Long-term associations between early-life family functioning and preadolescent white matter microstructure.


Journal

Psychological medicine
ISSN: 1469-8978
Titre abrégé: Psychol Med
Pays: England
ID NLM: 1254142

Informations de publication

Date de publication:
07 2023
Historique:
medline: 13 9 2023
pubmed: 26 5 2022
entrez: 25 5 2022
Statut: ppublish

Résumé

Causes of childhood behavior problems remain poorly understood. Enriched family environments and corresponding brain development may reduce the risk of their onset, but research investigating white matter neurodevelopmental pathways explaining associations between the family environment and behavior remains limited. We hypothesized that more positive prenatal and mid-childhood family functioning - a measure of a family's problem solving and supportive capacity - would be associated with two markers of preadolescent white matter neurodevelopment related to reduced behavior problems: higher global fractional anisotropy (FA) and lower global mean diffusivity (MD). Data are from 2727 families in the Generation R Study, the Netherlands. Mothers reported family functioning (McMaster Family Assessment Device, range 1-4, higher scores indicate healthier functioning) prenatally and in mid-childhood (mean age 6.1 years). In preadolescence (mean age 10.1), the study collected diffusion-weighted scans. We computed standardized global MD and FA values by averaging metrics from 27 white matter tracts, and we fit linear models adjusting for possible confounders to examine global and tract-specific outcomes. Prenatal and mid-childhood family functioning scores were moderately correlated, These results suggest high-functioning prenatal or perinatal family environments may confer lasting white matter neurodevelopmental benefits into preadolescence.

Sections du résumé

BACKGROUND
Causes of childhood behavior problems remain poorly understood. Enriched family environments and corresponding brain development may reduce the risk of their onset, but research investigating white matter neurodevelopmental pathways explaining associations between the family environment and behavior remains limited. We hypothesized that more positive prenatal and mid-childhood family functioning - a measure of a family's problem solving and supportive capacity - would be associated with two markers of preadolescent white matter neurodevelopment related to reduced behavior problems: higher global fractional anisotropy (FA) and lower global mean diffusivity (MD).
METHODS
Data are from 2727 families in the Generation R Study, the Netherlands. Mothers reported family functioning (McMaster Family Assessment Device, range 1-4, higher scores indicate healthier functioning) prenatally and in mid-childhood (mean age 6.1 years). In preadolescence (mean age 10.1), the study collected diffusion-weighted scans. We computed standardized global MD and FA values by averaging metrics from 27 white matter tracts, and we fit linear models adjusting for possible confounders to examine global and tract-specific outcomes.
RESULTS
Prenatal and mid-childhood family functioning scores were moderately correlated,
CONCLUSIONS
These results suggest high-functioning prenatal or perinatal family environments may confer lasting white matter neurodevelopmental benefits into preadolescence.

Identifiants

pubmed: 35611817
doi: 10.1017/S0033291722001404
pii: S0033291722001404
pmc: PMC10388303
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

4528-4538

Subventions

Organisme : NIMH NIH HHS
ID : T32 MH017119
Pays : United States
Organisme : NICHD NIH HHS
ID : F31 HD096820
Pays : United States

Auteurs

Scott W Delaney (SW)

Department of Social and Behavioral Sciences, Harvard T.H. Chan School of Public Health, Boston, MA USA.
Department of Child and Adolescent Psychiatry, Erasmus University Medical Center, Rotterdam, the Netherlands.
Lee Kum Sheung Center for Health and Happiness, Harvard T.H. Chan School of Public Health, Boston, MA USA.

Yllza Xerxa (Y)

Department of Child and Adolescent Psychiatry, Erasmus University Medical Center, Rotterdam, the Netherlands.
The Generation R Study Group, Erasmus University Medical Center, Rotterdam, the Netherlands.

Ryan L Muetzel (RL)

Department of Child and Adolescent Psychiatry, Erasmus University Medical Center, Rotterdam, the Netherlands.
Department of Epidemiology, Erasmus University Medical Center, Rotterdam, the Netherlands.

Tonya White (T)

Department of Child and Adolescent Psychiatry, Erasmus University Medical Center, Rotterdam, the Netherlands.
Department of Radiology and Nuclear Medicine, Erasmus University Medical Center, Rotterdam, the Netherlands.

Sebastien Haneuse (S)

Department of Biostatistics, Harvard T.H. Chan School of Public Health, Boston, MA USA.

Kerry J Ressler (KJ)

Department of Psychiatry, McLean Hospital, Harvard Medical School, Belmont, MA USA.

Henning Tiemeier (H)

Department of Social and Behavioral Sciences, Harvard T.H. Chan School of Public Health, Boston, MA USA.
Department of Child and Adolescent Psychiatry, Erasmus University Medical Center, Rotterdam, the Netherlands.

Laura D Kubzansky (LD)

Department of Social and Behavioral Sciences, Harvard T.H. Chan School of Public Health, Boston, MA USA.
Lee Kum Sheung Center for Health and Happiness, Harvard T.H. Chan School of Public Health, Boston, MA USA.

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Classifications MeSH