Effects of postnatal estradiol and progesterone replacement in extremely preterm infants

J Clin Endocrinol Metab. 1999 Dec;84(12):4531-5. doi: 10.1210/jcem.84.12.6180.


The fetus is supplied from the placenta with estradiol (E2) and progesterone (P) in increasing amounts during gestation. After delivery of a premature infant, placental supply is disrupted, resulting in a rapid decrease in E2 and P. Replacement of these placental hormones may restore intrauterine conditions and may be beneficial for bone mineral accretion, clinical course, and outcome. Thirty female infants with a median gestational age of 26.6 weeks (between 24.1-28.7) and a birth weight of 675 g (370-990) were randomized to receive E2 and P replacement, aiming to maintain plasma levels equaling the intrauterine levels, or no replacement. The E2 and P replacement was started iv and was followed by transepidermal administration for a total duration of 6 weeks. Repeated measurements included plasma levels of E2, P, FSH, and LH; uterine volume; calcium and phosphorus in spot urine specimens; and bone mineral accretion by single photon absorption densitometry. Further, the incidence of chronic lung disease and various clinical outcome data were recorded. The plasma levels of E2 and P were within the intrauterine range with median replacements of 2.30 mg/kg x day E2 (1.13-6.23) and 21.20 mg/kg x day P (11.23-27.36), iv. Three- and 6-fold higher doses of E2 and P were needed via the transepidermal route. The uterine volumes increased, and FSH and LH as indicators for biological effectiveness were significantly lowered with replacement. The bone mineral accretion rates tended to be higher, and the incidence of chronic lung disease tended to be lower (0% vs. 29%; P = 0.097). E2 and P replacement via iv and transepidermal routes is capable of maintaining plasma levels as high as those in utero with biological effectiveness. Trends toward improved postnatal bone mineral accretion and less chronic lung disease were found with the hormone replacement. Further and more extensive studies are warranted to address the role of this new approach in the care of extremely premature infants.

Publication types

  • Clinical Trial
  • Randomized Controlled Trial

MeSH terms

  • Birth Weight
  • Bone Density
  • Estradiol / administration & dosage
  • Estradiol / blood
  • Estradiol / therapeutic use*
  • Female
  • Follicle Stimulating Hormone / blood
  • Gestational Age
  • Hormone Replacement Therapy
  • Humans
  • Infant, Newborn
  • Infant, Premature*
  • Infusions, Intravenous
  • Luteinizing Hormone / blood
  • Progesterone / administration & dosage
  • Progesterone / blood
  • Progesterone / therapeutic use*
  • Weight Gain


  • Progesterone
  • Estradiol
  • Luteinizing Hormone
  • Follicle Stimulating Hormone