Bioavailability and Biological Effects of Vitamin D2 Contained in Mushroom

NCT ID: NCT01488734

Last Updated: 2017-04-14

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

47 participants

Study Classification

INTERVENTIONAL

Study Start Date

2011-11-30

Study Completion Date

2013-09-30

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

The purpose of this study is to compare the safety and efficacy of two different amounts of vitamin D2 (600 or 4000 International Units/day) provided by mushrooms added to one of the daily meals versus same doses of vitamin D3 provided as oral supplements sold in any drugstore in reaching adequate or optimal blood levels of 25(OH)D in people with Vitamin D deficiency and pre-diabetes (high blood sugar without full blown diabetes) or the metabolic syndrome. Metabolic syndrome is the name of a group of risk factors that raise the risk for heart disease and other health problems, such as diabetes and stroke as described by the US department of Health and Human Services.

This study will also attempt to demonstrate and compare the effect of the intervention with above two doses of vitamin D on blood levels of tests that show inflammation.

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Poor vitamin D status is now considered epidemic in North America. In addition to its effects on bone metabolism, Vitamin D has several other important biological effects including modulating the immune system, stimulating the production of insulin and decreasing renin production in the kidney. Furthermore, the active metabolite of vitamin D, 1,25 dihydroxyvitamin D (1,25(OH)2D), is a very potent inhibitor of cellular proliferation and inducer of terminal differentiation and vitamin D deficiency has been associated with higher prevalence of cancer, autoimmune diseases, including multiple sclerosis, rheumatoid arthritis, type 1 diabetes and hypertension.

The current recommendations for dietary vitamin D in North America are much too low to maintain optimal levels of 25(OH)D associated with disease prevention. The majority of circulating 25(0H) D originates from cutaneous synthesis upon exposure to adequate sunlight. However, seasonal changes, living at high latitudes or low polluted altitudes, dark skin pigmentation and aging are among the many factors that can impede this process requiring periodic reliance on dietary sources to supply the precursor to 25(OH)D.

In November of 2010, the Institute of Medicine (IOM) of the National Academy of Science established new DRI values for vitamin: EAR (Estimated Average Requirement) of 400 IU (10 µg; RDA ( Recommended Daily Intake) of 600 IU (15µg) for adults up to 70 years of age, and an UL of 4000 IU (50µg) (21). The IOM also discourages the taking of dietary supplements to achieve the RDA for vitamin D and encourages Americans to achieve their needed vitamin D through food sources.

The proposed study will be to provide meals with one serving of fresh mushroom per day that could have two different levels of vitamin D2 in it (600 IU or 4,000 IU/day, which are the 2011 currently recommended RDA to age 70 AI and UL, respectively) for four months and test both the bioavailability of vitamin D in mushroom, as reflected in blood 25(OH)D levels, as well as the effect of vitamin D on markers of disease (e.g. C-reactive protein (CRP), Hemoglobin A1c, etc). The vitamin D2 amount in mushrooms can easily be manipulated just by adjusting the time and distance of their UVB exposure. Two groups will be compared with controls who will receive the same dose of vitamin D3 in the form of tablets commercially available (600 IU or 4000 IU/day).

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Vitamin D Deficiency Metabolic Syndrome Prediabetes

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

TRIPLE

Participants Caregivers Outcome Assessors

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

Mushroom with 600 IU vitamin D2

Mushroom with 600 IU of vitamin D2 daily and placebo tablet

Group Type EXPERIMENTAL

Mushroom with 600 IU vitamin D2

Intervention Type DIETARY_SUPPLEMENT

Subjects in this group will eat daily meals containing mushrooms fortified with 600 IU of Vitamin D2. These subjects will also take one placebo tablet per day.

Placebo

Intervention Type DRUG

Placebo for the fortified mushroom arms

Mushroom with 4000 IU Vitamin D2

Mushroom with 4000 IU of Vitamin D2 daily and placebo tablet

Group Type EXPERIMENTAL

Mushroom with 4000 IU Vitamin D2

Intervention Type DIETARY_SUPPLEMENT

Subjects in this group will eat daily meals containing mushrooms fortified with 4000 IU of Vitamin D2. These subjects will also take one placebo tablet per day.

Placebo

Intervention Type DRUG

Placebo for the fortified mushroom arms

600 IU Vitamin D3 and untreated mushroom

Commercially available tablets with 600 IU/day of Vitamin D3 and untreated mushroom

Group Type ACTIVE_COMPARATOR

600 IU Vitamin D3 and untreated mushroom

Intervention Type DIETARY_SUPPLEMENT

Subjects in this group will take one commercially available tablet of 600 IU of Vitamin D3. These subjects will also eat one meal per day with untreated (inactive) mushrooms.

4000 IU Vitamin D3 and untreated mushroom

Commercially available tablets with 4000 IU/day of Vitamin D3 and untreated mushroom

Group Type ACTIVE_COMPARATOR

4000 IU Vitamin D3 and untreated mushroom

Intervention Type DIETARY_SUPPLEMENT

Subjects in this group will take one commercially available tablet of 4000 IU of Vitamin D3. These subjects will also eat one meal per day with untreated (inactive) mushrooms.

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

Mushroom with 600 IU vitamin D2

Subjects in this group will eat daily meals containing mushrooms fortified with 600 IU of Vitamin D2. These subjects will also take one placebo tablet per day.

Intervention Type DIETARY_SUPPLEMENT

Mushroom with 4000 IU Vitamin D2

Subjects in this group will eat daily meals containing mushrooms fortified with 4000 IU of Vitamin D2. These subjects will also take one placebo tablet per day.

Intervention Type DIETARY_SUPPLEMENT

600 IU Vitamin D3 and untreated mushroom

Subjects in this group will take one commercially available tablet of 600 IU of Vitamin D3. These subjects will also eat one meal per day with untreated (inactive) mushrooms.

Intervention Type DIETARY_SUPPLEMENT

4000 IU Vitamin D3 and untreated mushroom

Subjects in this group will take one commercially available tablet of 4000 IU of Vitamin D3. These subjects will also eat one meal per day with untreated (inactive) mushrooms.

Intervention Type DIETARY_SUPPLEMENT

Placebo

Placebo for the fortified mushroom arms

Intervention Type DRUG

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* Adult non-smoking subjects from ages 30 to 90, any race or gender
* Presence of at least two of the following characteristics:

* Waist circumference:

Men: \> 102 cm Women: \> 88 cm

* Blood pressure: \> 130/85 mm Hg (or use of anti-BP medication)
* HDL-cholesterol:

Men: \< 40 mg/dL Women: \< 50 mg/dL

* Triglycerides: \> 150 mg/dL (or use of medications for high triglycerides such as fibrates or nicotinic acid)
* Fasting blood sugar \> 100 mg/dl (or use of metformin), but a HbA1c \< 6.5%

Exclusion Criteria

* Blood levels of 25(OH)D \> 50 nmol/L
* Regular intake of vitamin D fortified milk exceeding approximately 3 glasses/day
* Lack of the ability to comprehend instructions and/or sign the consent form
* Inability to comply with the potential requirement to eat a daily portion of provided mushroom together with meals
* Inability to comply with the rule of avoiding any beach days during the duration of the study
* Any projected trip to sunny places such as Puerto Rico and the Caribbean during the period of study
* Any attendance to tanning studios during the period of study
* Women who regularly use a veil over their heads
* Any history of kidney stone formation
* Non-traumatic bone fracture over the past 3 years
* Any form of vitamin D supplement intake, including combined calcium and vitamin D products
* Active smoking
Minimum Eligible Age

30 Years

Maximum Eligible Age

90 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

Icahn School of Medicine at Mount Sinai

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Responsibility Role SPONSOR

Principal Investigators

Learn about the lead researchers overseeing the trial and their institutional affiliations.

Jaime Uribarri, MD

Role: PRINCIPAL_INVESTIGATOR

Icahn School of Medicine at Mount Sinai

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

Icahn School of Medicine at Mount Sinai

New York, New York, United States

Site Status

Countries

Review the countries where the study has at least one active or historical site.

United States

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

11-01366

Identifier Type: -

Identifier Source: secondary_id

GCO 11-0899

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.