Inhibitory control is related to fecal short-chain fatty acid concentrations in adults with overweight and obesity

Nutr Res. 2025 Jun:138:12-21. doi: 10.1016/j.nutres.2025.03.006. Epub 2025 Mar 27.

Abstract

Obesity is a pro-inflammatory condition with negative effects on executive functioning. Increased inflammation dysregulates gastrointestinal homeostasis and alters microbiota community composition. The gut microbiota produce immunomodulatory short-chain fatty acids (SCFA) that have been related to cognition in obesity, but the neural effects are not explored. Here, we hypothesized that greater fecal SCFA would be positively related to neuroelectric markers of inhibitory control and conflict monitoring in obesity. A cross-sectional cohort of 87 adults (35 ± 6 years, 53 females) with overweight and obesity (BMI = 32 ± 6 kg/m2) provided fresh fecal samples and participated in cognitive testing to assess response inhibition and conflict monitoring with electroencephalographic recording. Linear regressions, controlling for age, sex, BMI, and energy-adjusted dietary fiber intake, revealed positive relationships between NoGo N2 mean amplitude and fecal SCFA concentrations. Linear discriminant analysis effect size (LEfSe) revealed 16 amplicon sequence variants differentially abundant between high and low butyrate groups with Roseburia and Adlercreutzia individually related to NoGo N2 mean amplitude in MaAsLin2 modeling. Thus, greater fecal SCFA concentrations and SCFA producing microbiota (i.e., Roseburia) were related to markers of superior conflict monitoring in the NoGo task when adjusting for key covariates. These data highlight key associations between bacterial derived gut signaling molecules and neural regulation in cognitive domains particularly relevant to weight status that warrant further investigation.

MeSH terms

  • Adult
  • Cognition
  • Cross-Sectional Studies
  • Executive Function
  • Fatty Acids, Volatile* / analysis
  • Fatty Acids, Volatile* / metabolism
  • Feces* / chemistry
  • Feces* / microbiology
  • Female
  • Gastrointestinal Microbiome
  • Humans
  • Inhibition, Psychological*
  • Male
  • Middle Aged
  • Obesity* / metabolism
  • Obesity* / microbiology
  • Obesity* / psychology
  • Overweight* / metabolism
  • Overweight* / microbiology
  • Overweight* / psychology

Substances

  • Fatty Acids, Volatile