Frailty modeling under a selective sampling protocol: an application to type 1 diabetes related autoantibodies

dc.contributor.authorNevalainen Jaakko
dc.contributor.authorDatta Somnath
dc.contributor.authorToppari Jorma
dc.contributor.authorIlonen Jorma
dc.contributor.authorHyöty Heikki
dc.contributor.authorVeijola Riitta
dc.contributor.authorKnip Mikael
dc.contributor.authorVirtanen Suvi M
dc.contributor.organizationfi=biolääketieteen laitos|en=Institute of Biomedicine|
dc.contributor.organizationfi=lastentautioppi|en=Paediatrics and Adolescent Medicine|
dc.contributor.organizationfi=tyks, vsshp|en=tyks, varha|
dc.contributor.organizationfi=väestötutkimuskeskus|en=Centre for Population Health Research (POP Centre)|
dc.contributor.organization-code1.2.246.10.2458963.20.42471027641
dc.contributor.organization-code1.2.246.10.2458963.20.77952289591
dc.converis.publication-id67213595
dc.converis.urlhttps://research.utu.fi/converis/portal/Publication/67213595
dc.date.accessioned2022-10-27T12:24:25Z
dc.date.available2022-10-27T12:24:25Z
dc.description.abstract<p>Abstract<br></p><p>In studies following selective sampling protocols for secondary outcomes, conventional analyses regarding their appearance could provide misguided information. In the large type 1 diabetes prevention and prediction (DIPP) cohort study monitoring type 1 diabetes-associated autoantibodies, we propose to model their appearance via a multivariate frailty model, which incorporates a correlation component that is important for unbiased estimation of the baseline hazards under the selective sampling mechanism. As further advantages, the frailty model allows for systematic evaluation of the association and the differences in regression parameters among the autoantibodies. We demonstrate the properties of the model by a simulation study and the analysis of the autoantibodies and their association with background factors in the DIPP study, in which we found that high genetic risk is associated with the appearance of all the autoantibodies, whereas the association with sex and urban municipality was evident for IA-2A and IAA autoantibodies.<br></p>
dc.identifier.eissn1097-0258
dc.identifier.jour-issn0277-6715
dc.identifier.olddbid175291
dc.identifier.oldhandle10024/158385
dc.identifier.urihttps://www.utupub.fi/handle/11111/35852
dc.identifier.urnURN:NBN:fi-fe2021102752590
dc.language.isoen
dc.okm.affiliatedauthorToppari, Jorma
dc.okm.affiliatedauthorDataimport, Lastentautioppi
dc.okm.affiliatedauthorIlonen, Jorma
dc.okm.affiliatedauthorDataimport, tyks, vsshp
dc.okm.discipline3111 Biomedicineen_GB
dc.okm.discipline3111 Biolääketieteetfi_FI
dc.okm.internationalcopublicationinternational co-publication
dc.okm.internationalityInternational publication
dc.okm.typeA1 ScientificArticle
dc.publisherJohn Wiley and Sons Ltd
dc.publisher.countryUnited Kingdomen_GB
dc.publisher.countryBritanniafi_FI
dc.publisher.country-codeGB
dc.relation.doi10.1002/sim.9190
dc.relation.ispartofjournalStatistics in Medicine
dc.source.identifierhttps://www.utupub.fi/handle/10024/158385
dc.titleFrailty modeling under a selective sampling protocol: an application to type 1 diabetes related autoantibodies
dc.year.issued2021

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