Iron Bioavailability From Cereal-based Foods

September 26, 2022 updated by: Bruce R. Hamaker, Purdue University

The Potential of Food to Food Fortification to Improve Iron Bioavailability From Cereal-based Foods

Iron-deficient anemia is a chronic problem in sub-Saharan Africa and other developing areas of the world. From our previous research, the investigators have shown that certain local plant foods in Kenya and Senegal have an unusual action of improving in vitro iron bioaccessibility (nearly doubling the low value obtained in cereals). The investigators will assess absorption of stable isotopes of iron (57Fe, 54Fe and 58Fe) extrinsically labeled in a serving of porridge fortified with various combinations of moringa, baobab, mango, carrot and standard fortificant iron sulfate and the enhancer ascorbic acid.

Study Overview

Detailed Description

To better understand the potential for leveraging traditional plant-based ingredients in local fortification efforts in Africa, the proposed study will focus on assessment of acute iron bioavailability in participants consuming instant blended cereal porridges produced using whole grain white maize, with provitamin A (e.g. carrots/mango), moringa leaf powder and baobab fruit powder in specific combinations. The investigators hypothesize that: food-to-food fortified cereal-based porridge with with African baobab fruit and moringa leaf powder will effectively improve iron density and bioavailability in human participants as compared to a "gold standard" fortification (iron sulphate and ascorbic acid).

A randomized crossover design with 4 different white maize cereal-based porridges and a reference control porridge (with matching macronutrient contents) will be used, allowing each participant to serve as their own control. Porridges are designed to specifically compare: (1) Food to food fortification versus standard fortifications and (2) the ability of baobab fruit pulp to enhance iron absorption from both natural and standard sources. The porridges will be composed of locally sourced ingredients including: whole grain white maize, a pro-vitamin A source (oil and available vegetables e.g. carrot and mango) baobab fruit powder and moringa leaf powder.

The enrolled participants will come into the clinic 6 times to consume porridges or have blood drawn. Four times blood (1 for screening, 3 for study) will be drawn to determine the amount of the different forms of iron in participant's blood. On each day of porridge consumption (each visit except the final visit on Day 33), they will consume 2 x 350 g porridge meals and stay 90 mins after the participant has finished each of the meals, and then leave and come back to repeat for a total of 4 hours. After two weeks they will return to the clinic and the investigators will ask to draw some more blood to see if they have absorbed any of the different forms of iron. They will then have the next porridge. Importantly for each visit for both blood draws and the porridge consumption the participants will have to fast the previous night, so no food or beverages like tea or coffee can be consumed (only water allowed). During 5 visits when they will eat two portions of porridge during the day and will have to stay at the facility for 90 mins after each porridge consumption. During the last visit (Day 33), participants will need to give a blood sample, which will take about half an hour. Blood collected during these visits will be used to measure isotopic iron absorbed from the porridges.

Study Type

Interventional

Enrollment (Anticipated)

22

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Locations

    • Indiana
      • West Lafayette, Indiana, United States, 47907
        • Purdue University
        • Contact:

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years to 65 years (ADULT, OLDER_ADULT)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

Female

Description

Inclusion:

  • Female 18-65 Y
  • BMI 18.5-25 kg/m2
  • Stable weight past 3 month (+/- 2.5kg)
  • Clinically normal blood profiles
  • Fasting blood glucose < 110 and CRP below 3 mg/L

Exclusion:

  • Smokers and vapers
  • No heavy alcohol consumption (>2 drinks per day)
  • Diabetic
  • Presence of metabolic of intestinal disorder including lipid malabsorption or lactose intolerance
  • Male sex
  • Pregnant
  • Lactating
  • Long term use of medications
  • Blood donation in past 4 months
  • Previous participation in iron stable isotope bioavailability study
  • Following a weight reduction program or having one in past 3 months
  • Peri- or post-menopausal
  • Acute or chronic disease
  • Hypertension

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: BASIC_SCIENCE
  • Allocation: RANDOMIZED
  • Interventional Model: CROSSOVER
  • Masking: SINGLE

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
EXPERIMENTAL: Control Porridge
Wholegrain maize flour, Mango powder, Carrot powder, Ferrous sulfate, Corn starch
Maize porridge containing 54Fe as iron sulfate
EXPERIMENTAL: Reference Porride A
Wholegrain maize flour, Mango powder, Carrot powder, Ferrous sulfate, Ascorbic acid, Corn starch
Maize porridge counting 58Fe as iron sulfate with ascorbic acid
EXPERIMENTAL: Test Porridge B
Wholegrain maize flour, Moringa leaf powder, Mango powder, Carrot powder, Corn starch
Maize porridge containing 57Fe and fortified with Moringa leaf powder as iron source
EXPERIMENTAL: Test Porridge C
Wholegrain maize flour, Baobab fruit powder, Mango powder, Carrot powder, Ferrous sulfate, Corn starch
Maize porridge containing 57Fe and fortified with Boabab fruit powder as iron source
EXPERIMENTAL: Test Porridge D
Wholegrain maize flour, Baobab fruit powder, Moringa leaf powder, Mango powder, Carrot powder
Maize porridge containing 54Fe and fortified with Moringa leaf and Baobab fruit powder as iron source

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Iron absorption
Time Frame: Acute study but blood measurement to occur following 14 daysof acute consumption
Assessment whole blood for isotopic iron absorption from individual meals
Acute study but blood measurement to occur following 14 daysof acute consumption

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (ANTICIPATED)

November 1, 2022

Primary Completion (ANTICIPATED)

February 1, 2023

Study Completion (ANTICIPATED)

February 1, 2023

Study Registration Dates

First Submitted

September 20, 2021

First Submitted That Met QC Criteria

September 20, 2021

First Posted (ACTUAL)

September 29, 2021

Study Record Updates

Last Update Posted (ACTUAL)

September 28, 2022

Last Update Submitted That Met QC Criteria

September 26, 2022

Last Verified

September 1, 2022

More Information

Terms related to this study

Other Study ID Numbers

  • IRB-2019-764

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

IPD Plan Description

Individual participant data will not be shared with other researchers

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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