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Systemic Inflammation Predicts Alzheimer Pathology in Community Samples without Dementia.
Cherbuin, Nicolas; Walsh, Erin I; Leach, Liana; Brüstle, Anne; Burns, Richard; Anstey, Kaarin J; Sachdev, Perminder S; Baune, Bernhard T.
Afiliação
  • Cherbuin N; Research School of Population Health, Australian National University, Canberra, ACT 2601, Australia.
  • Walsh EI; Research School of Population Health, Australian National University, Canberra, ACT 2601, Australia.
  • Leach L; Research School of Population Health, Australian National University, Canberra, ACT 2601, Australia.
  • Brüstle A; John Curtin School of Medical Research, Australian National University, Canberra, ACT 2601, Australia.
  • Burns R; Research School of Population Health, Australian National University, Canberra, ACT 2601, Australia.
  • Anstey KJ; School of Psychology, University of New South Wales, Sydney, NSW 2052, Australia.
  • Sachdev PS; Neuroscience Research Australia, Sydney, NSW 2052, Australia.
  • Baune BT; Centre for Healthy Brain Ageing (CHeBA), Discipline of Psychiatry & Mental Health, University of New South Wales, Sydney, NSW 2052, Australia.
Biomedicines ; 10(6)2022 May 26.
Article em En | MEDLINE | ID: mdl-35740262
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-ß 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-ß 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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Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Prognostic_studies / Risk_factors_studies Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Prognostic_studies / Risk_factors_studies Idioma: En Ano de publicação: 2022 Tipo de documento: Article