Blunted nutrient-response pathways in adipose tissue following high fat meals in men with metabolic syndrome: A randomized postprandial transcriptomic study

A.L. Dordevic*, S.L. Coort, C.T. Evelo, C. Murgia, A.J. Sinclair, M.P. Bonham, A.E. Larsen, P. Gran, D. Cameron-Smith

*Corresponding author for this work

Research output: Contribution to journalArticleAcademicpeer-review

Abstract

Background: Excessive adipose tissue is central to disease burden posed by the Metabolic Syndrome (MetS). Whilst much is known of the altered transcriptomic regulation of adipose tissue under fasting conditions, little is known of the responses to high-fat meals. Methods: Nineteen middle-aged males (mean ? SD 52.0 ? 4.6 years), consumed two isocaloric high-fat, predominately dairy-based or soy-based, breakfast meals. Abdominal subcutaneous adipose biopsies were collected after overnight fast (0 h) and 4 h following each meal. Global gene expression profiling was performed by microarray (Illumina Human WG-6 v3). Results: In the fasted state, 13 genes were differently expressed between control and MetS adipose tissue ( 0.05). In response to the meals, the control participants had widespread in-creases in genes related to cellular nutrient responses ( 0.05; 2444 & 2367 genes; dairy & soy, respectively). There was blunted response in the MetS group ( 1.2 fold-change, p < 0.05; 332 336 genes; dairy & soy, respectively). Conclusions: In middle-aged males with MetS, a widespread suppression of the subcutaneous adipose tissue nutrient responsive gene expression suggests an inflexibility in the transcriptomic responsiveness both high-fat meals. ? 2020 The Authors. Published by Elsevier Ltd. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).

Original languageEnglish
Pages (from-to)1355-1366
Number of pages12
JournalClinical Nutrition
Volume40
Issue number3
DOIs
Publication statusPublished - 1 Mar 2021

Keywords

  • Adipose tissue
  • Metabolic syndrome
  • Nutrigenomics
  • Postprandial
  • Transcriptome
  • INSULIN-RESISTANCE
  • EXPRESSION
  • BIOPSY
  • HEALTH
  • MUSCLE
  • LIPIDS
  • CELLS
  • MTOR

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