Brain Connectivity Marker for Alzheimer's Disease (BRAINCONN)

Karolinska Institute

Status: Enrolling

Conditions: Alzheimer Disease

Treatments: Other: Neuroimaging

Study type: Observational

Funder types: Other

Identifiers

NCT06874231

Dnr 2023-00026-02

Details and patient eligibility

About

The main purpose of this project is to establish whether changes in brain connectivity can be used to predict the development of Alzheimer's disease (AD).

Full description

To achieve this aim, the investigators will perform six different studies that have been designed to achieve the following specific objectives:

1.1. Identify changes of brain connectivity in individuals who show abnormal AD amyloid biomarkers in the cerebrospinal fluid and blood.

1.2. To assess the correlation between brain connectivity changes and biomarkers of synaptic dysfunction and inflammation as well as alterations of electrical brain signals.

1.3. Establish whether alterations of brain connectivity could be improved after patients start treatment with cholinesterase inhibitors.

1.4. Assess differences in brain connectivity between patients receiving treatment with statins and those not taking this medication.

1.5. Determine whether brain connectivity changes can predict longitudinal cognitive decline and conversion to AD dementia.

1.6. Assess whether different microorganisms can grow more rapidly in the cerebrospinal fluid from AD patients compared to controls and whether their levels are associated with brain connectivity.

1.7. Evaluate the relationship between brain connectivity and the integrity of the locus coeruleus, which is the earliest site of AD pathology

Enrollment: 120 estimated patients

Sex: All

Ages: 40 to 85 years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

1. Inclusion criteria for subjects with subjective cognitive complaints:

   • MMSE (Mini-mental test) or MoCA (Montreal Cognitive Assessment) points between 26 and 30.
   • Absence of cognitive impairment.
   • Memory problems reported by the participant/family member.
   • Do not fulfill criteria for mild cognitive impairment or dementia.
   • Must speak and understand Swedish.

2. Inclusion criteria for patients with mild cognitive impairment:

   • MMSE (Mini-mental test) or MoCA (Montreal Cognitive Assessment) points between 24 and 30.
   • Impaired memory function.
   • Do not fulfill criteria for dementia.
   • Must speak and understand Swedish.
   • Must have abnormal cerebrospinal fluid amyloid-β 42/40 ratio levels, which is a biomarker of Alzheimer's disease.

3. Specific inclusion criteria for patients with Alzheimer's disease:

   • MMSE (Mini-mental test) or MoCA (Montreal Cognitive Assessment) points between 18 and 28.
   • Impaired memory function in addition to impaired executive abilities, language function, visuospatial ability and/or attention/psychomotor speed.
   • Meet NINCDS-ADRDA and DSM-IV criteria for probable Alzheimer's disease.
   • Must speak and understand Swedish.
   • Must have abnormal spinal fluid amyloid-β 42/40 ratio levels, which is a biomarker of Alzheimer's disease.

Exclusion criteria

• Alcohol or drug abuse.
• Unstable somatic disease or organ failure.
• Refuse to cerebrospinal fluid testing and/or blood sampling, neuropsychological testing, brain imaging, electroencephalogram or magnetoencephalogram.

In addition, participants who have claustrophobia or some form of metal implant in their body that may interfere with the brain imaging scan will be excluded from the study.

Trial design

120 participants in 4 patient groups

SCI normal

Description:

Subjects with subjective cognitive impairment with normal amyloid levels.

Treatment:

Other: Neuroimaging

SCI abnormal

Description:

Subjects with subjective cognitive impairment with low amyloid levels.

Treatment:

Other: Neuroimaging

MCI abnormal

Description:

Subjects with mild cognitive impairment with low amyloid levels.

Treatment:

Other: Neuroimaging

AD abnormal

Description:

Subjects with Alzheimer's disease with low amyloid levels.

Treatment:

Other: Neuroimaging