Neuroinflammation and Alzheimer's Pathology in POCD

University of Tennessee Graduate School of Medicine

Status: Unknown

Conditions: Post-Operative Confusion; Alzheimer Disease; Neuroinflammatory Response

Treatments: Behavioral: NACC Cognitive Battery; Behavioral: Montreal Cognitive Assessment; Behavioral: Grooved Pegboard; Diagnostic Test: 4AT Delirium; Behavioral: Stroop Test; Diagnostic Test: Cerebral Spinal Fluid Sample; Diagnostic Test: ERP Testing; Diagnostic Test: Blood Plasma and Serum sampling

Study type: Observational

Funder types: Other

Identifiers

NCT05378659

4790

Details and patient eligibility

About

The purpose of this project is to investigate the role of both neural inflammation and pre-existing neurodegenerative pathology in the risk and pathogenesis of post-operative cognitive dysfunction (POCD). To achieve this goal, the investigators will combine blood and cerebrospinal fluid (CSF) sampling, standardized cognitive tests, and dynamic neurophysiological markers of cortical network dysfunction in the form of event-related potentials (ERPs), to assess the link between neurodegeneration and neuroinflammation in the pathogenesis of POCD.

Full description

The purpose of this project is to investigate the role of both neural inflammation and pre-existing neurodegenerative pathology in the risk and pathogenesis of post-operative cognitive dysfunction (POCD) in 120 patients who will undergo a Total Knee Arthroscopy. The investigators will also explore neuropsychological, functional and biological measures as pre-operative risk indicators. To achieve this goal, the investigators will combine blood and cerebrospinal fluid (CSF) sampling, standardized cognitive tests, and dynamic neurophysiological markers of cortical network dysfunction in the form of event-related potentials (ERPs), to assess the link between neurodegeneration and neuroinflammation in the pathogenesis of POCD. To separate potential effects of general anesthesia from those of neuroinflammation, The investigators will recruit patients undergoing total knee replacement with the use of sedation and spinal anesthesia. To address the age risk factor, the investigators are targeting patients ages 60 and older. By using both validated and experimental biomarkers, this novel study design will isolate the effects of POCD due to systemic and neural inflammation and examine the links to pre-surgical cognitive impairment and underlying neurodegeneration as susceptibility factors.

Baseline (On the day of their final preoperative surgical visit prior to their TKA) the plan is to collect:

1. Cognitive assessments

   a. Montreal Cognitive Assessment b. Stroop Test c. Symbol Digit Modalities Test d. Oral Trail Making Test

2. Collect two 4-ml blood samples for biomarker evaluation

Visit 2 Pre-op (day of scheduled TKA surgery) the plan is to collect:

1. Repeat cognitive testing

   a. Montreal Cognitive Assessment b. Stroop Test c. Symbol Digit Modalities Test d. Oral Trail Making Test

2. Collect two 4-ml blood samples for biomarker evaluation

3. Collect 2cc of cerebral spinal fluid

Visit 2 Post-op:

1. 4 AT test for delirium
2. Collect two 4ml blood samples will be taken

Visit 3 (Forty-eight hours after discharge):

1. brief cognitive testing via telephone or video conferencing.

2. Blind Montreal Cognitive Assessment

3. Oral Trail Making Test

   Visit 4 (two weeks for their post-operative visit):

   1. Repeat cognitive testing

   2. Montreal Cognitive Assessment 2. Stroop Test 3. Symbol Digit Modalities Test 2. Oral Trail Making Test 3. Collect two 4ml blood samples for biomarker testing.

   For patients who had pre-operative cognitive impairment, their participation in the study will end here

   For 20 participants with no indication of pre-surgical cognitive impairment (10 with no post-operative impairment and 10 with presumed POCD)

   Visit 5 (~ 6 weeks post-op) the plan is to collect:

   1. Complete initial neurophysiological recording of event-related potentials (ERPs). This ERP session is performed to establish baseline cortical network function. Neurophysiological studies will be conducted using a 128-electrode EEG system.
   2. Collect two 4-ml blood samples

   Visit 6 End of Study (At 6 months):

   1. Collect a final assessment of cognition
   2. ERP assessment

Enrollment: 120 estimated patients

Sex: All

Ages: 60+ years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• Males and females 60 years or older in age
• Subjects scheduled to undergo TKA
• Fluent and literate in English
• Able to give consent for themselves based upon the MacArthur Competence Assessment Tool for Clinical Research
• Able to have a subarachnoid block with only intravenous sedation

Exclusion criteria

• Less than 60 years of age
• Cognitively impaired to the point where they are unable to give consent for themselves
• Blindness or partial blindness
• Pre-existing neurodegenerative conditions
• Contraindication for subarachnoid block and/or requiring general anesthesia

Trial design

120 participants in 2 patient groups

With Post-Operative Cognitive Dysfunction

Description:

Subjects determined to have post-operative cognitive dysfunction based on the results of: 1. 4AT Delirium Test 2. Scoring on : 1. Montreal Cognitive Assessment 2. Oral Trails Test 3. Stroop Test 4. Symbol Digit Modalities Test All subjects will undergo: 1. Blood sample collection 2. Cerebral spinal fluid collection 3. ERP testing 4. NACC Cognitive Battery 5. Grooved Pegboard testing

Treatment:

Diagnostic Test: ERP Testing

Behavioral: Stroop Test

Diagnostic Test: Blood Plasma and Serum sampling

Behavioral: NACC Cognitive Battery

Diagnostic Test: Cerebral Spinal Fluid Sample

Diagnostic Test: 4AT Delirium

Behavioral: Montreal Cognitive Assessment

Behavioral: Grooved Pegboard

Without Post-Operative Cognitive Dysfunction

Description:

Subjects determined to not have post-operative cognitive dysfunction based on the results of: 1. 4AT Delirium Test 2. Scoring on : 1. Montreal Cognitive Assessment 2. Oral Trails Test 3. Stroop Test 4. Symbol Digit Modalities Test All subjects will undergo: 1. Blood sample collection 2. Cerebral spinal fluid collection 3. ERP testing 4. NACC Cognitive Battery 5. Grooved Pegboard testing

Treatment:

Diagnostic Test: ERP Testing

Behavioral: Stroop Test

Diagnostic Test: Blood Plasma and Serum sampling

Behavioral: NACC Cognitive Battery

Diagnostic Test: Cerebral Spinal Fluid Sample

Diagnostic Test: 4AT Delirium

Behavioral: Montreal Cognitive Assessment

Behavioral: Grooved Pegboard