Vitamin D3-enhanced Eggs in Preschool Children (VD3-egg)

October 19, 2023 updated by: Mario Flores-Aldana, Instituto Nacional de Salud Publica, Mexico

Effect of the Consuption of Vitamin D3-enhanced Eggs on Serum 25-hydroxivitamin D[(25-OH)D3] and Parathyroid Hormone (PTH) in Preschool Children

This is double-blind, controlled fiel trial, to compare fortified egg with D3-or 25(OH)D3 and non-fortified eggs in healthy preschool-age children 12 to 60 months of age, affiliated to day-care centers at Secretaria de Desarrollo Social (SEDESOL).

The study aims to answer are:

  1. to evaluate the efficacy of fortified egg with vitamian D3 on serum concentrations of 25-hydroxyvitamin D3
  2. and to evaluate parathyroid hormone (PTH) in children aged 12 to 60 months of age.

    • Children would be given for breakfast fortified egg/non-foritfied egg three times per week for 12 weeks.
    • Blood samples will be taken at baseline and at the end of study.
    • Anthropometric meassurements weight /height will be taken at baseline and at end of study.

Study Overview

Detailed Description

  1. Vitamin D functions:

    Vitamin D (VD) is a fat-soluble vitamin. Its main function is to maintain optimal levels of calcium and phosphorus in the body; it also helps in neuromuscular transmission and bone mineralization, important in bone health and growth in children. There are VD receptors in bone, bone marrow, adipose tissue, adrenal, brain, stomach, small intestine, colon, pancreas, liver, lung, muscle, activated B and T lymphocytes, and in other organs, tissues, and cells. For this reason, various functions are assumed. VD serum concentrations above 75 mmol/l (30 ng/ml) have been shown to keep cell growth under control and prevent cells from becoming autonomous and malignant.

  2. Prevalences of vitamin D deficiencies and insufficiency:

    Worldwide, a high proportion of children, youth, and middle-aged adults are deficient in Vitamin D. It has been estimated that about one billion people in the world may be deficient in Vitamin D.

    In Latin America, only Mexico has representative population data on vitamin D deficiency. Recently it has been documented that the deficiency and insufficiency of Vitamin D are a public health problem in Mexico. In a national representative sample of 6,827 children aged 1 to 11 years who participated in the 2012 National Health and Nutrition Survey (ENSANUT), the prevalence of Vitamin D deficiency was 33% (25-OH-D <50 nmol/L), which means that there are 3 million children with Vitamin D deficiency in Mexico. On the other hand, insufficiency (25-OH-D of 50 <75 nmol/L) affects 56% of children. Likewise, it was found that less than 3% of children consume a supplement with Vitamin D.

  3. Vitamin D intake recommendations in children:

    The current vitamin D intake recommendations made by the APP since 2008 (Wagner CL, 2008) for children aged 1 to 8 years is an Adequate Intake of 400-600 IU (10-15µg), and for the Tolerable Upper Intake Level it is suggested do not exceed 2500 IU (63µg) in the case of children from 1 to 3 years and 3000 IU (75µg) in children from 4 to 8 years.

  4. Description of the study:

    A double-blind controlled cluster randomized field trial was developed.

    The participants were children from 6 day-care centers (SEDESOL) at Cuernavaca, Morelos, Mexico. The study sample had 275 children that completed the study (the protocol considered having at least 125 children in each treatment group), from 12 to 59 months, who attended 6 take care centers (SEDESOL), in Cuernavaca, Morelos.

  5. Objective

    To evaluate the efficacy of the consumption of fortified eggs with Vitamin D3 on the serum concentrations of 25-OH-D in children aged 12 to 59 months who attend take care centers (SEDESOL)in Cuernavaca.

  6. Treatment and control groups:

    The random assignments of the intervention group (fortified egg) and control group (unfortified egg) were done considering each day-care center as a unit of allocation.

    Three day-care centers were randomized to the intervention group and three to the control group. The study lasted 12 weeks.

    The treatment group consumed a fortified egg to provide 10 mcg of Vitamin D3 equivalent to 400 IU of Cholecalciferol, 3 times a week.

    The control group received unfortified egg (~ 43 IU Vitamin D) with the same frequency as the intervention group.

  7. Main Outcomes:

    The main outcome outcome variables were the serum levels of 25-hydroxyvitamin D3 (25-OH-D3) The second main outcome was to evaluate the parathyroid hormone (PTH).

    Other Variables:

    Blood parameters were taken: total cholesterol, HDL cholesterol, triglycerides, glucose, and hemoglobin.

    Anthropometric measurements of weight, height, age.

    Morbidity (diarrhea, constipation and respiratory tract infections) was evaluated three times per week and recorded.

    Standardized personnel weight the egg consumed before and after breakfast with a food weighing scale.

    Mothers were asked about children's usual diet by two diet questionnaires : a 24-hour dietary recall and a food frequency questionnaire at baseline and at the end of the study.

  8. Ethical considerations:

The protocol was submitted to he Research and Ethics Committee of the Medicine Research Division of the National Autonomous University of Mexico.The study was approved on May 8, 2018 with folio FM/DI/028/2018.

The children's mothers or guardians signed an informed consent letter.

Study Type

Interventional

Enrollment (Actual)

275

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 Locations

    • Morelos
      • Cuernavaca, Morelos, Mexico, 62100
        • Instituto Nacional de Salud Publica

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

  • Child

Accepts Healthy Volunteers

No

Description

Inclusion Criteria:

  • Children of either sex, from 12 to 59 months of age who attend take care SEDESOL centers
  • Children who consume eggs within their usual diet at least 5 times per month
  • Childrens whose parents or legal guardian agree to participate in the study and sign an informed consent letter

Exclusion Criteria:

  • Children with an egg allergy
  • Chldren with hypersensitivity to vitamin D
  • Children who have taken vitamin D supplements in the past month

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: Treatment
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Triple

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: vitamin D3-enhanced egg
The experimental group consumed an vitamin D3-enhanced egg (~ 400 IU). The randomization unit was the take care SEDESOL centers. All children in 3 day-care centers were given one vitamin D3-enhanced egg at breakfast, 3 times a week for 12 weeks (Monday, Wednesday and Friday).

In our study, the vitamin D3-enhanced eggs were produced by hens that received 23,500 IU of vitamin D3 per kg of feed. Which does not confer them any harm or danger of intoxication. This experiment was carried out at the Center for Teaching, Research and Extension in Poultry Production (CEIEPAv, FMVZ-UNAM) and lasted 40 weeks.

This ensured that the hens eggs were enhanced with vitamin D achieving a final concentration of approximately 400 IU of vitamin D

Placebo Comparator: Control
The control group consumed unfortified egg (~ 43 IU Vitamin D). The randomization unit was the 6 day-care centers (SEDESOL). All children in 3 day-care centers were given unfortified egg at breakfast, 3 times a week for 12 weeks (Monday, Wednesday and Friday).
Unfortified eggs were used for the control group with a concentration of approximately 43 IU of vitamin D

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Serum 25-OH-D
Time Frame: At baseline and at 12 weeks of intervention
nmol/L
At baseline and at 12 weeks of intervention

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Serum PTH
Time Frame: At baseline and at 12 weeks of intervention
pcg/mL
At baseline and at 12 weeks of intervention

Other Outcome Measures

Outcome Measure
Measure Description
Time Frame
Insulin
Time Frame: At baseline and at 12 weeks of intervention
ug/dL
At baseline and at 12 weeks of intervention
Weight
Time Frame: At baseline and at 12 weeks of intervention
kg
At baseline and at 12 weeks of intervention
Height
Time Frame: At baseline and at 12 weeks of intervention
cm
At baseline and at 12 weeks of intervention
Total Cholesterol
Time Frame: At baseline and at 12 weeks of intervention
mg/dL
At baseline and at 12 weeks of intervention
Triglicerids
Time Frame: At baseline and at 12 weeks of intervention
mg/dL
At baseline and at 12 weeks of intervention
HDLc
Time Frame: At baseline and at 12 weeks of intervention
mg/dL
At baseline and at 12 weeks of intervention
Glucose
Time Frame: At baseline and at 12 weeks of intervention
mg/dL
At baseline and at 12 weeks of intervention

Collaborators and Investigators

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

Investigators

  • Principal Investigator: Mario E Flores Aldana, PhD, National Institute of Public Health, Mexico

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 (Actual)

July 15, 2018

Primary Completion (Actual)

November 30, 2018

Study Completion (Actual)

December 21, 2019

Study Registration Dates

First Submitted

September 4, 2023

First Submitted That Met QC Criteria

October 19, 2023

First Posted (Actual)

October 23, 2023

Study Record Updates

Last Update Posted (Actual)

October 23, 2023

Last Update Submitted That Met QC Criteria

October 19, 2023

Last Verified

October 1, 2023

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

product manufactured in and exported from the U.S.

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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