Metabolic liability for weight gain in early adulthood

Cell Rep Med. 2024 May 21;5(5):101548. doi: 10.1016/j.xcrm.2024.101548. Epub 2024 May 3.

Abstract

While weight gain is associated with a host of chronic illnesses, efforts in obesity have relied on single "snapshots" of body mass index (BMI) to guide genetic and molecular discovery. Here, we study >2,000 young adults with metabolomics and proteomics to identify a metabolic liability to weight gain in early adulthood. Using longitudinal regression and penalized regression, we identify a metabolic signature for weight liability, associated with a 2.6% (2.0%-3.2%, p = 7.5 × 10-19) gain in BMI over ≈20 years per SD higher score, after comprehensive adjustment. Identified molecules specified mechanisms of weight gain, including hunger and appetite regulation, energy expenditure, gut microbial metabolism, and host interaction with external exposure. Integration of longitudinal and concurrent measures in regression with Mendelian randomization highlights the complexity of metabolic regulation of weight gain, suggesting caution in interpretation of epidemiologic or genetic effect estimates traditionally used in metabolic research.

Keywords: branched chain amino acids; metabolism; obesity; weight regulation.

MeSH terms

  • Adult
  • Body Mass Index*
  • Energy Metabolism
  • Female
  • Gastrointestinal Microbiome
  • Humans
  • Male
  • Metabolome
  • Metabolomics
  • Obesity / genetics
  • Obesity / metabolism
  • Proteomics / methods
  • Weight Gain*
  • Young Adult