Mixed Model with Correction for Case-Control Ascertainment Increases Association Power
We introduce a Liability Threshold Mixed Linear Model (LTMLM) association statistic for ascertained case-control studies that increases power vs. existing mixed model methods for diseases with low prevalence, with a well-controlled false-positive rate. Existing mixed model methods suffer a loss in p...
Gespeichert in:
Veröffentlicht in: | American journal of human genetics 2015-05, Vol.96 (5), p.720-730 |
---|---|
Hauptverfasser: | , , , , , , , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 730 |
---|---|
container_issue | 5 |
container_start_page | 720 |
container_title | American journal of human genetics |
container_volume | 96 |
creator | Hayeck, Tristan Zaitlen, Noah A. Loh, Po-Ru Vilhjalmsson, Bjarni Pollack, Samuela Gusev, Alexander Yang, Jian Chen, Guo-Bo Goddard, Michael E. Visscher, Peter M. Patterson, Nick Price, Alkes L. |
description | We introduce a Liability Threshold Mixed Linear Model (LTMLM) association statistic for ascertained case-control studies that increases power vs. existing mixed model methods for diseases with low prevalence, with a well-controlled false-positive rate. Existing mixed model methods suffer a loss in power under case-control ascertainment, but no solution has been proposed. Here, we solve this problem using a chi-square score statistic computed from posterior mean liabilities (PML) under the liability threshold model. Each individual’s PML is conditional not only on that individual’s case-control status, but also on every individual’s case-control status and on the genetic relationship matrix obtained from the data. The PML are estimated using a multivariate Gibbs sampler, with the liability-scale phenotypic covariance matrix based on the genetic relationship matrix (GRM) and a heritability parameter estimated via Haseman-Elston regression on case-control phenotypes followed by transformation to liability scale. In simulations of unrelated individuals, the LTMLM statistic was correctly calibrated and achieved higher power than existing mixed model methods for diseases with low prevalence, with the magnitude of the improvement depending on sample size and severity of case-control ascertainment. In a WTCCC2 multiple sclerosis data set with >10,000 samples, LTMLM was correctly calibrated and attained a 4.3% improvement (P=0.005) in chi-square statistics (vs. existing mixed model methods) at 75 known associated SNPs, consistent with simulations. Larger increases in power are expected at larger sample sizes. In conclusion, an increase in power over existing mixed model methods is available for ascertained case-control studies of diseases with low prevalence. |
doi_str_mv | 10.1016/j.ajhg.2015.03.004 |
format | Article |
fullrecord | <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_4570278</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0002929715001056</els_id><sourcerecordid>1680210596</sourcerecordid><originalsourceid>FETCH-LOGICAL-c553t-e99d1b394b8783462cdbdce756f329c42f78bb7c859792604955f618eb8688b33</originalsourceid><addsrcrecordid>eNp9kc1u1DAUhS0EosPAC7BAkdh0k3Btx44tIaQq4qdSK1gAWytxbjqOMnaxMy28PQ5TKmDBypLvd47v8SHkOYWKApWvpqqbdlcVAyoq4BVA_YBsqOBNKSWIh2QDAKzUTDcn5ElKEwClCvhjcsKE0oxSuiFfL913HIrLMOBc3LplV7QhRrSLC74YQyzaLmHZBr_EMBdnyWJcOuf36Jfi3NuIeZzyfQrWdb9En8Itxqfk0djNCZ_dnVvy5d3bz-2H8uLj-_P27KK0QvClRK0H2nNd96pRvJbMDv1gsRFy5Ezbmo2N6vvGKqEbzSTUWohRUoW9kkr1nG_Jm6Pv9aHfY5bmPbvZXEe37-IPEzpn_p54tzNX4cbUogGW39yS0zuDGL4dMC1m73LIee48hkMyVCpgFISWGX35DzqFQ_Q53koxqbVWK8WOlI0hpYjj_TIUzFqbmcxam1lrM8BNri2LXvwZ417yu6cMvD4CmD_zxmE0yTr0Fge3lmWG4P7n_xPaoakf</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1682699986</pqid></control><display><type>article</type><title>Mixed Model with Correction for Case-Control Ascertainment Increases Association Power</title><source>MEDLINE</source><source>Cell Press Free Archives</source><source>Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals</source><source>ScienceDirect Journals (5 years ago - present)</source><source>PubMed Central</source><creator>Hayeck, Tristan ; Zaitlen, Noah A. ; Loh, Po-Ru ; Vilhjalmsson, Bjarni ; Pollack, Samuela ; Gusev, Alexander ; Yang, Jian ; Chen, Guo-Bo ; Goddard, Michael E. ; Visscher, Peter M. ; Patterson, Nick ; Price, Alkes L.</creator><creatorcontrib>Hayeck, Tristan ; Zaitlen, Noah A. ; Loh, Po-Ru ; Vilhjalmsson, Bjarni ; Pollack, Samuela ; Gusev, Alexander ; Yang, Jian ; Chen, Guo-Bo ; Goddard, Michael E. ; Visscher, Peter M. ; Patterson, Nick ; Price, Alkes L.</creatorcontrib><description>We introduce a Liability Threshold Mixed Linear Model (LTMLM) association statistic for ascertained case-control studies that increases power vs. existing mixed model methods for diseases with low prevalence, with a well-controlled false-positive rate. Existing mixed model methods suffer a loss in power under case-control ascertainment, but no solution has been proposed. Here, we solve this problem using a chi-square score statistic computed from posterior mean liabilities (PML) under the liability threshold model. Each individual’s PML is conditional not only on that individual’s case-control status, but also on every individual’s case-control status and on the genetic relationship matrix obtained from the data. The PML are estimated using a multivariate Gibbs sampler, with the liability-scale phenotypic covariance matrix based on the genetic relationship matrix (GRM) and a heritability parameter estimated via Haseman-Elston regression on case-control phenotypes followed by transformation to liability scale. In simulations of unrelated individuals, the LTMLM statistic was correctly calibrated and achieved higher power than existing mixed model methods for diseases with low prevalence, with the magnitude of the improvement depending on sample size and severity of case-control ascertainment. In a WTCCC2 multiple sclerosis data set with >10,000 samples, LTMLM was correctly calibrated and attained a 4.3% improvement (P=0.005) in chi-square statistics (vs. existing mixed model methods) at 75 known associated SNPs, consistent with simulations. Larger increases in power are expected at larger sample sizes. In conclusion, an increase in power over existing mixed model methods is available for ascertained case-control studies of diseases with low prevalence.</description><identifier>ISSN: 0002-9297</identifier><identifier>EISSN: 1537-6605</identifier><identifier>DOI: 10.1016/j.ajhg.2015.03.004</identifier><identifier>PMID: 25892111</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Case-Control Studies ; Chromosome Mapping ; Computer Simulation ; Genetic Association Studies ; Genotype & phenotype ; Humans ; Matrix ; Models, Genetic ; Models, Theoretical ; Multiple sclerosis ; Multiple Sclerosis - genetics ; Multiple Sclerosis - pathology ; Phenotype ; Polymorphism, Single Nucleotide ; Regression analysis ; Sample Size ; Simulation</subject><ispartof>American journal of human genetics, 2015-05, Vol.96 (5), p.720-730</ispartof><rights>2015 The American Society of Human Genetics</rights><rights>Copyright © 2015 The American Society of Human Genetics. Published by Elsevier Inc. All rights reserved.</rights><rights>Copyright Cell Press May 7, 2015</rights><rights>2015 The American Society of Human Genetics. Published by Elsevier Ltd. All right reserved. 2015 The American Society of Human Genetics</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c553t-e99d1b394b8783462cdbdce756f329c42f78bb7c859792604955f618eb8688b33</citedby><cites>FETCH-LOGICAL-c553t-e99d1b394b8783462cdbdce756f329c42f78bb7c859792604955f618eb8688b33</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4570278/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.ajhg.2015.03.004$$EHTML$$P50$$Gelsevier$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,3550,27924,27925,45995,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25892111$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Hayeck, Tristan</creatorcontrib><creatorcontrib>Zaitlen, Noah A.</creatorcontrib><creatorcontrib>Loh, Po-Ru</creatorcontrib><creatorcontrib>Vilhjalmsson, Bjarni</creatorcontrib><creatorcontrib>Pollack, Samuela</creatorcontrib><creatorcontrib>Gusev, Alexander</creatorcontrib><creatorcontrib>Yang, Jian</creatorcontrib><creatorcontrib>Chen, Guo-Bo</creatorcontrib><creatorcontrib>Goddard, Michael E.</creatorcontrib><creatorcontrib>Visscher, Peter M.</creatorcontrib><creatorcontrib>Patterson, Nick</creatorcontrib><creatorcontrib>Price, Alkes L.</creatorcontrib><title>Mixed Model with Correction for Case-Control Ascertainment Increases Association Power</title><title>American journal of human genetics</title><addtitle>Am J Hum Genet</addtitle><description>We introduce a Liability Threshold Mixed Linear Model (LTMLM) association statistic for ascertained case-control studies that increases power vs. existing mixed model methods for diseases with low prevalence, with a well-controlled false-positive rate. Existing mixed model methods suffer a loss in power under case-control ascertainment, but no solution has been proposed. Here, we solve this problem using a chi-square score statistic computed from posterior mean liabilities (PML) under the liability threshold model. Each individual’s PML is conditional not only on that individual’s case-control status, but also on every individual’s case-control status and on the genetic relationship matrix obtained from the data. The PML are estimated using a multivariate Gibbs sampler, with the liability-scale phenotypic covariance matrix based on the genetic relationship matrix (GRM) and a heritability parameter estimated via Haseman-Elston regression on case-control phenotypes followed by transformation to liability scale. In simulations of unrelated individuals, the LTMLM statistic was correctly calibrated and achieved higher power than existing mixed model methods for diseases with low prevalence, with the magnitude of the improvement depending on sample size and severity of case-control ascertainment. In a WTCCC2 multiple sclerosis data set with >10,000 samples, LTMLM was correctly calibrated and attained a 4.3% improvement (P=0.005) in chi-square statistics (vs. existing mixed model methods) at 75 known associated SNPs, consistent with simulations. Larger increases in power are expected at larger sample sizes. In conclusion, an increase in power over existing mixed model methods is available for ascertained case-control studies of diseases with low prevalence.</description><subject>Case-Control Studies</subject><subject>Chromosome Mapping</subject><subject>Computer Simulation</subject><subject>Genetic Association Studies</subject><subject>Genotype & phenotype</subject><subject>Humans</subject><subject>Matrix</subject><subject>Models, Genetic</subject><subject>Models, Theoretical</subject><subject>Multiple sclerosis</subject><subject>Multiple Sclerosis - genetics</subject><subject>Multiple Sclerosis - pathology</subject><subject>Phenotype</subject><subject>Polymorphism, Single Nucleotide</subject><subject>Regression analysis</subject><subject>Sample Size</subject><subject>Simulation</subject><issn>0002-9297</issn><issn>1537-6605</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kc1u1DAUhS0EosPAC7BAkdh0k3Btx44tIaQq4qdSK1gAWytxbjqOMnaxMy28PQ5TKmDBypLvd47v8SHkOYWKApWvpqqbdlcVAyoq4BVA_YBsqOBNKSWIh2QDAKzUTDcn5ElKEwClCvhjcsKE0oxSuiFfL913HIrLMOBc3LplV7QhRrSLC74YQyzaLmHZBr_EMBdnyWJcOuf36Jfi3NuIeZzyfQrWdb9En8Itxqfk0djNCZ_dnVvy5d3bz-2H8uLj-_P27KK0QvClRK0H2nNd96pRvJbMDv1gsRFy5Ezbmo2N6vvGKqEbzSTUWohRUoW9kkr1nG_Jm6Pv9aHfY5bmPbvZXEe37-IPEzpn_p54tzNX4cbUogGW39yS0zuDGL4dMC1m73LIee48hkMyVCpgFISWGX35DzqFQ_Q53koxqbVWK8WOlI0hpYjj_TIUzFqbmcxam1lrM8BNri2LXvwZ417yu6cMvD4CmD_zxmE0yTr0Fge3lmWG4P7n_xPaoakf</recordid><startdate>20150507</startdate><enddate>20150507</enddate><creator>Hayeck, Tristan</creator><creator>Zaitlen, Noah A.</creator><creator>Loh, Po-Ru</creator><creator>Vilhjalmsson, Bjarni</creator><creator>Pollack, Samuela</creator><creator>Gusev, Alexander</creator><creator>Yang, Jian</creator><creator>Chen, Guo-Bo</creator><creator>Goddard, Michael E.</creator><creator>Visscher, Peter M.</creator><creator>Patterson, Nick</creator><creator>Price, Alkes L.</creator><general>Elsevier Inc</general><general>Cell Press</general><general>Elsevier</general><scope>6I.</scope><scope>AAFTH</scope><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>7TK</scope><scope>7TM</scope><scope>7U7</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>K9.</scope><scope>NAPCQ</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20150507</creationdate><title>Mixed Model with Correction for Case-Control Ascertainment Increases Association Power</title><author>Hayeck, Tristan ; Zaitlen, Noah A. ; Loh, Po-Ru ; Vilhjalmsson, Bjarni ; Pollack, Samuela ; Gusev, Alexander ; Yang, Jian ; Chen, Guo-Bo ; Goddard, Michael E. ; Visscher, Peter M. ; Patterson, Nick ; Price, Alkes L.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c553t-e99d1b394b8783462cdbdce756f329c42f78bb7c859792604955f618eb8688b33</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Case-Control Studies</topic><topic>Chromosome Mapping</topic><topic>Computer Simulation</topic><topic>Genetic Association Studies</topic><topic>Genotype & phenotype</topic><topic>Humans</topic><topic>Matrix</topic><topic>Models, Genetic</topic><topic>Models, Theoretical</topic><topic>Multiple sclerosis</topic><topic>Multiple Sclerosis - genetics</topic><topic>Multiple Sclerosis - pathology</topic><topic>Phenotype</topic><topic>Polymorphism, Single Nucleotide</topic><topic>Regression analysis</topic><topic>Sample Size</topic><topic>Simulation</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hayeck, Tristan</creatorcontrib><creatorcontrib>Zaitlen, Noah A.</creatorcontrib><creatorcontrib>Loh, Po-Ru</creatorcontrib><creatorcontrib>Vilhjalmsson, Bjarni</creatorcontrib><creatorcontrib>Pollack, Samuela</creatorcontrib><creatorcontrib>Gusev, Alexander</creatorcontrib><creatorcontrib>Yang, Jian</creatorcontrib><creatorcontrib>Chen, Guo-Bo</creatorcontrib><creatorcontrib>Goddard, Michael E.</creatorcontrib><creatorcontrib>Visscher, Peter M.</creatorcontrib><creatorcontrib>Patterson, Nick</creatorcontrib><creatorcontrib>Price, Alkes L.</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><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>Neurosciences Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Toxicology Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Premium</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>American journal of human genetics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hayeck, Tristan</au><au>Zaitlen, Noah A.</au><au>Loh, Po-Ru</au><au>Vilhjalmsson, Bjarni</au><au>Pollack, Samuela</au><au>Gusev, Alexander</au><au>Yang, Jian</au><au>Chen, Guo-Bo</au><au>Goddard, Michael E.</au><au>Visscher, Peter M.</au><au>Patterson, Nick</au><au>Price, Alkes L.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Mixed Model with Correction for Case-Control Ascertainment Increases Association Power</atitle><jtitle>American journal of human genetics</jtitle><addtitle>Am J Hum Genet</addtitle><date>2015-05-07</date><risdate>2015</risdate><volume>96</volume><issue>5</issue><spage>720</spage><epage>730</epage><pages>720-730</pages><issn>0002-9297</issn><eissn>1537-6605</eissn><abstract>We introduce a Liability Threshold Mixed Linear Model (LTMLM) association statistic for ascertained case-control studies that increases power vs. existing mixed model methods for diseases with low prevalence, with a well-controlled false-positive rate. Existing mixed model methods suffer a loss in power under case-control ascertainment, but no solution has been proposed. Here, we solve this problem using a chi-square score statistic computed from posterior mean liabilities (PML) under the liability threshold model. Each individual’s PML is conditional not only on that individual’s case-control status, but also on every individual’s case-control status and on the genetic relationship matrix obtained from the data. The PML are estimated using a multivariate Gibbs sampler, with the liability-scale phenotypic covariance matrix based on the genetic relationship matrix (GRM) and a heritability parameter estimated via Haseman-Elston regression on case-control phenotypes followed by transformation to liability scale. In simulations of unrelated individuals, the LTMLM statistic was correctly calibrated and achieved higher power than existing mixed model methods for diseases with low prevalence, with the magnitude of the improvement depending on sample size and severity of case-control ascertainment. In a WTCCC2 multiple sclerosis data set with >10,000 samples, LTMLM was correctly calibrated and attained a 4.3% improvement (P=0.005) in chi-square statistics (vs. existing mixed model methods) at 75 known associated SNPs, consistent with simulations. Larger increases in power are expected at larger sample sizes. In conclusion, an increase in power over existing mixed model methods is available for ascertained case-control studies of diseases with low prevalence.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>25892111</pmid><doi>10.1016/j.ajhg.2015.03.004</doi><tpages>11</tpages><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0002-9297 |
ispartof | American journal of human genetics, 2015-05, Vol.96 (5), p.720-730 |
issn | 0002-9297 1537-6605 |
language | eng |
recordid | cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_4570278 |
source | MEDLINE; Cell Press Free Archives; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; ScienceDirect Journals (5 years ago - present); PubMed Central |
subjects | Case-Control Studies Chromosome Mapping Computer Simulation Genetic Association Studies Genotype & phenotype Humans Matrix Models, Genetic Models, Theoretical Multiple sclerosis Multiple Sclerosis - genetics Multiple Sclerosis - pathology Phenotype Polymorphism, Single Nucleotide Regression analysis Sample Size Simulation |
title | Mixed Model with Correction for Case-Control Ascertainment Increases Association Power |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-01T17%3A50%3A00IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Mixed%20Model%20with%20Correction%20for%20Case-Control%20Ascertainment%20Increases%20Association%20Power&rft.jtitle=American%20journal%20of%20human%20genetics&rft.au=Hayeck,%20Tristan&rft.date=2015-05-07&rft.volume=96&rft.issue=5&rft.spage=720&rft.epage=730&rft.pages=720-730&rft.issn=0002-9297&rft.eissn=1537-6605&rft_id=info:doi/10.1016/j.ajhg.2015.03.004&rft_dat=%3Cproquest_pubme%3E1680210596%3C/proquest_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1682699986&rft_id=info:pmid/25892111&rft_els_id=S0002929715001056&rfr_iscdi=true |