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Transcriptomic Differences between Monozygotic Adolescent Twins Discordant for Metabolic Syndrome Following Weight Loss: A Case Study

Research output: Contribution to journalArticleOtherpeer-review

Abstract

This case reports peripheral blood mononuclear cell (PBMC) transcriptomic changes in a pair of male monozygotic pediatric twins with metabolic syndrome (MetS) undertaking assisted weight loss. These 14-year-old boys presented with similar baseline biochemistry and body composition. After a 16-week weight-loss intervention, percent body weight loss was similar (Twin A 12%, and Twin B 13%). MetS resolved in Twin A but Twin B maintained elevated triglycerides after weight loss. Analysis of the PBMC transcriptome before and after weight loss revealed very different changes in gene expression including differences in the direction of expression of genes related to immune cell activation. 48.7% of genes that were downregulated in Twin A were upregulated in Twin B. This case highlights a novel approach to report the influence of chronic low-grade inflammation and metabolic dysfunction on the PBMC transcriptome. It explores whether expression of genes related to immune functions may underlie the differences in response to weight loss or whether transcriptomic alterations in immune cells may precede more traditional biomarkers of chronic pro-inflammation. These monozygotic twins present an example of divergence of phenotypic outcomes despite identical genetic background and similar treatment response.

Original languageEnglish
Pages (from-to)196-201
Number of pages6
JournalTwin Research and Human Genetics
Volume25
Issue number4-5
DOIs
Publication statusPublished - 27 Oct 2022

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • gene expression
  • metabolic syndrome
  • Pediatric obesity
  • The alternate day fasting diet in adolescents with obesity: a randomised controlled trial

    Baur, L. A. (Primary Chief Investigator (PCI)), Truby, H. (Chief Investigator (CI)), Garnett, S. P. (Chief Investigator (CI)), Varady, K. (Chief Investigator (CI)), Cowell, C. T. (Chief Investigator (CI)), Collins, C. E. (Chief Investigator (CI)), Paxton, S. J. (Chief Investigator (CI)), Paxton, S. J. (Chief Investigator (CI)), Lister, N. B. (Chief Investigator (CI)), Gow, M. (Chief Investigator (CI)) & Brown, J. (Chief Investigator (CI))

    University of Sydney

    1/05/1731/05/21

    Project: Research

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