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Assessment of Breast Cancer Risk Factors Reveals Subtype Heterogeneity
Subtype heterogeneity for breast cancer risk factors has been suspected, potentially reflecting etiologic differences and implicating risk prediction. However, reports are conflicting regarding the presence of heterogeneity for many exposures. To examine subtype heterogeneity across known breast can...
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Published in: | Cancer research (Chicago, Ill.) Ill.), 2017-07, Vol.77 (13), p.3708-3717 |
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description | Subtype heterogeneity for breast cancer risk factors has been suspected, potentially reflecting etiologic differences and implicating risk prediction. However, reports are conflicting regarding the presence of heterogeneity for many exposures. To examine subtype heterogeneity across known breast cancer risk factors, we conducted a case-control analysis of 2,632 breast cancers and 15,945 controls in Sweden. Molecular subtype was predicted from pathology record-derived IHC markers by a classifier trained on PAM50 subtyping. Multinomial logistic regression estimated separate ORs for each subtype by the exposures parity, age at first birth, breastfeeding, menarche, hormone replacement therapy use, somatotype at age 18, benign breast disease, mammographic density, polygenic risk score, family history of breast cancer, and BRCA mutations. We found clear subtype heterogeneity for genetic factors and breastfeeding. Polygenic risk score was associated with all subtypes except for the basal-like (
< 0.0001). "Never breastfeeding" was associated with increased risk of basal-like subtype [OR 4.17; 95% confidence interval (CI) 1.89-9.21] compared with both nulliparity (reference) and breastfeeding. Breastfeeding was not associated with risk of HER2-overexpressing type, but protective for all other subtypes. The observed heterogeneity in risk of distinct breast cancer subtypes for germline variants supports heterogeneity in etiology and has implications for their use in risk prediction. The association between basal-like subtype and breastfeeding merits more research into potential causal mechanisms and confounders.
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doi_str_mv | 10.1158/0008-5472.CAN-16-2574 |
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< 0.0001). "Never breastfeeding" was associated with increased risk of basal-like subtype [OR 4.17; 95% confidence interval (CI) 1.89-9.21] compared with both nulliparity (reference) and breastfeeding. Breastfeeding was not associated with risk of HER2-overexpressing type, but protective for all other subtypes. The observed heterogeneity in risk of distinct breast cancer subtypes for germline variants supports heterogeneity in etiology and has implications for their use in risk prediction. The association between basal-like subtype and breastfeeding merits more research into potential causal mechanisms and confounders.
.</description><identifier>ISSN: 0008-5472</identifier><identifier>EISSN: 1538-7445</identifier><identifier>DOI: 10.1158/0008-5472.CAN-16-2574</identifier><identifier>PMID: 28512241</identifier><language>eng</language><publisher>United States: American Association for Cancer Research, Inc</publisher><subject>Breast cancer ; Breast feeding ; Breast Neoplasms - genetics ; Breast Neoplasms - pathology ; Breastfeeding & lactation ; Case-Control Studies ; ErbB-2 protein ; Etiology ; Exposure ; Female ; Genetic factors ; Genetics ; Health risk assessment ; Health risks ; Heterogeneity ; Hormone replacement therapy ; Humans ; Mammography ; Menarche ; Mutation ; Risk Factors ; Treatment Outcome</subject><ispartof>Cancer research (Chicago, Ill.), 2017-07, Vol.77 (13), p.3708-3717</ispartof><rights>2017 American Association for Cancer Research.</rights><rights>Copyright American Association for Cancer Research, Inc. Jul 1, 2017</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c526t-d6452ba8890f2b0e777364aade203e7a1897b95b23337cb9a77fd926a579b6093</citedby><cites>FETCH-LOGICAL-c526t-d6452ba8890f2b0e777364aade203e7a1897b95b23337cb9a77fd926a579b6093</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28512241$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Holm, Johanna</creatorcontrib><creatorcontrib>Eriksson, Louise</creatorcontrib><creatorcontrib>Ploner, Alexander</creatorcontrib><creatorcontrib>Eriksson, Mikael</creatorcontrib><creatorcontrib>Rantalainen, Mattias</creatorcontrib><creatorcontrib>Li, Jingmei</creatorcontrib><creatorcontrib>Hall, Per</creatorcontrib><creatorcontrib>Czene, Kamila</creatorcontrib><title>Assessment of Breast Cancer Risk Factors Reveals Subtype Heterogeneity</title><title>Cancer research (Chicago, Ill.)</title><addtitle>Cancer Res</addtitle><description>Subtype heterogeneity for breast cancer risk factors has been suspected, potentially reflecting etiologic differences and implicating risk prediction. However, reports are conflicting regarding the presence of heterogeneity for many exposures. To examine subtype heterogeneity across known breast cancer risk factors, we conducted a case-control analysis of 2,632 breast cancers and 15,945 controls in Sweden. Molecular subtype was predicted from pathology record-derived IHC markers by a classifier trained on PAM50 subtyping. Multinomial logistic regression estimated separate ORs for each subtype by the exposures parity, age at first birth, breastfeeding, menarche, hormone replacement therapy use, somatotype at age 18, benign breast disease, mammographic density, polygenic risk score, family history of breast cancer, and BRCA mutations. We found clear subtype heterogeneity for genetic factors and breastfeeding. Polygenic risk score was associated with all subtypes except for the basal-like (
< 0.0001). "Never breastfeeding" was associated with increased risk of basal-like subtype [OR 4.17; 95% confidence interval (CI) 1.89-9.21] compared with both nulliparity (reference) and breastfeeding. Breastfeeding was not associated with risk of HER2-overexpressing type, but protective for all other subtypes. The observed heterogeneity in risk of distinct breast cancer subtypes for germline variants supports heterogeneity in etiology and has implications for their use in risk prediction. The association between basal-like subtype and breastfeeding merits more research into potential causal mechanisms and confounders.
.</description><subject>Breast cancer</subject><subject>Breast feeding</subject><subject>Breast Neoplasms - genetics</subject><subject>Breast Neoplasms - pathology</subject><subject>Breastfeeding & lactation</subject><subject>Case-Control Studies</subject><subject>ErbB-2 protein</subject><subject>Etiology</subject><subject>Exposure</subject><subject>Female</subject><subject>Genetic factors</subject><subject>Genetics</subject><subject>Health risk assessment</subject><subject>Health risks</subject><subject>Heterogeneity</subject><subject>Hormone replacement therapy</subject><subject>Humans</subject><subject>Mammography</subject><subject>Menarche</subject><subject>Mutation</subject><subject>Risk Factors</subject><subject>Treatment Outcome</subject><issn>0008-5472</issn><issn>1538-7445</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><recordid>eNpdkF1LwzAUhoMobk5_glLwxpvOfDRNcjmLc8JQmHod0vZUOtd2Jqmwf2_K5i68OhzO874cHoSuCZ4SwuU9xljGPBF0ms1eYpLGlIvkBI0JZzIWScJP0fjIjNCFc-uwcoL5ORpRyQmlCRmj-cw5cK6B1kddFT1YMM5HmWkLsNGqdl_R3BS-sy5awQ-YjYve-tzvthAtwIPtPqGF2u8u0VkVjnB1mBP0MX98zxbx8vXpOZst44LT1MdlmnCaGykVrmiOQQjB0sSYEihmIAyRSuSK55QxJopcGSGqUtHUcKHyFCs2QXf73q3tvntwXje1K2CzMS10vdOhQAnFQiSgt__QddfbNnyniZKMcioxDRTfU4XtnLNQ6a2tG2N3mmA9iNaDRD1I1EG0JqkeRIfczaG9zxsoj6k_s-wXl9Z3Ww</recordid><startdate>20170701</startdate><enddate>20170701</enddate><creator>Holm, Johanna</creator><creator>Eriksson, Louise</creator><creator>Ploner, Alexander</creator><creator>Eriksson, Mikael</creator><creator>Rantalainen, Mattias</creator><creator>Li, Jingmei</creator><creator>Hall, Per</creator><creator>Czene, Kamila</creator><general>American Association for Cancer Research, Inc</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7T5</scope><scope>7TM</scope><scope>7TO</scope><scope>7U9</scope><scope>8FD</scope><scope>FR3</scope><scope>H94</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope></search><sort><creationdate>20170701</creationdate><title>Assessment of Breast Cancer Risk Factors Reveals Subtype Heterogeneity</title><author>Holm, Johanna ; 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< 0.0001). "Never breastfeeding" was associated with increased risk of basal-like subtype [OR 4.17; 95% confidence interval (CI) 1.89-9.21] compared with both nulliparity (reference) and breastfeeding. Breastfeeding was not associated with risk of HER2-overexpressing type, but protective for all other subtypes. The observed heterogeneity in risk of distinct breast cancer subtypes for germline variants supports heterogeneity in etiology and has implications for their use in risk prediction. The association between basal-like subtype and breastfeeding merits more research into potential causal mechanisms and confounders.
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subjects | Breast cancer Breast feeding Breast Neoplasms - genetics Breast Neoplasms - pathology Breastfeeding & lactation Case-Control Studies ErbB-2 protein Etiology Exposure Female Genetic factors Genetics Health risk assessment Health risks Heterogeneity Hormone replacement therapy Humans Mammography Menarche Mutation Risk Factors Treatment Outcome |
title | Assessment of Breast Cancer Risk Factors Reveals Subtype Heterogeneity |
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