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NCT Number: NCT03472820

Methylation Diet and Lifestyle Study

The maintenance of health and the progression of disease are associated with an individual's genetic make-up and environmental factors, including lifestyle choices (such as diet, exercise, behaviors, stressors, sleep, tobacco and alcohol use), environmental exposures and socioeconomic determinants. Environmental factors have been shown to influence, sometimes rapidly, epigenetic processes thereby influencing genetic expression. Regulation of the human genome by the epigenome is now regarded as a cornerstone, heritable, physiologic process, playing a key role in phenotypic expression of health and disease.

DNA methylation is a well-researched, primary epigenetic process. Aberrant DNA methylation resulting in hyper- or hypomethylated regions of the genome, generally results in inhibition or expression of certain genes and has been associated with the pathogenesis of numerous conditions, ranging from inflammation and accelerated aging, to cancer, autoimmunity, diabetes, heart disease, dementia, allergic disease, posttraumatic stress disease and others. Likewise, certain healthy diet and lifestyle habits have been demonstrated to favorably influence DNA methylation patterns.

Understanding that environmental factors can potently and sometimes rapidly, favorably or negatively influence epigenetic expression, a short-term diet and lifestyle intervention may significantly augment DNA methylation expression.

The purpose of this study is to evaluate a 9-week diet and lifestyle intervention on patient-reported quality of life, symptoms, and DNA and biochemical methylation-related biomarkers in healthy males ages 50-72.

Active, Not Recruiting

This study is active but is not currently recruiting participants.

Key information

Conditions

Lifestyle Diet Healthy

Age range

50 year–72 year

Sex eligibility

Male

Study type

Interventional

Phase

Not applicable

Primary location

NUNM Helfgott Research Institute

Portland, Oregon, 97201, United States

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • • Males, ages 50-72
  • Willing to adhere to 9 weeks of a dietary and lifestyle program including specific nutrition and exercise guidelines
  • Willing to avoid any over-the-counter medications, supplements or herbal products for the length of the study, except short-term use (<1 week) use at least 1 week before scheduled study visits
  • Willing to have blood drawn three times and abstain from food or beverage intake for 10-12 hours before blood draws
  • Willing to provide saliva samples
  • Willing to track food intake, sleep, stress management techniques, and exercise daily
  • Willing to drink a nutrient-enriched beverage and take a encapsulated probiotic daily
  • Willing and able to use electronic devices and connect to the internet
  • Able to speak, read and understand English

Exclusion criteria

  • • Currently taking any of the following prescription medications
  • Proton pump inhibitors: omeprazole (Prilosec, Prilosec OTC); aspirin and omeprazole (Yosprala); lansoprazole (Prevacid, Prevacid IV, Prevacid 24-Hour); ;dexlansoprazole (Dexilent, Dexilent Solutab); rabeprazole (Aciphex, Aciphex Sprinkle); pantoprazole (Protonix)
  • H2-blockers: nizatidine (Axid, Axid AR, Axid Pulvules); famotidine (Pepcid, Pepcid AC); cimetidine (Tagamet, Tagamet HB); ranitidine (Zantac)
  • These classes of medications are excluded due to direct (due to nutrient requirements for metabolism) and indirect (through impaired digestion and assimilation of nutrients).
  • Use of nutrition supplements or herbal products not prescribed by a licensed healthcare provider for a medical condition
  • Currently following a prescribed dietary/lifestyle program or initiate within the 30 days prior to baseline
  • Initiation of or changes to an exercise regimen within 30 days prior to baseline
  • Use of nicotine, marijuana or cannabinoids (including CBD products) or recreational drugs/substances (such as but not limited to cocaine, phencyclidine [PCP], and methamphetamine) current/within the last 30 days or use during the study
  • Have a diagnosis of cardiovascular disease, kidney disease, liver disease, diabetes, autoimmune disease, high blood pressure, or cancer (does not include basal cell carcinoma, squamous cell carcinoma, and/or carcinoma in situ of the cervix).
  • Have a diagnosis of an immunodeficiency condition, such as Human Immunodeficiency Virus (HIV) infection or Acquired Immune Deficiency Syndrome (AIDS)
  • Have a diagnosis of neurodegenerative conditions such as, amyotrophic lateral sclerosis (ALS), Parkinson's disease, Multiple Sclerosis, or Alzheimer's disease.
  • Excessive alcohol consumption (more than 4 drinks per day or 14 per week on average)
  • Known sensitivity, intolerance or allergy to ingredients in the study supplements or in the recommended dietary therapy
  • Currently receiving intravenous nutrient therapy
  • Currently participating in another interventional research study or participated in another interventional study within the last 3 weeks prior to baseline

Treatment and study plan

Diet Recommendations

Other

Specific dietary guidelines will be outlined for participants.

Lifestyle Recommendations

Other

Participants are encouraged to average a minimum of 7 hours of sleep per night.

Exercise Recommendations

Other

Participants will be encouraged to exercise a minimum of 30 minutes at least 5 days per week at an intensity of 60-80% of maximum perceived exertion.

Stress Management Recommendations

Other

Participants will utilize the Cleveland Clinic's Stress Free Now application to engage in a variety of guided stress reduction techniques, including meditation and mindful breathing. Recommended frequency is twice daily, preferably morning and evening.

PhytoGanix (tropical fruit flavor)

Other

Organic Superfruits & Greens Powder Drink Mix is a food-based phytonutrient blend. Participants will take 2 servings daily in divided doses.

UltraFlora Intensive Care

Other

Probiotic; Participants will take 2 capsules of UltraFlora Intensive Care probiotic daily in divided doses.

Primary outcomes

  1. Patient-Reported Outcomes Measurement Information System-29 (PROMIS-29)

    Time frame: 8 weeks

    PROMIS-29 will measure health-related quality of life and is a validated, 29 question survey divided into seven sub-domains of function including physical functioning, social function, pain interference, pain intensity, sleep, depression, and anxiety.

Secondary outcomes

  1. Measure Yourself Medical Outcome Profile (MYMOP)

    Time frame: 8 weeks

    MYMOP will measure change(s) in patient-reported symptoms and is a patient-centered outcome measure that allows for the participant to self-select their top health concern(s) or symptom(s) they are dealing with in their own words. The participant can also choose an activity that is limited by that health concern.

  2. National University of Natural Medicine Multi-system Symptom/Adverse Event Questionnaire

    Time frame: 8 weeks

    The NUNM Multi-system Symptom/Adverse Event Questionnaire measures change(s) in patient-reported symptoms and is a standardized ninety-one point monitoring form that requires asking questions pertaining to the following organ systems: eyes/ears/nose/throat, gastrointestinal, neurological/ musculoskeletal, psychological/general, cardiopulmonary, skin, genitourinary and whole body systems.

Other outcomes

  1. Infinium Methylation EPIC Index by Illumina

    Time frame: 8 weeks

    Infinium Methylation EPIC Index by Illumina measures the methylation status of CpG sites. Epigenetic profile that assesses methylation on over 850,000 CpG DNA sites. A saliva sample will collect approximately 2 mL (~1 teaspoon) into a cryovial.

  2. Methylation Profile by Doctor's Data

    Time frame: 8 weeks

    Methylation Profile by Doctor's Data measures the changes in the methylation related biomarkers and is a functional assessment of the phenotypic expression of common single nucleotide polymorphisms (SNPs) and provides a "methylation index," a ratio of S-Adenosylmethionine (SAM) to S-Adenosylhomocysteine (SAH).

  3. Folate Vitamer Panel by Doctor's Data

    Time frame: 8 weeks

    Folate Vitamer Panel by Doctor's Data measures the changes in the methylation related biomarkers and measures folate congeners affecting enzyme function in methylation pathways including unmodified Folic Acid (UMFA), 5-Methyltetrahydrofolate (5-MTHF), tetrahydrofolate (THF), folinic Acid (5-CHO-THF).

  4. Medical Symptom Questionnaire (MSQ)

    Time frame: 8 weeks

    The MSQ measures change(s) in patient-reported symptoms and is a 71-question measure that measures various health areas including: Digestive tract, Eyes, Energy/Activity, Emotions, Head, Heart, Joint/Muscles, Lungs, Mind, Mouth/Throat, Nose, Skin, Weight, and Other.

  5. DNA Methylation Pathway Profile by Doctor's Data

    Time frame: 8 weeks

    DNA Methylation Pathway Profile is a measurement of potential confounders and assesses changes to single nucleotide polymorphisms (SNPs) - DNA genotype which may affect enzymatic function which include, methionine metabolism, detoxification, hormones, and vitamin D. This is a blood spot test and requires collection of 5 drops of blood after a finger stick.

Sponsors and collaborators

Lead sponsor

National University of Natural Medicine

Other

Collaborators

  • Dr. Kara Fitzgerald, ND
  • Metagenics, Inc.

Registry information

Official study title

The Effects of Diet and Lifestyle on Quality of Life and Methylation-related Biomarkers in Vivo.

Acronym: MDL

Important dates

Study start
2018
Primary completion
2020
Study completion
2024
First posted
Mar 21, 2018
Registry last updated
Aug 6, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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