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| ID | Type | Description | Link |
|---|---|---|---|
| 1RF1NS117746-01 | U.S. NIH Grant/Contract | View source | |
| Protocol Version 4/6/2022 | Other Identifier | UW Madison | |
| A176000 | Other Identifier | UW Madison |
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| Name | Class |
|---|---|
| National Institute of Neurological Disorders and Stroke (NINDS) | NIH |
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Brain blood flow regulation will be measured in response to environmental changes using MRI.
Global brain blood flow decreases with advancing age; however, some adults have accelerated declines in brain blood flow, placing them at a greater risk of cognitive impairment. Similarly, brain reactivity to increased levels of carbon dioxide decreases with age, with a greater decline in adults with vascular risk factors and is impaired in early Alzheimer's disease. Preclinical models suggest that reduced brain blood flow, results in low levels of oxygen regionally. Currently, there are a lack of human studies that investigate the cause or consequence of altered blood flow regulation in the brain.
The research aims are:
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Controls | Healthy controls |
| |
| Vertebral Artery Hypoplasia | Healthy individuals with vertebral artery hypoplasia |
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| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| MRI | Device | Participants will undergo an MRI scan while participating in two breathing tests (hypercapnia and hypoxia) to measure brain blood flow. |
|
| Measure | Description | Time Frame |
|---|---|---|
| Cerebral Vascular Reactivity to Hypercapnia | The change in brain blood flow using MRI will be measured in response to a hypercapnic breathing test. The participants cerebral vascular reactivity to hypercapnia will be compared between the controls (without VAH) and those with VAH. | One study visit, up to 120 minutes in the MRI |
| Cerebral Blood Flow Response to Hypoxia | The change in brain blood flow using MRI will be measured in response to a hypoxic breathing test. The participants cerebral blood flow response to hypoxia will be compared between the controls (without VAH) and those with VAH. | One study visit, up to 120 minutes in the MRI |
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Inclusion Criteria:
Exclusion Criteria:
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Subjects for this study, will include healthy adults enrolled in the Wisconsin Alzheimer's Disease Research Clinical Core. Both men and women are eligible to participate in this study.
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| Name | Affiliation | Role |
|---|---|---|
| Jill N Barnes, PhD | University of Wisconsin, Madison | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| University of Wisconsin-Madison | Madison | Wisconsin | 53706 | United States |
| PubMed Identifier | Type | Citation | Retractions |
|---|---|---|---|
| 28515434 | Background | Kisler K, Nelson AR, Montagne A, Zlokovic BV. Cerebral blood flow regulation and neurovascular dysfunction in Alzheimer disease. Nat Rev Neurosci. 2017 Jul;18(7):419-434. doi: 10.1038/nrn.2017.48. Epub 2017 May 18. | |
| 32641520 | Background | Switzer AR, Cheema I, McCreary CR, Zwiers A, Charlton A, Alvarez-Veronesi A, Sekhon R, Zerna C, Stafford RB, Frayne R, Goodyear BG, Smith EE. Cerebrovascular reactivity in cerebral amyloid angiopathy, Alzheimer disease, and mild cognitive impairment. Neurology. 2020 Sep 8;95(10):e1333-e1340. doi: 10.1212/WNL.0000000000010201. Epub 2020 Jul 8. |
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Serum blood samples will be retained for future analysis.
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