{"title":"Population-based age-specific reference percentiles and Z-scores for AMH in women.","authors":"Ronit Machtinger, Rina Hemi, Ehud Barhod, Tomer Ziv-Baran","doi":"10.1080/14647273.2025.2610909","DOIUrl":null,"url":null,"abstract":"<p><p>Anti-Müllerian hormone (AMH) is a reliable biomarker for assessing ovarian reserve, offering insight into the quantity of a woman's remaining oocyte pool. As AMH levels naturally decline with age, establishing accurate reference values is crucial for fertility assessment and reproductive planning. While existing nomograms predominantly focus on infertile populations or small cohorts, the current study presents a comprehensive, population-based analysis of AMH levels in 5,230 women aged 25 to under 45 years. Serum samples were obtained through a central laboratory in a large tertiary hospital (Sheba Medical Center) which processes AMH tests collected primarily in the community. This unique setting provides a broadly representative sample of women from a community-based population. Utilizing these community-based serum samples measured using the Elecsys Cobas AMH assay; this cross-sectional study developed age-specific AMH percentiles and z-scores using the general additive model for location, scale and shape (GAMLSS). Participants were randomly split into a learning group (<i>n</i> = 4,000) and a validation group (<i>n</i> = 1,230), with similar median age (34.3 vs. 34.2 years, <i>p</i> = 0.499) and AMH (1.83 vs. 1.85 ng/mL, <i>p</i> = 0.584) levels. Median AMH values demonstrated a clear age-dependent decline, ranging from 3.03 ng/mL at age 25 to 0.31 ng/mL at age 44. The generated reference chart enables interpretation of AMH results in relation to age-matched peers, enhancing the clinical utility of AMH testing for counselling and decision-making in both individual and public health contexts. Importantly, this study addresses a gap in current literature by including a community-based population and avoiding the selection biases inherent in studies limited to women with infertility or polycystic ovary syndrome. The mean z-score in the validation group was approximately zero, confirming the model's robustness. These results reinforce the value of AMH as a tool for fertility assessment, while highlighting variability in AMH across populations and emphasising the need for standardised reference ranges. The newly established percentiles may support timely fertility preservation decisions and inform public health strategies aimed at fertility awareness in reproductive-aged women. As AMH testing becomes increasingly accessible, age-specific interpretation using robust population data will become essential in tailoring personalised reproductive care.</p>","PeriodicalId":13006,"journal":{"name":"Human Fertility","volume":"29 1","pages":"2610909"},"PeriodicalIF":2.0000,"publicationDate":"2026-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Human Fertility","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1080/14647273.2025.2610909","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2026/1/22 0:00:00","PubModel":"Epub","JCR":"Q2","JCRName":"OBSTETRICS & GYNECOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Anti-Müllerian hormone (AMH) is a reliable biomarker for assessing ovarian reserve, offering insight into the quantity of a woman's remaining oocyte pool. As AMH levels naturally decline with age, establishing accurate reference values is crucial for fertility assessment and reproductive planning. While existing nomograms predominantly focus on infertile populations or small cohorts, the current study presents a comprehensive, population-based analysis of AMH levels in 5,230 women aged 25 to under 45 years. Serum samples were obtained through a central laboratory in a large tertiary hospital (Sheba Medical Center) which processes AMH tests collected primarily in the community. This unique setting provides a broadly representative sample of women from a community-based population. Utilizing these community-based serum samples measured using the Elecsys Cobas AMH assay; this cross-sectional study developed age-specific AMH percentiles and z-scores using the general additive model for location, scale and shape (GAMLSS). Participants were randomly split into a learning group (n = 4,000) and a validation group (n = 1,230), with similar median age (34.3 vs. 34.2 years, p = 0.499) and AMH (1.83 vs. 1.85 ng/mL, p = 0.584) levels. Median AMH values demonstrated a clear age-dependent decline, ranging from 3.03 ng/mL at age 25 to 0.31 ng/mL at age 44. The generated reference chart enables interpretation of AMH results in relation to age-matched peers, enhancing the clinical utility of AMH testing for counselling and decision-making in both individual and public health contexts. Importantly, this study addresses a gap in current literature by including a community-based population and avoiding the selection biases inherent in studies limited to women with infertility or polycystic ovary syndrome. The mean z-score in the validation group was approximately zero, confirming the model's robustness. These results reinforce the value of AMH as a tool for fertility assessment, while highlighting variability in AMH across populations and emphasising the need for standardised reference ranges. The newly established percentiles may support timely fertility preservation decisions and inform public health strategies aimed at fertility awareness in reproductive-aged women. As AMH testing becomes increasingly accessible, age-specific interpretation using robust population data will become essential in tailoring personalised reproductive care.
期刊介绍:
Human Fertility is a leading international, multidisciplinary journal dedicated to furthering research and promoting good practice in the areas of human fertility and infertility. Topics included span the range from molecular medicine to healthcare delivery, and contributions are welcomed from professionals and academics from the spectrum of disciplines concerned with human fertility. It is published on behalf of the British Fertility Society.
The journal also provides a forum for the publication of peer-reviewed articles arising out of the activities of the Association of Biomedical Andrologists, the Association of Clinical Embryologists, the Association of Irish Clinical Embryologists, the British Andrology Society, the British Infertility Counselling Association, the Irish Fertility Society and the Royal College of Nursing Fertility Nurses Group.
All submissions are welcome. Articles considered include original papers, reviews, policy statements, commentaries, debates, correspondence, and reports of sessions at meetings. The journal also publishes refereed abstracts from the meetings of the constituent organizations.