Tau Networks in Psychotic Alzheimer's Disease
Study Details
Study Description
Brief Summary
This research project aims to understand the brain mechanisms behind the manifestation of psychotic symptoms in Alzheimer´s disease (AD), and nature of the unique relationship with tau pathology. Amongst the cognitive manifestations of psychosis are impairments related to frontal circuits (social cognition, working memory and executive function deficits). The investigator's previous work suggests a role of tau pathology (one of the hallmarks of AD neuropathology) in the manifestation of psychosis in AD. However, the cerebral mechanisms that underly this association remain poorly understood. The overarching aim of the study is is to investigate the mechanisms by which tau network pathology may promote the presentation of psychosis in AD.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
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Detailed Description
The specific aims of this application are:
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To measure the regional distribution of tau aggregation in AD patients with psychosis (AD+P) compared to AD without psychosis (AD-P) and Cognitively Unimpaired Healthy (CUH) participants with the PET radiotracer [18F]-PI2620;
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To measure structural and functional brain networks properties in AD+P compared to AD-P patients and CUH participants using MRI;
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To examine the association of tau pathology with structural/functional network properties; electrophysiologic biomarkers of neurotransmission and neuroplasticity; and psychotic symptoms. The current project will determine whether identification of tau pathology, and associated network connectivity disruptions and sensorimotor gating impairments, may be informing as potential biomarkers for psychosis in AD. As severe adverse events are associated with atypical antipsychotics in AD psychosis, this work will provide insights into whether anti-tau therapies such as monoclonal antibodies to tau, now being investigated in clinical trials, may be effective in the antipsychotic treatment of AD.
Study Design
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| Alzheimer's disease Age 65-85 years old. Diagnosis of probable AD dementia according to NIA-AA criteria. Mini-Mental State Examination (MMSE) score ≥ 10 and ≤ 26 at the screening visit. Clinical Dementia Rating (CDR) score ≥ 0.5. Logical Memory delay score of ≤8 for 16+ years of education, ≤4 for 8-15 years of education, and ≤2 for 0-7 years of education Participants will undergo neuropsychological examination, blood collection, sensorimotor gating/ERP testing, MRI and [18F]-PI2620 PET scan. |
Diagnostic Test: [18F]-PI2620 PET scan
The PET scan will measure the regional distribution of tau aggregation in AD patients with and without psychosis compared to Cognitively Unimpaired Healthy participants with the PET radiotracer [18F]-PI2620.
|
| Alzheimer's disease with psychosis - All the criteria for AD are met. Presence of one (or more) of the following symptoms: Visual or auditory hallucinations (e.g., seeing silent individuals standing in the room, seeing children in the yard, or seeing animals in the house). Delusions (fixed false beliefs that the patient believes to be true, e.g., that the spouse is unfaithful, that possessions are being stolen, or that one is not who one claims to be). Participants will undergo neuropsychological examination, blood collection, sensorimotor gating/ERP testing, MRI and [18F]-PI2620 PET scan. |
Diagnostic Test: [18F]-PI2620 PET scan
The PET scan will measure the regional distribution of tau aggregation in AD patients with and without psychosis compared to Cognitively Unimpaired Healthy participants with the PET radiotracer [18F]-PI2620.
|
| Cognitively Unimpaired Healthy Age 65-85 years old. No known genetic risk factors for dementia. No cognitive complaint Mini-Mental State Examination (MMSE) score ≥ 26 at the screening visit. Logical Memory delay score of ≥9 for 16+ years of education, ≥5 for 8-15 years of education, and ≥3 for 0-7 years of education Participants will undergo neuropsychological examination, blood collection, sensorimotor gating/ERP testing, MRI and [18F]-PI2620 PET scan. |
Diagnostic Test: [18F]-PI2620 PET scan
The PET scan will measure the regional distribution of tau aggregation in AD patients with and without psychosis compared to Cognitively Unimpaired Healthy participants with the PET radiotracer [18F]-PI2620.
|
Outcome Measures
Primary Outcome Measures
- Tau PET scan [5 years]
To measure the distribution of tau aggregation in AD patients with and without psychosis, compared to cognitively unimpaired healthy subjects with the PET radiotracer [18F]-PI2620.
Secondary Outcome Measures
- MRI of the brain [5 years]
To measure brain networks in AD patients with and without psychosis compared to Cognitively Unimpaired Healthy subjects.
Other Outcome Measures
- PPI (pre-pulse inhibition) testing [5 years]
To examine the association of tau pathology with electrophysiologic biomarkers of neurotransmission and neuroplasticity; and psychotic symptoms. The project will determine whether sensorimotor gating impairments may be informative as a potential biomarker for psychosis in AD.
Eligibility Criteria
Criteria
Inclusion Criteria Alzheimer´s disease (AD) participants:
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Age 65-85 years old.
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Diagnosis of probable AD dementia according to National Institute on Aging-Alzheimer's Association (NIA-AA) criteria.
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Mini-Mental State Examination (MMSE) score ≥ 10 and ≤ 26 at the screening visit.
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Clinical Dementia Rating (CDR) score ≥ 0.5.
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Logical Memory delay score of ≤8 for 16+ years of education, ≤4 for 8-15 years of education, and ≤2 for 0-7 years of education
Exclusion Criteria Alzheimer´s disease (AD) participants:
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Rosen-modified Hachinski Ischemia Score > 4 at the screening visit.
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History of stroke.
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Evidence of a clinically relevant neurological disorder other than probable AD at the screening visit. Participants with insulin dependent type 2 diabetes, a history of CVD, a history of epilepsy, a history of TBI with greater than 15 minutes of loss of consciousness, a movement disorder, autoimmune disease affecting the CNS, or delirium.
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Evidence of a clinically relevant or unstable psychiatric disorder, based on DSM-5 criteria, including schizophrenia or other psychotic disorder, bipolar disorder, delirium, or current/active major depression.
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History of alcoholism or drug dependency/abuse within the last 5 years before screening.
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Presence of metal implants such as pacemakers, ear implants, internal bullet fragments or shrapnel.
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Inability to lie flat for 1 hour approximately.
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hearing impairment as evidenced by the inability to hear 500, 1000 and 6000 Hz bilaterally on an OAE evaluation. Subjects with hearing aides will be allowed to participate if they meet minimum hearing requirements.
Specific Inclusion Criteria for Alzheimer´s disease (AD) with Psychotic symptoms:
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All the criteria for AD are met.
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Presence of one (or more) of the following symptoms:
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Visual or auditory hallucinations (e.g., seeing silent individuals standing in the room, seeing children in the yard, or seeing animals in the house).
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Delusions (fixed false beliefs that the patient believes to be true, e.g., that the spouse is unfaithful, that possessions are being stolen, or that one is not who one claims to be).
Inclusion Criteria Cognitively Unimpaired Healthy (CUH) participants:
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Age 65-85 years old.
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No known genetic risk factors for dementia.
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No cognitive complaint
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Mini-Mental State Examination (MMSE) score ≥ 26 at the screening visit.
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Logical Memory delay score of ≥9 for 16+ years of education, ≥5 for 8-15 years of education, and ≥3 for 0-7 years of education
Exclusion Criteria Cognitively Unimpaired Healthy (CUH) participants:
- Same criteria as AD participants above.
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | The Feinstein Institutes for Medical Research | Manhasset | New York | United States | 11030 |
Sponsors and Collaborators
- Northwell Health
Investigators
- Principal Investigator: Jeremy Koppel, MD, Northwell Health
Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- 22-0394