Cargando…

Association of Prenatal Exposure to Early-Life Adversity With Neonatal Brain Volumes at Birth

IMPORTANCE: Exposure to early-life adversity alters the structural development of key brain regions underlying neurodevelopmental impairments. The association between prenatal exposure to adversity and brain structure at birth remains poorly understood. OBJECTIVE: To examine whether prenatal exposur...

Descripción completa

Detalles Bibliográficos
Autores principales: Triplett, Regina L., Lean, Rachel E., Parikh, Amisha, Miller, J. Philip, Alexopoulos, Dimitrios, Kaplan, Sydney, Meyer, Dominique, Adamson, Christopher, Smyser, Tara A., Rogers, Cynthia E., Barch, Deanna M., Warner, Barbara, Luby, Joan L., Smyser, Christopher D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Medical Association 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9006107/
https://www.ncbi.nlm.nih.gov/pubmed/35412624
http://dx.doi.org/10.1001/jamanetworkopen.2022.7045
_version_ 1784686599926185984
author Triplett, Regina L.
Lean, Rachel E.
Parikh, Amisha
Miller, J. Philip
Alexopoulos, Dimitrios
Kaplan, Sydney
Meyer, Dominique
Adamson, Christopher
Smyser, Tara A.
Rogers, Cynthia E.
Barch, Deanna M.
Warner, Barbara
Luby, Joan L.
Smyser, Christopher D.
author_facet Triplett, Regina L.
Lean, Rachel E.
Parikh, Amisha
Miller, J. Philip
Alexopoulos, Dimitrios
Kaplan, Sydney
Meyer, Dominique
Adamson, Christopher
Smyser, Tara A.
Rogers, Cynthia E.
Barch, Deanna M.
Warner, Barbara
Luby, Joan L.
Smyser, Christopher D.
author_sort Triplett, Regina L.
collection PubMed
description IMPORTANCE: Exposure to early-life adversity alters the structural development of key brain regions underlying neurodevelopmental impairments. The association between prenatal exposure to adversity and brain structure at birth remains poorly understood. OBJECTIVE: To examine whether prenatal exposure to maternal social disadvantage and psychosocial stress is associated with neonatal global and regional brain volumes and cortical folding. DESIGN, SETTING, AND PARTICIPANTS: This prospective, longitudinal cohort study included 399 mother-infant dyads of sociodemographically diverse mothers recruited in the first or early second trimester of pregnancy and their infants, who underwent brain magnetic resonance imaging in the first weeks of life. Mothers were recruited from local obstetric clinics in St Louis, Missouri from September 1, 2017, to February 28, 2020. EXPOSURES: Maternal social disadvantage and psychosocial stress in pregnancy. MAIN OUTCOMES AND MEASURES: Confirmatory factor analyses were used to create latent constructs of maternal social disadvantage (income-to-needs ratio, Area Deprivation Index, Healthy Eating Index, educational level, and insurance status) and psychosocial stress (Perceived Stress Scale, Edinburgh Postnatal Depression Scale, Everyday Discrimination Scale, and Stress and Adversity Inventory). Neonatal cortical and subcortical gray matter, white matter, cerebellum, hippocampus, and amygdala volumes were generated using semiautomated, age-specific, segmentation pipelines. RESULTS: A total of 280 mothers (mean [SD] age, 29.1 [5.3] years; 170 [60.7%] Black or African American, 100 [35.7%] White, and 10 [3.6%] other race or ethnicity) and their healthy, term-born infants (149 [53.2%] male; mean [SD] infant gestational age, 38.6 [1.0] weeks) were included in the analysis. After covariate adjustment and multiple comparisons correction, greater social disadvantage was associated with reduced cortical gray matter (unstandardized β = −2.0; 95% CI, −3.5 to −0.5; P = .01), subcortical gray matter (unstandardized β = −0.4; 95% CI, −0.7 to −0.2; P = .003), and white matter (unstandardized β = −5.5; 95% CI, −7.8 to −3.3; P < .001) volumes and cortical folding (unstandardized β = −0.03; 95% CI, −0.04 to −0.01; P < .001). Psychosocial stress showed no association with brain metrics. Although social disadvantage accounted for an additional 2.3% of the variance of the left hippocampus (unstandardized β = −0.03; 95% CI, −0.05 to −0.01), 2.3% of the right hippocampus (unstandardized β = −0.03; 95% CI, −0.05 to −0.01), 3.1% of the left amygdala (unstandardized β = −0.02; 95% CI, −0.03 to −0.01), and 2.9% of the right amygdala (unstandardized β = −0.02; 95% CI, −0.03 to −0.01), no regional effects were found after accounting for total brain volume. CONCLUSIONS AND RELEVANCE: In this baseline assessment of an ongoing cohort study, prenatal social disadvantage was associated with global reductions in brain volumes and cortical folding at birth. No regional specificity for the hippocampus or amygdala was detected. Results highlight that associations between poverty and brain development begin in utero and are evident early in life. These findings emphasize that preventive interventions that support fetal brain development should address parental socioeconomic hardships.
format Online
Article
Text
id pubmed-9006107
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher American Medical Association
record_format MEDLINE/PubMed
spelling pubmed-90061072022-04-27 Association of Prenatal Exposure to Early-Life Adversity With Neonatal Brain Volumes at Birth Triplett, Regina L. Lean, Rachel E. Parikh, Amisha Miller, J. Philip Alexopoulos, Dimitrios Kaplan, Sydney Meyer, Dominique Adamson, Christopher Smyser, Tara A. Rogers, Cynthia E. Barch, Deanna M. Warner, Barbara Luby, Joan L. Smyser, Christopher D. JAMA Netw Open Original Investigation IMPORTANCE: Exposure to early-life adversity alters the structural development of key brain regions underlying neurodevelopmental impairments. The association between prenatal exposure to adversity and brain structure at birth remains poorly understood. OBJECTIVE: To examine whether prenatal exposure to maternal social disadvantage and psychosocial stress is associated with neonatal global and regional brain volumes and cortical folding. DESIGN, SETTING, AND PARTICIPANTS: This prospective, longitudinal cohort study included 399 mother-infant dyads of sociodemographically diverse mothers recruited in the first or early second trimester of pregnancy and their infants, who underwent brain magnetic resonance imaging in the first weeks of life. Mothers were recruited from local obstetric clinics in St Louis, Missouri from September 1, 2017, to February 28, 2020. EXPOSURES: Maternal social disadvantage and psychosocial stress in pregnancy. MAIN OUTCOMES AND MEASURES: Confirmatory factor analyses were used to create latent constructs of maternal social disadvantage (income-to-needs ratio, Area Deprivation Index, Healthy Eating Index, educational level, and insurance status) and psychosocial stress (Perceived Stress Scale, Edinburgh Postnatal Depression Scale, Everyday Discrimination Scale, and Stress and Adversity Inventory). Neonatal cortical and subcortical gray matter, white matter, cerebellum, hippocampus, and amygdala volumes were generated using semiautomated, age-specific, segmentation pipelines. RESULTS: A total of 280 mothers (mean [SD] age, 29.1 [5.3] years; 170 [60.7%] Black or African American, 100 [35.7%] White, and 10 [3.6%] other race or ethnicity) and their healthy, term-born infants (149 [53.2%] male; mean [SD] infant gestational age, 38.6 [1.0] weeks) were included in the analysis. After covariate adjustment and multiple comparisons correction, greater social disadvantage was associated with reduced cortical gray matter (unstandardized β = −2.0; 95% CI, −3.5 to −0.5; P = .01), subcortical gray matter (unstandardized β = −0.4; 95% CI, −0.7 to −0.2; P = .003), and white matter (unstandardized β = −5.5; 95% CI, −7.8 to −3.3; P < .001) volumes and cortical folding (unstandardized β = −0.03; 95% CI, −0.04 to −0.01; P < .001). Psychosocial stress showed no association with brain metrics. Although social disadvantage accounted for an additional 2.3% of the variance of the left hippocampus (unstandardized β = −0.03; 95% CI, −0.05 to −0.01), 2.3% of the right hippocampus (unstandardized β = −0.03; 95% CI, −0.05 to −0.01), 3.1% of the left amygdala (unstandardized β = −0.02; 95% CI, −0.03 to −0.01), and 2.9% of the right amygdala (unstandardized β = −0.02; 95% CI, −0.03 to −0.01), no regional effects were found after accounting for total brain volume. CONCLUSIONS AND RELEVANCE: In this baseline assessment of an ongoing cohort study, prenatal social disadvantage was associated with global reductions in brain volumes and cortical folding at birth. No regional specificity for the hippocampus or amygdala was detected. Results highlight that associations between poverty and brain development begin in utero and are evident early in life. These findings emphasize that preventive interventions that support fetal brain development should address parental socioeconomic hardships. American Medical Association 2022-04-12 /pmc/articles/PMC9006107/ /pubmed/35412624 http://dx.doi.org/10.1001/jamanetworkopen.2022.7045 Text en Copyright 2022 Triplett RL et al. JAMA Network Open. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the CC-BY License.
spellingShingle Original Investigation
Triplett, Regina L.
Lean, Rachel E.
Parikh, Amisha
Miller, J. Philip
Alexopoulos, Dimitrios
Kaplan, Sydney
Meyer, Dominique
Adamson, Christopher
Smyser, Tara A.
Rogers, Cynthia E.
Barch, Deanna M.
Warner, Barbara
Luby, Joan L.
Smyser, Christopher D.
Association of Prenatal Exposure to Early-Life Adversity With Neonatal Brain Volumes at Birth
title Association of Prenatal Exposure to Early-Life Adversity With Neonatal Brain Volumes at Birth
title_full Association of Prenatal Exposure to Early-Life Adversity With Neonatal Brain Volumes at Birth
title_fullStr Association of Prenatal Exposure to Early-Life Adversity With Neonatal Brain Volumes at Birth
title_full_unstemmed Association of Prenatal Exposure to Early-Life Adversity With Neonatal Brain Volumes at Birth
title_short Association of Prenatal Exposure to Early-Life Adversity With Neonatal Brain Volumes at Birth
title_sort association of prenatal exposure to early-life adversity with neonatal brain volumes at birth
topic Original Investigation
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9006107/
https://www.ncbi.nlm.nih.gov/pubmed/35412624
http://dx.doi.org/10.1001/jamanetworkopen.2022.7045
work_keys_str_mv AT triplettreginal associationofprenatalexposuretoearlylifeadversitywithneonatalbrainvolumesatbirth
AT leanrachele associationofprenatalexposuretoearlylifeadversitywithneonatalbrainvolumesatbirth
AT parikhamisha associationofprenatalexposuretoearlylifeadversitywithneonatalbrainvolumesatbirth
AT millerjphilip associationofprenatalexposuretoearlylifeadversitywithneonatalbrainvolumesatbirth
AT alexopoulosdimitrios associationofprenatalexposuretoearlylifeadversitywithneonatalbrainvolumesatbirth
AT kaplansydney associationofprenatalexposuretoearlylifeadversitywithneonatalbrainvolumesatbirth
AT meyerdominique associationofprenatalexposuretoearlylifeadversitywithneonatalbrainvolumesatbirth
AT adamsonchristopher associationofprenatalexposuretoearlylifeadversitywithneonatalbrainvolumesatbirth
AT smysertaraa associationofprenatalexposuretoearlylifeadversitywithneonatalbrainvolumesatbirth
AT rogerscynthiae associationofprenatalexposuretoearlylifeadversitywithneonatalbrainvolumesatbirth
AT barchdeannam associationofprenatalexposuretoearlylifeadversitywithneonatalbrainvolumesatbirth
AT warnerbarbara associationofprenatalexposuretoearlylifeadversitywithneonatalbrainvolumesatbirth
AT lubyjoanl associationofprenatalexposuretoearlylifeadversitywithneonatalbrainvolumesatbirth
AT smyserchristopherd associationofprenatalexposuretoearlylifeadversitywithneonatalbrainvolumesatbirth