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      Assessment of Neighborhood Poverty, Cognitive Function, and Prefrontal and Hippocampal Volumes in Children

      research-article
      , MA 1 , , , PhD 1 , , PhD 1 , , PhD 1 , 2 , 3
      JAMA Network Open
      American Medical Association

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          Key Points

          Question

          What are the associations between neighborhood poverty, child cognitive performance, and brain structure after accounting for household-level poverty?

          Findings

          This cross-sectional study of 11 875 children aged 9 and 10 years found an association between neighborhood poverty, prefrontal and hippocampal volume, and performance on cognitive tasks. These results remained even after controlling for individual household income.

          Meaning

          The findings of this study provide evidence that the broader neighborhood context uniquely contributes to prefrontal and hippocampal development and cognitive performance and should be considered in studies of early life poverty and adversity.

          Abstract

          This cross-sectional study evaluates whether neighborhood poverty is associated with cognitive function and prefrontal and hippocampal brain structure in ways that are dissociable from household socioeconomic status.

          Abstract

          Importance

          The association between poverty and unfavorable cognitive outcomes is robust, but most research has focused on individual household socioeconomic status (SES). There is increasing evidence that neighborhood context explains unique variance not accounted for by household SES.

          Objective

          To evaluate whether neighborhood poverty (NP) is associated with cognitive function and prefrontal and hippocampal brain structure in ways that are dissociable from household SES.

          Design, Setting, and Participants

          This cross-sectional study used a baseline sample of the ongoing longitudinal Adolescent Brain Cognitive Development (ABCD) Study. The ABCD Study will follow participants for assessments each year for 10 years. Data were collected at 21 US sites, mostly within urban and suburban areas, between September 2019 and October 2018. School-based recruitment was used to create a participant sample reflecting the US population. Data analysis was conducted from March to June 2019.

          Main Outcomes and Measures

          NP and household SES were included as factors potentially associated with National Institutes of Health Toolbox Cognitive Battery subtests and hippocampal and prefrontal (dorsolateral prefrontal cortex [DLPFC], dorsomedial PFC [DMPFC], superior frontal gyrus [SFG]) volumes. Independent variables were first considered individually and then together in mixed-effects models with age, sex, and intracranial volume as covariates. Structural equation modeling (SEM) was used to assess shared variance in NP to brain structure and cognitive task associations. The tested hypotheses were formulated after data collection.

          Results

          A total of 11 875 children aged 9 and 10 years (5678 [47.8%] girls) were analyzed. Greater NP was associated with lower scores across all cognitive domains (eg, total composite: β = −0.18; 95% CI, −0.21 to −0.15; P < .001) and with decreased brain volume in the DLPFC (eg, right DLPFC: β = −0.09; 95% CI, −0.12 to −0.07; P < .001), DMPFC (eg, right DMPC: β = −0.07; 95% CI, −0.09 to −0.05; P < .001), SFG (eg, right SFG: β = −0.05; 95% CI, −0.08 to −0.03; P < .001), and right hippocampus (β = −0.04; 95% CI, −0.06 to −0.01; P = .01), even when accounting for household income. Greater household income was associated with higher scores across all cognitive domains (eg, total composite: β = 0.30; 95% CI, 0.28 to 0.33; P < .001) and larger volume in all prefrontal and hippocampal brain regions (eg, right hippocampus: β = 0.04; 95% CI, 0.02 to 0.07; P < .001) even when accounting for NP. The SEM model was a good fit across all cognitive domains, with prefrontal regions being associated with NP relations to language (picture vocabulary: estimate [SE], –0.03 [0.01]; P < .001; oral reading: estimate [SE], –0.02 [0.01]; P < .001), episodic memory (picture sequence: estimate [SE], –0.02 [0.01]; P = .008), and working memory (dimensional card sort: estimate [SE], –0.02 [0.01]; P = .001; flanker inhibitory control: estimate [SE], –0.01 [0.01]; P = .01; list sorting: estimate [SE], –0.03 [0.01]; P < .001) and hippocampal regions being associated with NP associations with language (picture vocabulary: estimate [SE], –0.01 [0.004]; P < .001) and episodic memory (picture sequence: estimate [SE], –0.01 [0.004]; P < 0.001).

          Conclusions and Relevance

          In this study, NP accounted for unique variance in cognitive function and prefrontal and right hippocampal brain volume. These findings demonstrate the importance of including broader environmental influences when conceptualizing early life adversity.

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                Author and article information

                Journal
                JAMA Netw Open
                JAMA Netw Open
                JAMA Netw Open
                JAMA Network Open
                American Medical Association
                2574-3805
                3 November 2020
                November 2020
                3 November 2020
                : 3
                : 11
                : e2023774
                Affiliations
                [1 ]Department of Psychological and Brain Sciences, Washington University, St Louis, Missouri
                [2 ]Department of Psychiatry, Washington University, St Louis, Missouri
                [3 ]Department of Radiology, Washington University, St Louis, Missouri
                Author notes
                Article Information
                Accepted for Publication: September 1, 2020.
                Published: November 3, 2020. doi:10.1001/jamanetworkopen.2020.23774
                Open Access: This is an open access article distributed under the terms of the CC-BY License. © 2020 Taylor RL et al. JAMA Network Open.
                Corresponding Author: Rita L. Taylor, BA, Department of Psychological and Brain Sciences, Washington University, Box 1125, One Brookings Drive, St Louis, MO, 63130 ( ritaltaylor@ 123456wustl.edu ).
                Author Contributions: Ms Taylor had full access to all the data in the study and takes responsibility for the integrity of the data and the accuracy of the data analysis.
                Concept and design: Taylor, Barch.
                Acquisition, analysis, or interpretation of data: All authors.
                Drafting of the manuscript: Taylor.
                Critical revision of the manuscript for important intellectual content: All authors.
                Statistical analysis: Taylor, Cooper, Jackson.
                Obtained funding: Barch.
                Administrative, technical, or material support: Barch.
                Supervision: Barch.
                Conflict of Interest Disclosures: None reported.
                Funding/Support: The Adolescent Brain Cognitive Development (ABCD) Study was supported by National Institute on Drug Abuse, National Institute on Alcohol Abuse and Alcoholism, National Cancer Institute, National Institute of Mental Health, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Heart, Lung, and Blood Institute, National Institute of Neurological Disorders and Stroke, National Institute of Minority Health and Health Disparities, National Institutes of Health Office of Behavioral and Social Sciences Research, National Institutes of Health Office of Research on Women’s Health, US Centers for Disease Control and Prevention–Division of Violence and Prevention, National Institute of Justice, Canter for Disease Control and Prevention–Division of Adolescent and School Health, National Science Foundation, and National Endowment for the Arts.
                Role of the Funder/Sponsor: The funders had no role in the design and conduct of the study; collection, management, analysis, and interpretation of the data; preparation, review, or approval of the manuscript; and decision to submit the manuscript for publication.
                Additional Information: The ABCD data repository grows and changes over time. The ABCD data used in this report came from ABCD Release 2.0.1 161 (doi: 10.15154/1503209). See the ABCD website ( https://nda.nih.gov/abcd/query/abcd-curated-annual-release-2.0.html) for doi information.
                Article
                zoi200787
                10.1001/jamanetworkopen.2020.23774
                7610187
                33141160
                abd1b9fe-066d-45d3-a071-febf8112f068
                Copyright 2020 Taylor RL et al. JAMA Network Open.

                This is an open access article distributed under the terms of the CC-BY License.

                History
                : 18 May 2020
                : 1 September 2020
                Categories
                Research
                Original Investigation
                Online Only
                Pediatrics

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