First-trimester bleeding and twin pregnancy outcomes after in vitro fertilization

2016 ◽  
Vol 106 (1) ◽  
pp. 140-143 ◽  
Author(s):  
Jennifer L. Eaton ◽  
Xingqi Zhang ◽  
Ralph. R. Kazer
2018 ◽  
Vol 104 (4) ◽  
pp. 1005-1019 ◽  
Author(s):  
Tianyanxin Sun ◽  
Bora Lee ◽  
Jason Kinchen ◽  
Erica T Wang ◽  
Tania L Gonzalez ◽  
...  

Abstract Context 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. Objective To determine if maternal metabolomic profiles differ between spontaneous pregnancies and pregnancies conceived with fertility treatments that may explain the differences in pregnancy outcomes. Design Metabolon metabolomic analysis and ELISAs for 17-β-estradiol and progesterone were performed during the late first trimester of pregnancy. Setting Academic institution. Subjects 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]. Intervention Mode of conception. Main Outcome Measures Levels of of 806 metabolites within eight superpathways, 17-β-estradiol, and progesterone in maternal plasma in the late first trimester. Results 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. Conclusion 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.


Sign in / Sign up

Export Citation Format

Share Document