The MULTINUTRIENT Maize Project: Results of Human Feeding Trial

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

20 participants

Study Classification

INTERVENTIONAL

Study Start Date

2015-09-30

Study Completion Date

2016-03-31

Brief Summary

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The main objective of this human trial is the demonstration that β-carotene in fortified maize has good bioavailability as a plant source of vitamin A and that when humans ingest the biofortified product retinol levels are higher than when they ingest non biofortified white maize.

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Detailed Description

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Human feeding trial with fortified maize is part of the BIOFORCE project which aims to create transgenic cereal plants that will provide a near complete micronutrient complement for malnourished people. β-Carotene intake helps to balance inadequate retinol supply in significant parts of the world. In order for plants with enhanced levels of micronutrients to be useful, the micronutrients must be present in a bioavailable form that can be absorbed by the human body. To test the main hypothesis of the trial an open-label, randomized, three-way crossover trial consisting of three 7-day feeding periods has been designed. The study will compare three different feeding conditions: β-carotene fortified maize containing diet, white maize containing diet supplemented with a reference β-carotene dose and white maize diet. The study will test the hypothesis that a meal including fortified maize yields superior all-trans retinol area under the plasma concentration versus time curve (AUC) values than an isocaloric and isoprotein meal with normal maize.

After a first screen that will address physical conditions and lifestyle 18 volunteers (9 men and 9 women) who meet the eligibility criteria will be included in the study once they have read and sign the informed consent. The postprandial plasma all-trans retinol response to each test meal will be used to establish the bioavailability of provitamin A from fortified maize. The test meals will be consumed in random order separated by 1 week. Blood samples will be collected over 8 h. All-trans retinol will be analyzed in plasma by high pressure liquid chromatography (HPLC) with coulometric array electrochemical detection.

Mean AUC for all-trans retinol in plasma after ingestion of the β-carotene-fortified maize porridge, the white maize porridge with the β-carotene reference dose, and the white maize porridge will be compared.

Conditions

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Healthy

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

CROSSOVER

Primary Study Purpose

PREVENTION

Blinding Strategy

NONE

Study Groups

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β-carotene biofortified maize

Participants will ingest porridge bF: this will be the β-carotene fortified maize porridge where each 250 g will be made with 50 g of dry maize flour obtained from fortified corn seeds. The contents of β-carotene and other provitamin A carotenoids in this flour will be determined before preparing the porridges.

Group Type EXPERIMENTAL

β-carotene biofortified maize

Intervention Type OTHER

Determination of all-trans retinol AUC values after the ingestion of 200 g porridge made with 50 g of flour of β-carotene fortified maize

white maize supplemented with β-carotene

Participants will ingest porridge F: this will be also a β-carotene fortified maize porridge but in this case it will be made with 50 g of dry maize flour obtained from non fortified corn seeds and supplemented with a 500-1500 µg β-carotene reference dose. The exact dose of β-carotene that will be added to these porridges will be established according to the amount of β-carotene found in the flour used with porridges BF.

Group Type ACTIVE_COMPARATOR

β-carotene supplemented maize

Intervention Type OTHER

Determination of all-trans retinol AUC values after the ingestion of 200 g porridge made with 50 g of flour of β-carotene supplemented maize

white maize

Participants will ingest porridge N which will be the control porridge and will be made with 50 g of dry maize flour obtained from non fortified corn seeds.

Group Type SHAM_COMPARATOR

Normal (non biofortified) maize without added β-carotene

Intervention Type OTHER

Determination of all-trans retinol AUC values after the ingestion of 200 g porridge made with 50 g of flour of normal maize

Interventions

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β-carotene biofortified maize

Determination of all-trans retinol AUC values after the ingestion of 200 g porridge made with 50 g of flour of β-carotene fortified maize

Intervention Type OTHER

β-carotene supplemented maize

Determination of all-trans retinol AUC values after the ingestion of 200 g porridge made with 50 g of flour of β-carotene supplemented maize

Intervention Type OTHER

Normal (non biofortified) maize without added β-carotene

Determination of all-trans retinol AUC values after the ingestion of 200 g porridge made with 50 g of flour of normal maize

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Healthy persons
* Persons who had not taken vitamin A or β-carotene supplements within the past month

Exclusion Criteria

* Current or recent (previous 12 mo) cigarette smoking
* Frequent consumption of alcoholic beverages (1 drink/d)
* Current or recent (previous 1 mo) use of dietary supplements
* Current or recent (previous 6 mo) use of hormonal contraceptives
* Current or recent (previous 1 mo) use of medications known to affect lipid metabolism.
* History of restrictive eating
* BMI under 20 or over 30
* Lactose intolerance
* Vegetarians.
* Severe or symptomatic cardiac disease or hypertension
* History of bleeding disorders
* Chronic history of gastric, intestinal, liver, pancreatic, or renal disease
* Any portion of the stomach or the intestine removed (other than an appendectomy)
* History of intestinal obstruction, malabsorption, or use of antacid drugs; cancer (active or use of medications for a history of cancer treatment within the past 5 y)
* History of chronic alcoholism
* History of convulsive disorder
* Evidence of active drug abuse

Minimum Eligible Age

18 Years

Maximum Eligible Age

65 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes