Effects of Exogenous Ketones on Cognitive Function in Older Adults With Prediabetes?

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age60-75
SponsorUniversity of Alabama at Birmingham

About this trial

Brief Summary

The goal of this clinical trial is to learn whether older adults with prediabetes, but no diagnosed cognitive impairment, show early changes in brain energy use and thinking speed compared to older adults with normal blood sugar levels. The study will also test whether a single dose of an exogenous ketone supplement can improve brain energy use and cognitive processing speed.

The main questions it aims to answer are:

Do older adults with prediabetes have lower brain glucose uptake and slower cognitive processing speed compared to those with normal glucose levels?

Does a single dose of an exogenous ketone monoester supplement improve cognitive processing speed and brain glucose uptake?

Researchers will compare older adults with prediabetes to older adults with normal glucose levels to determine whether differences exist in brain glucose metabolism and cognitive performance. In a subset of participants, researchers will also compare brain and cognitive outcomes before and after consuming a ketone monoester supplement (DeltaG, Oxford, England).

Participants will:

Complete metabolic testing to determine glucose status

Undergo brain imaging using fluorodeoxyglucose positron emission tomography combined with magnetic resonance imaging (18FDG-PET/MRI) while performing a cognitive processing speed task

Consume a single dose of a commercially available ketone monoester supplement during one study visit

Complete cognitive testing during imaging to measure processing speed and brain activity

The results of this study will help determine whether early metabolic dysfunction is linked to reduced brain energy use and whether ketones can temporarily support brain function in individuals at risk for dementia.

Eligibility criteria

Qualifiers

Age 60 to 75 years

Able to provide written informed consent

Fluent in English

No diagnosed cognitive impairment or dementia

Disqualifiers

Diagnosis of mild cognitive impairment, dementia, or other neurodegenerative disorder

Diagnosis of type 1 diabetes or type 2 diabetes

Use of glucose-lowering medications (e.g., insulin, metformin, glucagon-like peptide-1 receptor agonists)

History of major neurological disorder (e.g., stroke, traumatic brain injury with loss of consciousness >30 minutes, epilepsy, multiple sclerosis)

Trial design

Treatments tested in this trial

  • Ketone Monoester (KE)
  • Placebo

Treatment groups

20 Participants
are divided into 2 treatment groups