Multi-target Dietary Supplement Tolerability in an Aging Population (MTDSST)
- Conditions
- Age-related Cognitive DeclineAging
- Interventions
- Dietary Supplement: Multi-target Dietary Supplement (MTDS)
- Registration Number
- NCT04641663
- Lead Sponsor
- Douglas Boreham
- Brief Summary
This study is being performed to determine if a multi-ingredient dietary supplement is safe and easy to take by healthy older adults. Participants will be required to take one of three different doses of the dietary supplement for 90 consecutive days and complete wellness surveys and a daily log while taking the supplement. Participants will also provide blood samples at the start of the study, after 30 days, and at the end of the study which will help determine how participants respond to the supplement.
- Detailed Description
Likely because of the highly complex nature of aging, there has been little success reducing age-related physical and cognitive deterioration. The predominant approach has been to manage emergent symptoms rather than mitigate the cellular mechanisms driving the degenerative processes underlying aging. Additionally, the multifaceted and complex etiology of aging makes it extremely difficult to provide effective interventions within current treatment paradigms. The medical community has established that preventative measures are the most effective means of slowing the progression of age-associated deterioration, however effective methods or interventions have not been established.
The Multi-Target Dietary Supplement (MTDS) was designed to simultaneously target and support the cellular processes implicated in the progression of the aging phenotype (oxidative stress, inflammatory processes, insulin resistance, and membrane and mitochondrial deterioration). The MTDS is unique in that it was specifically designed as a multi-target intervention to support the complex cellular perturbations associated with aging. Components of the formulation were chosen based on scientific consensus of documented effectiveness for one or more of the targeted processes, long-term evidence of safety, and synergistic or additive interactions between components.
In more than 20 years of pre-clinical research, the MTDS has demonstrated significant beneficial impacts in animal models of aging and age-associated disease. The MTDS has resulted in significant reductions in both acute and chronic oxidative stress, greatly improved mitochondrial function and efficiency, significantly reduced inflammatory processes and improved glucose metabolism. Signal transduction is normalized to youthful levels in aged animals, including key pathways implicated in aging (unpublished data). On a functional level, MTDS treatment has resulted in increased longevity of 10 to 28% in normal and accelerated aging phenotypes, respectively. Concomitant improvements in mobility, activity levels, muscle strength (exercise mimetic) and overall body condition in aged animals were observed. Dramatic reductions in the incidence of muscle wasting, arthritic processes, and cataracts were also observed. Sensory and cognitive acuity were protected and frequently enhanced in aged animals, with significant improvements in visual and olfactory function observed in a broad range of tasks. MTDS treatment has demonstrated profound sparing from age-related neuronal losses and corresponding protection of neurogenesis and enhanced synaptogenesis, resulting in dramatically improved cognition in aged animals. The quantity of data indicating MTDS efficacy in pre-clinical studies is considerable, however the effects of the MTDS in humans, although positive, remains anecdotal. This tolerability study is the critical first step to begin assessment of the efficacy of the MTDS in human populations. If even a portion of these protective effects of the MTDS are translatable from mice to humans, the positive impacts for the aging population and Ontario's healthcare system could be profound.
This is a multi-center, three-arm study designed to evaluate the safety of a dietary supplement at three dosing regimes for 90 days. Initially, 45 healthy volunteers will be randomly assigned to one of three dose regimes: 1) 100% of recommended daily dose (RDD), 2) 80% of recommended daily dose or 3) 60% of recommended daily dose. Dosing regimes are based on levels of the MORNING tablet doses, all groups will receive the full recommended dose for both EVENING and OMEGA doses. Written informed consent will be obtained and a medical history and health assessment will be performed. The investigator will determine whether the subject meets all inclusion and exclusion criteria. Health assessments will be made at baseline, 30 days and 90 days. Adverse events, concomitant medications, and product administration will be recorded throughout the study.
Compliance, safety, and tolerability parameters are the primary focus of this study; however the probability of serious adverse events is extremely low given the long safety history of safety of the vitamins and nutraceuticals that comprise the MTDS.
The primary objective is to evaluate the safety and tolerability of the MTDS regimen in terms of its administration at 3 dosing regimes for 90 consecutive days with respect to micronutrient levels, laboratory tests and adverse events.
The secondary objectives include:
1. monitoring compliance of taking the MTDS,
2. monitoring wellness as measured by the 36-Item Short Form Survey (SF-36) scale and daily journal, over the 90-day administration of the MTDS, and
3. to assess MTDS absorption through plasma micronutrient testing, at baseline, 30 days and 90 days following administration of the test agent.
Recruitment & Eligibility
- Status
- ENROLLING_BY_INVITATION
- Sex
- All
- Target Recruitment
- 70
- Male or Female subjects ages of 45 and older.
- Capable of providing informed consent
- Patients currently taking fluconazole, 3-hydroxy-3-methyl-glutaryl-CoA reductase (HMG-CoA) reductase inhibitors (i.e. "statin" drugs), or any other drug known to interfere with serum transaminase (i.e. liver enzymes), must have history of stable liver function test since first taking such drugs.
- Patients who usually and customarily take dietary supplements, including vitamins, must undergo a two-week washout period
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Exposure to any investigational drug within 90 days of the beginning of this study
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Known human immunodeficiency virus (HIV) seropositivity or Acquired Immunodeficiency Syndrome (AIDS); history of Hepatitis B (HBV), Hepatitis C (HCV) vital infection, unexplained elevated serum transaminase, or other hepatic disease. NOTE: HIV, HCV, and HBV testing will not be performed as part of screening.
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History of cancer within the last 5 years, except for basal or squamous cell cancer.
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Recent COVID-19 infection.
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Allergy to fish (specifically sardines, anchovies or mackerel) or any of the investigational product components
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Concomitant use, or use within less than a two-week period, of any other dietary supplement
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Concomitant use of any drug known to interfere with laboratory measures such as:
- Niaspan (extended release niacin)
- Lamisil (terbinafine HCl)
- Chronic use of acetaminophen (>1,500 mg/day) (occasional use for minor aches and pains is excluded from this restriction)
- Newly prescribed (< 90days) HMG-CoA reductase inhibitors ("statin medications"), or patients currently on statin medications who have previously shown evidence of elevated serum transaminases
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Currently diagnosed with multiple sclerosis, systemic lupus erythematosis, or other autoimmune disorders known to interfere with laboratory measures
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History of alcoholism or drug abuse, unless it is determined that such past use would not influence laboratory measures (DSN4 criteria)
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Any other active disease of a life-threatening nature or laboratory abnormality that, in the judgment of the investigator, may interfere with the interpretation, or increase risk of patient participation
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Conditions that require nutritional therapy, such as:
- Pernicious anemia
- Iron-deficiency anemia
- Hartnup Disease or Pellagra
- Scurvy
- Beriberi-induced Endemic Neuritis
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description 100 RDD Multi-target Dietary Supplement (MTDS) 100% of recommended daily dose (RDD) of the MORNING tablet dose (5 tablets), all groups will receive the full recommended dose for both EVENING (3 tablets) and OMEGA (2 softgels) doses. 60 RDD Multi-target Dietary Supplement (MTDS) 60% of recommended daily dose of the MORNING tablet dose (3 tablets), all groups will receive the full recommended dose for both EVENING (3 tablets) and OMEGA (2 softgels) doses. 80 RDD Multi-target Dietary Supplement (MTDS) 80% of recommended daily dose of the MORNING tablet dose (4 tablets), all groups will receive the full recommended dose for both EVENING (3 tablets) and OMEGA (2 softgels) doses.
- Primary Outcome Measures
Name Time Method Monocytes (10^9/L) out to 90 days Safety Assessment in Hematology
Total Bilirubin (umol/L) out to 90 days Safety Assessment in Serum Chemistry
High Sensitivity C-Reactive Protein (mg/L) out to 90 days Safety Assessment in Serum Chemistry
Hematocrit (%) out to 90 days Safety Assessment in Hematology
Eosinophils/Leukocytes (%) out to 90 days Safety Assessment in Hematology
Lymphocytes/Leukocytes (%) out to 90 days Safety Assessment in Hematology
Monocytes/Leukocytes (%) out to 90 days Safety Assessment in Hematology
Number of Participants With Treatment-Related Adverse Events (AE) as Assessed by CTCAE v5.0 out to 90 days Subjects are instructed to log any AEs that occur at any time during the study in the study journal. Participants will be contacted by phone after 7 days on the MTDS to assess any occurrence of AEs. Reported or observed AEs will be documented and followed to resolution.
Hemoglobin (g/L) out to 90 days Safety Assessment in Hematology
Serum Glucose (mmol/L) out to 90 days Safety Assessment in Serum Chemistry
Alanine Transaminase (U/L) out to 90 days Safety Assessment in Serum Chemistry
Erythrocytes (10^12/L) out to 90 days Safety Assessment in Hematology
Direct Bilirubin (umol/L) out to 90 days Safety Assessment in Serum Chemistry
Lactate Dehydrogenase (U/L) out to 90 days Safety Assessment in Serum Chemistry
Lymphocytes (10^9/L) out to 90 days Safety Assessment in Hematology
Neutrophils (10^9/L) out to 90 days Safety Assessment in Hematology
Chloride (mmol/L) out to 90 days Safety Assessment in Serum Chemistry
Urea (mmol/L) out to 90 days Safety Assessment in Serum Chemistry
Albumin (g/L) out to 90 days Safety Assessment in Serum Chemistry
Alkaline Phosphatase (U/L) out to 90 days Safety Assessment in Serum Chemistry
Leukocytes (10^9/L) out to 90 days Safety Assessment in Hematology
Basophils (10^3/uL) out to 90 days Safety Assessment in Hematology
Basophils/Leukocytes (%) out to 90 days Safety Assessment in Hematology
Eosinophils (10^9/L) out to 90 days Safety Assessment in Hematology
Neutrophils/Leukocytes (%) out to 90 days Safety Assessment in Hematology
Platelet Count (10^9/L) out to 90 days Safety Assessment in Hematology
Sodium (mmol/L) out to 90 days Safety Assessment in Serum Chemistry
Potassium (mmol/L) out to 90 days Safety Assessment in Serum Chemistry
Urate (umol/L) out to 90 days Safety Assessment in Serum Chemistry
Aspartate Phosphatase (U/L) out to 90 days Safety Assessment in Serum Chemistry
Gamma Glutamyl Transpeptidase (U/L) out to 90 days Safety Assessment in Serum Chemistry
Calcium (mmol/L) out to 90 days Safety Assessment in Serum Chemistry
Creatinine (umol/L) out to 90 days Safety Assessment in Serum Chemistry
- Secondary Outcome Measures
Name Time Method Zinc (mg/L) out to 90 days Plasma Micronutrient Levels
Copper (mg/L) out to 90 days Plasma Micronutrient Levels
Glutamine (mg/L) out to 90 days Plasma Micronutrient Levels
Carnitine (mg/L) out to 90 days Plasma Micronutrient Levels
Choline (mg/L) out to 90 days Plasma Micronutrient Levels
Inositol (mg/L) out to 90 days Plasma Micronutrient Levels
Coenzyme Q10 (mg/L) out to 90 days Plasma Micronutrient Levels
Vitamin B1 (mg/L) out to 90 days Plasma Micronutrient Levels
Biotin (mg/L) out to 90 days Plasma Micronutrient Levels
Vitamin K2 (mg/L) out to 90 days Plasma Micronutrient Levels
Vitamin B2 (mg/L) out to 90 days Plasma Micronutrient Levels
Vitamin B3 (mg/L) out to 90 days Plasma Micronutrient Levels
Vitamin B6 (mg/L) out to 90 days Plasma Micronutrient Levels
Pantothenate (mg/L) out to 90 days Plasma Micronutrient Levels
Vitamin C (mg/L) out to 90 days Plasma Micronutrient Levels
Vitamin A (mg/L) out to 90 days Plasma Micronutrient Levels
Vitamin B12 (mg/L) out to 90 days Plasma Micronutrient Levels
Glutathione (mg/L) out to 90 days Plasma Micronutrient Levels
Vitamin D3 (mg/L) out to 90 days Plasma Micronutrient Levels
Magnesium (mg/L) out to 90 days Plasma Micronutrient Levels
Alpha Lipoic Acid (mg/L) out to 90 days Plasma Micronutrient Levels
36-Item Short Form Survey (SF-36) up to 90 days The SF-36 wellness questionnaire will be used to assess the health status of subjects. There are 36 individual questions which identify eight different facets of wellness. These have been described as physical functioning, role-physical, bodily pain, general health, vitality, social functioning, role-emotional, and mental health. These facets are further collapsed into physical and mental component summaries. The eight scaled scores, which are the weighted sums of the questions in their section. Each scale is directly transformed into a 0-100 scale on the assumption that each question carries equal weight. The lower the score the more disability. The higher the score the less disability i.e., a score of zero is equivalent to maximum disability and a score of 100 is equivalent to no disability. This questionnaire will be included in the study booklet given to each subject, and will be self administered.
Folate (mg/L) out to 90 days Plasma Micronutrient Levels
Manganese (mg/L) out to 90 days Plasma Micronutrient Levels
Trial Locations
- Locations (2)
Northern Ontario School of Medicine - Elliot Lake site
🇨🇦Elliot Lake, Ontario, Canada
McMaster University - Behavioural Neurosciences
🇨🇦Hamilton, Ontario, Canada