Systemic Inflammation Predicts Alzheimer Pathology in Community Samples without Dementia

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2022

Authors

Cherbuin, N.
Walsh, E.I.
Leach, L.
Brüstle, A.
Burns, R.
Anstey, K.J.
Sachdev, P.S.
Baune, B.T.

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Biomedicines, 2022; 10(6):1240-1-1240-14

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Nicolas Cherbuin, Erin I. Walsh, Liana Leach, Anne Brüstle, Richard Burns, Kaarin J. Anstey, Perminder S. Sachdev, and Bernhard T. Baune

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Abstract

Neuroinflammation and oxidative stress (OS) are implicated in the pathophysiology of Alzheimer’s disease (AD). However, it is unclear at what stage of the disease process inflammation first becomes manifest. The aim of this study was to investigate the associations between specific plasma markers of inflammation and OS, tau, and Amyloid-beta 38, 40, and 42 levels in cognitively unimpaired middle-age and older individuals. Associations between inflammatory states identified through principal component analysis and AD biomarkers were investigated in middle-age (52–56 years, n = 335, 52% female) and older-age (72–76 years, n = 351, 46% female) participants without dementia. In middle-age, a component reflecting variation in OS was most strongly associated with tau and to a lesser extent amyloid-beta levels. In older-age, a similar component to that observed in middle-age was only associated with tau, while another component reflecting heightened inflammation independent of OS, was associated with all AD biomarkers. In middle and older-age, inflammation and OS states are associated with plasma AD biomarkers.

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© 2022 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https:// creativecommons.org/licenses/by/ 4.0/).

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