Nutrigenomics, PUFA, Iron and Cognition Amongst Under-two-year-old Indonesian Children

Not Applicable

• Conditions: Cognitive Ability, General
• Interventions: Dietary Supplement: DHA/EPA and iron supplementation

• Registration Number: NCT01504633
• Lead Sponsor: Indonesia University

Brief Summary

Rationale: Review on the positive effect of long chain polyunsaturated fatty acids (LCPUFA), especially docosahexanoic acid (DHA), supplementation on cognitive function in human using randomized controlled trials (RCTs) showed that results in RCTs were mixed and inconsistent. It has been suggested that the effect may be subtle, which is currently difficult to detect, but could be significant, or there may be individual variation which mediate the effect.

Objectives: This study aims to assess gene-nutrient inter-relation in explaining the effect of LCPUFAs i.e. DHA and/or iron on cognitive functioning of children \<24mo in Indonesia. Specifically the study's objectives are: (1) to assess effect of LCPUFA (as DHA oil) and iron (as iron supplement) in altering gene expressions, and (2) to assess the mediating effect of genes involved in fatty acid and iron metabolism in improving serum LCPUFA, alpha-linolenic acids (ALA), DHA and cognitive function.

Study design and study population: The study is a double-blind randomized controlled trial with children aged less than 24 months (window of opportunity). The study area is in East Lombok district, in West Nusa Tenggara province, Indonesia where nutrient intake including iron and presumably LCPUFA, is not optimal.

Intervention: The study is an intervention study, consisting of four groups: DHA, iron, DHA+iron, and placebo (60 subjects/group = 240 subjects in total). Capsule containing 100mg/d DHA or its placebo and syrup containing 16mg/d iron will be given daily for 24 weeks. Before and after the intervention child cognition (as Bayley Mental Developmental Index or MDI score), serum PUFA level, iron status (haemoglobin, transferrin receptor, ferritin), inflammation status (CRP, AGP), gene expression profiles, and potential confounders of child cognition such as lengt-for-age, weight-for-length, and weight-for-age Z-scores, stimulation/home environment, maternal characteristics will be collected.

Study outcome: The primary study outcomes will be cognitive score (as Bayley Mental Developmental Index or MDI score) and gene expression profiles. Secondary study outcomes will be serum PUFA level, iron status (haemoglobin, TfR, ferritin).

Nature and extent of the burden and risks benefit and group relatedness:

Subjects, who will be included into the study will invest 14 hours. The consumption of iron is not associated with any increased risk of iron overload both for infectious (including malaria) and chronic diseases nor consumption of n-3 fatty acids EPA and DHA exceed the US Food and Drug Administrator (FDA) Generally Recognized as Save (GRAS) limit. Venous blood of 5 mL will be drawn at baseline and endline. During screening, children with severe anaemia (Hb\<70g/L) will be excluded from the study and referred to the local public health center for further treatment.

Detailed Description

Not available

Study Timeline

• Study Start: 2011-12
• Study First Submitted: 2011-12-31
• Study First Submitted QC: 2012-01-03
• Study First Posted: 2012-01-05
• Status Verified: 2014-02
• Last Update Submitted: 2014-02-25
• Last Update Posted: 2014-02-26
• Primary Completion: 2014-12
• Study Completion: 2014-12

Recruitment & Eligibility

• Status: UNKNOWN
• Sex: All
• Target Recruitment: 240

Inclusion Criteria

• Child aged 12 to 17months old
• Both father and mother of Sasak ethnicity
• Currently breastfed

Exclusion Criteria

• Birth weight <2500 grams (LBW)
• Congenital malformation and/or disorder that interfered with adequate functioning in daily life
• Hemoglobin value below 70 g/L
• Malaria
• Maternal depression

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: FACTORIAL

Arm && Interventions

Group	Intervention	Description
DHA+EPA Group	DHA/EPA and iron supplementation	DHA/EPA capsule (100mg DHA + 20mg) and placebo syrup per day
Fe Group	DHA/EPA and iron supplementation	Placebo capsule and Fe syrup (16mg elemental iron) per day
DHA/EPA+Fe Group	DHA/EPA and iron supplementation	DHA/EPA capsule (100mg DHA + 20mg) and Fe syrup (16mg elemental iron) per day
Placebo Group	DHA/EPA and iron supplementation	Placebo capsule and placebo syrup

Primary Outcome Measures

Name	Time	Method
change in cognitive function (MDI score)	within 24 weeks after start of intervention	Mental Developmental Index (MDI) score of Bayley Scale of Infant Development (BSID)

Trial Locations

Locations (1)

SEAMEO Regional Center for Food and Nutrition (RECFON) University of Indonesia; 🇮🇩 Jakarta, DKI Jakarta, Indonesia