This intervention study will investigate the relationship between consumption of selenium-fortified biscuits fortified with selenium-enriched yeast (approximately 60mcg of selenium per day for 14 days) and both plasma selenium concentration and plasma selenoprotein P concentration in adult human volunteers. It will also investigate how selenium-status may affect changes in sensory perception of the fortified biscuits when consumed for 7 and 14 consecutive days (Flavour-Nutrient Learning).
There are different forms of selenium supplementation which may be used to improve selenium-status, one being selenium-enriched yeast. Selenium is an essential micronutrient consumed through food, however the selenium contents of foods is variable, and depends upon the soil the food has been grown in. The UK population may not consume enough selenium through their diet, due to selenium levels in British soil being low and the use of North American wheat flour being increasingly replaced with lower selenium European flour. It is therefore relevant to explore the ability of selenium-enriched yeast to improve selenium status if initially low. It is also important to investigate if the sensory attributes of selenium-fortified foods are different to unfortified foods. Additionally, investigating Flavour-Nutrient Learning (how selenium-status might change sensory perception of selenium-rich foods) could improve understanding of food choices. This study aims to investigate the following topics: 1. The relationship between selenium intake (through selenium-fortified biscuits) and selenium-status. 2. How selenium-status affects sensory perception of selenium-fortified biscuits (Flavour Nutrient Learning, FNL).
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
BASIC_SCIENCE
Masking
DOUBLE
Enrollment
102
Selenium-fortified biscuits, fortified with selenium-enriched yeast (approx. 60 mcg selenium per day, for 14 days). One of three novel flavours.
NU-Food
Newcastle upon Tyne, Tyne & Wear, United Kingdom
Change in preference for the intervention flavour over two other test flavours and plain flavour, after 14 days of consumption of Se-fortified intervention-flavoured biscuits.
Participants score their intervention flavour (the test flavour they eat for 14 days), two test flavours (not eaten for 14 days) and plain flavour using a visual analogue scale anchored by "not very"/0 and "very"/100. They do this for liking of smell, taste, texture, aftertaste and pleasantness of the overall eating experience. This is repeated three times (three plates of biscuits) in one food sensory test. Each attribute for each plate will have a 'preference score' calculated, using the following equation: Preference score = (score of intervention flavour) - (average score of other 3 flavours). Preference scores are then averaged across the three plates. Flavour preference change is calculated as the change in average flavour preference score from baseline (day 1 food sensory test) to after 14 days of intervention biscuit consumption at home (day 15 food sensory test): Preference change = day 15 score - day 1 score
Time frame: Day 1 (baseline) and day 15 (post-14 days of intervention biscuit consumption).
Change in preference for the intervention flavour over two other test flavours and plain flavour, after 7 days of consumption of Se-fortified biscuits flavoured with the intervention flavour.
Preference scores for each day are calculated using the formula in the primary outcome measure. Preference change is calculated using the following formula: Preference change = day 8 score - day 1 score
Time frame: Day 1 (baseline) and day 8 (post 7 days of intervention biscuit consumption).
Change in preference for the intervention flavour over two other test flavours, after 14 days of consumption of Se-fortified biscuits flavoured with the intervention flavour.
Preference scores for each day are calculated using the formula in the primary outcome measure, except without including the scores of the plain flavour. Preference change is measured using the formula in the primary outcome measure.
Time frame: Day 1 (baseline) and day 15 (post 14 days of intervention biscuit consumption).
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Change in preference for the intervention flavour over two other test flavours, after 7 days of consumption of Se-fortified biscuits flavoured with the intervention flavour.
Preference scores for each day are calculated using the formula in the primary outcome measure, except without including the scores of the plain flavour. Preference change is measured using the formula in the second outcome measure.
Time frame: Day 1 (baseline) and day 8 (post 7 days of intervention biscuit consumption).
Change in preference for the intervention flavour over plain flavour, after 14 days of consumption of Se-fortified biscuits flavoured with the intervention flavour.
Preference scores for each day are calculated using the formula in the primary outcome measure, except without including the scores of the two test flavour. Preference change is measured using the formula in the primary outcome measure.
Time frame: Day 1 (baseline) and day 15 (post 14 days of intervention biscuit consumption).
Change in preference for the intervention flavour compared with plain flavour, after 7 days of consumption of Se-fortified biscuits flavoured with the intervention flavour.
Preference scores for each day are calculated using the formula in the primary outcome measure, except without including the scores of the two test flavours. Preference change is measured using the formula in the second outcome measure.
Time frame: Day 1 (baseline) and day 8 (post 7 days of intervention biscuit consumption).
Change in plasma selenium concentration after consumption of selenium-fortified biscuits (approximately 60 micrograms of selenium per day) daily for 14 consecutive days.
Blood samples taken via venepuncture or finger-prick, centrifuged and plasma collected. Plasma analysed using inductively coupled plasma mass spectrometry (ICP-MS) after acid digestion. Change in plasma selenium concentration = concentration at day 15 (post 14 days of intervention biscuit consumption) - concentration at day 1 (baseline).
Time frame: Day 1 (baseline) and day 15 (post 14 days of intervention biscuit consumption).
Change in plasma selenium concentration after consumption of selenium-fortified biscuits (approximately 60 micrograms of selenium per day) daily for 7 consecutive days.
Blood samples taken via venepuncture or finger-prick, centrifuged and plasma collected. Plasma analysed using ICP-MS after acid digestion. Change in plasma selenium concentration = concentration at day 8 (post 7 days of intervention biscuit consumption) - concentration at day 1 (baseline).
Time frame: Day 1 (baseline) and day 8 (post 7 days of intervention biscuit consumption).
Change in plasma selenoprotein P (SEPP1) concentration after consumption of selenium-fortified biscuits (approximately 60 micrograms of selenium per day) daily for 14 consecutive days.
Blood samples taken via venepuncture, centrifuged and plasma collected. Plasma analysed using ELISA. Change in plasma selenoprotein P concentration = concentration at day 15 (post 14 days of intervention biscuit consumption) - concentration at day 1 (baseline).
Time frame: Day 1 (baseline) and day 15 (post 14 days of intervention biscuit consumption).
Change in plasma selenoprotein P (SEPP1) concentration after consumption of selenium-fortified biscuits (approximately 60 micrograms of selenium per day) daily for 7 consecutive days.
Blood samples taken via venepuncture, centrifuged and plasma collected. Plasma analysed using ELISA. Change in plasma selenoprotein P concentration = concentration at day 8 (post 7 days of intervention biscuit consumption) - concentration at day 1 (baseline).
Time frame: Day 1 (baseline) and day 8 (post 7 days of intervention biscuit consumption).
How many participants prefer a fortified test biscuit over an unfortified version of their intervention biscuit in a paired comparison test?
Participants are asked to indicate which they prefer from two biscuits on a plate. One biscuit will be a selenium-fortified test biscuit, and the other an unfortified version of their intervention biscuit. This is to test if preference is stronger for the intervention flavour or the Se-enriched yeast.
Time frame: Day 1 (baseline), day 8 (post-7 days intervention) and day 15 (post-14 days intervention).
How many participants prefer a fortified test biscuit over an unfortified test biscuit of a different flavour in a paired comparison test?
Participants are asked to indicate which they prefer from two biscuits on a plate. The biscuits will be the participant's two test flavours, one of which will be fortified. This is to test if a preference has developed for Se-enriched yeast flavour.
Time frame: Day 1 (baseline), day 8 (post-7 days intervention) and day 15 (post-14 days intervention).
How many participants prefer their fortified intervention biscuit over an unfortified test biscuit in a paired comparison test?
Participants are asked to indicate which they prefer from two biscuits on a plate. The biscuits will be the participant's fortified intervention biscuit, and an unfortified test biscuits. This is to test if participants prefer their intervention biscuit.
Time frame: Day 1 (baseline), day 8 (post-7 days intervention) and day 15 (post-14 days intervention).