Evidence map›Paper›PMID 35873737›Full record

ArticleBiological psychiatry global open science2022

Residence in High-Crime Neighborhoods Moderates the Association Between Interleukin 6 and Social and Nonsocial Reward Brain Responses.

Iris Ka-Yi Chat, Andrew A Gepty, Marin Kautz, Naoise Mac Giollabhui, Zoe V Adogli, Christopher L Coe, Lyn Y Abramson, Thomas M Olino, Lauren B Alloy

Open access · goldAbstract read
In one paragraph

Article in Biological psychiatry global open science, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
0.9field-weighted citation impact, top 32% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

16 citing papers in PubMed, 16 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors at 4 institutions in 1 country.

Iris Ka-Yi ChatDepartment of Psychology and Neuroscience (IK-YC, AAG, MK, NMG, ZVA, TMO, LBA), Temple University, Philadelphia, Pennsylvania; Psychological and Brain Sciences Department (AAG), George Washington University, Washington, District of Columbia; Depression Clinical Research Program (NMG), Massachusetts General Hospital, Boston, Massachusetts; and the Department of Psychology (CLC, LYA), University of Wisconsin, Madison, Wisconsin.
Andrew A GeptyDepartment of Psychology and Neuroscience (IK-YC, AAG, MK, NMG, ZVA, TMO, LBA), Temple University, Philadelphia, Pennsylvania; Psychological and Brain Sciences Department (AAG), George Washington University, Washington, District of Columbia; Depression Clinical Research Program (NMG), Massachusetts General Hospital, Boston, Massachusetts; and the Department of Psychology (CLC, LYA), University of Wisconsin, Madison, Wisconsin.
Marin KautzDepartment of Psychology and Neuroscience (IK-YC, AAG, MK, NMG, ZVA, TMO, LBA), Temple University, Philadelphia, Pennsylvania; Psychological and Brain Sciences Department (AAG), George Washington University, Washington, District of Columbia; Depression Clinical Research Program (NMG), Massachusetts General Hospital, Boston, Massachusetts; and the Department of Psychology (CLC, LYA), University of Wisconsin, Madison, Wisconsin.
Naoise Mac GiollabhuiDepartment of Psychology and Neuroscience (IK-YC, AAG, MK, NMG, ZVA, TMO, LBA), Temple University, Philadelphia, Pennsylvania; Psychological and Brain Sciences Department (AAG), George Washington University, Washington, District of Columbia; Depression Clinical Research Program (NMG), Massachusetts General Hospital, Boston, Massachusetts; and the Department of Psychology (CLC, LYA), University of Wisconsin, Madison, Wisconsin.
Zoe V AdogliDepartment of Psychology and Neuroscience (IK-YC, AAG, MK, NMG, ZVA, TMO, LBA), Temple University, Philadelphia, Pennsylvania; Psychological and Brain Sciences Department (AAG), George Washington University, Washington, District of Columbia; Depression Clinical Research Program (NMG), Massachusetts General Hospital, Boston, Massachusetts; and the Department of Psychology (CLC, LYA), University of Wisconsin, Madison, Wisconsin.
Christopher L CoeDepartment of Psychology and Neuroscience (IK-YC, AAG, MK, NMG, ZVA, TMO, LBA), Temple University, Philadelphia, Pennsylvania; Psychological and Brain Sciences Department (AAG), George Washington University, Washington, District of Columbia; Depression Clinical Research Program (NMG), Massachusetts General Hospital, Boston, Massachusetts; and the Department of Psychology (CLC, LYA), University of Wisconsin, Madison, Wisconsin.
Lyn Y AbramsonDepartment of Psychology and Neuroscience (IK-YC, AAG, MK, NMG, ZVA, TMO, LBA), Temple University, Philadelphia, Pennsylvania; Psychological and Brain Sciences Department (AAG), George Washington University, Washington, District of Columbia; Depression Clinical Research Program (NMG), Massachusetts General Hospital, Boston, Massachusetts; and the Department of Psychology (CLC, LYA), University of Wisconsin, Madison, Wisconsin.
Thomas M OlinoDepartment of Psychology and Neuroscience (IK-YC, AAG, MK, NMG, ZVA, TMO, LBA), Temple University, Philadelphia, Pennsylvania; Psychological and Brain Sciences Department (AAG), George Washington University, Washington, District of Columbia; Depression Clinical Research Program (NMG), Massachusetts General Hospital, Boston, Massachusetts; and the Department of Psychology (CLC, LYA), University of Wisconsin, Madison, Wisconsin.
Lauren B AlloyDepartment of Psychology and Neuroscience (IK-YC, AAG, MK, NMG, ZVA, TMO, LBA), Temple University, Philadelphia, Pennsylvania; Psychological and Brain Sciences Department (AAG), George Washington University, Washington, District of Columbia; Depression Clinical Research Program (NMG), Massachusetts General Hospital, Boston, Massachusetts; and the Department of Psychology (CLC, LYA), University of Wisconsin, Madison, Wisconsin.
Temple University Hospital · USUniversity of Wisconsin–Madison · USGeorge Washington University · USMassachusetts General Hospital · US

Funding

Integrated Reward-Inflammation Model Of First Onset Of Major Depression In Adolescence SupplementR01MH123473 · NIMH · TEMPLE UNIV OF THE COMMONWEALTH · PI ALLOY, LAUREN BERSH, NUSSLOCK, ROBIN · 2021 to 2025
$3.8M
Depression Surge in Adolescence & Gender Differences: Biocognitive MechanismsR01MH079369 · NIMH · TEMPLE UNIV OF THE COMMONWEALTH · PI ABRAMSON, LYN Y, ALLOY, LAUREN BERSH · 2008 to 2012
$3.4M
Risk for Adolescent Depression: Stress, Cognitive Vulnerability, & InflammationR01MH101168 · NIMH · TEMPLE UNIV OF THE COMMONWEALTH · PI ALLOY, LAUREN BERSH · 2013 to 2017
$3.2M
Reward-related Brain Functioning as an Endophenotype for DepressionK01MH092603 · NIMH · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI OLINO, THOMAS M · 2011 to 2015
$701k
Chronic Inflammation as a Pathway to Cognitive Dysfunction in Adolescents and Young Adults with a History of Elevated Depressive SymptomsF31MH118808 · NIMH · TEMPLE UNIV OF THE COMMONWEALTH · PI MAC GIOLLABHUI, NAOISE · 2019 to 2020
$67k
NIMH NIH HHS F31 MH118808NIMH NIH HHS K01 MH092603NIMH NIH HHS R01 MH079369NIMH NIH HHS R01 MH101168NIMH NIH HHS R01 MH123473
6 · The paper itself

Abstract

backgroundResidence in high-crime neighborhoods, especially in childhood, is linked to mental health issues later. Detecting distinct neurobiological processes underlying the effects of this environmental stressor may be critical to identifying prevention and intervention targets. This study examined the relationships of levels of a circulating inflammatory protein with social and monetary reward-related brain function among adolescents who lived in high- versus low-crime neighborhoods during childhood.

methodsA total of 70 participants (mean age = 16.3 years; 57% female) completed measures of inflammatory markers, depression history, and health and 2 functional magnetic resonance imaging tasks assessing responsivity to monetary and social rewards. Multivariate linear regression tested whether individuals with higher interleukin 6, an inflammatory cytokine, who also lived in neighborhoods with higher crime had distinct orbitofrontal cortex and nucleus accumbens activation to monetary reward and social acceptance.

resultsFor adolescents who lived in neighborhoods with more crime, higher interleukin 6 was associated with higher nucleus accumbens responses to social acceptance. We did not detect significant moderating effects of neighborhood crime rates on the associations of interleukin 6 with orbitofrontal cortex responses to social acceptance or orbitofrontal cortex/nucleus accumbens activation during monetary reward anticipation or outcome. These results were obtained before and after adjusting for neighborhood income and other covariates. We did not detect significant moderating effects of neighborhood income.

conclusionsHigh-threat residence environment and specific demands of the social context in childhood may have shaped the effect of peripheral immune activation on reward-related neural function in adolescence. The prevailing view that inflammation-associated behaviors are characterized by blunted responsiveness to reward may be oversimplistic.

Identifiers

PMID35873737
PMCPMC9306340
OpenAlexW4280604868

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.