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dc.date.accessioned2022-10-12T15:06:17Z
dc.date.available2022-10-12T15:06:17Z
dc.date.created2022-10-06T10:29:20Z
dc.date.issued2022
dc.identifier.citationDenault, William Robert Paul Bohlin, Jon Page, Christian Magnus Burgess, Stephen Jugessur, Astanand . Cross-fitted instrument: A blueprint for one-sample Mendelian randomization. PLoS Computational Biology. 2022, 18(8)
dc.identifier.urihttp://hdl.handle.net/10852/97223
dc.description.abstractBias from weak instruments may undermine the ability to estimate causal effects in instrumental variable regression (IVR). We present here a new approach to handling weak instrument bias through the application of a new type of instrumental variable coined ‘Cross-Fitted Instrument’ (CFI). CFI splits the data at random and estimates the impact of the instrument on the exposure in each partition. These estimates are then used to perform an IVR on each partition. We adapt CFI to the Mendelian randomization (MR) setting and term this adaptation ‘Cross-Fitting for Mendelian Randomization’ (CFMR). We show that, even when using weak instruments, CFMR is, at worst, biased towards the null, which makes it a conservative one-sample MR approach. In particular, CFMR remains conservative even when the two samples used to perform the MR analysis completely overlap, whereas current state-of-the-art approaches (e.g., MR RAPS) display substantial bias in this setting. Another major advantage of CFMR lies in its use of all of the available data to select genetic instruments, which maximizes statistical power, as opposed to traditional two-sample MR where only part of the data is used to select the instrument. Consequently, CFMR is able to enhance statistical power in consortia-led meta-analyses by enabling a conservative one-sample MR to be performed in each cohort prior to a meta-analysis of the results across all the cohorts. In addition, CFMR enables a cross-ethnic MR analysis by accounting for ethnic heterogeneity, which is particularly important in meta-analyses where the participating cohorts may have different ethnicities. To our knowledge, none of the current MR approaches can account for such heterogeneity. Finally, CFMR enables the application of MR to exposures that are either rare or difficult to measure, which would normally preclude their analysis in the regular two-sample MR setting.
dc.languageEN
dc.publisherPublic Library of Science (PLoS)
dc.rightsAttribution 4.0 International
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.titleCross-fitted instrument: A blueprint for one-sample Mendelian randomization
dc.title.alternativeENEngelskEnglishCross-fitted instrument: A blueprint for one-sample Mendelian randomization
dc.typeJournal article
dc.creator.authorDenault, William Robert Paul
dc.creator.authorBohlin, Jon
dc.creator.authorPage, Christian Magnus
dc.creator.authorBurgess, Stephen
dc.creator.authorJugessur, Astanand
cristin.unitcode185,15,13,25
cristin.unitnameStatistikk og Data Science
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode2
dc.identifier.cristin2059042
dc.identifier.bibliographiccitationinfo:ofi/fmt:kev:mtx:ctx&ctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.jtitle=PLoS Computational Biology&rft.volume=18&rft.spage=&rft.date=2022
dc.identifier.jtitlePLoS Computational Biology
dc.identifier.volume18
dc.identifier.issue8
dc.identifier.pagecount21
dc.identifier.doihttps://doi.org/10.1371/journal.pcbi.1010268
dc.type.documentTidsskriftartikkel
dc.type.peerreviewedPeer reviewed
dc.source.issn1553-734X
dc.type.versionPublishedVersion
cristin.articleide1010268
dc.relation.projectNFR/249779
dc.relation.projectNFR/262700


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