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dc.contributor.authorLupton MK
dc.contributor.authorBenyamin B
dc.contributor.authorProitsi P
dc.contributor.authorNyholt DR
dc.contributor.authorFerreira MA
dc.contributor.authorMontgomery GW
dc.contributor.authorHeath AC
dc.contributor.authorMadden PA
dc.contributor.authorMedland SE
dc.contributor.authorGordon SD
dc.contributor.authorLovestone S
dc.contributor.authorTsolaki M
dc.contributor.authorKloszewska I
dc.contributor.authorSoininen H
dc.contributor.authorMecocci P
dc.contributor.authorVellas B
dc.contributor.authorPowell JF
dc.contributor.authorBush AI
dc.contributor.authorWright MJ
dc.contributor.authorMartin NG
dc.contributor.authorWhitfield JB
dc.date.accessioned2017-06-19T11:56:11Z
dc.date.available2017-06-19T11:56:11Z
dc.date.issued2017
dc.identifier10.3233/JAD-170027fi_FI
dc.identifier.issn1387-2877
dc.identifier.urihttps://erepo.uef.fi/handle/123456789/2616
dc.descriptionArticle
dc.description.abstractIron deposition in the brain is a prominent feature of Alzheimer’s disease (AD). Recently, peripheral iron measures have also been shown to be associated with AD status. However, it is not known whether these associations are causal: do elevated or depleted iron levels throughout life have an effect on AD risk? We evaluate the effects of peripheral iron on AD risk using a genetic profile score approach by testing whether variants affecting iron, transferrin, or ferritin levels selected from GWAS meta-analysis of approximately 24,000 individuals are also associated with AD risk in an independent case-control cohort (n∼10,000). Conversely, we test whether AD risk variants from a GWAS meta-analysis of approximately 54,000 account for any variance in iron measures (n∼9,000). We do not identify a genetic relationship, suggesting that peripheral iron is not causal in the initiation of AD pathology.fi_FI
dc.language.isoENfi_FI
dc.publisherIOS Pressfi_FI
dc.relation.ispartofseriesJournal of Alzheimer's Disease
dc.relation.urihttp://dx.doi.org/10.3233/JAD-170027fi_FI
dc.rightsIn copyright 1.0
dc.subjectAlzheimer’s diseasefi_FI
dc.subjectapolipoproteins Efi_FI
dc.subjectdementiafi_FI
dc.subjectferritinfi_FI
dc.subjectgenetic profile scoresfi_FI
dc.subjectgenome-wide association studyfi_FI
dc.subjectironfi_FI
dc.subjectpopulation geneticsfi_FI
dc.subjecttransferrinfi_FI
dc.titleNo Genetic Overlap Between Circulating Iron Levels and Alzheimer's Diseasefi_FI
dc.typehttp://purl.org/eprint/type/JournalArticle
dc.description.versionfinal draftfi_FI
dc.contributor.departmentFaculty of Health Sciences, shared activities
uef.solecris.id47618144
eprint.statushttp://purl.org/eprint/status/PeerReviewedfi_FI
dc.type.publicationinfo:eu-repo/semantics/article
uef.citationinfo.issuePublished: 30 May 2017
dc.relation.doi10.3233/JAD-170027
dc.description.reviewstatushttp://purl.org/eprint/status/PeerReviewed
dc.relation.issn1387-2877
dc.relation.issuePublished: 30 May 2017
dc.rights.accesslevelopenAccess
dc.rights.copyright© IOS Press and the authors
dc.type.displayTypearticleen
dc.type.displayTypeartikkelifi
dc.rights.urlhttps://rightsstatements.org/page/InC/1.0/


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