Not provided
Not provided
| ID | Type | Description | Link |
|---|---|---|---|
| 2016-002016-40 | EudraCT Number | ||
| CMO 2016-2598 | Other Identifier | CMO Regio Arnhem-Nijmegen |
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
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.
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
| Label | Type | Description | Intervention Names |
|---|---|---|---|
| POCD | Patients with postoperative cognitive decline (POCD) after coronary artery bypass grafting (CABG) surgery |
| |
| no POCD | Patients without postoperative cognitive decline (POCD) after coronary artery bypass grafting (CABG) surgery |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| 18F-DPA-714 PET/CT neuroimaging | Diagnostic Test |
|
| Measure | Description | Time Frame |
|---|---|---|
| Change in TSPO PET tracer uptake at 3-7 days post-surgery | 18F-DPA-714 | 3-7 days post-surgery minus preoperative (= day before surgery) |
| Measure | Description | Time Frame |
|---|---|---|
| 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. |
Not provided
Inclusion Criteria:
Exclusion Criteria:
Not provided
Not provided
Not provided
Not provided
Patients >50 years that are planned to undergo elective coronary artery bypass grafting (CABG) surgery by the cardiothoracic surgery department of the Radboud university medical center in Nijmegen (NL).
Not provided
| Name | Affiliation | Role |
|---|---|---|
| Wilson F Abdo, MD PhD | Radboud University Medical Center | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Department of Intensive Care Medicine, Radboud university medical center | Nijmegen | 6500HB | Netherlands |
| PubMed Identifier | Type | Citation | Retractions |
|---|---|---|---|
| 33980522 | Background | Peters van Ton AM, Duindam HB, van Tuijl J, Li WW, Dieker HJ, Riksen NP, Meijer FA, Kessels RP, Kohn N, van der Hoeven JG, Pickkers P, Rijpkema M, Abdo WF. Neuroinflammation in cognitive decline post-cardiac surgery (the FOCUS study): an observational study protocol. BMJ Open. 2021 May 11;11(5):e044062. doi: 10.1136/bmjopen-2020-044062. |
| Label | URL |
|---|---|
| Pubmed link to publication of complete study protocol | View source |
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
| ID | Term |
|---|---|
| D000079690 | Postoperative Cognitive Complications |
| D003324 | Coronary Artery Disease |
| ID | Term |
|---|---|
| D011183 | Postoperative Complications |
| D010335 | Pathologic Processes |
| D013568 | Pathological Conditions, Signs and Symptoms |
| D060825 | Cognitive Dysfunction |
Not provided
Not provided
Not provided
Not provided
Not provided
|
| 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 | 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 | 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 | 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 | Day before surgery, 3-7 days and 6 weeks after surgery |
| Complete blood count | including leukocyte differentiation measured on an automated hematology analyzer | 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 healthy donor monocytes, after exposure to patient serum obtained during CABG surgery | Healthy donor monocytes will be exposed to patient serum obtained during surgery, to see whether this changes the ex vivo cytokine producing capacity (TNFa, IL6, IL10) | Perioperatively at stop extracorporeal circulation (ECC) |
| Number of newly developed (ischemic and hemorrhagic) brain and vascular wall lesions | pre- and 3-7 days post-surgery |
| Delta brain activity in three large scale brain networks involved in stress reactivity on resting-state fMRI | pre- and 3-7 days post-surgery |
| D003072 | Cognition Disorders |
| D019965 | Neurocognitive Disorders |
| D001523 | Mental Disorders |
| D003327 | Coronary Disease |
| D017202 | Myocardial Ischemia |
| D006331 | Heart Diseases |
| D002318 | Cardiovascular Diseases |
| D001161 | Arteriosclerosis |
| D001157 | Arterial Occlusive Diseases |
| D014652 | Vascular Diseases |