» Articles » PMID: 28433372

Intrinsic Fertility of Human Oocytes

Overview
Journal Fertil Steril
Date 2017 Apr 24
PMID 28433372
Citations 23
Authors
Affiliations
Soon will be listed here.
Abstract

Objective: To study the intrinsic fertility of the human oocyte.

Design: A large retrospective study of natural cycle single embryo transfer (ET) IVF cycles.

Setting: Private IVF clinic, university, and private hospital.

Patient(s): Patients were enrolled consecutively over an 8-year period in a single ET natural cycle protocol.

Intervention(s): A total of 13,949 oocyte retrievals with natural IVF single ET. Software package R (version 3.2.5) was used for statistical calculations.

Main Outcome Measure(s): Live baby rate per oocyte according to age.

Result(s): A total of 14,185 natural cycle oocytes resulted in 1,913 live babies from single ET. The number of oocytes required to make one live baby in this large series varied with the age of the female partner. For those under 35, the live baby born per oocyte was 26%. For over age 42 it decreased to 1%. These results fit very robustly with a logistic function curve, which is at first steady (horizontal), followed by a linear decline after age 35 with a 10% loss every year until age 43, and then a flattening out (horizontal) by age 44.

Conclusion(s): The intrinsic fertility per oocyte in natural cycle is far greater than reported in hyperstimulated cycles, varying robustly from 26% to 4% with age from <35 to 42 years. The curve is relatively flat until age 34, and then declines rapidly 10% per year thereafter.

Citing Articles

Unraveling the Clinical FSH Conundrum: Insights From the Small Ovarian Reserve Heifer Model.

Ireland J, Karl K, Latham K Mol Reprod Dev. 2025; 92(2):e70007.

PMID: 39935023 PMC: 11814505. DOI: 10.1002/mrd.70007.


Who freezes her eggs and why? psychological predictors, reasons, and outcomes of social egg freezing.

Schmid J, Weber S, Ehlert U Reprod Biol Endocrinol. 2025; 23(1):7.

PMID: 39815288 PMC: 11734346. DOI: 10.1186/s12958-024-01342-3.


Mitochondrial DNA Damage and Its Repair Mechanisms in Aging Oocytes.

Kobayashi H, Imanaka S Int J Mol Sci. 2024; 25(23).

PMID: 39684855 PMC: 11642581. DOI: 10.3390/ijms252313144.


The stromal microenvironment and ovarian aging: mechanisms and therapeutic opportunities.

Shen L, Liu J, Luo A, Wang S J Ovarian Res. 2023; 16(1):237.

PMID: 38093329 PMC: 10717903. DOI: 10.1186/s13048-023-01300-4.


Melatonin enhances the developmental potential of immature oocytes from older reproductive-aged women by improving mitochondrial function.

Yang D, Mu Y, Wang J, Zou W, Zou H, Yang H Heliyon. 2023; 9(9):e19366.

PMID: 37681148 PMC: 10480597. DOI: 10.1016/j.heliyon.2023.e19366.