The Genetic Effects on Vitamin D Supplementation
Vitamin D Deficiency
About this trial
This is an interventional basic science trial for Vitamin D Deficiency
Eligibility Criteria
Inclusion Criteria: Healthy adults female and male 18-65 years completion of physical activity readiness questionnaire (PAR-Q). Exclusion Criteria: Below 18 years above 65 years individuals taking medications that could interact with vitamin D status Individuals regularly taking daily Vitamin D supplementation during the 3 months before the intervention start date major dietary changes in vitamin D intake during the intervention period
Sites / Locations
- St Mary's University TwickenhamRecruiting
Arms of the Study
Arm 1
Arm 2
Arm 3
Experimental
Experimental
Experimental
Control (Low risk genotype)
Intervention (Medium risk genotype)
Intervention (High risk genotype)
Participants with no genetic variation in their VDR, GC and CYP2R1 genes that would increase their risk of vitamin D deficiency. Participants will be given 10µg vitamin D supplements for 90 days. This group is a control against the medium and high-risk intervention groups.
Participants with genetic variation in their VDR, GC and CYP2R1 genes that moderately increase their risk of vitamin D deficiency. Participants will be given 10µg vitamin D supplements for 90 days. This group will be compared against the low-risk control group to determine the effect of genetic variations on vitamin D status.
Participants with genetic variation in their VDR, GC and CYP2R1 genes that increase their risk of vitamin D deficiency. Participants will be given 10µg vitamin D supplements for 90 days. This group will be compared against the low-risk control group to determine the effect of genetic variations on vitamin D status.