Cognitive Change, Inflammation, Neurodegenerative Diseases
Conditions
Brief summary
The goal of this clinical trial is to learn whether Nicotinamide adenine dinucleotide (NAD+) can influence cognition and biomarkers in healthy, cognitively intact women aged 40-80. The main questions it aims to answer are: Will cognitive functioning change in response to NAD+? Will inflammatory markers and serum indicators of neurodegeneration change in response to NAD+? Researchers will compare individuals receiving NAD+ to those receiving placebo to see if the results differ. Participants will: Complete an online questionnaire, Visit the lab for computerized cognitive testing and a blood draw, Take NAD+ or a placebo every day for 4 weeks, Visit the lab for computerized cognitive testing and a blood draw
Interventions
Participants will take a supplement for four weeks. The supplement will either be Nicotinamide adenine dinucleotide or a placebo.
Participants will take a supplement for four weeks. The supplement will either be Nicotinamide adenine dinucleotide or a placebo pill.
Sponsors
Study design
Eligibility
Inclusion criteria
* Identify as Female * Have a BMI of 18.5 or above * Must be able to swallow tablets
Exclusion criteria
* Those who are pregnant, breastfeeding, or taking hormone medication
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Neurocognition | four weeks | NIH Toolkit Cognition Battery, Automated Neuropsychological Assessment Metrics |
| Neurodegenerative disease panel | four weeks | BDNF, Cathespin D, MPO, PAI-1 (total), PDGF-AA, PDGF-AB/BB, RANTES, slCAM-1, sNCAM, sVCAM-1 |
| Markers of systemic inflammation | four weeks | GM-CSF, IFNγ, IL-1β, IL-2, IL-4, IL-5, IL-6, IL-8, IL-10, IL-12p70, IL-13, IL-17A, IL-23, TNFα |
Countries
United States