Resumen
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.
| Idioma original | English |
|---|---|
| Páginas (desde-hasta) | 1281-1297 |
| Número de páginas | 17 |
| Publicación | Journal of Alzheimer's Disease |
| Volumen | 80 |
| N.º | 3 |
| DOI | |
| Estado | Published - 2021 |
Nota bibliográfica
Publisher Copyright:© 2021 - The authors. Published by IOS Press.
Financiación
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.
| Financiadores | Número del financiador |
|---|---|
| Duke Anesthesiology Department | |
| National Institutes of Health (NIH) | T32GM008600, R03 AG050918 |
| National Institutes of Health (NIH) | |
| National Institute on Aging | K76AG057022 |
| National Institute on Aging | |
| International Anesthesia Research Society | P30AG028716, UH3AG056925 |
| International Anesthesia Research Society |
ODS de las Naciones Unidas
Este resultado contribuye a los siguientes Objetivos de Desarrollo Sostenible
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Good health and well being
ASJC Scopus subject areas
- General Neuroscience
- Clinical Psychology
- Geriatrics and Gerontology
- Psychiatry and Mental health
Huella
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