Performance of Disease Risk Score Matching in Nested Case-Control Studies: A Simulation Study
In a case-control study, matching on a disease risk score (DRS), which includes many confounders, should theoretically result in greater precision than matching on only a few confounders; however, this has not been investigated. We simulated 1,000 hypothetical cohorts with a binary exposure, a time-...
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Veröffentlicht in: | American journal of epidemiology 2016-05, Vol.183 (10), p.949-957 |
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creator | Desai, Rishi J Glynn, Robert J Wang, Shirley Gagne, Joshua J |
description | In a case-control study, matching on a disease risk score (DRS), which includes many confounders, should theoretically result in greater precision than matching on only a few confounders; however, this has not been investigated. We simulated 1,000 hypothetical cohorts with a binary exposure, a time-to-event outcome, and 13 covariates. Each cohort comprised 2 subcohorts of 10,000 patients each: a historical subcohort and a concurrent subcohort. DRS were estimated in the historical subcohorts and applied to the concurrent subcohorts. Nested case-control studies were conducted in the concurrent subcohorts using incidence density sampling with 2 strategies-matching on age and sex, with adjustment for additional confounders, and matching on DRS-followed by conditional logistic regression for 9 outcome-exposure incidence scenarios. In all scenarios, DRS matching yielded lower average standard errors and mean squared errors than did matching on age and sex. In 6 scenarios, DRS matching also resulted in greater empirical power. DRS matching resulted in less relative bias than did matching on age and sex at lower outcome incidences but more relative bias at higher incidences. Post-hoc analysis revealed that the effect of DRS model misspecification might be more pronounced at higher outcome incidences, resulting in higher relative bias. These results suggest that DRS matching might increase the statistical efficiency of case-control studies, particularly when the outcome is rare. |
doi_str_mv | 10.1093/aje/kwv269 |
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We simulated 1,000 hypothetical cohorts with a binary exposure, a time-to-event outcome, and 13 covariates. Each cohort comprised 2 subcohorts of 10,000 patients each: a historical subcohort and a concurrent subcohort. DRS were estimated in the historical subcohorts and applied to the concurrent subcohorts. Nested case-control studies were conducted in the concurrent subcohorts using incidence density sampling with 2 strategies-matching on age and sex, with adjustment for additional confounders, and matching on DRS-followed by conditional logistic regression for 9 outcome-exposure incidence scenarios. In all scenarios, DRS matching yielded lower average standard errors and mean squared errors than did matching on age and sex. In 6 scenarios, DRS matching also resulted in greater empirical power. DRS matching resulted in less relative bias than did matching on age and sex at lower outcome incidences but more relative bias at higher incidences. Post-hoc analysis revealed that the effect of DRS model misspecification might be more pronounced at higher outcome incidences, resulting in higher relative bias. These results suggest that DRS matching might increase the statistical efficiency of case-control studies, particularly when the outcome is rare.</description><identifier>ISSN: 0002-9262</identifier><identifier>EISSN: 1476-6256</identifier><identifier>DOI: 10.1093/aje/kwv269</identifier><identifier>PMID: 27189330</identifier><language>eng</language><publisher>United States: Oxford Publishing Limited (England)</publisher><subject>Age ; Case-Control Studies ; Cohort Studies ; Computer Simulation ; Confounding Factors (Epidemiology) ; Disease ; Epidemiologic Methods ; Gender ; Health risk assessment ; Humans ; Incidence ; Logistic Models ; Risk Assessment</subject><ispartof>American journal of epidemiology, 2016-05, Vol.183 (10), p.949-957</ispartof><rights>The Author 2016. Published by Oxford University Press on behalf of the Johns Hopkins Bloomberg School of Public Health. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.</rights><rights>Copyright Oxford Publishing Limited(England) May 15, 2016</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c351t-e400d746d30f0463bf8ef3515595b0f041ef713464676c250faff100867a7b83</citedby><cites>FETCH-LOGICAL-c351t-e400d746d30f0463bf8ef3515595b0f041ef713464676c250faff100867a7b83</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>315,781,785,27928,27929</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/27189330$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Desai, Rishi J</creatorcontrib><creatorcontrib>Glynn, Robert J</creatorcontrib><creatorcontrib>Wang, Shirley</creatorcontrib><creatorcontrib>Gagne, Joshua J</creatorcontrib><title>Performance of Disease Risk Score Matching in Nested Case-Control Studies: A Simulation Study</title><title>American journal of epidemiology</title><addtitle>Am J Epidemiol</addtitle><description>In a case-control study, matching on a disease risk score (DRS), which includes many confounders, should theoretically result in greater precision than matching on only a few confounders; however, this has not been investigated. We simulated 1,000 hypothetical cohorts with a binary exposure, a time-to-event outcome, and 13 covariates. Each cohort comprised 2 subcohorts of 10,000 patients each: a historical subcohort and a concurrent subcohort. DRS were estimated in the historical subcohorts and applied to the concurrent subcohorts. Nested case-control studies were conducted in the concurrent subcohorts using incidence density sampling with 2 strategies-matching on age and sex, with adjustment for additional confounders, and matching on DRS-followed by conditional logistic regression for 9 outcome-exposure incidence scenarios. In all scenarios, DRS matching yielded lower average standard errors and mean squared errors than did matching on age and sex. In 6 scenarios, DRS matching also resulted in greater empirical power. DRS matching resulted in less relative bias than did matching on age and sex at lower outcome incidences but more relative bias at higher incidences. Post-hoc analysis revealed that the effect of DRS model misspecification might be more pronounced at higher outcome incidences, resulting in higher relative bias. These results suggest that DRS matching might increase the statistical efficiency of case-control studies, particularly when the outcome is rare.</description><subject>Age</subject><subject>Case-Control Studies</subject><subject>Cohort Studies</subject><subject>Computer Simulation</subject><subject>Confounding Factors (Epidemiology)</subject><subject>Disease</subject><subject>Epidemiologic Methods</subject><subject>Gender</subject><subject>Health risk assessment</subject><subject>Humans</subject><subject>Incidence</subject><subject>Logistic Models</subject><subject>Risk Assessment</subject><issn>0002-9262</issn><issn>1476-6256</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpdkMtOwzAQRS0EgvLY8AHIEhuEFDqOEzthh8pTKg9RtihykzG4TWKwExB_j0sLC1Yj3Tm6mjmE7DM4YZDzoZrhcP75EYt8jQxYIkUk4lSskwEAxFEei3iLbHs_A2AsT2GTbMWSZTnnMCDPD-i0dY1qS6RW03PjUXmkj8bP6aS0Dumt6spX075Q09I79B1WdBSQaGTbztmaTrq-MuhP6RmdmKavVWds-5N-7ZINrWqPe6u5Q54uL55G19H4_upmdDaOSp6yLsIEoJKJqDhoSASf6gx12KRpnk4XEUMtGU9EIqQo4xS00poBZEIqOc34Djla1r45-96HE4vG-BLrWrVoe18wmYffhRAsoIf_0JntXRuOW1AxzzKQEKjjJVU6671DXbw50yj3VTAoFs6L4LxYOg_wwaqynzZY_aG_kvk3xTR7ew</recordid><startdate>20160515</startdate><enddate>20160515</enddate><creator>Desai, Rishi J</creator><creator>Glynn, Robert J</creator><creator>Wang, Shirley</creator><creator>Gagne, Joshua J</creator><general>Oxford Publishing Limited (England)</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>7QP</scope><scope>7T2</scope><scope>7TK</scope><scope>7U7</scope><scope>7U9</scope><scope>C1K</scope><scope>H94</scope><scope>K9.</scope><scope>NAPCQ</scope><scope>7X8</scope></search><sort><creationdate>20160515</creationdate><title>Performance of Disease Risk Score Matching in Nested Case-Control Studies: A Simulation Study</title><author>Desai, Rishi J ; Glynn, Robert J ; Wang, Shirley ; Gagne, Joshua J</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c351t-e400d746d30f0463bf8ef3515595b0f041ef713464676c250faff100867a7b83</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Age</topic><topic>Case-Control Studies</topic><topic>Cohort Studies</topic><topic>Computer Simulation</topic><topic>Confounding Factors (Epidemiology)</topic><topic>Disease</topic><topic>Epidemiologic Methods</topic><topic>Gender</topic><topic>Health risk assessment</topic><topic>Humans</topic><topic>Incidence</topic><topic>Logistic Models</topic><topic>Risk Assessment</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Desai, Rishi J</creatorcontrib><creatorcontrib>Glynn, Robert J</creatorcontrib><creatorcontrib>Wang, Shirley</creatorcontrib><creatorcontrib>Gagne, Joshua J</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Health and Safety Science Abstracts (Full archive)</collection><collection>Neurosciences Abstracts</collection><collection>Toxicology Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Premium</collection><collection>MEDLINE - Academic</collection><jtitle>American journal of epidemiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Desai, Rishi J</au><au>Glynn, Robert J</au><au>Wang, Shirley</au><au>Gagne, Joshua J</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Performance of Disease Risk Score Matching in Nested Case-Control Studies: A Simulation Study</atitle><jtitle>American journal of epidemiology</jtitle><addtitle>Am J Epidemiol</addtitle><date>2016-05-15</date><risdate>2016</risdate><volume>183</volume><issue>10</issue><spage>949</spage><epage>957</epage><pages>949-957</pages><issn>0002-9262</issn><eissn>1476-6256</eissn><abstract>In a case-control study, matching on a disease risk score (DRS), which includes many confounders, should theoretically result in greater precision than matching on only a few confounders; however, this has not been investigated. 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subjects | Age Case-Control Studies Cohort Studies Computer Simulation Confounding Factors (Epidemiology) Disease Epidemiologic Methods Gender Health risk assessment Humans Incidence Logistic Models Risk Assessment |
title | Performance of Disease Risk Score Matching in Nested Case-Control Studies: A Simulation Study |
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