Association of Preterm Birth and Socioeconomic Status With Neonatal Brain Structure.


Journal

JAMA network open
ISSN: 2574-3805
Titre abrégé: JAMA Netw Open
Pays: United States
ID NLM: 101729235

Informations de publication

Date de publication:
01 05 2023
Historique:
medline: 2 6 2023
pubmed: 31 5 2023
entrez: 31 5 2023
Statut: epublish

Résumé

Preterm birth and socioeconomic status (SES) are associated with brain structure in childhood, but the relative contributions of each during the neonatal period are unknown. To investigate associations of birth gestational age (GA) and SES with neonatal brain morphology by testing 3 hypotheses: GA and SES are associated with brain morphology; associations between SES and brain morphology vary with GA; and associations between SES and brain structure and morphology depend on how SES is operationalized. This cohort study recruited participants from November 2016 to September 2021 at a single center in the United Kingdom. Participants were 170 extremely and very preterm infants and 91 full-term or near-term infants. Exclusion criteria were major congenital malformation, chromosomal abnormality, congenital infection, cystic periventricular leukomalacia, hemorrhagic parenchymal infarction, and posthemorrhagic ventricular dilatation. Birth GA and SES, operationalized at the neighborhood level (using the Scottish Index of Multiple Deprivation), the family level (using parental education and occupation), and subjectively (World Health Organization Quality of Life measure). Brain volume (85 parcels) and 5 whole-brain cortical morphology measures (gyrification index, thickness, sulcal depth, curvature, surface area) at term-equivalent age (median [range] age, 40 weeks, 5 days [36 weeks, 2 days to 45 weeks, 6 days] and 42 weeks [38 weeks, 2 days to 46 weeks, 1 day] for preterm and full-term infants, respectively). Participants were 170 extremely and very preterm infants (95 [55.9%] male; 4 of 166 [2.4%] Asian, 145 of 166 [87.3%] White) and 91 full-term or near-term infants (50 [54.9%] male; 3 of 86 [3.5%] Asian, 78 of 86 [90.7%] White infants) with median (range) birth GAs of 30 weeks, 0 days (22 weeks, 1 day, to 32 weeks, 6 days) and 39 weeks, 4 days (36 weeks, 3 days, to 42 weeks, 1 day), respectively. In fully adjusted models, birth GA was associated with a higher proportion of brain volumes (27 of 85 parcels [31.8%]; β range, -0.20 to 0.24) than neighborhood-level SES (1 of 85 parcels [1.2%]; β = 0.17 [95% CI, -0.16 to 0.50]) or family-level SES (maternal education: 4 of 85 parcels [4.7%]; β range, 0.09 to 0.15; maternal occupation: 1 of 85 parcels [1.2%]; β = 0.06 [95% CI, 0.02 to 0.11] respectively). There were interactions between GA and both family-level and subjective SES measures on regional brain volumes. Birth GA was associated with cortical surface area (β = 0.10 [95% CI, 0.02 to 0.18]) and gyrification index (β = 0.16 [95% CI, 0.07 to 0.25]); no SES measure was associated with cortical measures. In this cohort study of UK infants, birth GA and SES were associated with neonatal brain morphology, but low GA had more widely distributed associations with neonatal brain structure than SES. Further work is warranted to elucidate the mechanisms underlying the association of both GA and SES with early brain development.

Identifiants

pubmed: 37256618
pii: 2805445
doi: 10.1001/jamanetworkopen.2023.16067
pmc: PMC10233421
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e2316067

Subventions

Organisme : Medical Research Council
ID : G1002033
Pays : United Kingdom
Organisme : Wellcome Trust
ID : 108890/Z/15/Z
Pays : United Kingdom

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Auteurs

Katie Mckinnon (K)

Medical Research Council Centre for Reproductive Health, University of Edinburgh, Edinburgh, United Kingdom.

Paola Galdi (P)

Medical Research Council Centre for Reproductive Health, University of Edinburgh, Edinburgh, United Kingdom.

Manuel Blesa-Cábez (M)

Medical Research Council Centre for Reproductive Health, University of Edinburgh, Edinburgh, United Kingdom.

Gemma Sullivan (G)

Medical Research Council Centre for Reproductive Health, University of Edinburgh, Edinburgh, United Kingdom.
Centre for Clinical Brain Sciences, University of Edinburgh, Edinburgh, United Kingdom.

Kadi Vaher (K)

Medical Research Council Centre for Reproductive Health, University of Edinburgh, Edinburgh, United Kingdom.

Amy Corrigan (A)

Medical Research Council Centre for Reproductive Health, University of Edinburgh, Edinburgh, United Kingdom.

Jill Hall (J)

Medical Research Council Centre for Reproductive Health, University of Edinburgh, Edinburgh, United Kingdom.

Lorena Jiménez-Sánchez (L)

Centre for Clinical Brain Sciences, University of Edinburgh, Edinburgh, United Kingdom.

Michael Thrippleton (M)

Centre for Clinical Brain Sciences, University of Edinburgh, Edinburgh, United Kingdom.

Mark E Bastin (ME)

Centre for Clinical Brain Sciences, University of Edinburgh, Edinburgh, United Kingdom.

Alan J Quigley (AJ)

Department of Radiology, Royal Hospital for Children and Young People, Edinburgh, United Kingdom.

Evdoxia Valavani (E)

Usher Institute, Edinburgh Medical School, University of Edinburgh, Edinburgh, United Kingdom.

Athanasios Tsanas (A)

Usher Institute, Edinburgh Medical School, University of Edinburgh, Edinburgh, United Kingdom.
Alan Turing Institute, London, United Kingdom.

Hilary Richardson (H)

School of Philosophy, Psychology, and Language Sciences, University of Edinburgh, Edinburgh, United Kingdom.

James P Boardman (JP)

Centre for Clinical Brain Sciences, University of Edinburgh, Edinburgh, United Kingdom.

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