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Plasma protein biomarkers of Alzheimer's disease endophenotypes in asymptomatic older twins: early cognitive decline and regional brain volumes

Kiddle, SJ (author)
Steves, CJ (author)
Mehta, M (author)
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Simmons, A (author)
Karolinska Institutet
Xu, X (author)
Newhouse, S (author)
Sattlecker, M (author)
Ashton, NJ (author)
Bazenet, C (author)
Killick, R (author)
Adnan, J (author)
Westman, E (author)
Karolinska Institutet
Nelson, S (author)
Soininen, H (author)
Kloszewska, I (author)
Mecocci, P (author)
Tsolaki, M (author)
Vellas, B (author)
Curtis, C (author)
Breen, G (author)
Williams, SCR (author)
Lovestone, S (author)
Spector, TD (author)
Dobson, RJB (author)
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 (creator_code:org_t)
2015-06-16
2015
English.
In: Translational psychiatry. - : Springer Science and Business Media LLC. - 2158-3188. ; 5, s. e584-
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • There is great interest in blood-based markers of Alzheimer’s disease (AD), especially in its pre-symptomatic stages. Therefore, we aimed to identify plasma proteins whose levels associate with potential markers of pre-symptomatic AD. We also aimed to characterise confounding by genetics and the effect of genetics on blood proteins in general. Panel-based proteomics was performed using SOMAscan on plasma samples from TwinsUK subjects who are asymptomatic for AD, measuring the level of 1129 proteins. Protein levels were compared with 10-year change in CANTAB-paired associates learning (PAL; n=195), and regional brain volumes (n=34). Replication of proteins associated with regional brain volumes was performed in 254 individuals from the AddNeuroMed cohort. Across all the proteins measured, genetic factors were found to explain ~26% of the variability in blood protein levels on average. The plasma level of the mitogen-activated protein kinase (MAPK) MAPKAPK5 protein was found to positively associate with the 10-year change in CANTAB-PAL in both the individual and twin difference context. The plasma level of protein MAP2K4 was found to suggestively associate negatively (Q<0.1) with the volume of the left entorhinal cortex. Future studies will be needed to assess the specificity of MAPKAPK5 and MAP2K4 to eventual conversion to AD.

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