What hormone checks ovarian reserve?

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Last updated: November 19, 2025View editorial policy

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Ovarian Reserve Assessment

Anti-Müllerian hormone (AMH) and antral follicle count (AFC) are the primary markers used to assess ovarian reserve, with AMH being the most convenient and reliable hormonal indicator. 1

Primary Hormonal Markers

Anti-Müllerian Hormone (AMH)

  • AMH is the best currently available hormonal measure of ovarian reserve and accurately reflects the pool of growing follicles in the ovary 1, 2
  • AMH is produced exclusively by granulosa cells of small, growing ovarian follicles and correlates strongly with the number of antral follicles 1, 3
  • Key advantage: AMH does not vary significantly by menstrual cycle day and is not affected by exogenous estrogen or progesterone, making it convenient for testing at any time 1, 4
  • AMH is superior to age, basal FSH, estradiol, and inhibin B for assessing ovarian reserve in healthy women 1
  • Very low AMH levels (below 0.7 ng/mL) indicate ovarian failure or severely diminished ovarian reserve 1, 5

Antral Follicle Count (AFC)

  • AFC measured by transvaginal ultrasound is the most established method for assessing ovarian reserve and correlates well with AMH 1
  • AFC directly visualizes the pool of small antral follicles available for recruitment 1

Secondary Hormonal Markers

Follicle-Stimulating Hormone (FSH) and Estradiol

  • FSH remains a late marker of ovarian dysfunction and is less sensitive than AMH for early detection of diminished ovarian reserve 1
  • Baseline FSH and estradiol should be measured on days 3-6 of the menstrual cycle for women with regular cycles 4
  • FSH >35 IU/L suggests ovarian failure 4
  • FSH is useful for diagnosing premature ovarian insufficiency (POI) but has limited predictive value for future fertility 1

Clinical Application Algorithm

For women ≥25 years with regular cycles:

  • AMH testing is the preferred initial assessment, as validated normative data are available for this age group 1
  • AFC can be added for comprehensive evaluation 1

For women <25 years:

  • AMH interpretation is less reliable, as there is no evidence that low AMH indicates reduced fertility in this age group 1
  • AFC by transvaginal ultrasound remains the gold standard 1

For women with irregular cycles or amenorrhea:

  • AMH is particularly useful since it does not require cycle-specific timing 4
  • FSH and estradiol should be measured to evaluate for POI 1

Important Caveats

  • AMH assays lack international standardization, so results should be interpreted using laboratory-specific reference ranges 5, 6
  • AMH reflects the "functional ovarian reserve" (growing follicles responsive to gonadotropins) rather than the total primordial follicle pool 7, 6
  • Women using hormonal contraceptives should discontinue them at least 2 months before testing if assessing baseline reproductive function 4
  • AMH has limited value in predicting actual pregnancy success or live birth rates, though it effectively predicts ovarian response to stimulation 6, 2

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Research

The role of anti-Müllerian hormone (AMH) in ovarian disease and infertility.

Journal of assisted reproduction and genetics, 2020

Guideline

Hormonal Indicators of Ovulation

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

Implications of Low AMH Levels on Fertility

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Research

Anti-Müllerian Hormone and Ovarian Reserve: Update on Assessing Ovarian Function.

The Journal of clinical endocrinology and metabolism, 2020

Research

The role of anti-müllerian hormone (AMH) in assessing ovarian reserve.

The Journal of clinical endocrinology and metabolism, 2011

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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