ABSTRACT
Transient hypothyroxinemia without elevated thyroid-stimulating hormone (TSH) levels
is common in prematurity, especially in very-low-birth-weight (VLBW) infants. The
transient hypothyroxinemia of prematurity (THOP) has been seen as a ``benign'' condition
not requiring medical treatment. However, some recent large observational studies
have revealed a relationship between THOP and abnormal neurodevelopment. Furthermore,
one study showed THOP had twice the risk of brain echolucency, which was the best
predictable neurodevelopmental dysfunction, than the premature infants with normal
or higher thyroxine levels. The relationships among THOP, illness severity, and neurodevelopmental
dysfunction remain unclear. We propose a hypothesis that THOP is associated with abnormal
ultrasound and illness severity. We studied 54 infants who were admitted more than
14 days at our neonatal intensive care unit (NICU) with a birth weight <2000 g from
March 1999 to March 2000. The infants received serum thyroxine (T4), free-T4, and
TSH measurement during the first weeks of life. Most of them had serum thyroxine levels
measured at approximately 2 weeks of age. The infants enrolled in the study were examined
by at least 1 of 3 cranial ultrasounds during the first weeks of life, illness severity
evaluation according to the neonatal therapeutic intervention scoring system (NTISS)
score, as well as NICU hospital stay period. Infant were classified as THOP by T4
value <5.3 μg/dL (68 nmol/L), which is 2.6 SD below the mean for term infants in Massachusetts,
without elevated TSH value (<20 μIU/mL). After adjusting for some confounding factors,
such as gestational age, birth weight, duration of mechanical ventilation, infants
with THOP were associated with abnormal cranial ultrasound, illness severity, and
lower 1-minute Apgar score. In our studies, THOP was related with brain ultrasound
anomaly, neonatal illness, and lower Apgar score at 1 minute. Does early thyroxine
intervention improve the prognosis and neurodevelopmental dysfunction? This question
requires further investigation.
KEYWORD
Preterm - hypothyroxinemia - brain echolucency - thyroxine - NTISS - illness severity