<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Ziegler G</submitter><funding>UCLH Biomedical Research Centre</funding><funding>Jacobs Foundation</funding><funding>Medical Research Council</funding><funding>National Institute for Health Research (NIHR)</funding><funding>Brain and Behavior Research Foundation</funding><funding>Wellcome Trust</funding><pagination>3392-3402</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC7375075</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>41(12)</volume><pubmed_abstract>Socio-economic disadvantage increases exposure to life stressors. Animal research suggests early life stressors impact later neurodevelopment, including myelin developmental growth. To determine how early life disadvantage may affect myelin growth in adolescence and young adulthood, we analysed data from an accelerated longitudinal neuroimaging study measuring magnetisation transfer (MT), a myelin-sensitive marker, in 288 participants (149 female) between 14 and 25 years of age at baseline. We found that early life economic disadvantage before age 12, measured by a neighbourhood poverty index, was associated with slower myelin growth. This association was observed for magnetization transfer in cortical, subcortical and core white matter regions, and also in key subcortical nuclei. Particip</pubmed_abstract><journal>Human brain mapping</journal><pubmed_title>Childhood socio-economic disadvantage predicts reduced myelin growth across adolescence and young adulthood.</pubmed_title><pmcid>PMC7375075</pmcid><funding_grant_id>NIHR200256</funding_grant_id><funding_grant_id>095844</funding_grant_id><funding_grant_id>098362/Z/12/Z</funding_grant_id><funding_grant_id>211155/Z/18/Z</funding_grant_id><funding_grant_id>NF‐SI‐0514‐10157</funding_grant_id><funding_grant_id>2017-1261-04</funding_grant_id><funding_grant_id>NF-SI-0514-10157</funding_grant_id><funding_grant_id>27023</funding_grant_id><funding_grant_id>NF-SI-0513-10051</funding_grant_id><funding_grant_id>Collaboration for Leadership in Applied Health Res</funding_grant_id><funding_grant_id>NF-SI-0510-10228</funding_grant_id><funding_grant_id>2017‐1261‐04</funding_grant_id><funding_grant_id>Senior Investigator Award</funding_grant_id><funding_grant_id>095844/7/11/Z</funding_grant_id><funding_grant_id>MC_G0802534</funding_grant_id><pubmed_authors>Goodyer IM</pubmed_authors><pubmed_authors>Dolan RJ</pubmed_authors><pubmed_authors>Moutoussis M</pubmed_authors><pubmed_authors>Hauser TU</pubmed_authors><pubmed_authors>Fearon P</pubmed_authors><pubmed_authors>Jones PB</pubmed_authors><pubmed_authors>Ziegler G</pubmed_authors><pubmed_authors>Lindenberger U</pubmed_authors><pubmed_authors>Fonagy P</pubmed_authors><pubmed_authors>Bullmore ET</pubmed_authors></additional><is_claimable>false</is_claimable><name>Childhood socio-economic disadvantage predicts reduced myelin growth across adolescence and young adulthood.</name><description>Socio-economic disadvantage increases exposure to life stressors. Animal research suggests early life stressors impact later neurodevelopment, including myelin developmental growth. To determine how early life disadvantage may affect myelin growth in adolescence and young adulthood, we analysed data from an accelerated longitudinal neuroimaging study measuring magnetisation transfer (MT), a myelin-sensitive marker, in 288 participants (149 female) between 14 and 25 years of age at baseline. We found that early life economic disadvantage before age 12, measured by a neighbourhood poverty index, was associated with slower myelin growth. This association was observed for magnetization transfer in cortical, subcortical and core white matter regions, and also in key subcortical nuclei. Particip</description><dates><release>2020-01-01T00:00:00Z</release><publication>2020 Aug</publication><modification>2025-04-19T11:40:02.816Z</modification><creation>2025-04-19T11:40:02.816Z</creation></dates><accession>S-EPMC7375075</accession><cross_references><pubmed>32432383</pubmed><doi>10.1002/hbm.25024</doi></cross_references></HashMap>