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Human Ovarian Reserve from Conception to the Menopause

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TLDR
This model allows us to estimate the number of NGFs present in the ovary at any given age, suggests that 81% of the variance in NGF populations is due to age alone, and shows for the first time, to the knowledge, that the rate of N GF recruitment increases from birth to age 14 years then declines with age until menopause.
Abstract
The human ovary contains a fixed number of non-growing follicles (NGFs) established before birth that decline with increasing age culminating in the menopause at 50-51 years. The objective of this study is to model the age-related population of NGFs in the human ovary from conception to menopause. Data were taken from eight separate quantitative histological studies (n = 325) in which NGF populations at known ages from seven weeks post conception to 51 years (median 32 years) were calculated. The data set was fitted to 20 peak function models, with the results ranked by obtained r2 correlation coefficient. The highest ranked model was chosen. Our model matches the log-adjusted NGF population from conception to menopause to a five-parameter asymmetric double Gaussian cumulative (ADC) curve (r2 = 0.81). When restricted to ages up to 25 years, the ADC curve has r2 = 0.95. We estimate that for 95% of women by the age of 30 years only 12% of their maximum pre-birth NGF population is present and by the age of 40 years only 3% remains. Furthermore, we found that the rate of NGF recruitment towards maturation for most women increases from birth until approximately age 14 years then decreases towards the menopause. To our knowledge, this is the first model of ovarian reserve from conception to menopause. This model allows us to estimate the number of NGFs present in the ovary at any given age, suggests that 81% of the variance in NGF populations is due to age alone, and shows for the first time, to our knowledge, that the rate of NGF recruitment increases from birth to age 14 years then declines with age until menopause. An increased understanding of the dynamics of human ovarian reserve will provide a more scientific basis for fertility counselling for both healthy women and those who have survived gonadotoxic cancer treatments.

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A Validated Model of Serum Anti-Müllerian Hormone from Conception to Menopause

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A validated model of serum anti-Mullerian hormone from conception to menopause

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References
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Journal ArticleDOI

The timing of normal puberty and the age limits of sexual precocity: variations around the world, secular trends, and changes after migration

TL;DR: These observations urge further study of the onset of puberty as a possible sensitive and early marker of the interactions between environmental conditions and genetic susceptibility that can influence physiological and pathological processes.
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Accelerated disappearance of ovarian follicles in mid-life: implications for forecasting menopause

TL;DR: This model shows follicle numbers decline bi-exponentially rather than as a simple exponential function of age, as had been assumed, with a first exponential rate parameter of -0.097 and a second of - 0.237, and predicts the impact of step reductions of follicles numbers on the prospective span of menstrual life was predicted.
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Germline stem cells and follicular renewal in the postnatal mammalian ovary

TL;DR: It is shown that juvenile and adult mouse ovaries possess mitotically active germ cells that, based on rates of oocyte degeneration (atresia) and clearance, are needed to continuously replenish the follicle pool.
Journal ArticleDOI

TGF-beta superfamily members and ovarian follicle development.

TL;DR: Advances in the understanding of intraovarian regulatory mechanisms should facilitate the development of new approaches for monitoring and manipulating ovarian function and improving fertility in domesticated livestock, endangered species and man.
Journal ArticleDOI

A quantitative and cytological study of germ cells in human ovaries

TL;DR: Foetal, neonatal and post-natal human ovaries were studied with the object of correlating cytological changes in the germ cells with fluctuations in their numbers, and three ‘waves’ of degeneration were observed, affecting oogonia undergoing mitosis, oocytes principally at the pachytene stage and oocytes at the diplotene stage.
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