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American Heart Association

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Final ID: 4122507

Fetal Socioeconomic and Environmental Exposures Influence Fetal Brain Growth and Risk of Neonatal Brain Injury in Congenital Heart Disease

Abstract Body (Do not enter title and authors here): Introduction:
Fetuses with CHD have smaller total brain volume (TBV) and are at risk for acquired brain white matter injury (WMI), both of which are linked to neurodevelopmental impairments. Social determinants of health (SDOH) and other fetal environmental factors have been linked to fetal brain health in other populations. Our aim was to test our hypothesis that these exposures influence fetal brain growth and postnatal WMI risk in severe CHD.

Methods:
Our prospective longitudinal cohort study enrolled fetuses with severe CHD to undergo fetal brain MRI and postnatal pre-operative brain MRI. Participants completed home environment surveys on individual SDOH and exposures. Community SDOH metrics were determined using Child Opportunity Index (COI) based on home address. An ‘at risk’ fetus composite was created if there was exposure to: personal/household smoking, welfare/food stamps, or poverty. TBV was calculated at both time points. Presence/degree of WMI was determined on postnatal MRI. Repeated measures analysis and logistic regression were performed to determine association between individual and community SDOH metrics with rate of TBV growth and risk of WMI.

Results:
55 participants enrolled (54 fetal scans: mean GA 33.9 wks, 95%CI: 33.7,34.1; 47 neonatal scans: mean GA 39.3 wks 95%CI: 38.9,39.6). Fetal sex, smoking exposure, and several individual SDOH were associated with TBV growth. Adjusting for fetal sex and GA at scan, rate of TBV growth was slower with smoking exposure (coeff: -5.2, 95%CI: -10.3, -0.2, p= 0.04) and trended towards significance for those with welfare/food stamps or poverty. ‘At risk’ fetuses had slower rate of TBV growth than those without risk (coeff: -2.5, 95%CI: -5.0, -0.07, p= 0.04) (Figure 1). There were lower odds of pre-operative WMI with high COI compared to low after adjusting for GA at scan (OR= 0.16, 95%CI: 0.03, 0.9, p= 0.04).

Conclusion:
Smoking exposure and individual-level SDOH influence brain growth, while community COI is associated with risk of postnatal pre-op WMI in CHD. Our findings identify targets for intervention to optimize brain growth and outcomes in the CHD population, including smoking cessation programs, and nutritional and needs assessment during pregnancy.
  • Derose, Lesje  ( UCSF Department of Pediatrics , San Francisco , California , United States )
  • Martin, Megan  ( UCSF Department of Pediatrics , San Francisco , California , United States )
  • Luna Silva, Karla  ( UCSF Department of Pediatrics , San Francisco , California , United States )
  • Nunez Gallegos, Flora  ( UCSF Department of Pediatrics , San Francisco , California , United States )
  • Steurer, Martina  ( UCSF Department of Pediatrics , San Francisco , California , United States )
  • George, Elizabeth  ( UCSF Department of Pediatrics , San Francisco , California , United States )
  • Xu, Duan  ( UCSF Department of Pediatrics , San Francisco , California , United States )
  • Mcquillen, Patrick  ( UCSF Department of Pediatrics , San Francisco , California , United States )
  • Peyvandi, Shabnam  ( UCSF Department of Pediatrics , San Francisco , California , United States )
  • Author Disclosures:
    Lesje DeRose: DO NOT have relevant financial relationships | Megan Martin: DO NOT have relevant financial relationships | Karla Luna Silva: No Answer | Flora Nunez Gallegos: DO NOT have relevant financial relationships | Martina Steurer: DO NOT have relevant financial relationships | Elizabeth George: DO NOT have relevant financial relationships | Duan Xu: No Answer | Patrick McQuillen: DO NOT have relevant financial relationships | Shabnam Peyvandi: DO NOT have relevant financial relationships
Meeting Info:

Scientific Sessions 2024

2024

Chicago, Illinois

Session Info:

Young Hearts Early Career Investigator Competition

Saturday, 11/16/2024 , 09:45AM - 10:45AM

Abstract Oral Session

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