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Maternal Pre-Gravid Obesity Changes Gene Expression Profiles Towards Greater Inflammation and Reduced Insulin Sensitivity in Umbilical Cord

BACKGROUND: Maternal obesity is associated with unfavorable outcomes, which may be reflected in the as yet undiscovered gene expression profiles of the umbilical cord (UC). METHODS: UCs from 12 lean (pre-gravid BMI < 24.9) and 10 overweight/obese (OW/OB, pre-gravid BMI ≥25) women without gestatio...

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Autores principales: Thakali, Keshari M., Saben, Jessica, Faske, Jennifer B., Lindsey, Forrest, Gomez-Acevedo, Horacio, Lowery, Curtis L., Badger, Thomas M., Andres, Aline, Shankar, Kartik
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4135718/
https://www.ncbi.nlm.nih.gov/pubmed/24819376
http://dx.doi.org/10.1038/pr.2014.72
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author Thakali, Keshari M.
Saben, Jessica
Faske, Jennifer B.
Lindsey, Forrest
Gomez-Acevedo, Horacio
Lowery, Curtis L.
Badger, Thomas M.
Andres, Aline
Shankar, Kartik
author_facet Thakali, Keshari M.
Saben, Jessica
Faske, Jennifer B.
Lindsey, Forrest
Gomez-Acevedo, Horacio
Lowery, Curtis L.
Badger, Thomas M.
Andres, Aline
Shankar, Kartik
author_sort Thakali, Keshari M.
collection PubMed
description BACKGROUND: Maternal obesity is associated with unfavorable outcomes, which may be reflected in the as yet undiscovered gene expression profiles of the umbilical cord (UC). METHODS: UCs from 12 lean (pre-gravid BMI < 24.9) and 10 overweight/obese (OW/OB, pre-gravid BMI ≥25) women without gestational diabetes were collected for gene expression analysis using Human Primeview microarrays (Affymetrix). Metabolic parameters were assayed in mother’s plasma and cord blood. RESULTS: Although offspring birth weight and adiposity (at 2-wk) did not differ between groups, expression of 232 transcripts was affected in UC from OW/OB compared to those of lean mothers. GSEA analysis revealed an up-regulation of genes related to metabolism, stimulus and defense response and inhibitory to insulin signaling in the OW/OB group. We confirmed that EGR1, periostin, and FOSB mRNA expression was induced in UCs from OW/OB moms, while endothelin receptor B, KFL10, PEG3 and EGLN3 expression was decreased. Messenger RNA expression of EGR1, FOSB, MEST and SOCS1 were positively correlated (p<0.05) with mother’s first trimester body fat mass (%). CONCLUSIONS: Our data suggest a positive association between maternal obesity and changes in UC gene expression profiles favoring inflammation and insulin resistance, potentially predisposing infants to develop metabolic dysfunction later on in life.
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spelling pubmed-41357182015-02-01 Maternal Pre-Gravid Obesity Changes Gene Expression Profiles Towards Greater Inflammation and Reduced Insulin Sensitivity in Umbilical Cord Thakali, Keshari M. Saben, Jessica Faske, Jennifer B. Lindsey, Forrest Gomez-Acevedo, Horacio Lowery, Curtis L. Badger, Thomas M. Andres, Aline Shankar, Kartik Pediatr Res Article BACKGROUND: Maternal obesity is associated with unfavorable outcomes, which may be reflected in the as yet undiscovered gene expression profiles of the umbilical cord (UC). METHODS: UCs from 12 lean (pre-gravid BMI < 24.9) and 10 overweight/obese (OW/OB, pre-gravid BMI ≥25) women without gestational diabetes were collected for gene expression analysis using Human Primeview microarrays (Affymetrix). Metabolic parameters were assayed in mother’s plasma and cord blood. RESULTS: Although offspring birth weight and adiposity (at 2-wk) did not differ between groups, expression of 232 transcripts was affected in UC from OW/OB compared to those of lean mothers. GSEA analysis revealed an up-regulation of genes related to metabolism, stimulus and defense response and inhibitory to insulin signaling in the OW/OB group. We confirmed that EGR1, periostin, and FOSB mRNA expression was induced in UCs from OW/OB moms, while endothelin receptor B, KFL10, PEG3 and EGLN3 expression was decreased. Messenger RNA expression of EGR1, FOSB, MEST and SOCS1 were positively correlated (p<0.05) with mother’s first trimester body fat mass (%). CONCLUSIONS: Our data suggest a positive association between maternal obesity and changes in UC gene expression profiles favoring inflammation and insulin resistance, potentially predisposing infants to develop metabolic dysfunction later on in life. 2014-05-12 2014-08 /pmc/articles/PMC4135718/ /pubmed/24819376 http://dx.doi.org/10.1038/pr.2014.72 Text en http://www.nature.com/authors/editorial_policies/license.html#terms Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use:http://www.nature.com/authors/editorial_policies/license.html#terms
spellingShingle Article
Thakali, Keshari M.
Saben, Jessica
Faske, Jennifer B.
Lindsey, Forrest
Gomez-Acevedo, Horacio
Lowery, Curtis L.
Badger, Thomas M.
Andres, Aline
Shankar, Kartik
Maternal Pre-Gravid Obesity Changes Gene Expression Profiles Towards Greater Inflammation and Reduced Insulin Sensitivity in Umbilical Cord
title Maternal Pre-Gravid Obesity Changes Gene Expression Profiles Towards Greater Inflammation and Reduced Insulin Sensitivity in Umbilical Cord
title_full Maternal Pre-Gravid Obesity Changes Gene Expression Profiles Towards Greater Inflammation and Reduced Insulin Sensitivity in Umbilical Cord
title_fullStr Maternal Pre-Gravid Obesity Changes Gene Expression Profiles Towards Greater Inflammation and Reduced Insulin Sensitivity in Umbilical Cord
title_full_unstemmed Maternal Pre-Gravid Obesity Changes Gene Expression Profiles Towards Greater Inflammation and Reduced Insulin Sensitivity in Umbilical Cord
title_short Maternal Pre-Gravid Obesity Changes Gene Expression Profiles Towards Greater Inflammation and Reduced Insulin Sensitivity in Umbilical Cord
title_sort maternal pre-gravid obesity changes gene expression profiles towards greater inflammation and reduced insulin sensitivity in umbilical cord
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4135718/
https://www.ncbi.nlm.nih.gov/pubmed/24819376
http://dx.doi.org/10.1038/pr.2014.72
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