Cerebrospinal Fluid Proteome Changes in Older Non-Cardiac Surgical Patients with Postoperative Cognitive Dysfunction

Author:

VanDusen Keith W.1,Li Yi-Ju23,Cai Victor1,Hall Ashley1,Hiles Sarah4,Thompson J. Will4,Moseley M. Arthur4,Cooter Mary1,Acker Leah1,Levy Jerrold H.1,Ghadimi Kamrouz1,Quiñones Quintin J.1,Devinney Michael J.1,Chung Stacey1,Terrando Niccolò1,Moretti Eugene W.1,Browndyke Jeffrey N.567,Mathew Joseph P.1,Berger Miles1111,

Affiliation:

1. Department of Anesthesiology, Duke University Medical Center, Durham, NC, USA

2. Department of Biostatistics and Bioinformatics, Duke University, Durham, NC, USA

3. Duke Molecular Physiology Institute, Duke University, Durham, NC, USA

4. Duke Center for Genomic and Computational Biology, Duke University, Durham, NC, USA

5. Department of Psychiatry & Behavioral Sciences, Division of Geriatric Behavioral Health, Duke University Medical Center, Durham, NC, USA

6. Duke Institute for Brain Sciences, Duke University, Durham, NC, USA

7. Center for Cognitive Neuroscience, Duke University Medical Center, Durham, NC, USA

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.

Publisher

IOS Press

Subject

Psychiatry and Mental health,Geriatrics and Gerontology,Clinical Psychology,General Medicine,General Neuroscience

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