4.3 Article

Redox Imbalance and Methylation Disturbances in Early Childhood Obesity

Journal

OXIDATIVE MEDICINE AND CELLULAR LONGEVITY
Volume 2021, Issue -, Pages -

Publisher

HINDAWI LTD
DOI: 10.1155/2021/2207125

Keywords

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Funding

  1. National Institute of General Medical Sciences of the National Institutes of Health under a COBRE Award [P20GM109096]
  2. Arkansas Biosciences Institute/Arkansas Children' Research Institute
  3. European Regional Development Fund, through the Centro 2020 Regional Operational Programme Healthy Aging2020 [CENTRO-01-0145-FEDER-000012]
  4. European Regional Development Fund, through COMPETE 2020-Operational Programme for Competitiveness and Internationalisation
  5. Portuguese national funds via FCT-Fundacao para a Ciencia e a Tecnologia [POCI-01-0145-FEDER-007440, POCI-01-0145-FEDER-022184, UIDB/04539/2020, UIDP/04539/2020, UIDP/04501/2020, SFRH/BD/143849/2019]
  6. NIH/NIGMS [UL1 TR003107, KL2 TR003108]
  7. USDA/ARS [6026-51000-012-06-S]
  8. Fundação para a Ciência e a Tecnologia [UIDP/04501/2020, SFRH/BD/143849/2019] Funding Source: FCT

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The study revealed novel metabolic alterations in the transmethylation and transsulfuration pathways in prepubertal children with obesity, as well as early changes in adipocyte secretory function. These findings may serve as early metabolic markers of disease in this population.
Obesity is increasing worldwide in prepubertal children, reducing the age of onset of associated comorbidities, including type 2 diabetes. Sulfur-containing amino acids, methionine, cysteine, and their derivatives play important roles in the transmethylation and transsulfuration pathways. Dysregulation of these pathways leads to alterations in the cellular methylation patterns and an imbalanced redox state. Therefore, we tested the hypothesis that one-carbon metabolism is already dysregulated in prepubertal children with obesity. Peripheral blood was collected from 64 children, and the plasma metabolites from transmethylation and transsulfuration pathways were quantified by HPLC. The cohort was stratified by BMI z-scores and HOMA-IR indices into healthy lean (HL), healthy obese (HO), and unhealthy obese (UHO). Fasting insulin levels were higher in the HO group compared to the HL, while the UHO had the highest. All groups presented normal fasting glycemia. Furthermore, high-density lipoprotein (HDL) was lower while triglycerides and lactate levels were higher in the UHO compared to HO subjects. S-adenosylhomocysteine (SAH) and total homocysteine levels were increased in the HO group compared to HL. Additionally, glutathione metabolism was also altered. Free cystine and oxidized glutathione (GSSG) were increased in the HO as compared to HL subjects. Importantly, the adipocyte secretory function was already compromised at this young age. Elevated circulating leptin and decreased adiponectin levels were observed in the UHO as compared to the HO subjects. Some of these alterations were concomitant with alterations in the DNA methylation patterns in the obese group, independent of the impaired insulin levels. In conclusion, our study informs on novel and important metabolic alterations in the transmethylation and the transsulfuration pathways in the early stages of obesity. Moreover, the altered secretory function of the adipocyte very early in life may be relevant in identifying early metabolic markers of disease that may inform on the increased risk for specific future comorbidities in this population.

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