Transcriptomic Differences Between Monozygotic Adolescent Twins Discordant For Metabolic Syndrome Following Weight Loss: A Case Study.
Kaitlin DayAlan J McCubbinChiara MurgiaMelissa C SoutheyJustin BrownHelen TrubyPublished in: Twin research and human genetics : the official journal of the International Society for Twin Studies (2022)
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.
Keyphrases
- weight loss
- bariatric surgery
- single cell
- roux en y gastric bypass
- metabolic syndrome
- gene expression
- body composition
- genome wide
- gastric bypass
- rna seq
- low grade
- peripheral blood
- oxidative stress
- glycemic control
- poor prognosis
- obese patients
- insulin resistance
- dna methylation
- type diabetes
- mental health
- clinical trial
- stem cells
- physical activity
- bone mineral density
- resistance training
- postmenopausal women
- binding protein
- mesenchymal stem cells
- transcription factor