Data-Mining Approach on Transcriptomics and Methylomics Placental Analysis Highlights Genes in Fetal Growth Restriction.

Front Genet

Unité Mixte de Recherche (UMR) MITOVASC, Équipe Mitolab, Centre National de la Recherche Scientifique (CNRS) 6015, Institut National de la Santé et de la Recherche Médicale (INSERM) U1083, Université d'Angers, Angers, France.

Published: January 2020

AI Article Synopsis

  • IUGR impacts about 8% of newborns, leading to increased health risks even later in life, and previous studies show various genetic, epigenetic, and metabolic changes associated with it, but the overall mechanisms remain unclear.
  • Researchers conducted a detailed study using placental samples to analyze over 1,200 genes, applying a mix of methylomics and transcriptomics along with data-mining methods to gain insights into IUGR.
  • They used machine learning to identify phenotypic subgroups related to IUGR (like premature birth and birth weight) and found significant alterations in various biological processes, enhancing the understanding of IUGR's underlying mechanisms and relevant genetic factors.

Article Abstract

Intrauterine Growth Restriction (IUGR) affects 8% of newborns and increases morbidity and mortality for the offspring even during later stages of life. Single omics studies have evidenced epigenetic, genetic, and metabolic alterations in IUGR, but pathogenic mechanisms as a whole are not being fully understood. An in-depth strategy combining methylomics and transcriptomics analyses was performed on 36 placenta samples in a case-control study. Data-mining algorithms were used to combine the analysis of more than 1,200 genes found to be significantly expressed and/or methylated. We used an automated text-mining approach, using the bulk textual gene annotations of the discriminant genes. Machine learning models were then used to explore the phenotypic subgroups (premature birth, birth weight, and head circumference) associated with IUGR. Gene annotation clustering highlighted the alteration of cell signaling and proliferation, cytoskeleton and cellular structures, oxidative stress, protein turnover, muscle development, energy, and lipid metabolism with insulin resistance. Machine learning models showed a high capacity for predicting the sub-phenotypes associated with IUGR, allowing a better description of the IUGR pathophysiology as well as key genes involved.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6962302PMC
http://dx.doi.org/10.3389/fgene.2019.01292DOI Listing

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