Open AccessThe neuroinflammatory marker sTNFR2 relates to worse cognition and tau in women across the Alzheimer's disease spectrum
Author(s) -
Bernier Rachel A.,
Banks Sarah J.,
Panizzon Matthew S.,
Andrews Murray J.,
Jacobs Emily G.,
Galasko Douglas R.,
Shepherd Alyx L.,
Akassoglou Katerina,
Sundermann Erin E.
Publication year - 2022
Publication title -
alzheimer's and dementia: diagnosis, assessment and disease monitoring
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.497
H-Index - 37
ISSN - 2352-8729
DOI - 10.1002/dad2.12284
Subject(s) - neuroinflammation , dementia , psychology , cognition , medicine , neuroimaging , cognitive reserve , cognitive decline , disease , hyperintensity , oncology , neuroscience , magnetic resonance imaging , radiology
Despite women showing greater Alzheimer's disease (AD) prevalence, tau burden, and immune/neuroinflammatory response, whether neuroinflammation impacts cognition differently in women versus men and the biological basis of this impact remain unknown. We examined sex differences in how cerebrospinal fluid (CSF) neuroinflammation relates to cognition across the aging–mild cognitive impairment (MCI)–AD continuum and the mediating role of phosphorylated tau (p‐tau) versus other AD biomarkers. Methods Participants included 284 individuals from the Alzheimer's Disease Neuroimaging Initiative study. CSF neuroinflammatory markers included interleukin‐6, tumor necrosis factor α, soluble tumor necrosis factor receptor 2 (sTNFR2), and chitinase‐3‐like protein 1. AD biomarkers were CSF p‐tau 181 and amyloid beta 1‐42 levels and magnetic resonance imaging measures of hippocampal and white matter hyperintensity volumes. Results We found a sex‐by‐sTNFR2 interaction on Mini‐Mental State Examination and Clinical Dementia Rating‐Sum of Boxes. Higher levels of sTNFR2 related to poorer cognition in women only. Among biomarkers, only p‐tau 181 eliminated the female‐specific relationships between neuroinflammation and cognition. Discussion Women may be more susceptible than men to the adverse effects of sTNFR2 on cognition with a potential etiological link with tau to these effects.