Prior Safety Data
This treatment has already been tested in at least one earlier human trial.
Healthy Volunteers Welcome
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Review the details below, then apply to join this clinical trial.
At a Glance
Age
50 and older
Sex
Any
Trial phase
Phase 2
Study type
Interventional
Purpose
Treatment
Participants needed
118 (estimated)
Sponsor
Douglas Seals · Other
Who this trial is looking for
This trial is looking for middle-aged and older adults with elevated blood pressure. Participants will take a supplement called nicotinamide riboside and be monitored over time.
Are You a Good Fit for This Trial?
You may be able to join if
I can provide informed consent
I am willing to accept random assignment to condition
I have systolic blood pressure between 120 and 159 mmHg
I have a body mass index under 40 kg/m2
I have been weight stable in the last 3 months
I do not have other clinical diseases
I have a normal ankle-brachial index
My fasting plasma glucose is under 126 mg/dL
You may not be able to join if
I have systolic blood pressure below 120 or 160 mmHg or higher
I am currently taking antihypertensive medications
I have a chronic medical condition like diabetes or cancer
I smoke
I have alcohol dependence or abuse
I have uncontrolled thyroid disease
I have an abnormal blood pressure response to exercise
I do regular vigorous aerobic exercise
Summarized in plain language from this trial's official eligibility criteria.
The full criteria are further down this page — only the research team can
confirm whether you qualify.
Think this trial could be right for you?
Answer three quick questions written from this study's own rules to see if you may qualify. No account needed to find out.
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 st…
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.
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Eligibility Criteria
Inclusion Criteria:
* 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 th…
Inclusion Criteria:
* 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
Exclusion Criteria:
* Systolic blood pressure \<120 or \>/= 160 mmHg
* Currently taking antihypertensive medications
* Other chronic medical condition (e.g., diabetes, chronic kidney disease, cancer)
* Current smoker
* Alcohol dependence or abuse
* Uncontrolled thyroid disease or change in thyroid medication within previous 3 months
* Abnormal blood pressure response to exercise (drop in SBP below resting pressure or SBP \>160 mmHg or DBP \>115 mmHg)
* Regular vigorous aerobic/endurance exercise (\>4 bouts/weeks, \>30 min/bout at a workload \>6 METS)
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