<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Michels KB</submitter><funding>World Cancer Research Fund</funding><funding>World Cancer Research Fund UK (WCRF UK)</funding><funding>Foundation for the National Institutes of Health</funding><funding>NCI NIH HHS</funding><funding>Division of Cancer Prevention, National Cancer Institute</funding><funding>PCI Proyecto</funding><funding>NIGMS NIH HHS</funding><funding>FONDECYT</funding><pagination>104</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC7531086</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>22(1)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>Systemic inflammation may play a role in shaping breast composition, one of the strongest risk factors for breast cancer. Pubertal development presents a critical window of breast tissue susceptibility to exogenous and endogenous factors, including pro-inflammatory markers. However, little is known about the role of systemic inflammation on adolescent breast composition and pubertal development among girls.&lt;h4>Methods&lt;/h4>We investigated associations between circulating levels of inflammatory markers (e.g., interleukin-6 (IL-6), tumor necrosis factor receptor 2 (TNFR2), and C-reactive protein (CRP)) at Tanner stages 2 and 4 and breast composition at Tanner stage 4 in a cohort of 397 adolescent girls in Santiago, Chile (Growth and Obesity Cohort Study, 2006-2018). Multiva</pubmed_abstract><journal>Breast cancer research : BCR</journal><pubmed_title>Association between indicators of systemic inflammation biomarkers during puberty with breast density and onset of menarche.</pubmed_title><pmcid>PMC7531086</pmcid><funding_grant_id>K07 CA225856</funding_grant_id><funding_grant_id>REDI170060</funding_grant_id><funding_grant_id>11170670</funding_grant_id><funding_grant_id>R01CA158313</funding_grant_id><funding_grant_id>R01 CA158313</funding_grant_id><funding_grant_id>P20 GM113134</funding_grant_id><funding_grant_id>2010/245</funding_grant_id><funding_grant_id>K07CA225856</funding_grant_id><pubmed_authors>Shepherd J</pubmed_authors><pubmed_authors>Corvalan C</pubmed_authors><pubmed_authors>Kim CE</pubmed_authors><pubmed_authors>Pereira A</pubmed_authors><pubmed_authors>Binder AM</pubmed_authors><pubmed_authors>Keller K</pubmed_authors><pubmed_authors>Santos JL</pubmed_authors><pubmed_authors>Michels KB</pubmed_authors></additional><is_claimable>false</is_claimable><name>Association between indicators of systemic inflammation biomarkers during puberty with breast density and onset of menarche.</name><description>&lt;h4>Background&lt;/h4>Systemic inflammation may play a role in shaping breast composition, one of the strongest risk factors for breast cancer. Pubertal development presents a critical window of breast tissue susceptibility to exogenous and endogenous factors, including pro-inflammatory markers. However, little is known about the role of systemic inflammation on adolescent breast composition and pubertal development among girls.&lt;h4>Methods&lt;/h4>We investigated associations between circulating levels of inflammatory markers (e.g., interleukin-6 (IL-6), tumor necrosis factor receptor 2 (TNFR2), and C-reactive protein (CRP)) at Tanner stages 2 and 4 and breast composition at Tanner stage 4 in a cohort of 397 adolescent girls in Santiago, Chile (Growth and Obesity Cohort Study, 2006-2018). Multiva</description><dates><release>2020-01-01T00:00:00Z</release><publication>2020 Oct</publication><modification>2025-04-26T13:28:22.066Z</modification><creation>2020-10-29T08:40:07Z</creation></dates><accession>S-EPMC7531086</accession><cross_references><pubmed>33004039</pubmed><doi>10.1186/s13058-020-01338-y</doi></cross_references></HashMap>