No genetic overlap between circulating iron levels and Alzheimer's disease

Iron 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 e...

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Bibliographic Details
Main Authors: Lupton, MK, Benyamin, B, Proitsi, P, Nyholt, DR, Ferreira, MA, Montgomery, GW, Heath, AC, Madden, PA, Medland, SE, Gordon, SD, GERAD1 Consortium, Alzheimer’s Disease Neuroimaging Initiative, Lovestone, S, Tsolaki, M, Kloszewska, I, Soininen, H, Mecocci, P, Vellas, B, Powell, JF, Bush, AI, Wright, MJ, Martin, NG, Whitfield, JB
Format: Journal article
Language:English
Published: IOS Press 2017
Description
Summary:Iron 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.