Skip to content

M1 Schizophrenia PET Study

Muscarinic M1 Receptor Availability and Cognition in Schizophrenia

Status
Completed
Phases
Phase 1
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05105542
Enrollment
18
Registered
2021-11-03
Start date
2021-04-20
Completion date
2023-10-31
Last updated
2024-11-12

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Healthy, Schizoaffective Disorder, Schizophrenia

Keywords

Schizophrenia, Muscarinic M1 Receptor, M1 AChR, [11C]EMO, PET Scan, MRI Scan

Brief summary

This exploratory study seeks to examine M1 receptor availability in SZ patients and to relate M1 receptor availability to proximal and distal measures of cognitive performance, namely evoked ɣ oscillations in the EEG and verbal memory. Furthermore, the relationship between hippocampal \[11C\]EMO availability (BPND), evoked ɣ oscillations, verbal memory, and measures of illness severity will be explored.

Detailed description

Converging lines of evidence from postmortem studies provide strong evidence that brain muscarinic M1 receptor deficit is present in a subset of schizophrenia (SZ) patients. M1 receptors are an important target for cognitive deficits in SZ. However, until now, it has not been possible to examine the heterogeneity of SZ with respect to M1 receptor availability in vivo. The development of a novel positron emission tomography (PET) ligand, \[11C\]EMO, at Yale PET Center provides a unique opportunity to, for the first time, examine in vivo brain muscarinic M1 receptor availability in SZ and, concurrently, elucidate the relationship of M1 receptors to cognitive deficits in SZ. The investigators will compare M1 receptor availability in SZ patients and age-, gender-matched healthy controls using \[11C\]EMO and the High Resolution Research Tomograph (HRRT), a PET scanner with high sensitivity and resolution available for human brain imaging. This study will explore the relationship between: hippocampal \[11C\]EMO binding (as a measure of hippocampal M1 AChR availability), encoding-related γ power during a verbal memory task, verbal memory, gender, and serum acetylcholine level. This exploratory study will provide the necessary pilot data to conduct a larger study to fully investigate the heterogeneity of SZ with respect to M1 receptor availability.

Interventions

DRUG11C-EMO - A Novel PET Radiotracer for Muscarinic M1 Receptor

The radiotracer, \[11C\]EMO, will be administered at the beginning of each PET scan.

DEVICEPET Scan

PET scanner with high sensitivity and resolution available for human brain imaging

Sponsors

National Institute of Mental Health (NIMH)
CollaboratorNIH
Yale University
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
DIAGNOSTIC
Masking
NONE

Intervention model description

Two groups will be studied: 1.) patients diagnosed with schizophrenia or schizoaffective disorder, and 2.) age and gender-matched healthy controls. Both groups will undergo neuroimaging, cognitive assessments, etc.

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
Yes

Inclusion criteria

* Men and women aged 18- 65 years that are physically and mentally healthy with the exception of DSM-5 schizophrenia or schizoaffective disorder diagnosis * Subjects with no metal in the body that may pose a risk during MRI scanning * No significant medical history, including head trauma and bleeding disorders

Exclusion criteria

* Men and women with a history or presence of clinically significant medical conditions * People who suffer from claustrophobia, have MRI incompatible implants, or other contraindications for MRI and PET scans

Design outcomes

Primary

MeasureTime frameDescription
Hippocampal M1 availability10 daysMeasured by \[11C\]EMO availability (BPND)

Secondary

MeasureTime frameDescription
evoked ɣ oscillations10 daysMeasured by EEG
verbal memory10 daysMeasured by cognitive assessments

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026