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Mammographic microcalcifications and risk of breast cancer

BACKGROUND: Mammographic microcalcifications are considered early signs of breast cancer (BC). We examined the association between microcalcification clusters and the risk of overall and subtype-specific BC. Furthermore, we studied how mammographic density (MD) influences the association between mic...

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Autores principales: Azam, Shadi, Eriksson, Mikael, Sjölander, Arvid, Gabrielson, Marike, Hellgren, Roxanna, Czene, Kamila, Hall, Per
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8405644/
https://www.ncbi.nlm.nih.gov/pubmed/34127810
http://dx.doi.org/10.1038/s41416-021-01459-x
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author Azam, Shadi
Eriksson, Mikael
Sjölander, Arvid
Gabrielson, Marike
Hellgren, Roxanna
Czene, Kamila
Hall, Per
author_facet Azam, Shadi
Eriksson, Mikael
Sjölander, Arvid
Gabrielson, Marike
Hellgren, Roxanna
Czene, Kamila
Hall, Per
author_sort Azam, Shadi
collection PubMed
description BACKGROUND: Mammographic microcalcifications are considered early signs of breast cancer (BC). We examined the association between microcalcification clusters and the risk of overall and subtype-specific BC. Furthermore, we studied how mammographic density (MD) influences the association between microcalcification clusters and BC risk. METHODS: We used a prospective cohort (n = 53,273) of Swedish women with comprehensive information on BC risk factors and mammograms. The total number of microcalcification clusters and MD were measured using a computer-aided detection system and the STRATUS method, respectively. Cox regressions and logistic regressions were used to analyse the data. RESULTS: Overall, 676 women were diagnosed with BC. Women with ≥3 microcalcification clusters had a hazard ratio [HR] of 2.17 (95% confidence interval [CI] = 1.57–3.01) compared to women with no clusters. The estimated risk was more pronounced in premenopausal women (HR = 2.93; 95% CI = 1.67–5.16). For postmenopausal women, microcalcification clusters and MD had a similar influence on BC risk. No interaction was observed between microcalcification clusters and MD. Microcalcification clusters were significantly associated with in situ breast cancer (odds ratio: 2.03; 95% CI = 1.13–3.63). CONCLUSIONS: Microcalcification clusters are an independent risk factor for BC, with a higher estimated risk in premenopausal women. In postmenopausal women, microcalcification clusters have a similar association with BC as baseline MD.
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spelling pubmed-84056442021-09-16 Mammographic microcalcifications and risk of breast cancer Azam, Shadi Eriksson, Mikael Sjölander, Arvid Gabrielson, Marike Hellgren, Roxanna Czene, Kamila Hall, Per Br J Cancer Article BACKGROUND: Mammographic microcalcifications are considered early signs of breast cancer (BC). We examined the association between microcalcification clusters and the risk of overall and subtype-specific BC. Furthermore, we studied how mammographic density (MD) influences the association between microcalcification clusters and BC risk. METHODS: We used a prospective cohort (n = 53,273) of Swedish women with comprehensive information on BC risk factors and mammograms. The total number of microcalcification clusters and MD were measured using a computer-aided detection system and the STRATUS method, respectively. Cox regressions and logistic regressions were used to analyse the data. RESULTS: Overall, 676 women were diagnosed with BC. Women with ≥3 microcalcification clusters had a hazard ratio [HR] of 2.17 (95% confidence interval [CI] = 1.57–3.01) compared to women with no clusters. The estimated risk was more pronounced in premenopausal women (HR = 2.93; 95% CI = 1.67–5.16). For postmenopausal women, microcalcification clusters and MD had a similar influence on BC risk. No interaction was observed between microcalcification clusters and MD. Microcalcification clusters were significantly associated with in situ breast cancer (odds ratio: 2.03; 95% CI = 1.13–3.63). CONCLUSIONS: Microcalcification clusters are an independent risk factor for BC, with a higher estimated risk in premenopausal women. In postmenopausal women, microcalcification clusters have a similar association with BC as baseline MD. Nature Publishing Group UK 2021-06-14 2021-08-31 /pmc/articles/PMC8405644/ /pubmed/34127810 http://dx.doi.org/10.1038/s41416-021-01459-x Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Azam, Shadi
Eriksson, Mikael
Sjölander, Arvid
Gabrielson, Marike
Hellgren, Roxanna
Czene, Kamila
Hall, Per
Mammographic microcalcifications and risk of breast cancer
title Mammographic microcalcifications and risk of breast cancer
title_full Mammographic microcalcifications and risk of breast cancer
title_fullStr Mammographic microcalcifications and risk of breast cancer
title_full_unstemmed Mammographic microcalcifications and risk of breast cancer
title_short Mammographic microcalcifications and risk of breast cancer
title_sort mammographic microcalcifications and risk of breast cancer
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8405644/
https://www.ncbi.nlm.nih.gov/pubmed/34127810
http://dx.doi.org/10.1038/s41416-021-01459-x
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