In this study, two intervention strategies to address iodine deficiency and prevent iodine deficiency disorders in breast-fed weaning infants will be evaluated in a mild to moderate iodine-deficient population in Zamboanga del Norte, Philippines, Southeast Asia.
Universal salt iodization (USI) is the most effective means to ensure optimal population iodine status and prevent iodine deficiency. In countries where USI is well implemented it is generally assumed that iodine requirements of infants are covered through breast milk. As infants wean from breast milk, at the age of 4-6 months, iodized salt programs likely contribute little to their iodine intakes. Home-prepared complementary foods have low native iodine content and pediatric guidelines recommend no extra salt be given to infants during the first year making the dietary sources of iodine limited. Weaning infants may therefore be particularly vulnerable to iodine deficiency and its effects. Iodine is an essential micronutrient and an integral component of the thyroid hormones, needed for normal growth and development, particularly of the brain. Thyroid hormones play a critical role for development of the central nervous system from early fetal life until well after birth. Thyroid hormone insufficiency during postnatal development is associated with sensorimotor and language deficits and hypothyroidism in infancy is associated with poorer language, memory skills, fine motor, auditory processing, attention and executive processing. In iodine deficient areas where iodized salt coverage is poor, WHO, UNICEF and the International Council for the Control of Iodine Deficiency Disorders (ICCIDD) recommend infants between 7 and 24 months be given a daily dose of 90 µg iodine (potassium iodate) or an annual dose of 200 mg iodine (iodised oil). The scientific evidence for this recommendation is weak, however, and it is uncertain under what conditions the two prevention strategies may be applied and which of the two is best when. The objective of this study is to evaluate the efficacy and safety of the two recommended intervention strategies in iodine-deficient weaning infants. The need for high-quality controlled studies to better understand the potential contribution and synergy of alternative strategies to help achieve optimal iodine nutrition in different population groups and settings has recently been defined as a major research priority. Following a cross-sectional, pilot study, we will conduct a randomized controlled trial to assess the efficacy of two daily doses of iodine as potassium iodate (90 µg, 100% of the WHO recommended dose, and 45 µg, 50% of the WHO recommended dose) and the annual dose of 200 mg iodine in iodised oil, via a randomized, controlled trial in weaning infants of lactating mothers living in an area affected by mild to moderate iodine deficiency in Zamboanga del Norte, Philippines, Southeast Asia. We will compare the efficacy of each of the iodine doses against each other, and against micro-nutrients given alone, estimate the optimal level of iodine for inclusion in MNPs, and report on the safety of these interventions in weaning infants. This study will provide important guidance to public health experts, governments and international organisations to ensure normal infant thyroid function and growth and development.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
TRIPLE
90 µg iodine-fortified micronutrient powder sachet (14 micronutrients); oral route; 1 daily
45 µg iodine-fortified micronutrient powder sachet (14 micronutrients); oral route; 1 daily
200 mg iodine oil capsule; oral route; once at study start
Infant urinary iodine concentration (UIC)
Time frame: 24 weeks
Infant dried blood spot thyroglobulin (DBS-Tg)
Time frame: 24 weeks
Infant dried blood spot TSH (DBS-TSH)
Time frame: 24 weeks
Infant dried blood spot total T4 (DBS-T4)
Time frame: 24 weeks
Infant somatic growth (head circumference, weight, length)
Time frame: 24 weeks, and if results significant at this point, 52 weeks
Thyroid autoimmunity
Measurement of thyroid antibodies
Time frame: 24 weeks
Safety (Composite measure of infant morbidities and infant mortality)
Composite measure of infant morbidities and infant mortality
Time frame: 24 weeks
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Non-iodised evening primrose oil capsule; oral route; once at study start
Un-fortified powder sachet (maltodextrin, no micronutrients); oral route; 1 daily
Un-fortified micronutrient powder sachet (14 micronutrients); oral route; 1 daily