Ag. Vanwassenaer et al., THYROID-FUNCTION IN VERY PRETERM INFANTS - INFLUENCES OF GESTATIONAL-AGE AND DISEASE, Pediatric research, 42(5), 1997, pp. 604-609
It is not known how immaturity and disease influence postnatal thyroid
function in infants <30 wk of gestational age. We performed serial me
asurements of plasma thyroxine (T-4), free T-4 (FT4), triiodothyronine
(T-3), reverse T-3 (rT(3)), TSH, and T-4-binding globulin (TBG) in 10
0 infants of <30 wk of gestation, during the first 8 postnatal weeks,
to investigate the influences of disease and gestational age on the ti
me course of thyroid hormones. One hundred infants were divided twice
into two groups: 1) in a group of 25-28 and of 28-30 wk of gestation;
and 2) in a sick and a healthy group, with similar gestational ages. T
he time course of T-4, FT4, T-3, TSH, and TBG, but not rT(3) differed
significantly (p < 0.005) between the gestational age groups. T-4 and
FT4 decreased to levels below the cord blood value with a deeper FT4 n
adir on d 7 in the youngest group. Disease decreased T-4, FT4, T-3, TS
H, and TBG concentrations especially during the 1st wk after birth (p
< 0.005), However, the FT4 nadir on d 7 was similar in sick and health
y infants, After 3 wk, T-4, FT4, T-3, and TBG were higher in the sick
group compared with the healthy group, rT(3) levels were not increased
in sick infants. We conclude that the extent of the FT4 decrease afte
r birth in infants of <30 wk gestation is mainly influenced by gestati
onal age and probably reflects a transient depletion of thyroidal horm
one reserves. rT(3) cannot be used as a marker of nonthyroidal illness
in very preterm infants.