The association between cerebrospinal fluid interleukin-6, soluble interleukin-6 receptor, and interleukin-6 trans-signalling binary complex with postoperative delirium: an observational cohort study
Background: Postoperative delirium causes significant morbidity and mortality. Delirium is associated with the presence of plasma and CSF biomarkers, including interleukin-6 (IL-6). When IL-6 binds to the non-membrane-bound soluble IL-6 receptor (sIL-6R), the resultant binary complex, IL-6·sIL-6R, triggers pro-inflammatory processes called trans-signalling. While murine models implicate central IL-6 trans-signalling in perioperative cognitive dysfunction, there are few clinical reports addressing its role in delirium. The primary aim was to investigate whether postoperative changes in CSF IL-6, sIL-6R and IL-6·sIL-6R complexes were associated with the incidence and severity of postoperative delirium. We also explored whether CSF sIL-6R was related to peripheral inflammation and blood-brain barrier permeability. Methods: We performed an exploratory analysis of data from an ongoing observational cohort study on perioperative delirium in patients undergoing major surgery, with delirium incidence (3-Minute Diagnostic Confusion Assessment Method or Confusion Assessment Method for the Intensive Care Unit) and severity (Delirium Rating Scale-Revised-98), plasma, and CSF samples collected on postoperative days 1-7. Biomarkers were analysed using enzyme-linked immunosorbent assay. Results: =0.01). CSF soluble sgp130, the natural inhibitor of the trans-signalling pathway, did not correlate with delirium. CSF sIL-6R was also significantly correlated with peripheral inflammation (plasma IL-6 and IL-8) and blood-brain barrier permeability (CSF:plasma albumin ratio and plasma S100B). Conclusions: Interleukin-6 trans-signalling may be implicated in postoperative delirium, which raises the future possibility of targeted immunomodulatory therapy in susceptible individuals to prevent and/or reverse postoperative co gnitive decline. Clinical trial registration: NCT02926417.
Authors
- David Kunkel (ORCID: https://orcid.org/0000-0003-1812-8312)
- Robert D. Sanders (ORCID: https://orcid.org/0000-0003-0113-0328)
- Justin G. Wu (ORCID: https://orcid.org/0000-0002-5443-5478)
- Jennifer Taylor (ORCID: https://orcid.org/0000-0003-2152-4287)
- Richard Lennertz (ORCID: https://orcid.org/0000-0003-3273-9056)
- Mervyn Maze (ORCID: https://orcid.org/0000-0001-9794-2472)
- Robert A. Pearce (ORCID: https://orcid.org/0000-0002-1516-6260)
Institutions
- The University of Sydney (AU)
- University of Wisconsin–Madison (US)
- University of California, San Francisco (US)
- Royal Prince Alfred Hospital (AU)
- Sydney Local Health District (AU)
- National Health and Medical Research Council (AU)
Publication Details
- Journal
- BJA Open
- Published
- 2026-04-10
- DOI
- https://doi.org/10.1016/j.bjao.2026.100546
- Primary Topic
- Intensive Care Unit Cognitive Disorders
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- National Institutes of Health