Neuroinflammation in Cognitive Decline Post-cardiac Surgery

N/ACompletedNCT04520802

Radboud University Medical Center15 enrolled

Overview

Major cardiovascular surgery is associated with postoperative cognitive decline (POCD), with a deterioration in memory, attention and speed of information processing. A multifactorial pathophysiology is presumed but this study focuses on the role of (neuro)inflammation in the development of POCD after coronary artery bypass grafting (CABG) surgery.

Systemic inflammation can activate the innate immune cells of the brain inducing neuroinflammation, which plays an important role in the pathogenesis of neurodegenerative disease. Major cardiovascular surgery induces a severe systemic inflammatory response.There is growing support that neuroinflammation is a pivotal factor in the development of postoperative cognitive decline (POCD) due to surgery-related systemic inflammation. Although the neuroinflammatory hypothesis is scientifically accepted, in vivo human data supporting the role of neuroinflammation in severe systemic inflammation such as major surgery are still lacking. In the last decades, several nuclear imaging tracers have been developed that can quantitatively measure microglial and astrocytic activation in vivo, by targeting the mitochondrial 18kDa translocator protein (TSPO). The investigators hypothesize that cardiac surgery induces a neuroinflammatory response and that its presence is related to acute and long term brain dysfunction postoperatively. This will be studied by pre- and postoperative PET brain imaging using a 18F-DPA-714 tracer targeting TSPO, combined with longitudinal neuropsychological examinations. Structural changes in the brain will be recorded on MRI prior to and after cardiac surgery to enable us to correct for the potentially confounding effects of neurovascular events on cognitive outcomes after CABG surgery.

Study Type

OBSERVATIONAL

Enrollment

Conditions

Postoperative Cognitive Dysfunction Coronary Artery Disease Pathophysiology

Interventions

18F-DPA-714 PET/CT neuroimagingDIAGNOSTIC_TEST

* Pre- and postoperative neuroimaging using 18F-DPA-714 PET/CT and brain MRI. * Longitudinal neuropsychological examinations (up to 6 months postoperatively) * Blood samples are drawn to assess the severity of the systemic inflammatory response

Eligibility

Sex: ALLMin age: 50 Years

Medical Language ↔ Plain English

Inclusion Criteria: * Age \> 50 years * Planned for on-pump coronary artery bypass grafting surgery * High-affinity binder or mixed-affinity binders based on rs6971 polymorphism for TSPO * Chronic use of statins (defined as pre-hospital use) Exclusion Criteria: * Previous cardiac surgery. * Pregnancy or wish to become pregnant within 2 weeks after PET-CT scan * Contra-indication to undergo a PET/CT or MRI scan, including claustrophobia. * Low-affinity binder based on rs6971 polymorphism for TSPO, or unable to determine rs6971 polymorphism. * Patients with cognitive disorders that have not recovered enough to be able to understand the study leaflets and information for participation. * Brain or spinal surgery within the last 6 months. * Meningitis or brain infection within the last 6 months. * Pre-existing dementia or neurodegenerative disease or cognitive impairment interfering with the ability to understand informational material about this research project. * Presence of a CSF catheter or shunt. * Patients with known brain tumors. * Patients with brain injury (e.g. acute stroke, or subarachnoid hemorrhage) within the last 6 months. * Severe brain trauma in previous medical history. * Chronic (\>2 weeks) use of immunosuppressive agents (see table 3.3.A). * Concomitant diseases resulting in severe immunosuppression (e.g. HIV). * Auto-immune or auto-inflammatory disease * Active infection \< 2 weeks prior to inclusion (defined as fever \>38.5 or antibiotic treatment) * Kidney failure, defined by a MDRD-GFR\<15 ml/min/1.73m2 * Known contrast allergy for gadolinium * Chronic use of neuroleptics, defined as pre-hospital use. * Patients that do not speak Dutch or have disabilities that prevent accurate delirium diagnosis. * Analphabetic patients. * No written informed consent obtained.

Locations (1)

Department of Intensive Care Medicine, Radboud university medical center

Nijmegen, Netherlands

Outcomes

Primary Outcomes

Change in TSPO PET tracer uptake at 3-7 days post-surgery

18F-DPA-714

Time frame: 3-7 days post-surgery minus preoperative (= day before surgery)

Secondary Outcomes

Occurrence of postoperative cognitive dysfunction (POCD)

POCD diagnosis based on neuropsychological assessments including TMT A\&B, Stroop I, II, III, WAIS-IV - digit span, LDST, RAVLT, RCFT, RBMT-3 face recognition, LFT and token test. POCD diagnosis is made when patients are newly impaired in one or more cognitive domains (memory, executive functioning, speed of processing and language), or when the average test rating has declined in more than one domain compared to baseline.

Time frame: Baseline (preoperative), postoperative (3-7 days after surgery, 6 weeks and 6 months)

Whole brain TSPO PET tracer uptake pre- and 3-7 days post-surgery

18F-DPA-714

Time frame: pre- and 3-7 days post-surgery

Pro- and anti-inflammatory in vivo cytokine concentrations [in pg/ml]

TNFa, IL6, IL-1B, IL10, IL-1RA

Time frame: Day before surgery, during surgery (stop extracorporeal circulation (ECC)), after surgery (6 hours after stop ECC, 24 hours after incision, 3-7 days post-surgery and 6 weeks after surgery)

Ex vivo cytokine production of stimulated monocytes [in ng/10^9 monocytes]

TNFa, IL6, IL1B, MCP1, IL10

Time frame: Day before surgery, 3-7 days and 6 weeks after surgery

Flowcytometry analysis to study the inflammatory phenotype of the cells

HLA-DR, CCR2, CD11b, CD14, CD16

Time frame: Day before surgery, 3-7 days and 6 weeks after surgery

Data from ClinicalTrials.gov

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