggests that targeting early interventions to correct EFAD and promote FA absorption in children with EED may facilitate childhood growth in high-risk settings.
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spelling pubmed-101422002023-04-29 Essential Fatty Acid Deficiency Associates with Growth Faltering and Environmental Enteric Dysfunction in Children Narvaez-Rivas, Monica Setchell, Kenneth D. R. Galandi, Stephanie L. Zhao, Xueheng Iqbal, Najeeha Talat Ahmed, Sheraz Iqbal, Junaid Syed, Sana Ali, Syed Asad Moore, Sean R. Metabolites Article Environmental enteric dysfunction (EED) is characterized by intestinal inflammation, malabsorption and growth-faltering in children with heightened exposure to gut pathogens. The aim of this study was to characterize serum non-esterified fatty acids (NEFA), in association with childhood undernutrition and EED, as potential biomarkers to predict growth outcomes. The study comprised a cohort of undernourished rural Pakistani infants (n = 365) and age-matched controls followed prospectively up to 24 months of age. Serum NEFA were quantified at ages 3–6 and 9 months and correlated with growth outcomes, serum bile acids and EED histopathological biomarkers. Serum NEFA correlated with linear growth-faltering and systemic and gut biomarkers of EED. Undernourished children exhibited essential fatty acid deficiency (EFAD), with low levels of linoleic acid and total n-6 polyunsaturated fatty acids, compensated by increased levels of oleic acid and increased elongase and desaturase activities. EFAD correlated with reduced anthropometric Z scores at 3–6 and 9 months of age. Serum NEFA also correlated with elevated BA and liver dysfunction. Essential fatty acid depletion and altered NEFA metabolism were highly prevalent and associated with acute and chronic growth-faltering in EED. The finding suggests that targeting early interventions to correct EFAD and promote FA absorption in children with EED may facilitate childhood growth in high-risk settings. MDPI 2023-03-29 /pmc/articles/PMC10142200/ /pubmed/37110148 http://dx.doi.org/10.3390/metabo13040489 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
Narvaez-Rivas, Monica
Setchell, Kenneth D. R.
Galandi, Stephanie L.
Zhao, Xueheng
Iqbal, Najeeha Talat
Ahmed, Sheraz
Iqbal, Junaid
Syed, Sana
Ali, Syed Asad
Moore, Sean R.
Essential Fatty Acid Deficiency Associates with Growth Faltering and Environmental Enteric Dysfunction in Children
title Essential Fatty Acid Deficiency Associates with Growth Faltering and Environmental Enteric Dysfunction in Children
title_full Essential Fatty Acid Deficiency Associates with Growth Faltering and Environmental Enteric Dysfunction in Children
title_fullStr Essential Fatty Acid Deficiency Associates with Growth Faltering and Environmental Enteric Dysfunction in Children
title_full_unstemmed Essential Fatty Acid Deficiency Associates with Growth Faltering and Environmental Enteric Dysfunction in Children
title_short Essential Fatty Acid Deficiency Associates with Growth Faltering and Environmental Enteric Dysfunction in Children
title_sort essential fatty acid deficiency associates with growth faltering and environmental enteric dysfunction in children
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10142200/
https://www.ncbi.nlm.nih.gov/pubmed/37110148
http://dx.doi.org/10.3390/metabo13040489
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