Every year, around 7,500 extremely preterm babies are born in the UK, and many develop a dangerous shortage of thyroid hormone that can damage their developing brains. This hormone, thyroxine, is essential for normal brain development, but these infants cannot make enough of it because their intravenous nutrition lacks iodide—the raw material the thyroid needs to produce thyroxine. Current feeding solutions leave these babies in negative iodide balance, meaning they lose more iodide than they take in. This trial will recruit infants born between 24 and 31 weeks from 21 UK neonatal units, randomly giving half a daily iodide supplement until they reach 34 weeks gestation. The researchers will track thyroid hormone levels and later assess each child’s neurodevelopment at age two using standard developmental tests. If iodide supplementation proves effective, it could become a simple, cheap addition to standard neonatal care—preventing brain damage in thousands of children each year without requiring expensive new technology or complex procedures. The impact would be measured in improved cognitive outcomes, reduced disability rates, and lower long-term healthcare costs for a generation of preterm survivors.
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Thyroxine is a hormone produced by the thyroid gland and is essential for normal brain development. Low serum thyroxine levels (hypothyroxinaemia) are common in extreme preterm infants (under 31 weeks gestation) and this hypothyroxinaemia is associated with neurodevelopmental compromise. About 7500 extreme preterm infants are born per annum in the UK; with an estimated 20% disability rate, assuming 70% survival. Iodide is required for synthesis of thyroxine. Extreme preterm infants are initially exclusively parenterally fed (directly into the blood stream) and enteral feeds (directly into the gastro-intestinal tract) are gradually introduced and increased as clinically appropriate. Parenteral nutrition solutions are severely iodide deficient and infants are in negative iodide balance while on total parenteral nutrition. Our study aims to determine whether nutritional supplementation with iodide compared to non-supplemented infants enables extreme preterm infants to achieve a positive iodide balance and whether this protects brain development in this group of infants. This study will recruit infants born between 24 and 31 weeks gestation from a pool of 21 neonatal units in the UK. Infants will be randomised to receive a daily iodide supplement or not until they are the equivalent of 34 weeks gestation. Thyroid hormone levels will be measured during the trial and data will be collected about illnesses and events during the prenatal and postnatal periods. Neurodevelopment will be assessed in all infants at two years of age using established developmental tests. For further background information see www.euthyroid.org
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