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Accès ouvert déclaré 2026 article

Limbic System Microstructure in Neonates With Antenatal Opioid Exposure

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10Institutions déclarées
1Pays d’affiliation déclarés

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Le résumé fourni par la source

Importance: There is limited research examining the association of antenatal opioid exposure with neonatal brain microstructure, particularly within the limbic system, which contains high concentrations of opioid receptors. Prior studies investigating microstructural changes in major white matter tracts were underpowered and lacked matched controls. Objective: To compare limbic system microstructure between neonates who were opioid exposed and unexposed. Design, Setting, and Participants: This case-control study assessed diffusion tensor imaging of neonates enrolled in the Outcomes of Babies With Opioid Exposure (OBOE) study and scanned between August 2020 and December 2023 at 4 US sites. Participants were term neonates with antenatal exposure and unexposed controls. Data were analyzed from July 2024 to April 2026. Exposure: Neonates were antenatally exposed to methadone, buprenorphine, oxycodone, hydromorphone, fentanyl, hydrocodone, heroin, morphine, or some combination of these opioids. Main Outcomes and Measures: The primary outcome was limbic system diffusion metric comparisons between neonates who were exposed and unexposed. Diffusion tensor imaging data in term neonates were acquired using harmonized protocols on Siemens and Philips 3T magnetic resonance imaging scanners, preprocessed using a neonatal-optimized pipeline, and analyzed. Using analysis of covariance, fractional anisotropy, mean diffusivity, radial diffusivity, and axial diffusivity were compared in the limbic system of neonates who were unexposed vs opioid exposed. In secondary, exploratory analyses, diffusion metrics in the limbic system were compared between subgroups of opioid exposure (methadone, buprenorphine, and other opioids) and controls. False discovery rate (FDR) was used to correct for multiple comparisons. Results: Among 201 enrolled neonates, 75 were unexposed (mean [SD] postmenstrual age, 42.76 [2.05] weeks; 45 male [60.0%]) and 126 were antenatally opioid exposed (mean [SD] postmenstrual age, 42.72 [2.06] weeks; 65 male [51.6%]), of which 79 were exposed to buprenorphine, 30 to methadone, and 14 to other opioids. Neonates who were opioid exposed showed a significantly lower mean diffusivity (mean difference [β] = -0.06 × 10-3 mm2/s [95% CI, -0.11 to -0.01 × 10-3 mm2/s]; FDR P = .04) and radial diffusivity (β = -0.07 × 10-3 mm2/s [95% CI, -0.12 to -0.02 × 10-3 mm2/s]; FDR P = .04) in the fornix. Secondary, exploratory analyses revealed buprenorphine-specific associations (eg, higher mean diffusivity in the left parahippocampal gyrus vs no opioid exposure: β = 0.02 × 10⁻3 mm2/s [95% CI, 0.00 to 0.04 × 10⁻3 mm2/s]) and other opioid-specific associations (eg, higher fractional anisotropy in the left thalamus for other opioids vs unexposed: β = 0.01 [95% CI, 0.01 to 0.02]) in GM limbic system structures. Conclusions and Relevance: This study found altered limbic system microstructure, particularly in the fornix, in neonates with antenatal opioid exposure, and exploratory analyses showed different patterns of limbic system microstructure across opioid exposure subgroups. Clinical correlation is needed.

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Le contrôle bibliographique ouvert

DOI retrouvé dans Crossref DOI retrouvé ; titre concordant.

Titre Crossref
Limbic System Microstructure in Neonates With Antenatal Opioid Exposure
Date Crossref
02/07/2026
Éditeur
American Medical Association (AMA)
Type
journal-article

Ce recoupement confirme des métadonnées liées au DOI. Il ne confirme ni la méthode ni les conclusions de l’étude, et il ne compte pas comme une seconde source scientifique indépendante.

Où se fait cette recherche

  • Children's National pays non établi dans la notice
    Établissement de santé
  • Cincinnati Children's Hospital Medical Center pays non établi dans la notice
    Établissement de santé
  • University of Cincinnati Department of Pediatrics pays non établi dans la notice
    Université ou école supérieure
  • RTI International pays non établi dans la notice
    Organisation à but non lucratif
  • Children's Hospital of Philadelphia pays non établi dans la notice
    Organisme public
  • University of Pennsylvania pays non établi dans la notice
    Université ou école supérieure
  • University of Alabama at Birmingham pays non établi dans la notice
    Université ou école supérieure
  • Case Western Reserve University pays non établi dans la notice
    Université ou école supérieure
  • Emory University pays non établi dans la notice
    Université ou école supérieure
  • Tufts University pays non établi dans la notice
    Université ou école supérieure
  • Developing Brain Institute pays non établi dans la notice
    Structure de recherche
  • Perinatal Institute pays non établi dans la notice
    Structure de recherche

Children's National, Cincinnati Children's Hospital Medical Center et Department of Pediatrics — University of Cincinnati, avec 9 autres affiliations.

Une affiliation ne permet pas de déduire la nationalité d’un auteur.

Les sujets associés

Prenatal Substance Exposure EffectsOpioid Use Disorder TreatmentNeonatal and fetal brain pathology

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