Mechanisms of Impaired Brain Blood Flow With Aging

Not Applicable

Completed

• Conditions: Aging

• Registration Number: NCT03775382
• Lead Sponsor: University of Delaware

Brief Summary

Aging is the primary risk factor for Alzheimer's disease (AD), which is a rapidly growing public health concern. Understanding the mechanisms of normal brain aging may provide insight into the factors linking advancing age to increased risk for AD and thereby lead to new therapeutic targets for preventing or slowing AD progression. Cardiovascular changes, including impaired cerebrovascular function, occur with aging and may increase risk for AD; however, the mechanisms by which cerebrovascular function becomes impaired in older adults are incompletely understood. The overall goal of this project is to examine potential mechanisms of age-related declines in cerebrovascular function in humans. The investigators hypothesize that brain macro-vascular endothelial dysfunction, secondary to oxidative stress, plays an important role in mediating age-related changes in brain blood flow and cerebrovascular reactivity. The results of this pilot study have the potential to identify novel targets of cerebrovascular aging and will help guide the design of future clinical trials aimed at improving cerebral blood flow in older adults.

Detailed Description

Not available

Study Timeline

• Study Start: 2017-10-30
• Study First Submitted: 2018-12-06
• Study First Submitted QC: 2018-12-12
• Study First Posted: 2018-12-13
• Primary Completion: 2022-06-01
• Study Completion: 2022-06-01
• Status Verified: 2023-05
• Last Update Submitted: 2023-05-08
• Last Update Posted: 2023-05-10

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 34

Inclusion Criteria

• 18-29 or 55-79 years old

Exclusion Criteria

• Pregnancy or breastfeeding;
• Blood chemistries indicative of abnormal renal, liver, thyroid and adrenal function (i.e., outside of normal reference range); estimated glomerular filtration rate using the MDRD prediction equation must be >60 ml/min/1.73 m2;
• Abnormal blood chemistry that is clinically relevant or any blood chemistry marker that is +/-2.5x the upper or lower limit;
• Lack of a suitable temporal window for cerebrovascular assessments;
• Current smoking;
• Chronic clinical diseases (e.g., coronary artery, peripheral artery, or cerebrovascular diseases, diabetes, chronic kidney disease, COPD);
• Major psychiatric disorder (e.g. Alzheimer's disease or other form of dementia, schizophrenia, bipolar disorder, major depression within past two years);
• Neurological or autoimmune conditions affecting cognition (e.g. Parkinson's disease, epilepsy, multiple sclerosis, head trauma with loss of consciousness greater than 30 min, large vessel infarct);
• Current medication use likely to affect CNS functions (e.g. long active benzodiazepines);
• Having past or present alcohol dependence or abuse, as defined by the American Psychiatry Association, Diagnostic and Statistical Manual of Mental Disorders;
• Body mass index (BMI) >40 kg/m2 (FMD measurements can be inaccurate in severely obese patients).

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: CROSSOVER

Primary Outcome Measures

Name	Time	Method
Change from baseline in internal carotid artery (ICA) diameter after acute infusion of the antioxidant ascorbic acid	Change from baseline to 30 minutes post-infusion	Cerebrovascular reactivity to hypercapnia

Secondary Outcome Measures

Name	Time	Method
Change from baseline in middle cerebral artery (MCA) diameter after acute infusion of the antioxidant ascorbic acid	Change from baseline to 30 minutes post-infusion	Cerebrovascular reactivity to hypercapnia

Trial Locations

Locations (1)

Neurovascular Aging Laboratory; 🇺🇸 Newark, Delaware, United States