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Lipid-lowering drugs, dyslipidemia, and breast cancer risk in a Medicare population
Purpose We sought to disentangle the effects of statins and other lipid-lowering drugs and the underlying dyslipidemia for which they are prescribed on breast cancer risk. Methods We conducted a case–control study within the linked Surveillance, Epidemiology, and End results (SEER)-Medicare data. Ca...
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Published in: | Breast cancer research and treatment 2018-06, Vol.169 (3), p.607-614 |
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description | Purpose
We sought to disentangle the effects of statins and other lipid-lowering drugs and the underlying dyslipidemia for which they are prescribed on breast cancer risk.
Methods
We conducted a case–control study within the linked Surveillance, Epidemiology, and End results (SEER)-Medicare data. Cases were women with invasive breast cancer aged 66 + years (
N
= 30,004) identified by SEER registries (years 2007–2011). Controls were women (
N
= 198,969) identified from a 5% random sample of Medicare recipients alive and breast cancer free in year of selection. Participants had a minimum of 13 months of Part A, Part B non-health maintenance organization Medicare and Part D Medicare coverage at least 13 months preceding cancer diagnosis/selection. Exposures were assessed until 12 months before diagnosis/control selection. Odds ratios (OR) and 99.9% confidence intervals (CI) were estimated using adjusted unconditional and multinomial logistic regression.
Results
ORs of invasive breast cancer associated with dyslipidemia, statins, and non-statin lipid-lowering drugs were 0.86 (99.9% CI 0.81–0.90), 1.07 (99.9% CI 1.03–1.13) and 1.03 (99.9% CI 0.95–1.11), respectively. Risk reductions with dyslipidemia were slightly greater when untreated than treated and did not vary much by time between dyslipidemia and breast cancer diagnosis. Whether treated or untreated, dyslipidemia was associated with greater reductions in risk for later stage than earlier stage breast cancer (
p
-heterogeneity |
doi_str_mv | 10.1007/s10549-018-4680-7 |
format | article |
fullrecord | <record><control><sourceid>gale_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_6705395</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><galeid>A538907901</galeid><sourcerecordid>A538907901</sourcerecordid><originalsourceid>FETCH-LOGICAL-c568t-4a3c45bcf71a1b1c6f3cc6d5bd1495e8e68bac087fbb52ac5e16bedda62228803</originalsourceid><addsrcrecordid>eNp1kkFv1DAQhS1ERbeFH8AFWULi1JSxE9vJBamqKCBtxQE4W4492XXJ2sFOivrvSbSl7UogHyx5vvfkmXmEvGZwzgDU-8xAVE0BrC4qWUOhnpEVE6osFGfqOVkBk6qYC_KYnOR8AwCNguYFOeZNJUAqsSLf1n7wrujjb0w-bKhL0yafUXeX-6WAO2_OqAmOtglNHqk1wWKiyeef1Adq6DU6b01COsRh6s3oY3hJjjrTZ3x1f5-SH1cfv19-LtZfP325vFgXVsh6LCpT2kq0tlPMsJZZ2ZXWSidax6pGYI2ybo2FWnVtK7ixApls0TkjOed1DeUp-bD3HaZ2h85iGJPp9ZD8zqQ7HY3Xh5Xgt3oTb7VUIMpGzAZv7w1S_DVhHvVNnFKY_6w5AC8V5w17pDamR-1DF2czu_PZ6gtR1g2oBhbq_B_UfJYZ2hiw8_P7geDdE8EWTT9uc-ynZYL5EGR70KaYc8LuoUMGesmB3udAzznQSw60mjVvno7mQfF38TPA90Aelr1jemz9_65_ALgJvTI</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2002372291</pqid></control><display><type>article</type><title>Lipid-lowering drugs, dyslipidemia, and breast cancer risk in a Medicare population</title><source>Springer Nature</source><creator>Schairer, Catherine ; Freedman, D. Michal ; Gadalla, Shahinaz M. ; Pfeiffer, Ruth M.</creator><creatorcontrib>Schairer, Catherine ; Freedman, D. Michal ; Gadalla, Shahinaz M. ; Pfeiffer, Ruth M.</creatorcontrib><description>Purpose
We sought to disentangle the effects of statins and other lipid-lowering drugs and the underlying dyslipidemia for which they are prescribed on breast cancer risk.
Methods
We conducted a case–control study within the linked Surveillance, Epidemiology, and End results (SEER)-Medicare data. Cases were women with invasive breast cancer aged 66 + years (
N
= 30,004) identified by SEER registries (years 2007–2011). Controls were women (
N
= 198,969) identified from a 5% random sample of Medicare recipients alive and breast cancer free in year of selection. Participants had a minimum of 13 months of Part A, Part B non-health maintenance organization Medicare and Part D Medicare coverage at least 13 months preceding cancer diagnosis/selection. Exposures were assessed until 12 months before diagnosis/control selection. Odds ratios (OR) and 99.9% confidence intervals (CI) were estimated using adjusted unconditional and multinomial logistic regression.
Results
ORs of invasive breast cancer associated with dyslipidemia, statins, and non-statin lipid-lowering drugs were 0.86 (99.9% CI 0.81–0.90), 1.07 (99.9% CI 1.03–1.13) and 1.03 (99.9% CI 0.95–1.11), respectively. Risk reductions with dyslipidemia were slightly greater when untreated than treated and did not vary much by time between dyslipidemia and breast cancer diagnosis. Whether treated or untreated, dyslipidemia was associated with greater reductions in risk for later stage than earlier stage breast cancer (
p
-heterogeneity < 0.0001).
Conclusions
Lipid-lowering drugs did not account for the lower breast cancer risk associated with dyslipidemia. Our data do not support using statins or other lipid-lowering drugs to prevent breast cancer.</description><identifier>ISSN: 0167-6806</identifier><identifier>EISSN: 1573-7217</identifier><identifier>DOI: 10.1007/s10549-018-4680-7</identifier><identifier>PMID: 29450675</identifier><language>eng</language><publisher>New York: Springer US</publisher><subject>Aged ; Aged, 80 and over ; Breast cancer ; Breast Neoplasms - epidemiology ; Breast Neoplasms - etiology ; Cancer prevention ; Cancer research ; Case-Control Studies ; Diagnosis ; Drugs ; Dyslipidemia ; Dyslipidemias - complications ; Dyslipidemias - drug therapy ; Epidemiology ; Female ; Health aspects ; Health maintenance organizations ; Health risk assessment ; HMOs ; Hormone replacement therapy ; Humans ; Hypolipidemic Agents - adverse effects ; Hypolipidemic Agents - therapeutic use ; Invasiveness ; Lipids ; Mammography ; Medical diagnosis ; Medicare ; Medicine ; Medicine & Public Health ; Metabolic disorders ; Odds Ratio ; Oncology ; Risk Assessment ; Risk Factors ; Statins ; United States - epidemiology</subject><ispartof>Breast cancer research and treatment, 2018-06, Vol.169 (3), p.607-614</ispartof><rights>This is a U.S. government work and its text is not subject to copyright protection in the United States; however, its text may be subject to foreign copyright protection 2018</rights><rights>COPYRIGHT 2018 Springer</rights><rights>Breast Cancer Research and Treatment is a copyright of Springer, (2018). All Rights Reserved.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c568t-4a3c45bcf71a1b1c6f3cc6d5bd1495e8e68bac087fbb52ac5e16bedda62228803</citedby><cites>FETCH-LOGICAL-c568t-4a3c45bcf71a1b1c6f3cc6d5bd1495e8e68bac087fbb52ac5e16bedda62228803</cites><orcidid>0000-0001-7671-4972</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,776,780,881,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/29450675$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Schairer, Catherine</creatorcontrib><creatorcontrib>Freedman, D. Michal</creatorcontrib><creatorcontrib>Gadalla, Shahinaz M.</creatorcontrib><creatorcontrib>Pfeiffer, Ruth M.</creatorcontrib><title>Lipid-lowering drugs, dyslipidemia, and breast cancer risk in a Medicare population</title><title>Breast cancer research and treatment</title><addtitle>Breast Cancer Res Treat</addtitle><addtitle>Breast Cancer Res Treat</addtitle><description>Purpose
We sought to disentangle the effects of statins and other lipid-lowering drugs and the underlying dyslipidemia for which they are prescribed on breast cancer risk.
Methods
We conducted a case–control study within the linked Surveillance, Epidemiology, and End results (SEER)-Medicare data. Cases were women with invasive breast cancer aged 66 + years (
N
= 30,004) identified by SEER registries (years 2007–2011). Controls were women (
N
= 198,969) identified from a 5% random sample of Medicare recipients alive and breast cancer free in year of selection. Participants had a minimum of 13 months of Part A, Part B non-health maintenance organization Medicare and Part D Medicare coverage at least 13 months preceding cancer diagnosis/selection. Exposures were assessed until 12 months before diagnosis/control selection. Odds ratios (OR) and 99.9% confidence intervals (CI) were estimated using adjusted unconditional and multinomial logistic regression.
Results
ORs of invasive breast cancer associated with dyslipidemia, statins, and non-statin lipid-lowering drugs were 0.86 (99.9% CI 0.81–0.90), 1.07 (99.9% CI 1.03–1.13) and 1.03 (99.9% CI 0.95–1.11), respectively. Risk reductions with dyslipidemia were slightly greater when untreated than treated and did not vary much by time between dyslipidemia and breast cancer diagnosis. Whether treated or untreated, dyslipidemia was associated with greater reductions in risk for later stage than earlier stage breast cancer (
p
-heterogeneity < 0.0001).
Conclusions
Lipid-lowering drugs did not account for the lower breast cancer risk associated with dyslipidemia. Our data do not support using statins or other lipid-lowering drugs to prevent breast cancer.</description><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Breast cancer</subject><subject>Breast Neoplasms - epidemiology</subject><subject>Breast Neoplasms - etiology</subject><subject>Cancer prevention</subject><subject>Cancer research</subject><subject>Case-Control Studies</subject><subject>Diagnosis</subject><subject>Drugs</subject><subject>Dyslipidemia</subject><subject>Dyslipidemias - complications</subject><subject>Dyslipidemias - drug therapy</subject><subject>Epidemiology</subject><subject>Female</subject><subject>Health aspects</subject><subject>Health maintenance organizations</subject><subject>Health risk assessment</subject><subject>HMOs</subject><subject>Hormone replacement therapy</subject><subject>Humans</subject><subject>Hypolipidemic Agents - adverse effects</subject><subject>Hypolipidemic Agents - therapeutic use</subject><subject>Invasiveness</subject><subject>Lipids</subject><subject>Mammography</subject><subject>Medical diagnosis</subject><subject>Medicare</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Metabolic disorders</subject><subject>Odds Ratio</subject><subject>Oncology</subject><subject>Risk Assessment</subject><subject>Risk Factors</subject><subject>Statins</subject><subject>United States - epidemiology</subject><issn>0167-6806</issn><issn>1573-7217</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><recordid>eNp1kkFv1DAQhS1ERbeFH8AFWULi1JSxE9vJBamqKCBtxQE4W4492XXJ2sFOivrvSbSl7UogHyx5vvfkmXmEvGZwzgDU-8xAVE0BrC4qWUOhnpEVE6osFGfqOVkBk6qYC_KYnOR8AwCNguYFOeZNJUAqsSLf1n7wrujjb0w-bKhL0yafUXeX-6WAO2_OqAmOtglNHqk1wWKiyeef1Adq6DU6b01COsRh6s3oY3hJjjrTZ3x1f5-SH1cfv19-LtZfP325vFgXVsh6LCpT2kq0tlPMsJZZ2ZXWSidax6pGYI2ybo2FWnVtK7ixApls0TkjOed1DeUp-bD3HaZ2h85iGJPp9ZD8zqQ7HY3Xh5Xgt3oTb7VUIMpGzAZv7w1S_DVhHvVNnFKY_6w5AC8V5w17pDamR-1DF2czu_PZ6gtR1g2oBhbq_B_UfJYZ2hiw8_P7geDdE8EWTT9uc-ynZYL5EGR70KaYc8LuoUMGesmB3udAzznQSw60mjVvno7mQfF38TPA90Aelr1jemz9_65_ALgJvTI</recordid><startdate>20180601</startdate><enddate>20180601</enddate><creator>Schairer, Catherine</creator><creator>Freedman, D. Michal</creator><creator>Gadalla, Shahinaz M.</creator><creator>Pfeiffer, Ruth M.</creator><general>Springer US</general><general>Springer</general><general>Springer Nature B.V</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>3V.</scope><scope>7TO</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>H94</scope><scope>K9-</scope><scope>K9.</scope><scope>M0R</scope><scope>M0S</scope><scope>M1P</scope><scope>M2O</scope><scope>MBDVC</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0001-7671-4972</orcidid></search><sort><creationdate>20180601</creationdate><title>Lipid-lowering drugs, dyslipidemia, and breast cancer risk in a Medicare population</title><author>Schairer, Catherine ; Freedman, D. Michal ; Gadalla, Shahinaz M. ; Pfeiffer, Ruth M.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c568t-4a3c45bcf71a1b1c6f3cc6d5bd1495e8e68bac087fbb52ac5e16bedda62228803</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Breast cancer</topic><topic>Breast Neoplasms - epidemiology</topic><topic>Breast Neoplasms - etiology</topic><topic>Cancer prevention</topic><topic>Cancer research</topic><topic>Case-Control Studies</topic><topic>Diagnosis</topic><topic>Drugs</topic><topic>Dyslipidemia</topic><topic>Dyslipidemias - complications</topic><topic>Dyslipidemias - drug therapy</topic><topic>Epidemiology</topic><topic>Female</topic><topic>Health aspects</topic><topic>Health maintenance organizations</topic><topic>Health risk assessment</topic><topic>HMOs</topic><topic>Hormone replacement therapy</topic><topic>Humans</topic><topic>Hypolipidemic Agents - adverse effects</topic><topic>Hypolipidemic Agents - therapeutic use</topic><topic>Invasiveness</topic><topic>Lipids</topic><topic>Mammography</topic><topic>Medical diagnosis</topic><topic>Medicare</topic><topic>Medicine</topic><topic>Medicine & Public Health</topic><topic>Metabolic disorders</topic><topic>Odds Ratio</topic><topic>Oncology</topic><topic>Risk Assessment</topic><topic>Risk Factors</topic><topic>Statins</topic><topic>United States - epidemiology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Schairer, Catherine</creatorcontrib><creatorcontrib>Freedman, D. Michal</creatorcontrib><creatorcontrib>Gadalla, Shahinaz M.</creatorcontrib><creatorcontrib>Pfeiffer, Ruth M.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>Health & Medical Collection (Proquest)</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>ProQuest Public Health Database</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep (ProQuest)</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Consumer Health Database</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Family Health Database (Proquest)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>PML(ProQuest Medical Library)</collection><collection>ProQuest research library</collection><collection>Research Library (Corporate)</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest Central Basic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Breast cancer research and treatment</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Schairer, Catherine</au><au>Freedman, D. Michal</au><au>Gadalla, Shahinaz M.</au><au>Pfeiffer, Ruth M.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Lipid-lowering drugs, dyslipidemia, and breast cancer risk in a Medicare population</atitle><jtitle>Breast cancer research and treatment</jtitle><stitle>Breast Cancer Res Treat</stitle><addtitle>Breast Cancer Res Treat</addtitle><date>2018-06-01</date><risdate>2018</risdate><volume>169</volume><issue>3</issue><spage>607</spage><epage>614</epage><pages>607-614</pages><issn>0167-6806</issn><eissn>1573-7217</eissn><abstract>Purpose
We sought to disentangle the effects of statins and other lipid-lowering drugs and the underlying dyslipidemia for which they are prescribed on breast cancer risk.
Methods
We conducted a case–control study within the linked Surveillance, Epidemiology, and End results (SEER)-Medicare data. Cases were women with invasive breast cancer aged 66 + years (
N
= 30,004) identified by SEER registries (years 2007–2011). Controls were women (
N
= 198,969) identified from a 5% random sample of Medicare recipients alive and breast cancer free in year of selection. Participants had a minimum of 13 months of Part A, Part B non-health maintenance organization Medicare and Part D Medicare coverage at least 13 months preceding cancer diagnosis/selection. Exposures were assessed until 12 months before diagnosis/control selection. Odds ratios (OR) and 99.9% confidence intervals (CI) were estimated using adjusted unconditional and multinomial logistic regression.
Results
ORs of invasive breast cancer associated with dyslipidemia, statins, and non-statin lipid-lowering drugs were 0.86 (99.9% CI 0.81–0.90), 1.07 (99.9% CI 1.03–1.13) and 1.03 (99.9% CI 0.95–1.11), respectively. Risk reductions with dyslipidemia were slightly greater when untreated than treated and did not vary much by time between dyslipidemia and breast cancer diagnosis. Whether treated or untreated, dyslipidemia was associated with greater reductions in risk for later stage than earlier stage breast cancer (
p
-heterogeneity < 0.0001).
Conclusions
Lipid-lowering drugs did not account for the lower breast cancer risk associated with dyslipidemia. Our data do not support using statins or other lipid-lowering drugs to prevent breast cancer.</abstract><cop>New York</cop><pub>Springer US</pub><pmid>29450675</pmid><doi>10.1007/s10549-018-4680-7</doi><tpages>8</tpages><orcidid>https://orcid.org/0000-0001-7671-4972</orcidid><oa>free_for_read</oa></addata></record> |
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source | Springer Nature |
subjects | Aged Aged, 80 and over Breast cancer Breast Neoplasms - epidemiology Breast Neoplasms - etiology Cancer prevention Cancer research Case-Control Studies Diagnosis Drugs Dyslipidemia Dyslipidemias - complications Dyslipidemias - drug therapy Epidemiology Female Health aspects Health maintenance organizations Health risk assessment HMOs Hormone replacement therapy Humans Hypolipidemic Agents - adverse effects Hypolipidemic Agents - therapeutic use Invasiveness Lipids Mammography Medical diagnosis Medicare Medicine Medicine & Public Health Metabolic disorders Odds Ratio Oncology Risk Assessment Risk Factors Statins United States - epidemiology |
title | Lipid-lowering drugs, dyslipidemia, and breast cancer risk in a Medicare population |
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