Association between plasma tau and postoperative delirium incidence and severity: a prospective observational study

Postoperative delirium is associated with increases in the neuronal injury biomarker, neurofilament light (NfL). Here we tested whether two other biomarkers, glial fibrillary acidic protein (GFAP) and tau, are associated with postoperative delirium. A total of 114 surgical patients were recruited in...

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Veröffentlicht in:British journal of anaesthesia : BJA 2021-02, Vol.126 (2), p.458-466
Hauptverfasser: Ballweg, Tyler, White, Marissa, Parker, Margaret, Casey, Cameron, Bo, Amber, Farahbakhsh, Zahra, Kayser, Austin, Blair, Alexander, Lindroth, Heidi, Pearce, Robert A., Blennow, Kaj, Zetterberg, Henrik, Lennertz, Richard, Sanders, Robert D.
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container_issue 2
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container_title British journal of anaesthesia : BJA
container_volume 126
creator Ballweg, Tyler
White, Marissa
Parker, Margaret
Casey, Cameron
Bo, Amber
Farahbakhsh, Zahra
Kayser, Austin
Blair, Alexander
Lindroth, Heidi
Pearce, Robert A.
Blennow, Kaj
Zetterberg, Henrik
Lennertz, Richard
Sanders, Robert D.
description Postoperative delirium is associated with increases in the neuronal injury biomarker, neurofilament light (NfL). Here we tested whether two other biomarkers, glial fibrillary acidic protein (GFAP) and tau, are associated with postoperative delirium. A total of 114 surgical patients were recruited into two prospective biomarker cohort studies with assessment of delirium severity and incidence. Plasma samples were sent for biomarker analysis including tau, NfL, and GFAP, and a panel of 10 cytokines. We determined a priori to adjust for interleukin-8 (IL-8), a marker of inflammation, when assessing associations between biomarkers and delirium incidence and severity. GFAP concentrations showed no relationship to delirium. The change in tau from preoperative concentrations to postoperative Day 1 was greater in patients with postoperative delirium (P
doi_str_mv 10.1016/j.bja.2020.08.061
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Here we tested whether two other biomarkers, glial fibrillary acidic protein (GFAP) and tau, are associated with postoperative delirium. A total of 114 surgical patients were recruited into two prospective biomarker cohort studies with assessment of delirium severity and incidence. Plasma samples were sent for biomarker analysis including tau, NfL, and GFAP, and a panel of 10 cytokines. We determined a priori to adjust for interleukin-8 (IL-8), a marker of inflammation, when assessing associations between biomarkers and delirium incidence and severity. GFAP concentrations showed no relationship to delirium. The change in tau from preoperative concentrations to postoperative Day 1 was greater in patients with postoperative delirium (P&lt;0.001) and correlated with delirium severity (ρ=0.39, P&lt;0.001). The change in tau correlated with increases in IL-8 (P&lt;0.001) and IL-10 (P=0.0029). Linear regression showed that the relevant clinical predictors of tau changes were age (P=0.037), prior stroke/transient ischaemic attack (P=0.001), and surgical blood loss (P&lt;0.001). After adjusting for age, sex, preoperative cognition, and change in IL-8, tau remained significantly associated with delirium severity (P=0.026). Using linear mixed effect models, only tau (not NfL or IL-8) predicted recovery from delirium (P&lt;0.001). The change in plasma tau was associated with delirium incidence and severity, and resolved over time in parallel with delirium features. The impact of this putative perioperative neuronal injury biomarker on long-term cognition merits further investigation. 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Linear regression showed that the relevant clinical predictors of tau changes were age (P=0.037), prior stroke/transient ischaemic attack (P=0.001), and surgical blood loss (P&lt;0.001). After adjusting for age, sex, preoperative cognition, and change in IL-8, tau remained significantly associated with delirium severity (P=0.026). Using linear mixed effect models, only tau (not NfL or IL-8) predicted recovery from delirium (P&lt;0.001). The change in plasma tau was associated with delirium incidence and severity, and resolved over time in parallel with delirium features. The impact of this putative perioperative neuronal injury biomarker on long-term cognition merits further investigation. 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Here we tested whether two other biomarkers, glial fibrillary acidic protein (GFAP) and tau, are associated with postoperative delirium. A total of 114 surgical patients were recruited into two prospective biomarker cohort studies with assessment of delirium severity and incidence. Plasma samples were sent for biomarker analysis including tau, NfL, and GFAP, and a panel of 10 cytokines. We determined a priori to adjust for interleukin-8 (IL-8), a marker of inflammation, when assessing associations between biomarkers and delirium incidence and severity. GFAP concentrations showed no relationship to delirium. The change in tau from preoperative concentrations to postoperative Day 1 was greater in patients with postoperative delirium (P&lt;0.001) and correlated with delirium severity (ρ=0.39, P&lt;0.001). The change in tau correlated with increases in IL-8 (P&lt;0.001) and IL-10 (P=0.0029). 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subjects Aged
Anesthesiology
biomarker
Biomarkers - blood
delirium
Delirium - blood
Delirium - diagnosis
Delirium - epidemiology
Female
glial fibrillary acidic protein
Glial Fibrillary Acidic Protein - blood
Humans
Incidence
inflammation
Interleukin-8 - blood
Life Sciences & Biomedicine
Male
neuronal injury
Neuroscience and Neuroanaesthesia
Neurosciences
Neurovetenskaper
postoperative
Postoperative Complications - blood
Postoperative Complications - diagnosis
Postoperative Complications - epidemiology
Predictive Value of Tests
Prospective Studies
Science & Technology
Severity of Illness Index
surgery
tau
tau Proteins - blood
Time Factors
title Association between plasma tau and postoperative delirium incidence and severity: a prospective observational study
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