Clinical Trial Details
— Status: Completed
Administrative data
NCT number |
NCT04009629 |
Other study ID # |
STUDY00142822 |
Secondary ID |
R21AG061548 |
Status |
Completed |
Phase |
N/A
|
First received |
|
Last updated |
|
Start date |
October 25, 2019 |
Est. completion date |
October 28, 2021 |
Study information
Verified date |
May 2022 |
Source |
University of Kansas Medical Center |
Contact |
n/a |
Is FDA regulated |
No |
Health authority |
|
Study type |
Interventional
|
Clinical Trial Summary
Research suggests that physical exercise supports brain health and cognition as we age. The
goal of this project is to examine the specific changes in brain blood flow and biological
factors in the blood immediately after exercise in older adults who have the APOE4 gene, a
genetic risk factor for developing Alzheimer's. Results from this study will help researchers
and clinicians understand and measure changes in the body and brain as a function of
exercise, and how those changes relate to Alzheimer's risk.
Description:
The brain and cardiovascular system share common risk factors for age-related diseases such
as hypertension, hypercholesterolemia, and genetics (e.g. APOE4). Because of this link, much
work has focused on the role of cerebrovascular health in reducing dementia risk. Regular
aerobic exercise has well-established benefits for cardiovascular health and has been
repeatedly linked to better cognition, brain health, and lower risk of Alzheimer's disease
(AD). Despite strong evidence for sustained cognitive and brain outcomes, the mechanisms
relating aerobic exercise with brain health and cognition remain imprecisely defined. Amongst
many potential mechanisms, cerebral blood flow (CBF) and blood-based biomarkers, such as
neurotrophins, are promising targets for their shared association to brain and cardiovascular
health. Prior investigations have largely attempted to measure change in these mechanisms
under resting conditions after an extended exercise intervention with mixed and conflicting
results. Further, studies have often not accounted for genetic differences that may blunt the
effect of exercise. Unlike prior work, our innovative approach is to begin by characterizing
the dynamic changes that result from an acute exercise challenge. A single bout of aerobic
exercise temporarily increases CBF and prompts neurotrophin release. These transient changes
ultimately drive long-term physiologic adaptation to exercise. Therefore, the study team will
characterize the dynamic response to an acute, standardized bout of aerobic exercise in a
group of nondemented older adults, comparing those who do and do not carry the APOE4 allele.
The first aim will test if CBF response to an acute exercise challenge is blunted in APOE4
carriers. The second aim will similarly test the acute exercise response of blood-based
biomarkers such as brain derived neurotrophic factor, insulin-like growth factor, and
vascular endothelial growth factor in APOE4 carriers versus non-carriers. The study team
expects that more accurately understanding the acute effects will provide valuable insight
into how aerobic exercise supports cognitive function and brain health. Armed with this
knowledge the field can optimize biomarker measurement for future exercise intervention
randomized controlled trials, informing our long-term goal of identifying precision exercise
prescription for AD prevention.