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 volunteersQualifiers
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
Case-control
Cross-sectional
Treatments tested in this trial
[18F]FDG PET
Diagnostic testRegional glucose metabolism as well as glucose transport will be assessed.
[11C]PIB
Diagnostic testEarly perfusion PET after acetazolamide infusion as well as late amyloid load will be assessed.
Treatment groups
Trial outcomes
Primary outcomes
Glucose transport
Regional flux of glucose to brain regions, (mmol/mL/min )
Secondary outcomes
Glucose metabolism
Regional glucose metabolism, (μmol 100 g-1 min-1)
Amyloid load
Regional SUVR of amyloid
Stress perfusion
Perfusion relative to cerebellum during acetazolamide vasodilation. SUVR
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