Division of Reproductive Endocrinology and Infertility, Center for Reproductive Medicine, Cedars-Sinai Medical Center, Los Angeles, California.
Metabolon, Inc., Durham, North Carolina.
J Clin Endocrinol Metab. 2019 Apr 1;104(4):1005-1019. doi: 10.1210/jc.2018-01118.
Maternal metabolic status reflects underlying physiological changes in the maternal-placental-fetal unit that may help identify contributors to adverse pregnancy outcomes associated with infertility and treatments used.
To determine if maternal metabolomic profiles differ between spontaneous pregnancies and pregnancies conceived with fertility treatments that may explain the differences in pregnancy outcomes.
Metabolon metabolomic analysis and ELISAs for 17-β-estradiol and progesterone were performed during the late first trimester of pregnancy.
Academic institution.
Women in the Spontaneous/Medically Assisted/Assisted Reproductive Technology cohort (N = 409), 208 of whom conceived spontaneously and 201 with infertility [non in vitro fertilization treatments (NIFT), n=90; in vitro fertilization (IVF), n=111].
Mode of conception.
Levels of of 806 metabolites within eight superpathways, 17-β-estradiol, and progesterone in maternal plasma in the late first trimester.
Metabolomic differences in the lipid superpathway (i.e., steroid metabolites, lipids with docosahexaenoyl acyl chains, acyl cholines), and xanthine and benzoate metabolites (P < 0.05) were significant among the spontaneous and two infertility groups, with greatest differences between the spontaneous and IVF groups. 17-β-estradiol and progesterone levels were significantly elevated in the infertility groups, with greatest differences between the spontaneous and IVF groups.
Metabolomic profiles differ between spontaneous and infertility pregnancies, likely driven by IVF. Higher levels of steroids and their metabolites are likely due to increased hormone production from placenta reprogrammed from fertility treatments, which may contribute to adverse outcomes associated with infertility and the treatments used.
母体代谢状态反映了母体-胎盘-胎儿单位的潜在生理变化,这些变化可能有助于确定与不孕和治疗相关的不良妊娠结局的原因。
确定自然妊娠和接受生育治疗的妊娠之间的母体代谢组谱是否存在差异,这些差异可能解释了妊娠结局的差异。
在妊娠早期晚期进行代谢组学分析和 17-β-雌二醇和孕激素的 ELISA 检测。
学术机构。
自然/医学辅助/辅助生殖技术队列中的女性(N=409),其中 208 名自然受孕,201 名因不孕[非体外受精治疗(NIFT),n=90;体外受精(IVF),n=111]受孕。
受孕方式。
妊娠早期晚期母体血浆中 806 种代谢物、17-β-雌二醇和孕激素的 8 个超级途径水平。
脂质超级途径(即类固醇代谢物、具有二十二碳六烯酰酰链的脂质、酰胆碱)和黄嘌呤和苯甲酸代谢物的代谢组差异在自然和两种不孕组之间具有统计学意义(P<0.05),自然和 IVF 组之间的差异最大。不孕组中 17-β-雌二醇和孕激素水平显著升高,自然和 IVF 组之间的差异最大。
自然妊娠和不孕妊娠的代谢组谱存在差异,可能是由 IVF 引起的。类固醇及其代谢物水平升高可能是由于来自生育治疗的胎盘重新编程导致激素产生增加,这可能导致与不孕和治疗相关的不良结局。