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

Study Overview: This is a randomized, double-blind, placebo-controlled, parallel design, single site phase IIa clinical trial assessing the efficacy of nicotinamide riboside supplementation to lower systolic blood pressure (SBP) and aortic stiffness in middle-aged to older (MA/O) adults (50-79 years) with elevated to stage-1 systolic hypertension (SBP: 120-139 mmHg). Nicotinamide riboside is an endogenously occurring precursor of NAD+ and a novel caloric restriction mimetic in humans that is now commercially available as a dietary ingredient/supplement. We have recently demonstrated that chronic supplementation with nicotinamide riboside lowers SBP and carotid-femoral pulse wave velocity (CFPWV; gold-standard measure of aortic stiffness and independent risk factor for cardiovascular diseases) in a small pilot study of healthy MA/O adults; the greatest reductions in SBP were observed in a subgroup with baseline SBP in the elevated/stage-1 hypertension range. As a next translational step, the present study proposes to assess the efficacy of 3 months of nicotinamide riboside supplementation for decreasing SBP (primary outcome) and aortic stiffness (secondary outcome) in a larger cohort of MA/O men and women with SBP in the elevated/stage-1 hypertension range. As secondary aims, we will also assess safety and tolerability of long-term nicotinamide riboside supplementation, and the effects of nicotinamide riboside supplementation vs. placebo on NAD+ metabolites and circulating biomarkers of vasoconstriction, oxidative stress and inflammation. Subject Enrollment and Screening: Potential participants will be made aware of the proposed study through described recruitment efforts (see Recruitment and Retention section). Interested participants will contact a staff research assistant via phone or email (contact information supplied with recruitment materials) and will complete a general screening form online through the Research Electronic Data Capture (REDCap) system to determine eligibility. REDCap is a secure web-based application designed to support data capture for research studies. After hearing a thorough study description and having all questions answered by the staff research assistant, those eligible and interested in participating in the study will provide written and verbal informed consent, and undergo in-person screening at the CU Boulder Clinical Translational Research Center (CTRC). Informed consent will only be obtained by members of the research team who have been observed and approved by the CTRC Research Subject Advocate (see Protection of Human Subjects). We plan to consent 148 subjects in order to meet our enrollment targets (to account for an \~25% rate of exclusion base on in-person screening). In-person screening will include: review of medical history; physical exam; resting heart rate; resting blood pressure; blood draw for metabolic profile, lipid profile, complete blood count, and thyroid stimulating hormone; measurement of ankle-brachial index; and a 12-lead ECG at rest and during graded exercise testing (see the Eligibility Criteria section for detailed inclusion/exclusion criteria). Resting blood pressure will be measured on a second occasion within one week of the initial screening to establish baseline blood pressure status; SBP measured on the two separate days will be averaged and must be in the elevated to stage-1 hypertension range (120-139 mmHg) for enrollment into the study. Participant Randomization and Subject/Investigator Blinding: After completing screening, eligible subjects will be randomized to either the nicotinamide riboside or placebo group. A randomized block design will be used to balance groups for sex, age (mid-life: 50-64 years vs. older: 65-79 years) and hypertension status (elevated vs. stage-1 systolic hypertension). Randomization will be carried out by an unblinded staff research assistant who is not involved in data collection or analysis. Subjects will be categorized based on the block randomization scheme and then a random number generator will be used to assign subjects to either nicotinamide riboside or placebo treatment. Researchers involved in collection of outcome data will be blinded to the assigned intervention. Subjects will be blinded to their assigned intervention and will receive capsules in coded blister packs; nicotinamide riboside and placebo capsules will appear identical. CTRC clinical staff involved with subject check-in visits and/or data collection will also be blinded (in the case of a serious adverse event, blinding of the CTRC staff will be broken, as necessary to ensure appropriate medical treatment). Assessment of Study Outcomes: All subjects will undergo baseline testing for all primary, secondary, and other outcome measures. All measurements will be made after a 12 hour fast from food and caffeine (water allowed) and 24 hours after abstaining from alcohol and exercise. All tests will take place in the CU Boulder CTRC. The protocol for baseline testing is as follows: * Urine sample collection; * Assessment of casual SBP; * Placement of IV in an antecubital vein followed by 30 minutes of rest in a supine position; - Collection of blood samples by a trained CTRC provider; * Assessment of aortic stiffness by CFPWV. Following completion of outcome measure testing, the below non-outcome measures will be made in order to ensure that participant characteristics known to affect cardiovascular function are unaltered during the intervention: * 3-day diet records to ensure that daily fluid and caloric intake remain stable; * The Community Healthy Activities Model Program for Seniors (CHAMPS) questionnaire will be completed and physical activity will be assessed by accelerometers (ActiGraph, 3-day recordings) to document stability of physical activity levels; * Maximal oxygen consumption using indirect calorimetry during incremental treadmill exercise (Balke protocol) will be measured to document unchanged aerobic fitness; and * Body composition will be assessed by dual energy x-ray absorptiometry (DEXA) and anthropometry to confirm unaltered body composition; body mass will also be determined during safety and check in visits with CTRC nursing staff. Following all CTRC testing procedures, subjects will be outfitted with an ambulatory blood pressure monitor pre-programmed to automatically measure blood pressure every 20 minutes. A study team member will provide the subject with written and verbal instructions on how to operate the monitor. Subjects will wear the monitor for 24 hours before returning it to the investigators. Ambulatory blood pressure data will be evaluated for completeness immediately upon return of the monitor; if an inadequate number of blood pressure measurements (\<67% of expected) were made to properly characterize 24-hour SBP the subject will be re-outfitted with the ambulatory monitor, be re-instructed on its use, and wear it for a second 24-hour period. The Research Strategy and Outcome Measures sections provide a more detailed description of these procedures. Similar protocols and procedures are well established in the Seals laboratory and the CU Boulder CTRC. Delivery of the Intervention: After completing baseline testing, subjects will begin their assigned intervention (nicotinamide riboside or placebo). Subjects will be instructed to take 2 x 250 mg capsules in the morning and 2 x 250 mg capsules in the evening (4 capsules/day). This will result in a dosing of 500 mg nicotinamide riboside 2x/day in the nicotinamide riboside group (1000 mg/day total). Subjects will return to the CU Boulder CTRC once every two weeks for check-in and to receive capsules. Capsules will be prepared by the manufacturer in blister packs to promote adherence and will be stored and dispensed by the CTRC pharmacist (unblinded) and distributed by a CTRC nurse (blinded). Subjects will return their blister packs at each check-in visit and after follow-up testing to assess adherence to the intervention. During each visit to the CTRC, subjects will be monitored for treatment-emergent adverse events by blinded CTRC clinical staff. Post-Testing: After completing 3 months of treatment with either nicotinamide riboside or placebo, subjects will return to the CU Boulder CTRC for reassessment of all outcome measures, including: casual SBP, 24-h ambulatory SBP, CFPWV, venous blood draw, and urine sample. Non-outcome control measures (3-day diet record, CHAMPS survey, activity monitor, maximal oxygen consumption test, body composition) will also be reassessed. These measures will be made under the same experimental conditions, in the same order, and with the same techniques as baseline testing. Intervention Duration and Study Sample Size: The expected duration for a participant to complete the entire protocol from screening to follow-up testing is 18 weeks. Based on our power analysis, we need to complete the entire protocol on a total of 94 participants (47/group) to detect a significant difference between treatment conditions in our primary outcome measure (SBP). We intend to enroll 118 subjects (59/group) to account for an \~20% dropout rate. Based on this, we will enroll 2-3 subjects per month, which will allow for completion of data collection by month 55 of this award; this rate of testing is achievable based on previous pharmacological interventions carried out in the Seals laboratory and the availability of the CTRC facilities and staff. Data Collection and Analysis (including blinding): Collection of primary and secondary outcome measures will be performed by postdoctoral fellow, Dr. Craighead, with the assistance of members of the laboratory. IV placement and blood draws will be performed by experienced CTRC clinical staff. Data analysis will be performed by Dr. Craighead. Having a single investigator perform all data collection and analysis will remove the potential for inter-investigator variation. Dr. Craighead and other research and clinical staff involved in data acquisition will remain blinded throughout data collection and analysis. All data will be analyzed as outlined in the Research Strategy section and Outcome Measures section; data analysis and dissemination of results will be completed by the end of this award.