Association Between Intakes of Protein, Calcium and Milk With Gene Expression and Linear Growth of School Aged Children

NCT ID: NCT03895151

Last Updated: 2019-12-03

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: NA
• Total Enrollment: 150 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2018-01-24
• Study Completion Date: 2019-06-30

Brief Summary

Protein is one type of nutrients known as the cause of stunting in developing countries since the mid-1970s (1) but then less attention on protein intake with the assumption that protein intake is sufficient. Compilation of published and non-published dietary intake research among Indonesian children aged 3-12 years (2), 0-18 years old (3) and 1-3 years old (3) found that protein intake among Indonesian children was sufficient (4). This finding is also confirmed by some other studies in 6 low-income countries and lead to the conclusion that growth restriction is not due to protein deficiency (5). Since then, micronutrient received main attention for the past 4 decades (1) to improve the health and survival of young children in developing countries. Issues on the need to re-examined protein recently emerge after the paper of Semba (1,6) regarding the low circulating amino acid among stunted children. It was hypothesized that the correlation between the low level of circulating amino acid with linear growth was through the mechanism of rapamycin complex C1 (mTORC1) and general control nonderepressible 2 (GCN2) pathway that contributes in the synthesis of sphingolipids and glycerophospholipids (6). However, the mechanism on how amino acid link to linear growth remains unclear.

Fortification among Asian children revealed that only milk as food vehicles reported a significant effect on linear growth (2). It is likely that the effect on linear growth is influenced not only on micronutrient content of the fortified foods but also on protein and amino acid profiles of milk as the food vehicle.

Detailed Description

Background:

The understanding of stunting has shifted from attention to protein and micronutrients in 60-80s to amino acids and calcium in the past two decades. Amino acids are suspected to be nutrients that determine to stunting because recent studies have shown that growth can be carried out by the information pathway through the mTOR pathway (the mechanistic target of rapamycin). mTOR is a serine/threonine protein kinase from the PI3K family related kinases which are the main subunits of 2 complex proteins, namely mTORC1 and mTORC2. The mTORC1 protein includes 5 main parts for cell growth, nutrition, growth factors, oxygen, energy, and stress. The mTORC2 protein is used in the cytoskeletal organization and cell survival. The activated mTORC1 protein initiates anabolic processes such as synthetic proteins, lipids, and nucleotides and inhibits catabolic processes such as autophagy. mTORC1 consists of three core proteins: mTOR, Raptor (regulatory protein associated with mTOR) and mLST8 (deadly mammals with Sec13 protein 8).

Activation of the mTORC1 pathway as a controller of growth and metabolism is in accordance with the adequacy of intracellular essential amino acids. Deficiency of leucine, isoleucine, and valine determines mTOR downregulation. Inadequate intake of essential amino acids will repress protein and lipid synthesis as well as cell growth that will affect bone and chondral palate growth, skeletal muscle growth, nervous system myelinization, immune function and the size of the organ formed (Saxton & Sabatini, 2017). Research by Semba, et.al (2016) shows that in stunting children's serum, the levels of the nine essential amino acids are very low. Given that the body does not form essential amino acids directly, the intake of amino acids from food becomes very important (Nuss & Tanumihardjo, 2011). Essential amino acids are mostly contained in animal protein, but consumption in developing countries is still limited. Consumption of animal food sources is associated with a lower risk of stunting.

Study of the mTORC1 pathway that has been done in vitro studies and experimental animals. In humans, the evidence of amino acid signaling through the mTORC1 pathway by using metabolomic aspects and proteomic and transcriptomic characteristics is still unknown. Analysis of genes related to MTORC1 pathway may answer this question

The scope of services:

1. To assess intakes of energy, macronutrients (protein, fat, carbohydrate), calcium and other micronutrients related to growth (zinc, iron, magnesium)

2. To assess linear growth

3. To assess gene expression of the mTORC1 pathway in school-age children in Malang, East Java.

The objective of research:

1. To assess energy and nutrient intake (especially for protein and calcium)

2. To assess the expression of mTOR gene

3. To assess the linear growth (height)

4. To assess the association between intake of protein, calcium, milk with gene expression of mTOR and linear growth of children who received food-based intervention with or without milk with comparable calcium and protein intakes

Conditions

Nutritional Stunting; Nutritional Anemia; Nutritional Deficiency; Nutrigenetic; Nutrigenomic; Linear Programming; Food Based Recommendation

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: SINGLE

Study Groups

Milk supplementation

Children will receive 130 ml fresh milk, 6 days/week for 20 weeks (January-June 2019).

Milk will be provided and delivered by appointed supplier directly to school. Milk will be distributed with name of the student on the bottle - during break time.

Subjects must be consumed with supervision of the teacher at school during the break.

If they can not finish the milk at once, they can store it in the provided cool box. Student then can consume it again before they go home. Teacher have to record the remaining milk in each bottle that corresponds to every child name and record it in the provided form.

Prior to holiday, student will be given the milk according to school leave days.

Enumerators should collect the form every 3 days and make a recap in the provided form.

Group Type: EXPERIMENTAL

Milk supplementation

Intervention Type: DIETARY_SUPPLEMENT

Fresh milk from local farmer. No artificial sweetener and preservatives. Brandless.

Food Based Recommendation (FBR) nutrition education

FBR group will received nutrition education delivered by trained teacher under the supervision of researcher/research assistant once a week. Those who received nutrition education is not only the recruited subjects but also includes their classmates.

Group Type: EXPERIMENTAL

Food Based Recommendation (FBR) nutrition education

Intervention Type: OTHER

Food Based Recommendation is result of OPTIFOOD WHO that analysed local food to optimize nutritional status according to problem nutrient.

Control

Control group will receive standard nutrition education

Group Type: NO_INTERVENTION

No interventions assigned to this group

Interventions

Milk supplementation

Fresh milk from local farmer. No artificial sweetener and preservatives. Brandless.

Intervention Type: DIETARY_SUPPLEMENT

Food Based Recommendation (FBR) nutrition education

Food Based Recommendation is result of OPTIFOOD WHO that analysed local food to optimize nutritional status according to problem nutrient.

Intervention Type: OTHER

Eligibility Criteria

Inclusion Criteria

• Primary school children
• Willing to take part in the research and taken venous blood sampling as evidence by the signing of an informed consent from the parents
• Does not suffer from disability
• No complaint such as diarrhea, vomiting or nausea after drinking milk (based on the information of parents during screening)

Exclusion Criteria

• The child not present when taking blood
• Having a history of bleeding such as hemophilia
• Children have plans to move schools within the next 6 months from the baseline data collection.

• Minimum Eligible Age: 8 Years
• Maximum Eligible Age: 10 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

Direktorat Riset dan Pengabdian Masyarakat Universitas Indonesia

UNKNOWN

Sponsor Role: collaborator

University of Brawijaya

OTHER

Sponsor Role: collaborator

SEAMEO Regional Centre for Food and Nutrition

OTHER

Sponsor Role: lead

Responsible Party

Dr.Umi Fahmida

Dr. Umi Fahmida

Responsibility Role: PRINCIPAL_INVESTIGATOR

Principal Investigators

Umi Fahmida Fahmida, Dr

Role: PRINCIPAL_INVESTIGATOR

SEAMEO RECFON

Locations

Universitas Brawijaya

Malang, East Java, Indonesia

Countries

Indonesia

Other Identifiers

NGMilkMalang

Identifier Type: -

Identifier Source: org_study_id