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Study of neuroinflammation and aging of Alzheimer's dementia using multimodal neuroimaging (MRI and PET)

Study of neuroinflammation and aging of Alzheimer's dementia using multimodal neuroimaging (MRI and PET)

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CRIS
Registry ID
KCT0005431
Enrollment
360
Registered
2020-09-24
Start date
2020-01-28
Completion date
Unknown
Last updated
2025-03-03

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

Conditions

None listed

Interventions

None listed

Sponsors

Gachon University Gil Medical Center
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: - Cognitively Normal (CN) • Normal cognition will be defined according to neuropsychological testing, which didn't fall within 1.5 SD, and Clinical Dementia Rating (CDR) was 0 . - Mild cognitive impairment (MCI): • CDR was 0.5 • Subjects were not be clinically diagnosed with dementia according to Diagnostic and Statistical Manual of Mental Disorders, 4th. Edition, Text-revision (DSM-IV-TR) criteria. - Dementia (AD) - Alzheimer's disease (AD): • CDR = 0.5 • subjects were diagnosed with dementia according to DSM-IV-TR. • subjects were diagnosed with probable AD or possible AD according to the National Institute of Neurological and Communicative Disorders and Stroke and the Alzheimer’s Disease and Related Disorders Association (NINCDS-ADRDA) criteria.

Exclusion criteria

Exclusion criteria: - Subjects who do not meet the inclusion criteria. - Subjects who have history of any significant neurological disease other than AD or VD , such as traumatic brain injury, Parkinson's disease, Huntington's disease, motor neuron disease, or multiple sclerosis. - Subjects who have history of brain tumor, normal presure hydrocephalus, encephalitis, or metabolic encephalopathy. - Subjects who have history of a massive stroke in cerebrum, brain strem or cerebellum. - Subjects who have history of psychiatric disorder. - Subjects unable to undergo MRI or PET scanning. - Pregnent or reast feeding women.

Design outcomes

Primary

MeasureTime frame
Quantitative,topographical analysis, and standardized uptake value ratio (SUVR) map generation for 18F-Flutemetamol PET and 18F-DPA-714 PET;Generation of the cortical cortical thickness map through anatomical MRI;Generation of structural connectivity and fiber tractography through Diffusion MRI;Generation of functional connectivity map through Resting-state fMRI

Secondary

MeasureTime frame
Comparison of cognitive function and brain structure changes between groups during follow-up;Comparison of cognitive function and neuroinflammation between groups during follow-up;Analysis of effect on cognitive impairment and brain atrophy during follow-up

Countries

Korea, Republic of

Contacts

Public ContactYoung Noh

Gachon University Gil Medical Center

ynoh@gachon.ac.kr+82-32-460-9043

Outcome results

None listed

Source: CRIS (via WHO ICTRP) · Data processed: Feb 4, 2026