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Association between indicators of systemic inflammation biomarkers during puberty with breast density and onset of menarche

BACKGROUND: 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, litt...

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Autores principales: Michels, Karin B., Keller, Kristen, Pereira, Ana, Kim, Claire E., Santos, José L., Shepherd, John, Corvalan, Camila, Binder, Alexandra M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7531086/
https://www.ncbi.nlm.nih.gov/pubmed/33004039
http://dx.doi.org/10.1186/s13058-020-01338-y
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author Michels, Karin B.
Keller, Kristen
Pereira, Ana
Kim, Claire E.
Santos, José L.
Shepherd, John
Corvalan, Camila
Binder, Alexandra M.
author_facet Michels, Karin B.
Keller, Kristen
Pereira, Ana
Kim, Claire E.
Santos, José L.
Shepherd, John
Corvalan, Camila
Binder, Alexandra M.
author_sort Michels, Karin B.
collection PubMed
description BACKGROUND: 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. METHODS: 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). Multivariable linear models were used to examine the association between breast composition and each inflammatory marker, stratifying by Tanner stage at inflammatory marker measurement. Accelerated failure time models were used to evaluate the association between inflammatory markers concentrations at each Tanner stage and time to menarche. RESULTS: In age-adjusted linear regression models, a doubling of TNFR2 at Tanner 2 was associated with a 26% (95% CI 7–48%) increase in total breast volume at Tanner 4 and a 22% (95% CI 10–32%) decrease of fibroglandular volume at Tanner 4. In multivariable models further adjusted for body fatness and other covariates, these associations were attenuated to the null. The time to menarche was 3% (95% CI 1–5%) shorter among those in the highest quartile of IL-6 at Tanner 2 relative to those in the lowest quartile in fully adjusted models. Compared to those in the lowest quartile of CRP at Tanner 4, those in the highest quartile experienced 2% (95% CI 0–3%) longer time to menarche in multivariable models. CONCLUSIONS: Systemic inflammation during puberty was not associated with breast volume or breast density at the conclusion of breast development among pubertal girls after adjusting for body fatness; however, these circulating inflammation biomarkers, specifically CRP and IL-6, may affect the timing of menarche onset.
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spelling pubmed-75310862020-10-05 Association between indicators of systemic inflammation biomarkers during puberty with breast density and onset of menarche Michels, Karin B. Keller, Kristen Pereira, Ana Kim, Claire E. Santos, José L. Shepherd, John Corvalan, Camila Binder, Alexandra M. Breast Cancer Res Research Article BACKGROUND: 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. METHODS: 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). Multivariable linear models were used to examine the association between breast composition and each inflammatory marker, stratifying by Tanner stage at inflammatory marker measurement. Accelerated failure time models were used to evaluate the association between inflammatory markers concentrations at each Tanner stage and time to menarche. RESULTS: In age-adjusted linear regression models, a doubling of TNFR2 at Tanner 2 was associated with a 26% (95% CI 7–48%) increase in total breast volume at Tanner 4 and a 22% (95% CI 10–32%) decrease of fibroglandular volume at Tanner 4. In multivariable models further adjusted for body fatness and other covariates, these associations were attenuated to the null. The time to menarche was 3% (95% CI 1–5%) shorter among those in the highest quartile of IL-6 at Tanner 2 relative to those in the lowest quartile in fully adjusted models. Compared to those in the lowest quartile of CRP at Tanner 4, those in the highest quartile experienced 2% (95% CI 0–3%) longer time to menarche in multivariable models. CONCLUSIONS: Systemic inflammation during puberty was not associated with breast volume or breast density at the conclusion of breast development among pubertal girls after adjusting for body fatness; however, these circulating inflammation biomarkers, specifically CRP and IL-6, may affect the timing of menarche onset. BioMed Central 2020-10-01 2020 /pmc/articles/PMC7531086/ /pubmed/33004039 http://dx.doi.org/10.1186/s13058-020-01338-y Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research Article
Michels, Karin B.
Keller, Kristen
Pereira, Ana
Kim, Claire E.
Santos, José L.
Shepherd, John
Corvalan, Camila
Binder, Alexandra M.
Association between indicators of systemic inflammation biomarkers during puberty with breast density and onset of menarche
title Association between indicators of systemic inflammation biomarkers during puberty with breast density and onset of menarche
title_full Association between indicators of systemic inflammation biomarkers during puberty with breast density and onset of menarche
title_fullStr Association between indicators of systemic inflammation biomarkers during puberty with breast density and onset of menarche
title_full_unstemmed Association between indicators of systemic inflammation biomarkers during puberty with breast density and onset of menarche
title_short Association between indicators of systemic inflammation biomarkers during puberty with breast density and onset of menarche
title_sort association between indicators of systemic inflammation biomarkers during puberty with breast density and onset of menarche
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7531086/
https://www.ncbi.nlm.nih.gov/pubmed/33004039
http://dx.doi.org/10.1186/s13058-020-01338-y
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