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Bioavailability of Vitamin D Photoisomers From UVB-exposed Button Mushrooms

Bioavailability of Vitamin D Photoisomers From UVB-exposed Button Mushrooms

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05668832
Enrollment
36
Registered
2022-12-30
Start date
2023-01-09
Completion date
2024-07-30
Last updated
2022-12-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Dietary Exposure, Safety Issues

Keywords

lumisterol, tachysterol, hydroxy-photoisomers, vitamin D

Brief summary

The European Food Safety Authority has approved many applications for UVB light treated foods (e.g. UVB-exposed button mushrooms) in the last years. The UVB light treatment is used to increase the vitamin D content in foods and improve the vitamin D status of subjects. However, UVB irradiation is accompanied by the formation of vitamin D photoisomers such as lumisterol and tachysterol. The current study aims to investigated whether these vitamin D photoisomers can enter the circulation and are metabolised in humans that consume UVB-treated mushrooms.

Detailed description

according to protocol

Interventions

DIETARY_SUPPLEMENTUVB-exposed button mushrooms

Healthy subjects will be randomized into two groups and received either UVB-exposed button mushrooms or non-UVB-exposed button mushrooms for 7 days. Blood samples from each subject will be taken at baseline (before the intake of the mushrooms, 3 h and 6 h thereafter, and at day 8. Three months later, another blood sample was taken.

Sponsors

Martin-Luther-Universität Halle-Wittenberg
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
Yes

Inclusion criteria

* Healthy subjects * Age between 18 and 65 years * Body Mass Index in the range of 18.5 to 29.9 kg/m2

Exclusion criteria

* Acute or chronic illnesses (high blood pressure, heart disease, diabetes, kidney disease, liver disease, alcohol dependence, etc.) * Taking medication (except oral contraceptives) * Pregnancy or breastfeeding * Food intolerances or allergies to mushrooms and dairy products * Smokers * Visits to solariums or previous holidays in southern countries or in the Alps or other high mountains * Participation in another study * Blood donation during the last 2 months before the start of the study * Dieting * Severe weight loss or weight loss (≥ 3 kg) within the last month

Design outcomes

Primary

MeasureTime frameDescription
Circulating vitamin D photoisomersat baseline (before the intervention), 3 hours postprandial, 6 hours postprandial, at day 8, changes from baseline at 3 monthsPlasma concentrations of vitamin D photoisomers (such as lumisterol, tachysterol and their hydroxy derivates) after the consumption of the UVB-exposed versus non UVB-exposed button mushrooms

Secondary

MeasureTime frameDescription
Parameters of vitamin D metabolismat baseline (before the intervention), 3 hours postprandial, 6 hours postprandial, at day 8, changes from baseline at 3 monthsPlasma concentrations of vitamin D metabolites (vitamin D2, vitamin D3, 25-hydroxyvitamin D2, 25-hydroxyvitamin D3, 24,25-dihydroxyvitamin D2, calcitriol, ergosterol)
Parameters of mineral metabolismat baseline (before the intervention), 3 hours postprandial, 6 hours postprandial, at day 8, changes from baseline at 3 monthsPlasma calcium, phosphate, parathyroid hormone, fibroblast growth factor-23
Plasma lipidsat baseline (before the intervention), 3 hours postprandial, 6 hours postprandial, at day 8, changes from baseline at 3 monthsPlasma triglycerides, cholesterol
Inflammation markersat baseline (before the intervention), 3 hours postprandial, 6 hours postprandial, at day 8, changes from baseline at 3 monthsPlasma CRP, Interleukin-6
mRNA and protein expression in peripheral mononuclear blood cellsat baseline (before the intervention), 3 hours postprandial, 6 hours postprandial, at day 8, changes from baseline at 3 monthsVitamin D receptor target genes, CYP enzymes

Contacts

Primary ContactGabriele I Stangl, Prof. Dr.
gabriele.stangl@landw.uni-halle.de+493455522707

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026