Brain Blood Flow and Sugar Transport in Alzheimer's Disease With and Without Diabetes - A Pilot Imaging Study

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age60-90
SponsorRigshospitalet, Denmark

About this trial

Alzheimer's disease is the most common cause of dementia and affects a growing number of older adults. Although harmful proteins build up in the brain, we still do not fully understand why some brain regions are affected earlier or more severely than others. Many people with Alzheimer's disease also have problems with blood flow and sugar handling in the brain, and these changes may play an important role in disease development. People with type 2 diabetes are at especially high risk of developing Alzheimer's disease and often experience a more severe disease course.

This pilot study aims to improve our understanding of how brain blood flow and sugar use are altered in Alzheimer's disease, and whether these changes differ in people with and without type 2 diabetes. We will study three groups: people with Alzheimer's disease without diabetes, people with Alzheimer's disease and type 2 diabetes, and healthy older individuals. By comparing these groups, we aim to identify early brain changes that may contribute to cognitive decline.

Participants will undergo advanced brain imaging using positron emission tomography (PET) scans. One scan uses a radioactive sugar tracer to measure how the brain takes up and uses glucose. Importantly, a new non-invasive method will also allow us to estimate how efficiently glucose is transported from the blood into the brain. This is a key process that may be impaired in Alzheimer's disease, but has previously required invasive procedures. The new approach avoids arterial cannulation, making the study safer and more comfortable for participants.

A second PET scan will assess brain blood flow and blood vessel function, including how well the vessels can respond to increased demand. Participants will also complete cognitive tests to assess memory and thinking abilities.

Ultimately, this research may contribute to earlier diagnosis, better monitoring of disease progression, and development of new treatment strategies for Alzheimer's disease.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

suspected Alzheimer's disease

type 2 diabetes (group A)

able and willing to comply with study protocoil´´l

Disqualifiers

type 2 diabetes (group B and C)

significant brain disease apart from dementia (group A and B)

significant vascular or neurological disease (group C)

active cancer treatment

Trial population

Patients are recruited from the memory clinica at Herlev Hospital, Copenhagen, Denmark

Trial design

Design model

Case-control

Time perspective

Cross-sectional

Treatments tested in this trial

  • [18F]FDG PET

    Diagnostic test

    Regional glucose metabolism as well as glucose transport will be assessed.

  • [11C]PIB

    Diagnostic test

    Early perfusion PET after acetazolamide infusion as well as late amyloid load will be assessed.

Treatment groups

60 Participants
are divided into 3 treatment groups
Group A: Alzheimer's disease with type 2 diabetes2 interventions
Group B: Alzheimer's disease without type 2 diabetes2 interventions
Group C: Healthy subjects2 interventions

Trial outcomes

Primary outcomes

1

Glucose transport

Regional flux of glucose to brain regions, (mmol/mL/min )

Time frame
at inclusion

Secondary outcomes

1

Glucose metabolism

Regional glucose metabolism, (μmol 100 g-1 min-1)

Time frame
at inclusion
2

Amyloid load

Regional SUVR of amyloid

Time frame
at inclusion
3

Stress perfusion

Perfusion relative to cerebellum during acetazolamide vasodilation. SUVR

Time frame
at inclusion

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Rigshospitalet, Denmark

Lead sponsor

Copenhagen University Hospital at Herlev

Sponsor institution

Copenhagen University Hospital at Herlev

Collaborator