AI Article Synopsis

  • The study investigates how renal disease and thyroid conditions affect the excretion of epidermal growth factor (EGF) in infants, focusing on the perinatal period.
  • Urine samples were collected from infants with congenital renal disease, hypothyroidism, and hyperthyroidism to compare their EGF and creatinine excretion levels against a healthy control group of 190 infants.
  • Results show that EGF excretion tends to increase earlier in gestation compared to creatinine; however, it is reduced in cases of renal disease and hypothyroidism, while hyperthyroidism leads to greater EGF excretion.

Article Abstract

We have previously demonstrated that changes in urinary epidermal growth factor/creatinine ratios relate to gestational age and gender. It is unclear what controls this developmental pattern although chronic renal disease and thyroid aberrations have significant effects on epidermal growth factor and creatinine excretion in childhood and in adults. Therefore, we chose to explore the effects of these disease states on epidermal growth factor excretion during the perinatal time period. We collected urine samples from 8 infants with congenital renal disease and 45 infants with low T4 and normal TSH values who 'failed' the newborn screen. In addition, 2 infants with hypothyroidism and 2 infants with neonatal Grave's disease had urine samples examined. Values were compared with the epidermal growth factor and creatinine excretion from 190 infants. We demonstrated that epidermal growth factor excretion increased earlier in gestation than does creatinine excretion. In infants with renal disease or hypothyroidism, epidermal growth factor excretion was decreased while hyperthyroidism enhanced excretion. Epidermal growth factor excretion increased with relief of an obstruction but still remained low and creatinine excretion was unchanged. We confirm that in preterm infants as in childhood there are similar effects of thyroid and renal diseases on epidermal growth factor excretion.

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http://dx.doi.org/10.1530/acta.0.1210505DOI Listing

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