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| Name | Class |
|---|---|
| Biotechnology and Biological Sciences Research Council | OTHER |
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Vitamin D deficiency is considered a public health priority in the UK, with approximately 30-40% of the UK population being deemed vitamin D deficient during winter months. Current government strategies to improve vitamin D status amongst the UK population involve dietary supplementation, however, it has been shown that excess adiposity reduces the impact of dietary supplementation with vitamin D. One potential explanation for this observation is that vitamin D becomes sequestered in adipose tissue. We hypothesise that exercise may facilitate the mobilisation of vitamin D from adipose tissue and thus increase circulating vitamin D (25OHD) concentrations. Little is currently known as to whether a single bout of exercise affects vitamin D status, with a handful of studies demonstrating contradictory findings. This research will examine the effect of an acute bout of exercise (treadmill-based at 60% VO2 Max for 60 minutes) on vitamin D status (serum 25(OH)D) in healthy community-dwelling adults.
This study is a random crossover design and will require 34 participants to visit the University of Bath on 6 separate occasions in total.
Individuals who express an interest in taking part will be invited to attend an initial screening meeting at the University so that the eligibility can be assessed for the study, and the all procedures explained verbally. If the participant is eligible and is happy to participate in the study, they will attend a second visit prior to two trials to undertake a treadmill-based maximal exercise test (VO2 Max), resting metabolic rate measure and several measures will be taken to assess body composition. Trials will involve a 60-minute exercise bout at 60% of the participant's maximum oxygen uptake or a 60-minute resting period (both followed by a further hour of rest). The order in which these trials occur will be randomised for each participant and the participant will not be told of this order prior to the trials.
During both trials, a cannula will be inserted into a vein in the arm prior to exercise and 10ml blood samples will be drawn at baseline (pre-exercise) and immediately after the exercise session and 1 hour post exercise from the antecubital vein. The participant will return to the university the day after each trial for a 10ml venous blood sample (24hr post-exercise) which will be taken via venepuncture. In the 24 hours following a trial, participants will be provided with standardised meals in order to ensure energy balance. Other controls which will be applied during the study period will include the provision of factor 50 sunscreen (if the participant is undertaking trials between March and October) to aid in mitigating against the cutaneous synthesis of vitamin D, and guidance on avoiding any strenuous activity 24 hours prior to trial days. Participants will also be provided with a physical activity monitor (MotionWatch8, CamNTech) to wear during trial days after leaving the lab.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Participants | This study follows a randomised crossover design. All participants will undergo a single 60-minute treadmill-based exercise intervention, and a resting period for equal duration in a randomised order. |
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| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Treadmill-Based Exercise (60% VO2 Max for 60 minutes) | Other | Each participant will undergo a single 60-minute treadmill-based exercise intervention in a randomised order. Treadmill settings are generated based on settings which correspond to participants exercising at 60% VO2 max from their maximal exercise test on visit 2. To confirm that participants are exercising at 60% during the hour session, 1 minute samples of expired air are taken at 15 minute intervals and immediately analysed to check % VO2 max. Participants heart rate and RPE measures are also taken at 15 minute intervals throughout the exercise session and cross-checked against predicted values at 60% VO2 Max. |
| Measure | Description | Time Frame |
|---|---|---|
| Serum vitamin D concentration | As assessed by serum 25(OH)D via LC-MS | 24 hours- change from baseline to 24 hours post exercise |
| Measure | Description | Time Frame |
|---|---|---|
| Markers of lipid mobilisation | As assessed by plasma NEFA, triacyglycerol and glycerol | 24 hours- change from baseline to 24 hours post exercise |
| Calcium | As assessed by serum calcium |
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Inclusion Criteria:
Exclusion Criteria:
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Healthy, community-dwelling adults (aged 25-65 years old)
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| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Sophie Ella Davies | Bath | Somerset | BA1 6AW | United Kingdom |
| PubMed Identifier | Type | Citation | Retractions |
|---|---|---|---|
| 39097829 | Derived | Davies SE, Perkin OJ, Betts JA, Gonzalez JT, Hewison M, Jenkinson C, Jones KS, Meadows SR, Parkington DA, Koulman A, Thompson D. The effect of an acute bout of exercise on circulating vitamin D metabolite concentrations: a randomised crossover study in healthy adults. J Physiol. 2024 Sep;602(17):4157-4170. doi: 10.1113/JP286395. Epub 2024 Aug 4. |
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| ID | Term |
|---|---|
| C092779 | RE1-silencing transcription factor |
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Human Plasma and Serum
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| Rest (60 minutes) | Other | Each participant will undergo a 60-minute rest period in a randomised order. |
|
| 24 hours- change from baseline to 24 hours post exercise |
| Other vitamin D metabolites | As assessed by serum 1,25(OH)D and other forms of serum vitamin D via LC-MS | 24 hours- change from baseline to 24 hours post exercise |