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Prediagnostic Immune Cell Profiles and Breast Cancer

IMPORTANCE: Higher overall leukocyte counts in women may be associated with increased risk of breast cancer, but the association of specific leukocyte subtypes with breast cancer risk remains unknown. OBJECTIVE: To determine associations between circulating leukocyte subtypes and risk of breast canc...

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Autores principales: Kresovich, Jacob K., O’Brien, Katie M., Xu, Zongli, Weinberg, Clarice R., Sandler, Dale P., Taylor, Jack A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Medical Association 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6991268/
https://www.ncbi.nlm.nih.gov/pubmed/31951276
http://dx.doi.org/10.1001/jamanetworkopen.2019.19536
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author Kresovich, Jacob K.
O’Brien, Katie M.
Xu, Zongli
Weinberg, Clarice R.
Sandler, Dale P.
Taylor, Jack A.
author_facet Kresovich, Jacob K.
O’Brien, Katie M.
Xu, Zongli
Weinberg, Clarice R.
Sandler, Dale P.
Taylor, Jack A.
author_sort Kresovich, Jacob K.
collection PubMed
description IMPORTANCE: Higher overall leukocyte counts in women may be associated with increased risk of breast cancer, but the association of specific leukocyte subtypes with breast cancer risk remains unknown. OBJECTIVE: To determine associations between circulating leukocyte subtypes and risk of breast cancer. DESIGN, SETTING, AND PARTICIPANTS: Between 2003 and 2009, the Sister Study enrolled 50 884 women who had a sister previously diagnosed with breast cancer but were themselves breast cancer free. A case-cohort subsample was selected in July 2014 from the full Sister Study cohort. Blood samples were obtained at baseline, and women were followed up through October 2016. Data analysis was performed in April 2019. MAIN OUTCOMES AND MEASURES: The main outcome was the development of breast cancer in women. Whole-blood DNA methylation was measured, and methylation values were deconvoluted using the Houseman method to estimate proportions of 6 leukocyte subtypes (B cells, natural killer cells, CD8(+) and CD4(+) T cells, monocytes, and granulocytes). Leukocyte subtype proportions were dichotomized at their population median value, and Cox proportional hazard models were used to estimate associations with breast cancer. RESULTS: Among 2774 non-Hispanic white women included in the analysis (mean [SD] age at enrollment, 56.6 [8.8] years), 1295 women were randomly selected from the full cohort (of whom 91 developed breast cancer) along with an additional 1479 women who developed breast cancer during follow-up (mean [SD] time to diagnosis, 3.9 [2.2] years). Circulating proportions of B cells were positively associated with later breast cancer (hazard ratio [HR], 1.17; 95% CI, 1.01-1.36; P = .04). Among women who were premenopausal at blood collection, the association between B cells and breast cancer was significant (HR, 1.38; 95% CI, 1.05-1.82; P = .02), and an inverse association for circulating proportions of monocytes was found (HR, 0.75; 95% CI, 0.57-0.99; P = .05). Among all women, associations between leukocyte subtypes and breast cancer were time dependent: higher monocyte proportions were associated with decreased near-term risk (within 1 year of blood collection, HR, 0.62; 95% CI, 0.43-0.89; P = .01), whereas higher B cell proportions were associated with increased risk 4 or more years after blood collection (HR, 1.38; 95% CI, 1.15-1.67; P = .001). CONCLUSIONS AND RELEVANCE: Circulating leukocyte profiles may be altered before clinical diagnoses of breast cancer and may be time-dependent markers for breast cancer risk, particularly among premenopausal women.
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spelling pubmed-69912682020-02-11 Prediagnostic Immune Cell Profiles and Breast Cancer Kresovich, Jacob K. O’Brien, Katie M. Xu, Zongli Weinberg, Clarice R. Sandler, Dale P. Taylor, Jack A. JAMA Netw Open Original Investigation IMPORTANCE: Higher overall leukocyte counts in women may be associated with increased risk of breast cancer, but the association of specific leukocyte subtypes with breast cancer risk remains unknown. OBJECTIVE: To determine associations between circulating leukocyte subtypes and risk of breast cancer. DESIGN, SETTING, AND PARTICIPANTS: Between 2003 and 2009, the Sister Study enrolled 50 884 women who had a sister previously diagnosed with breast cancer but were themselves breast cancer free. A case-cohort subsample was selected in July 2014 from the full Sister Study cohort. Blood samples were obtained at baseline, and women were followed up through October 2016. Data analysis was performed in April 2019. MAIN OUTCOMES AND MEASURES: The main outcome was the development of breast cancer in women. Whole-blood DNA methylation was measured, and methylation values were deconvoluted using the Houseman method to estimate proportions of 6 leukocyte subtypes (B cells, natural killer cells, CD8(+) and CD4(+) T cells, monocytes, and granulocytes). Leukocyte subtype proportions were dichotomized at their population median value, and Cox proportional hazard models were used to estimate associations with breast cancer. RESULTS: Among 2774 non-Hispanic white women included in the analysis (mean [SD] age at enrollment, 56.6 [8.8] years), 1295 women were randomly selected from the full cohort (of whom 91 developed breast cancer) along with an additional 1479 women who developed breast cancer during follow-up (mean [SD] time to diagnosis, 3.9 [2.2] years). Circulating proportions of B cells were positively associated with later breast cancer (hazard ratio [HR], 1.17; 95% CI, 1.01-1.36; P = .04). Among women who were premenopausal at blood collection, the association between B cells and breast cancer was significant (HR, 1.38; 95% CI, 1.05-1.82; P = .02), and an inverse association for circulating proportions of monocytes was found (HR, 0.75; 95% CI, 0.57-0.99; P = .05). Among all women, associations between leukocyte subtypes and breast cancer were time dependent: higher monocyte proportions were associated with decreased near-term risk (within 1 year of blood collection, HR, 0.62; 95% CI, 0.43-0.89; P = .01), whereas higher B cell proportions were associated with increased risk 4 or more years after blood collection (HR, 1.38; 95% CI, 1.15-1.67; P = .001). CONCLUSIONS AND RELEVANCE: Circulating leukocyte profiles may be altered before clinical diagnoses of breast cancer and may be time-dependent markers for breast cancer risk, particularly among premenopausal women. American Medical Association 2020-01-17 /pmc/articles/PMC6991268/ /pubmed/31951276 http://dx.doi.org/10.1001/jamanetworkopen.2019.19536 Text en Copyright 2020 Kresovich JK et al. JAMA Network Open. http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the CC-BY License.
spellingShingle Original Investigation
Kresovich, Jacob K.
O’Brien, Katie M.
Xu, Zongli
Weinberg, Clarice R.
Sandler, Dale P.
Taylor, Jack A.
Prediagnostic Immune Cell Profiles and Breast Cancer
title Prediagnostic Immune Cell Profiles and Breast Cancer
title_full Prediagnostic Immune Cell Profiles and Breast Cancer
title_fullStr Prediagnostic Immune Cell Profiles and Breast Cancer
title_full_unstemmed Prediagnostic Immune Cell Profiles and Breast Cancer
title_short Prediagnostic Immune Cell Profiles and Breast Cancer
title_sort prediagnostic immune cell profiles and breast cancer
topic Original Investigation
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6991268/
https://www.ncbi.nlm.nih.gov/pubmed/31951276
http://dx.doi.org/10.1001/jamanetworkopen.2019.19536
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