Particulate Matter Exposure and Default Mode Network Equilibrium During Early Adolescence

Brain Connect. 2024 Aug;14(6):307-318. doi: 10.1089/brain.2023.0072. Epub 2024 Jul 3.

Abstract

Background: Air pollution exposure has been associated with adverse cognitive and mental health outcomes in children, adolescents, and adults, although youth may be particularly susceptible given ongoing brain development. However, the neurodevelopmental mechanisms underlying the associations among air pollution, cognition, and mental health remain unclear. We examined the impact of particulate matter (PM2.5) on resting-state functional connectivity (rsFC) of the default mode network (DMN) and three key attention networks: dorsal attention, ventral attention, and cingulo-opercular. Methods: Longitudinal changes in rsFC within/between networks were assessed from baseline (9-10 years) to the 2-year follow-up (11-12 years) in 10,072 youth (M ± SD = 9.93 + 0.63 years; 49% female) from the Adolescent Brain Cognitive Development (ABCD®) study. Annual ambient PM2.5 concentrations from the 2016 calendar year were estimated using hybrid ensemble spatiotemporal models. RsFC was estimated using functional neuroimaging. Linear mixed models were used to test associations between PM2.5 and change in rsFC over time while adjusting for relevant covariates (e.g., age, sex, race/ethnicity, parental education, and family income) and other air pollutants (O3, NO2). Results: A PM2.5 × time interaction was significant for within-network rsFC of the DMN such that higher PM2.5 concentrations were associated with a smaller increase in rsFC over time. Further, significant PM2.5 × time interactions were observed for between-network rsFC of the DMN and all three attention networks, with varied directionality. Conclusion: PM2.5 exposure was associated with alterations in the development and equilibrium of the DMN-a network implicated in self-referential processing-and anticorrelated attention networks, which may impact trajectories of cognitive and mental health symptoms across adolescence.

Keywords: Developmental biology; Psychiatry; Resting-state networks.

MeSH terms

  • Adolescent
  • Air Pollutants / adverse effects
  • Air Pollution* / adverse effects
  • Attention / drug effects
  • Attention / physiology
  • Brain* / diagnostic imaging
  • Brain* / growth & development
  • Child
  • Cognition / physiology
  • Connectome / methods
  • Default Mode Network* / diagnostic imaging
  • Environmental Exposure / adverse effects
  • Female
  • Humans
  • Longitudinal Studies
  • Magnetic Resonance Imaging*
  • Male
  • Nerve Net / diagnostic imaging
  • Nerve Net / growth & development
  • Particulate Matter* / adverse effects

Substances

  • Particulate Matter
  • Air Pollutants