Effect of Hyperinsulinemia and Insulin Resistance on Endocrine, Metabolic, and Reproductive Outcomes in Non-PCOS Women Undergoing Assisted Reproduction: A Retrospective Cohort Study

To evaluate the effect of hyperinsulinemia (HI) and insulin resistance (IR) on endocrine, metabolic, and reproductive outcomes in women without polycystic ovary syndrome (PCOS) undergoing assisted reproduction. The study included 1,104 non-PCOS women undergoing fertilization/intracytoplasmic sperm i...

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Veröffentlicht in:Frontiers in medicine 2022-01, Vol.8, p.736320-736320
Hauptverfasser: Cai, Wang-Yu, Luo, Xi, Song, Jianyuan, Ji, Danpin, Zhu, Jun, Duan, Cuicui, Wu, Wei, Wu, Xiao-Ke, Xu, Jian
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Sprache:eng
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Zusammenfassung:To evaluate the effect of hyperinsulinemia (HI) and insulin resistance (IR) on endocrine, metabolic, and reproductive outcomes in women without polycystic ovary syndrome (PCOS) undergoing assisted reproduction. The study included 1,104 non-PCOS women undergoing fertilization/intracytoplasmic sperm injection-fresh embryo transfer. HI was evaluated by serum fasting insulin (FIN), and IR was evaluated by homeostatic model assessment of insulin resistance index (HOMA-IR). In addition, biometric, sex hormone, and metabolic parameters were measured. Independent -test, linear, and logistic regression examined associations between HI, IR, and endocrine, metabolic, ovarian stimulation characteristics, and reproductive outcomes. Women with HI and IR had lower levels of progesterone, luteinizing hormone, follicle-stimulating hormone, estradiol, high-density lipoproteins, and increased levels of triglycerides low-density lipoproteins. For ovarian stimulation characteristics, those with HI and IR had a longer duration of stimulation, a higher total gonadotropin dose, and a lower peak estradiol level. Linear regression confirmed these associations. For reproductive outcomes, HI and IR were not associated with clinical pregnancy, live birth, and miscarriage. HI and IR did not impair reproductive outcomes in non-PCOS women undergoing assisted reproduction.
ISSN:2296-858X
2296-858X
DOI:10.3389/fmed.2021.736320