Cerebrospinal fluid proteome changes in older non-cardiac surgical patients with postoperative cognitive dysfunction

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10 Scopus citations

Abstract

Background: Postoperative cognitive dysfunction (POCD), a syndrome of cognitive deficits occurring 1-12 months after surgery primarily in older patients, is associated with poor postoperative outcomes. POCD is hypothesized to result from neuroinflammation; however, the pathways involved remain unclear. Unbiased proteomic analyses have been used to identify neuroinflammatory pathways in multiple neurologic diseases and syndromes but have not yet been applied to POCD. Objective: To utilize unbiased mass spectrometry-based proteomics to identify potential neuroinflammatory pathways underlying POCD. Methods: Unbiased LC-MS/MS proteomics was performed on immunodepleted cerebrospinal fluid (CSF) samples obtained before, 24 hours after, and 6 weeks after major non-cardiac surgery in older adults who did (n = 8) or did not develop POCD (n = 6). Linear mixed models were used to select peptides and proteins with intensity differences for pathway analysis. Results: Mass spectrometry quantified 8,258 peptides from 1,222 proteins in > 50%of patient samples at all three time points. Twelve peptides from 11 proteins showed differences in expression over time between patients with versus without POCD (q < 0.05), including proteins previously implicated in neurodegenerative disease pathophysiology. Additionally, 283 peptides from 182 proteins were identified with trend-level differences (q < 0.25) in expression over time between these groups. Among these, pathway analysis revealed that 50 were from 17 proteins mapping to complement and coagulation pathways (q = 2.44∗10-13). Conclusion: These data demonstrate the feasibility of performing unbiased mass spectrometry on perioperative CSF samples to identify pathways associated with POCD. Additionally, they provide hypothesis-generating evidence for CSF complement and coagulation pathway changes in patients with POCD.

Original languageEnglish
Pages (from-to)1281-1297
Number of pages17
JournalJournal of Alzheimer's Disease
Volume80
Issue number3
DOIs
StatePublished - 2021

Bibliographical note

Publisher Copyright:
© 2021 - The authors. Published by IOS Press.

Funding

This study was supported by a Duke Anesthesiology DREAM Innovation Grant (to MB), NIH R03 AG050918 (to MB), NIH T32GM008600, and a mentored research award from the International Anesthesia Research Society (to MB). MB also acknowledges additional support from NIH grants K76AG057022, P30AG028716, and UH3AG056925, and from the Duke Anesthesiology Department.

FundersFunder number
Duke Anesthesiology Department
National Institutes of Health (NIH)T32GM008600, R03 AG050918
National Institutes of Health (NIH)
National Institute on AgingK76AG057022
National Institute on Aging
International Anesthesia Research SocietyP30AG028716, UH3AG056925
International Anesthesia Research Society

    Keywords

    • Inflammation
    • Mass spectrometry
    • Neurocognitive disorders
    • Postoperative cognitive dysfunction
    • Proteomics

    ASJC Scopus subject areas

    • General Neuroscience
    • Clinical Psychology
    • Geriatrics and Gerontology
    • Psychiatry and Mental health

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