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Abstract
Background
Anti-Müllerian hormone (AMH) is a product of growing ovarian follicles. The concentration of AMH in blood may also reflect the non-growing follicle (NGF) population, i.e. the ovarian reserve, and be of value in predicting reproductive lifespan. A full description of AMH production up to the menopause has not been previously reported.
Methodology/Principal Findings
By searching the published literature for AMH concentrations in healthy pre-menopausal females, and using our own data (combined ) we have generated and robustly validated the first model of AMH concentration from conception to menopause. This model shows that 34% of the variation in AMH is due to age alone. We have shown that AMH peaks at age 24.5 years, followed by a decline to the menopause. We have also shown that there is a neonatal peak and a potential pre-pubertal peak. Our model allows us to generate normative data at all ages.
Conclusions/Significance
These data highlight key inflection points in ovarian follicle dynamics. This first validated model of circulating AMH in healthy females describes a transition period in early adulthood, after which AMH reflects the progressive loss of the NGF pool. The existence of a neonatal increase in gonadal activity is confirmed for females. An improved understanding of the relationship between circulating AMH and age will lead to more accurate assessment of ovarian reserve for the individual woman.
Anti-Müllerian hormone (AMH) is a product of growing ovarian follicles. The concentration of AMH in blood may also reflect the non-growing follicle (NGF) population, i.e. the ovarian reserve, and be of value in predicting reproductive lifespan. A full description of AMH production up to the menopause has not been previously reported.
Methodology/Principal Findings
By searching the published literature for AMH concentrations in healthy pre-menopausal females, and using our own data (combined ) we have generated and robustly validated the first model of AMH concentration from conception to menopause. This model shows that 34% of the variation in AMH is due to age alone. We have shown that AMH peaks at age 24.5 years, followed by a decline to the menopause. We have also shown that there is a neonatal peak and a potential pre-pubertal peak. Our model allows us to generate normative data at all ages.
Conclusions/Significance
These data highlight key inflection points in ovarian follicle dynamics. This first validated model of circulating AMH in healthy females describes a transition period in early adulthood, after which AMH reflects the progressive loss of the NGF pool. The existence of a neonatal increase in gonadal activity is confirmed for females. An improved understanding of the relationship between circulating AMH and age will lead to more accurate assessment of ovarian reserve for the individual woman.
Original language | English |
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Article number | e22024 |
Number of pages | 7 |
Journal | PLoS ONE |
Volume | 6 |
Issue number | 7 |
DOIs | |
Publication status | Published - 15 Jul 2011 |
Fingerprint
Dive into the research topics of 'A validated model of serum anti-Müllerian hormone from conception to menopause'. Together they form a unique fingerprint.Projects
- 1 Finished
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A Constraint Solver Synthesiser: A Constraint Solver Synthesiser
Miguel, I. J. (PI), Balasubramaniam, D. (CoI), Gent, I. P. (CoI), Kelsey, T. (CoI) & Linton, S. A. (CoI)
1/10/09 → 30/09/14
Project: Standard
Research output
- 2 Article
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Can Anti-Müllerian hormone predict the diagnosis of polycystic ovary syndrome? A systematic review and meta-analysis of extracted data
Iliodromiti, S., Kelsey, T., Anderson, R. & Nelson, S., Aug 2013, In: Journal of Clinical Endocrinology & Metabolism. 98, 8, p. 3332-3340 9 p.Research output: Contribution to journal › Article › peer-review
Open AccessFile -
Interpreting human follicular recruitment and antimullerian hormone concentrations throughout life
Fleming, R., Kelsey, T., Anderson, R., Wallace, H. & Nelson, S., 2012, In: Fertility and Sterility. 98, 5, p. 1097-1102Research output: Contribution to journal › Article › peer-review