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Childhood Malnutrition and Association of Lean Mass with Metabolome and Hormone Profile in Later Life

This study aimed to determine the associations of targeted metabolomics and hormone profiles data with lean mass index (LMI), which were estimated using bioelectrical impedance, in survivors of child severe malnutrition (SM) (n = 69) and controls (n = 77) in Malawi 7 years after being treated. Linea...

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Autores principales: Gonzales, Gerard Bryan, Lelijveld, Natasha, Bourdon, Celine, Chimwezi, Emmanuel, Nyirenda, Moffat J., Wells, Jonathan C., Kerac, Marko, Bandsma, Robert H. J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7700560/
https://www.ncbi.nlm.nih.gov/pubmed/33238545
http://dx.doi.org/10.3390/nu12113593
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author Gonzales, Gerard Bryan
Lelijveld, Natasha
Bourdon, Celine
Chimwezi, Emmanuel
Nyirenda, Moffat J.
Wells, Jonathan C.
Kerac, Marko
Bandsma, Robert H. J.
author_facet Gonzales, Gerard Bryan
Lelijveld, Natasha
Bourdon, Celine
Chimwezi, Emmanuel
Nyirenda, Moffat J.
Wells, Jonathan C.
Kerac, Marko
Bandsma, Robert H. J.
author_sort Gonzales, Gerard Bryan
collection PubMed
description This study aimed to determine the associations of targeted metabolomics and hormone profiles data with lean mass index (LMI), which were estimated using bioelectrical impedance, in survivors of child severe malnutrition (SM) (n = 69) and controls (n = 77) in Malawi 7 years after being treated. Linear associations between individual metabolite or hormone and LMI were determined, including their interaction with nutrition status 7 years prior. Path analysis was performed to determine structural associations. Lastly, predictive models for LMI were developed using the metabolome and hormone profile by elastic net regularized regression (EN). Metabolites including several lipids, amino acids, and hormones were individually associated (p < 0.05 after false discovery rate correction) with LMI. However, plasma FGF21 (Control: β = −0.02, p = 0.59; Case: β = −0.14, p < 0.001) and tryptophan (Control: β = 0.15, p = 0.26; Case: β = 0.70, p < 0.001) were associated with LMI among cases but not among controls (both interaction p-values < 0.01). Moreover, path analysis revealed that tryptophan mediates the association between child SM and LMI. EN revealed that most predictors of LMI differed between groups, further indicating altered metabolic mechanisms driving lean mass accretion among SM survivors later in life.
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spelling pubmed-77005602020-11-30 Childhood Malnutrition and Association of Lean Mass with Metabolome and Hormone Profile in Later Life Gonzales, Gerard Bryan Lelijveld, Natasha Bourdon, Celine Chimwezi, Emmanuel Nyirenda, Moffat J. Wells, Jonathan C. Kerac, Marko Bandsma, Robert H. J. Nutrients Article This study aimed to determine the associations of targeted metabolomics and hormone profiles data with lean mass index (LMI), which were estimated using bioelectrical impedance, in survivors of child severe malnutrition (SM) (n = 69) and controls (n = 77) in Malawi 7 years after being treated. Linear associations between individual metabolite or hormone and LMI were determined, including their interaction with nutrition status 7 years prior. Path analysis was performed to determine structural associations. Lastly, predictive models for LMI were developed using the metabolome and hormone profile by elastic net regularized regression (EN). Metabolites including several lipids, amino acids, and hormones were individually associated (p < 0.05 after false discovery rate correction) with LMI. However, plasma FGF21 (Control: β = −0.02, p = 0.59; Case: β = −0.14, p < 0.001) and tryptophan (Control: β = 0.15, p = 0.26; Case: β = 0.70, p < 0.001) were associated with LMI among cases but not among controls (both interaction p-values < 0.01). Moreover, path analysis revealed that tryptophan mediates the association between child SM and LMI. EN revealed that most predictors of LMI differed between groups, further indicating altered metabolic mechanisms driving lean mass accretion among SM survivors later in life. MDPI 2020-11-23 /pmc/articles/PMC7700560/ /pubmed/33238545 http://dx.doi.org/10.3390/nu12113593 Text en © 2020 by the authors. 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 (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Gonzales, Gerard Bryan
Lelijveld, Natasha
Bourdon, Celine
Chimwezi, Emmanuel
Nyirenda, Moffat J.
Wells, Jonathan C.
Kerac, Marko
Bandsma, Robert H. J.
Childhood Malnutrition and Association of Lean Mass with Metabolome and Hormone Profile in Later Life
title Childhood Malnutrition and Association of Lean Mass with Metabolome and Hormone Profile in Later Life
title_full Childhood Malnutrition and Association of Lean Mass with Metabolome and Hormone Profile in Later Life
title_fullStr Childhood Malnutrition and Association of Lean Mass with Metabolome and Hormone Profile in Later Life
title_full_unstemmed Childhood Malnutrition and Association of Lean Mass with Metabolome and Hormone Profile in Later Life
title_short Childhood Malnutrition and Association of Lean Mass with Metabolome and Hormone Profile in Later Life
title_sort childhood malnutrition and association of lean mass with metabolome and hormone profile in later life
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7700560/
https://www.ncbi.nlm.nih.gov/pubmed/33238545
http://dx.doi.org/10.3390/nu12113593
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