{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"submitter":["Michels KB"],"funding":["World Cancer Research Fund","World Cancer Research Fund UK (WCRF UK)","Foundation for the National Institutes of Health","NCI NIH HHS","Division of Cancer Prevention, National Cancer Institute","PCI Proyecto","NIGMS NIH HHS","FONDECYT"],"pagination":["104"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC7531086"],"repository":["biostudies-literature"],"omics_type":["Unknown"],"volume":["22(1)"],"pubmed_abstract":["<h4>Background</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.<h4>Methods</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"],"journal":["Breast cancer research : BCR"],"pubmed_title":["Association between indicators of systemic inflammation biomarkers during puberty with breast density and onset of menarche."],"pmcid":["PMC7531086"],"funding_grant_id":["K07 CA225856","REDI170060","11170670","R01CA158313","R01 CA158313","P20 GM113134","2010/245","K07CA225856"],"pubmed_authors":["Shepherd J","Corvalan C","Kim CE","Pereira A","Binder AM","Keller K","Santos JL","Michels KB"],"additional_accession":[]},"is_claimable":false,"name":"Association between indicators of systemic inflammation biomarkers during puberty with breast density and onset of menarche.","description":"<h4>Background</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.<h4>Methods</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","dates":{"release":"2020-01-01T00:00:00Z","publication":"2020 Oct","modification":"2025-04-26T13:28:22.066Z","creation":"2020-10-29T08:40:07Z"},"accession":"S-EPMC7531086","cross_references":{"pubmed":["33004039"],"doi":["10.1186/s13058-020-01338-y"]}}