Nicotinamide Riboside Supplementation for Treating Elevated Systolic Blood Pressure and Arterial Stiffness in Middle-aged and Older Adults

Who is this study for? Middle-aged and older adults with elevated systolic blood pressure and arterial stiffness
What treatments are being studied? Nicotinamide riboside
Status: Recruiting
Location: See location...
Intervention Type: Drug, Other
Study Type: Interventional
Study Phase: Phase 2
SUMMARY

Aging is the primary risk factor for cardiovascular diseases (CVD), the number one cause of death in developed societies. Systolic blood pressure (SBP) increase with age and is a key intermediary factor linking aging to increased CVD risk. The primary mechanisms underlying the age-associated increase in SBP is stiffening of the large elastic arteries, which is mediated by increases in oxidative stress, inflammation, and vascular smooth muscle tone. Regular caloric restriction is effective at lowering SBP in middle-aged and older adults; however, adherence to caloric restriction is poor and may be detrimental to normal weight older adults due to reduced skeletal muscle mass and bone mineral density. Therefore, identification of more practical alternative interventions that mimic the beneficial effects of caloric restriction, with stronger adherence and less risk of adverse consequences, is of significant biomedical importance. Nicotinamide riboside is a naturally occurring precursor of nicotinamide adenine dinucleotide (NAD+), a critical mediator of the beneficial effects of caloric restriction, and therefore a novel caloric restriction mimetic compound. We recently completed the first pilot study of nicotinamide riboside supplementation in healthy middle-aged and older adults and demonstrated that 6 weeks of supplementation decreased systolic blood pressure (SBP) by 8 mmHg in individuals with baseline SBP of 120-139 mmHg (elevated SBP/stage 1 hypertension) compared with placebo, and lowered arterial stiffness, a strong independent predictor of CVD and related morbidity and mortality. As a next translational step, we will conduct a randomized, placebo-controlled, double-blind clinical trial to further assess the safety and efficacy of oral nicotinamide riboside (3 months vs placebo) for decreasing SBP and arterial stiffness in middle-aged and older men and women with SBP between 120 and 139 mmHg at baseline.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 50
Healthy Volunteers: t
View:

• Ability to provide informed consent

• Willing to accept random assignment to condition

• Systolic blood pressure between 120 and 159 mmHg

• Body mass index \<40 kg/m2

• Weight stable in the prior 3 months (\<2 kg weight change) and willing to remain weight stable throughout the study

• Absence of other clinical disease as determined by medical history, physical examination, blood chemistries, ankle-brachial index, and 12-lead ECG at rest and during graded treadmill exercise

‣ Ankle-brachial index \>0.7

⁃ Total cholesterol \<240 mg/dL

⁃ Fasting plasma glucose \<126 mg/dL

⁃ Normal 12-lead ECG at rest and during graded treadmill exercise to fatigue

Locations
United States
Colorado
Integrative Physiology of Aging Laboratory
RECRUITING
Boulder
Contact Information
Primary
Daniel H Craighead, PhD
daniel.craighead@colorado.edu
303-492-7702
Time Frame
Start Date: 2019-05-10
Estimated Completion Date: 2025-06-01
Participants
Target number of participants: 118
Treatments
Experimental: Nicotinamide riboside
Subjects will take 500 mg of the vitamin B3-precursor, nicotinamide riboside (NIAGEN) twice per day (1,000 mg per day total) for 3 months.
Placebo_comparator: Placebo
Subjects will take placebo pills twice a day for 3 months.
Related Therapeutic Areas
Sponsors
Leads: Douglas Seals

This content was sourced from clinicaltrials.gov

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