Assisted Reproduction · Safety and Risks

Supraphysiologic estradiol is an independent predictor of low birth weight in full-term singletons born after fresh embryo transfer

Pereira N, Elias RT, Christos PJ, Petrini AC, Hancock K, Lekovich JP, Rosenwaks Z

Published July 2017 Human reproduction (Oxford, England)
DOI 10.1093/humrep/dex095 PMID 28505290 PMC PMC6251696

RRM Academy Synopsis

High estradiol in fresh IVF is linked to term low birth weight

Higher estradiol in fresh IVF stimulation was linked to more term low-birth-weight singleton babies. This retrospective cohort analyzed 4071 live singleton births to normal responders under 40 at one New York center, 2005 to 2014. Estradiol was measured on trigger day. Preterm birth did not rise as estradiol rose in this cohort.

Key Findings

  • Of 6419 women with live births after fresh IVF, 4071 had live singleton births and were analyzed. Term low birth weight (under 2500 g) affected 143/4071 (3.5%).
  • Between a lower and a higher estradiol band, low birth weight rose from 6.43% to 20.7% and term low birth weight rose from 5.1% to 10.3%.
  • Odds of term low birth weight were 6.1 to 7.9 times higher in the higher estradiol groups than in the reference group.
  • Estradiol showed no such effect for preterm birth (adjusted OR 1.1, 95% CI 0.4 to 2.9) or very low birth weight (adjusted OR 1.9, 95% CI 0.2 to 25.1).
  • A higher-versus-lower estradiol split gave an adjusted odds ratio of 10.8 (95% CI 9.2 to 12.5) for term low birth weight. Estradiol had an AUC (prediction score) of 0.85 as a predictor.

Interpretation

The authors reviewed records from one New York IVF center. They adjusted for age, parity, BMI, race, infertility diagnosis and stimulation details. They suggest estradiol remained an independent predictor of term low birth weight in these normal responders. Only normal responders under 40 were studied. High responders were excluded. The authors state that high blood pressure in pregnancy and placental problems were not analyzed, progesterone was not accounted for, and a prospective study is needed.

RRM Context

Restorative reproductive medicine looks for the cause of infertility and works with the woman's own ovulatory cycle. IVF bypasses the cause and adds a stimulated hormone environment. In the cohort, higher estradiol levels during stimulation were associated with low birth weight at term. The authors cite a study of 65,868 live singletons. Its researchers reported higher odds of low birth weight after an excessive ovarian response.

Abstract

Study Question

Is supraphysiologic estradiol (E2) an independent predictor of low birth weight (LBW) in singletons born after fresh IVF-embryo transfer (ET) cycles?

Summary Answer

Our results suggest that E2 > 2500 pg/ml is an independent predictor for LBW in full-term singletons born to normal responder patients undergoing fresh IVF-ET cycles.

What Is Known Already

The pathogenesis of LBW in IVF singletons remains unknown. However, recent studies have suggested that the hyperestrogenic milieu generated during ovarian stimulation may create a sub-optimal peri-implantation environment, leading to placental dysfunction, and therefore, LBW.

Study Design, Size, Duration

Retrospective cohort study of normal responder patients, <40 years old, undergoing fresh IVF-ET cycles resulting in live singleton births between January 2005 and June 2014.

Participants/Materials, Setting, Methods

A total of 6419 patients had live births after fresh IVF-ET during the study period, of which 2348 (36.6%) patients were excluded due to multiple gestation, vanishing twins or incomplete records. Perinatal outcomes recorded for all patients included birth weight, gestational age (GA) at delivery, mode of delivery and gender. Term birth, preterm birth (PTB) and LBW incidence proportions were plotted against E2 level on the day of trigger. The term LBW incidence proportion (i.e. singletons born at GA ≥ 37 weeks with birth weight <2500 g) was considered the primary outcome of interest.

Main Results and the Role of Chance

A total of 4071 patients with live singleton births were included. The median age, BMI, E2 level and birth weight for the study cohort was 36 (33-39) years, 22.3 (20.4-25.0) kg/m2, 1554 (1112.7-2179) pg/ml and 3289 (2920-3628) g, respectively. The incidence proportion of LBW rose from 6.4% (E2 2001-2500 pg/ml) to 20.7% (E2 3501-4000 pg/ml), without a corresponding rise in the incidence proportion of PTB. The odds of term LBW with E2 > 2500 pg/ml were 6.1-7.9 times higher compared to the referent E2 group. Multivariable logistic regression analysis revealed that E2 was an independent predictor for term LBW, even after adjusting for age, BMI, race, parity, infertility diagnosis, duration of ovarian stimulation, gonadotropin dosage and method of insemination (adjusted odds ratio 10.8, 95% CI 9.2-12.5). Receiver operating characteristic analysis generated an AUC estimate of 0.85 for E2 level as a predictor of LBW.

Limitations, Reasons for Caution

The current study did not include analyses of hypertensive disorders of pregnancy or placental abnormalities. Furthermore, all patients were normal responders and of normal BMI, possibly limiting the overall generalizability of the study. Finally, as with any retrospective study, prospective data are required to validate the role of E2 in predicting LBW.

Wider Implications of the Findings

Our results emphasize the importance of minimizing the supraphysiologic elevations of E2 levels during ovarian stimulation in fresh IVF-ET cycles. This, in turn, can optimize the early peri-implantation environment and mitigate adverse perinatal outcomes such as LBW.

Study Funding/Competing Interests

Dr Paul J. Christos was partially supported by the following grant: Clinical and Translational Science Center at Weill Cornell Medical College (UL1-TR000457-06).

Trial Registration

N/A.

Topics

Related research

Assisted Reproduction › Safety and Risks › Neonatal and Birth Outcomes · Reproductive Endocrinology › Ovarian Hormones › Estrogen · Pregnancy › Neonatal Outcomes › Birth Weight
PMID 28505290 28505290 DOI 10.1093/humrep/dex095 10.1093/humrep/dex095 Pereira et al. 2017, Pereira 2017