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What is the best way to measure what people eat? Comparing self-reported habitual and actual dietary intakes with metabolite markers of dietary intakes.

Comparing self-reported habitual and actual dietary intakes with metabolite markers of dietary intakes in healthy adults: a randomised crossover feeding study

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12622001036707
Enrollment
24
Registered
2022-07-25
Start date
2022-08-30
Completion date
2022-10-19
Last updated
2023-01-16

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

Conditions

None listed

Brief summary

The proposed research is a feeding study to consider the use of metabolites found in blood and urine as markers of dietary intake. Current clinical and population advice, as well as research, is almost entirely based on self-reported dietary intakes, which are prone to bias. We will conduct a crossover trial of three interventions where specific foods in known amounts are given to 24 participants. This will allow us to compare self-reported intakes and blood and urine metabolite concentrations with the participants’ true intakes. An example of the metabolites are alkylresorcinols, which are found in the bran layer of grains. We have used these in previous studies to show that when whole grains are provided to participants, they report eating them, and the alkylresorcinols in the blood go up. Here we seek to consider the use of a range of metabolites to comment on the broader dietary profile, such as intakes of vegetables, fruit, legumes, red meat, fish, whole grains, and dairy.

Interventions

There are three interventions in the proposed study, each two days long. The first day of each intervention is a standardisation day, the second is a day where all foods of known amounts are provided. For the standardisation days, participants will be instructed to eat, move, and sleep as they normally would, with no extremes in physical activity or other behaviours. This advice will be given for the first day of each of the three interventions. In the morning of each standardisation day partici

There are three interventions in the proposed study, each two days long. The first day of each intervention is a standardisation day, the second is a day where all foods of known amounts are provided. For the standardisation days, participants will be instructed to eat, move, and sleep as they normally would, with no extremes in physical activity or other behaviours. This advice will be given for the first day of each of the three interventions. In the morning of each standardisation day participants will start to collect a 24-hour urine sample and complete it the following morning. On each intervention day, participants will provide a fasted blood sample, as well as collect another 24-hour urine sample over the course of the day. Following the blood sample, participants will then present to the metabolic facility to complete a 24-hour recall of food eaten the day before, and eat their breakfast of a prepared food while under observation. Participants will receive and eat all meals (breakfast, lunch, and dinner) in this manner on each intervention day. Meals are prepared and administered by a Dietitian within two-hour windows for each breakfast, lunch, and dinner. On intervention days, participants will be provided with snack foods of known weights to consume outside of the facility if they feel hunger, or wish to eat more. In the morning of the day after each intervention day, participants return any unconsumed snacks, their completed their 24-hour urine samples, provide a fasted blood sample and complete a 24-hour recall. The three interventions will be separated by at least three days washout, so that study requirements are not too onerous on participants. Trial recruitment will be run out of the University of Otago Dunedin campus, in New Zealand. The interventions differ in the food provided each day for meals and snacks. In one intervention: meals will be of whole grains, seafood, and dairy while snacks will be of vegetables, red meat, nuts and seeds. On this day no fruit, chicken, egg, or legumes will be consumed. In a second intervention: meals will be of vegetables, red meat, nuts and seeds while snacks will be of fruit, chicken, egg, and legume. No whole grains, seafood, or dairy will be consumed. In a third intervention: meals will be of fruit, chicken, egg, and legumes while snacks will be of whole grains, seafood, and dairy. No vegetables, red meats, and nuts and seeds will be consumed. The meals provided each day will provide slightly less energy intake (kJ) than participants require each day, to ensure they are consumed in full, with access to the snack foods unrestricted per day to allow participants to eat until full or for other reasons. The purpose of these three interventions is to see how metabolite biomarkers of dietary intakes change in fasted plasma and 24 hour urine in response to foods of known values, as well as compare the metabolite measures with self-reported dietary assessment techniques: a food frequency questionnaire and three 24-hour recalls captured on intervention days.

Sponsors

Universilty of Otago
Lead SponsorUniversity

Study design

Allocation
Randomised controlled trial
Intervention model
Crossover
Primary purpose
Diagnosis
Masking
Blinded (masking used) (Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
All
Age
18 Years to 40 Years
Healthy volunteers
Yes

Inclusion criteria

Adults aged 18-40 willing to adhere with the study requirements to standardise their lifestyle habits (physical activity, food choice, alcohol intake and sleep routine) over the three weeks of the data capture, eat the prepared foods on three feeding days, record or report their dietary intakes both habitually and on six days, provide six fasted plasma and 24-hour urine samples

Exclusion criteria

Those with food sensitivities, food allergies, or eating disorders that might interfere with their ability to adhere with the study requirements. Those with gastro-intestinal issues (e.g., IBS, IBD, etc.), renal issues and liver issues (i.e. any health issues affecting digestion, metabolism and clearance) or other characteristics that might interfere with their ability to adhere with the study requirements.

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026