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Association of CSF Alzheimer's disease biomarkers with postoperative delirium in older adults

INTRODUCTION: The interaction between delirium and dementia is complex. We examined if Alzheimer's disease (AD) biomarkers in patients without clinical dementia are associated with increased risk of postoperative delirium, and whether AD biomarkers demonstrate a graded association with delirium...

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Autores principales: Fong, Tamara G., Vasunilashorn, Sarinnapha M., Gou, Yun, Libermann, Towia A., Dillon, Simon, Schmitt, Eva, Arnold, Steven E., Kivisäkk, Pia, Carlyle, Becky, Oh, Esther S., Vlassakov, Kamen, Kunze, Lisa, Hshieh, Tammy, Jones, Richard N., Marcantonio, Edward R., Inouye, Sharon K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7968120/
https://www.ncbi.nlm.nih.gov/pubmed/33748398
http://dx.doi.org/10.1002/trc2.12125
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author Fong, Tamara G.
Vasunilashorn, Sarinnapha M.
Gou, Yun
Libermann, Towia A.
Dillon, Simon
Schmitt, Eva
Arnold, Steven E.
Kivisäkk, Pia
Carlyle, Becky
Oh, Esther S.
Vlassakov, Kamen
Kunze, Lisa
Hshieh, Tammy
Jones, Richard N.
Marcantonio, Edward R.
Inouye, Sharon K.
author_facet Fong, Tamara G.
Vasunilashorn, Sarinnapha M.
Gou, Yun
Libermann, Towia A.
Dillon, Simon
Schmitt, Eva
Arnold, Steven E.
Kivisäkk, Pia
Carlyle, Becky
Oh, Esther S.
Vlassakov, Kamen
Kunze, Lisa
Hshieh, Tammy
Jones, Richard N.
Marcantonio, Edward R.
Inouye, Sharon K.
author_sort Fong, Tamara G.
collection PubMed
description INTRODUCTION: The interaction between delirium and dementia is complex. We examined if Alzheimer's disease (AD) biomarkers in patients without clinical dementia are associated with increased risk of postoperative delirium, and whether AD biomarkers demonstrate a graded association with delirium severity. METHODS: Participants (n = 59) were free of clinical dementia, age [Formula: see text] 70 years, and scheduled for elective total knee or hip arthroplasties. Cerebrospinal fluid (CSF) was collected at the time of induction for spinal anesthesia. CSF AD biomarkers were measured by enzyme‐linked immunosorbent assay (ELISA) (ADX/Euroimmun); cut points for amyloid, tau, and neurodegeneration (ATN) biomarker status were A = amyloid beta (Aβ)(42) <175 pg/mL or Aβ(42/40) ratio <0.07; T = p‐tau >80 pg/mL; and N = t‐tau >700 pg/mL. Confusion Assessment Method (CAM) and CAM‐Severity (CAM‐S) were rated daily post‐operatively for delirium and delirium severity, respectively. RESULTS: Aβ(42), tau, and p‐tau mean pg/mL (SD) were 361.5 (326.1), 618.3 (237.1), and 97.1 (66.1), respectively, for those with delirium, and 550.4 (291.6), 518.3 (213.5), and 54.6 (34.5), respectively, for those without delirium. Thirteen participants (22%) were ATN positive. Delirium severity by peak CAM‐S [mean difference (95% confidence interval)] was 1.48 points higher (0.29‐2.67), P = 0.02 among the ATN positive. Delirium in the ATN‐positive group trended toward but did not reach statistical significance (23% vs. 7%, p = 0.10). Peak CAM‐S [mean (SD)] in the delirium group was 7 (2.8) compared to no delirium group 2.5 (1.3), but when groups were further classified by ATN status, an incremental effect on delirium severity was observed, such that patients who were both ATN and delirium negative had the lowest mean (SD) peak CAM‐S scores of 2.5 (1.3) points, whereas those who were ATN and delirium positive had CAM‐S scores of 8.7 (2.3) points; other groups (either ATN or delirium positive) had intermediate CAM‐S scores. DISCUSSION: The presence of AD biomarkers adds important information in predicting delirium severity. Future studies are needed to confirm this relationship and to better understand the role of AD biomarkers, even in pre‐clinical phase, in delirium.
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spelling pubmed-79681202021-03-19 Association of CSF Alzheimer's disease biomarkers with postoperative delirium in older adults Fong, Tamara G. Vasunilashorn, Sarinnapha M. Gou, Yun Libermann, Towia A. Dillon, Simon Schmitt, Eva Arnold, Steven E. Kivisäkk, Pia Carlyle, Becky Oh, Esther S. Vlassakov, Kamen Kunze, Lisa Hshieh, Tammy Jones, Richard N. Marcantonio, Edward R. Inouye, Sharon K. Alzheimers Dement (N Y) Research Articles INTRODUCTION: The interaction between delirium and dementia is complex. We examined if Alzheimer's disease (AD) biomarkers in patients without clinical dementia are associated with increased risk of postoperative delirium, and whether AD biomarkers demonstrate a graded association with delirium severity. METHODS: Participants (n = 59) were free of clinical dementia, age [Formula: see text] 70 years, and scheduled for elective total knee or hip arthroplasties. Cerebrospinal fluid (CSF) was collected at the time of induction for spinal anesthesia. CSF AD biomarkers were measured by enzyme‐linked immunosorbent assay (ELISA) (ADX/Euroimmun); cut points for amyloid, tau, and neurodegeneration (ATN) biomarker status were A = amyloid beta (Aβ)(42) <175 pg/mL or Aβ(42/40) ratio <0.07; T = p‐tau >80 pg/mL; and N = t‐tau >700 pg/mL. Confusion Assessment Method (CAM) and CAM‐Severity (CAM‐S) were rated daily post‐operatively for delirium and delirium severity, respectively. RESULTS: Aβ(42), tau, and p‐tau mean pg/mL (SD) were 361.5 (326.1), 618.3 (237.1), and 97.1 (66.1), respectively, for those with delirium, and 550.4 (291.6), 518.3 (213.5), and 54.6 (34.5), respectively, for those without delirium. Thirteen participants (22%) were ATN positive. Delirium severity by peak CAM‐S [mean difference (95% confidence interval)] was 1.48 points higher (0.29‐2.67), P = 0.02 among the ATN positive. Delirium in the ATN‐positive group trended toward but did not reach statistical significance (23% vs. 7%, p = 0.10). Peak CAM‐S [mean (SD)] in the delirium group was 7 (2.8) compared to no delirium group 2.5 (1.3), but when groups were further classified by ATN status, an incremental effect on delirium severity was observed, such that patients who were both ATN and delirium negative had the lowest mean (SD) peak CAM‐S scores of 2.5 (1.3) points, whereas those who were ATN and delirium positive had CAM‐S scores of 8.7 (2.3) points; other groups (either ATN or delirium positive) had intermediate CAM‐S scores. DISCUSSION: The presence of AD biomarkers adds important information in predicting delirium severity. Future studies are needed to confirm this relationship and to better understand the role of AD biomarkers, even in pre‐clinical phase, in delirium. John Wiley and Sons Inc. 2021-03-17 /pmc/articles/PMC7968120/ /pubmed/33748398 http://dx.doi.org/10.1002/trc2.12125 Text en © 2020 The Authors. Alzheimer's & Dementia: Translational Research & Clinical Interventions published by Wiley Periodicals, Inc. on behalf of Alzheimer's Association. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Research Articles
Fong, Tamara G.
Vasunilashorn, Sarinnapha M.
Gou, Yun
Libermann, Towia A.
Dillon, Simon
Schmitt, Eva
Arnold, Steven E.
Kivisäkk, Pia
Carlyle, Becky
Oh, Esther S.
Vlassakov, Kamen
Kunze, Lisa
Hshieh, Tammy
Jones, Richard N.
Marcantonio, Edward R.
Inouye, Sharon K.
Association of CSF Alzheimer's disease biomarkers with postoperative delirium in older adults
title Association of CSF Alzheimer's disease biomarkers with postoperative delirium in older adults
title_full Association of CSF Alzheimer's disease biomarkers with postoperative delirium in older adults
title_fullStr Association of CSF Alzheimer's disease biomarkers with postoperative delirium in older adults
title_full_unstemmed Association of CSF Alzheimer's disease biomarkers with postoperative delirium in older adults
title_short Association of CSF Alzheimer's disease biomarkers with postoperative delirium in older adults
title_sort association of csf alzheimer's disease biomarkers with postoperative delirium in older adults
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7968120/
https://www.ncbi.nlm.nih.gov/pubmed/33748398
http://dx.doi.org/10.1002/trc2.12125
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