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Androstenedione

Drugs and Chemicals · NLM MeSH · updated 2026-10-31 · version 1

Citations verified against PubMedNot yet clinician-reviewed10 referencesApproximately 5 min read

A delta-4 C19 steroid that is produced not only in the testis, but also in the ovary and the adrenal cortex.

Table of Contents

1. Definition2. Research landscape3. Reading the evidence4. Open-access studies5. Key reviews6. References7. About this article

Definition and research guide

This page combines a MeSH definition, publication statistics and selected research abstracts. It is a starting point for reading the literature, not a medical textbook or a systematic evidence review.

Content available: 4 complete abstracts (901 words), 10 references. Full article text is not stored or reproduced here; follow the PMID, DOI or PMC links to read the original sources and their access terms.

Definition

A delta-4 C19 steroid that is produced not only in the testis, but also in the ovary and the adrenal cortex. Depending on the tissue type, androstenedione can serve as a precursor to testosterone as well as estrone and estradiol.

Definition: NLM Medical Subject Headings (MeSH) scope note (Public domain (U.S. National Library of Medicine); attribution requested). View the MeSH record.

Also known as: 4-Androstene-3,17-dione; 4 Androstene 3,17 dione; delta-4-Androstenedione; delta 4 Androstenedione.

Where it fits in the MeSH classification

Broader topics
Androstenes; 17-Ketosteroids; Testosterone Congeners

Related concepts

  • Testis
  • Ovary
  • Adrenal Cortex
  • Testosterone
  • Estrone
  • Estradiol

Research landscape

PubMed indexes 7,318 records tagged with the MeSH heading “Androstenedione” (counts retrieved 2026-10-31). 414 of them (5.7%) were published from 2020 onward, and the busiest period so far is through 1999 with 4,818 records.

Reviews account for 254 records (3.5%) and meta-analyses for 17. Randomized controlled trials number 212 (2.9%) as a share of all records on the topic.

PubMed records by publication periodthrough 1999: 4,818 records; 2000-2009: 1,247 records; 2010-2019: 839 records; 2020 onward: 414 records4,818through 19991,2472000-20098392010-20194142020 onward
Records in PubMed indexed with this heading, by publication period. Real counts from NCBI E-utilities; the final period covers only part of the current year. Volume reflects how much has been published, not how strong the evidence is.
Show the data
PeriodRecords
through 19994,818
2000-20091,247
2010-2019839
2020 onward414
Share of records by publication typeReviews: 3.5 percent; Meta-analyses: 0.2 percent; Randomized controlled trials: 2.9 percentReviews3.5% (254)Meta-analyses0.2% (17)Randomized controlled trials2.9% (212)
Share of all PubMed records on this heading that carry each publication type. Types overlap with other records, so the shares do not sum to 100%.
Publication-type chart data
Publication types among 7,318 PubMed records
TypeRecordsShare
Reviews2543.5%
Meta-analyses170.2%
Randomized controlled trials2122.9%

Method: PubMed query "Androstenedione"[MeSH Terms] with publication-type and date filters, retrieved 2026-10-31.

Reading the evidence in drugs and chemicals

Studies of a chemical or drug can answer very different questions: what it is and how it behaves in cells and animals, how the body handles it, and whether it changes outcomes in people. Laboratory and animal findings often do not carry over to patients, and observational studies of exposures are confounded by who uses a substance and why. Nothing on this page is a recommendation to use, avoid, start or stop any substance or medicine; talk to a qualified clinician or pharmacist about your own situation. Check the dose, the species, the comparison group and whether a patient-relevant outcome was measured.

Evidence from open-access studies

These open-access studies come from PubMed’s best-match results for this heading (papers whose main topic it is), ranked here by citation count, with one recent addition. Each abstract is reproduced in full under its recorded open licence so that you can read the authors’ own words. They illustrate the literature; they are not a systematic summary of it. Citation counts measure attention, not reliability or clinical benefit.

Study comparison — selected abstracts, not a systematic review
Study / authorsYearSource label / designEurope PMC citationsLicence / source
Hyperandrogenemia in polycystic ovary syndrome: exploration of the role of free testosterone and androstenedione in metabolic phenotype
Lerchbaum E, Schwetz V, Rabe T, Giuliani A, Obermayer-Pietsch B
2014Research article
Design not recorded in structured metadata
67cc by
PMID 25310562 · DOI · PMC4195601
The clinical and endocrine effects of 4-hydroxyandrostenedione alone and in combination with goserelin in premenopausal women with advanced breast cancer
Stein RC, Dowsett M, Hedley A, Gazet JC, Ford HT, Coombes RC
1990Clinical trial
Design not recorded in structured metadata
65cc by
PMID 2145964 · DOI · PMC1971476
Altered theca and cumulus oocyte complex gene expression, follicular arrest and reduced fertility in cows with dominant follicle follicular fluid androgen excess
Summers AF, Pohlmeier WE, Sargent KM, Cole BD, Vinton RJ, Kurz SG, et al.
2014Research article
Design not recorded in structured metadata
46cc0
PMID 25330369 · DOI · PMC4199720
Development and validation of a predictive model for cervical insufficiency incorporating AMH and androstenedione
Zhao X, Ma M, Liu Y, Ma Y, Li R, Wang Y
2025Research article
Design not recorded in structured metadata
1cc by
PMID 41387944 · DOI · PMC12808648

Hyperandrogenemia in polycystic ovary syndrome: exploration of the role of free testosterone and androstenedione in metabolic phenotype [1]

Research article Lerchbaum E, Schwetz V, Rabe T, Giuliani A, Obermayer-Pietsch B · · 2014 · cited 67 times (Europe PMC)

Abstract reading summary — source excerpts
Opening excerpt
ObjectiveTo evaluate the association between androstenedione, testosterone, and free testosterone and metabolic disturbances in polycystic ovary syndrome.
Closing excerpt
Further, a higher androstenedione/free testosterone-ratio was independently associated with a beneficial metabolic profile.
Interpretation limits
Verbatim excerpts from the authors’ abstract; the closing excerpt may describe a finding, limitation or recommendation. Design, population, effect size and uncertainty have not been independently extracted or appraised. Read the complete abstract and linked paper before interpreting the findings.
Read complete abstract (161 words)

ObjectiveTo evaluate the association between androstenedione, testosterone, and free testosterone and metabolic disturbances in polycystic ovary syndrome.MethodsWe analyzed the association between androstenedione, testosterone, and free testosterone and metabolic parameters in a cross-sectional study including 706 polycystic ovary syndrome and 140 BMI-matched healthy women. Polycystic ovary syndrome women were categorized into 4 groups: normal androstenedione and normal free testosterone (NA/NFT), elevated androstenedione and normal free testosterone (HA/NFT), normal androstenedione and elevated free testosterone (NA/HFT), elevated androstenedione and free testosterone (HA/HFT).ResultsPolycystic ovary syndrome women with elevated free testosterone levels (HA/HFT and NA/HFT) have an adverse metabolic profile including 2 h glucose, HbA1c, fasting and 2 h insulin, area under the insulin response curve, insulin resistance, insulin sensitivity index (Matsuda), triglycerides, total and high density lipoprotein cholesterol levels compared to NA/NFT (pConclusionsPolycystic ovary syndrome women with elevated free testosterone levels but not with isolated androstenedione elevation have an adverse metabolic phenotype. Further, a higher androstenedione/free testosterone-ratio was independently associated with a beneficial metabolic profile.

Abstract reproduced from the open-access article under the recorded cc by licence; © the authors. PMID 25310562 · DOI · PMC4195601

The clinical and endocrine effects of 4-hydroxyandrostenedione alone and in combination with goserelin in premenopausal women with advanced breast cancer [2]

Clinical trial Stein RC, Dowsett M, Hedley A, Gazet JC, Ford HT, Coombes RC · · 1990 · cited 65 times (Europe PMC)

Abstract reading summary — source excerpts
Opening excerpt
The aromatase inhibitor, 4-hydroxyandrostenedione (4OHA) is an effective treatment for advanced post-menopausal breast cancer.
Closing excerpt
The combination of LHRH analogue and aromatase inhibitor may prove to be a superior treatment to LHRH analogue alone in these patients.
Interpretation limits
Verbatim excerpts from the authors’ abstract; the closing excerpt may describe a finding, limitation or recommendation. Design, population, effect size and uncertainty have not been independently extracted or appraised. Read the complete abstract and linked paper before interpreting the findings.
Read complete abstract (230 words)

The aromatase inhibitor, 4-hydroxyandrostenedione (4OHA) is an effective treatment for advanced post-menopausal breast cancer. The clinical and endocrine effects of 4OHA treatment were studied in five pre- and perimenopausal women with metastatic breast cancer. Serum oestradiol levels were not significantly reduced as a result of treatment with 500 mg of 4OHA by weekly i.m. injections and no patient had a tumour response. Four patients were subsequently treated with the luteinising hormone releasing hormone (LHRH) analogue, gosereline, and three had objective responses. The endocrine effects of combined treatment with goserelin (Zoladex), and 4OHA were studied in a further five premenopausal women. Serum oestradiol levels after treatment with goserelin alone were typical of post-menopausal women. Addition of 4OHA led to a further suppression of oestradiol to within the range observed in post-menopausal patients treated with further suppression of oestradiol to within the range observed in post-menopausal patients treated with 4OHA. Six patients whose tumours had regressed as a result of goserelin treatment and who subsequently relapsed were then given combined treatment. Four of the six experienced a second remission. We conclude that while 4OHA alone is unlikely to be a satisfactory treatment for premenopausal patients with advanced breast cancer, 4OHA in conjunction with goserelin leads to profound suppression of oestradiol. The combination of LHRH analogue and aromatase inhibitor may prove to be a superior treatment to LHRH analogue alone in these patients.

Abstract reproduced from the open-access article under the recorded cc by licence; © the authors. PMID 2145964 · DOI · PMC1971476

Altered theca and cumulus oocyte complex gene expression, follicular arrest and reduced fertility in cows with dominant follicle follicular fluid androgen excess [3]

Research article Summers AF, Pohlmeier WE, Sargent KM, Cole BD, Vinton RJ, Kurz SG, et al. · · 2014 · cited 46 times (Europe PMC)

Abstract reading summary — source excerpts
Opening excerpt
Aspiration of bovine follicles 12-36 hours after induced corpus luteum lysis serendipitously identified two populations of cows, one with High androstenedione (A4; >40 ng/ml; mean = 102) and another with Low A4 (<20 ng/ml; mean = 9) in follicular fluid.
Closing excerpt
These data suggest that the dominant follicle environment of High A4 cows including reduced estrogen conversion and androgen excess contributes to infertility in part through altered follicular and oocyte development.
Interpretation limits
Verbatim excerpts from the authors’ abstract; the closing excerpt may describe a finding, limitation or recommendation. Design, population, effect size and uncertainty have not been independently extracted or appraised. Read the complete abstract and linked paper before interpreting the findings.
Read complete abstract (258 words)

Aspiration of bovine follicles 12-36 hours after induced corpus luteum lysis serendipitously identified two populations of cows, one with High androstenedione (A4; >40 ng/ml; mean = 102) and another with Low A4 (<20 ng/ml; mean = 9) in follicular fluid. We hypothesized that the steroid excess in follicular fluid of dominant follicles in High A4 cows would result in reduced fertility through altered follicle development and oocyte maternal RNA abundance. To test this hypothesis, estrous cycles of cows were synchronized and ovariectomy was performed 36 hours later. HPLC MS/MS analysis of follicular fluid showed increased dehydroepiandrosterone (6-fold), A4 (158-fold) and testosterone (31-fold) in the dominant follicle of High A4 cows. However, estrone (3-fold) and estradiol (2-fold) concentrations were only slightly elevated, suggesting a possible inefficiency in androgen to estrogen conversion in High A4 cows. Theca cell mRNA expression of LHCGR, GATA6, CYP11A1, and CYP17A1 was greater in High A4 cows. Furthermore, abundance of ZAR1 was decreased 10-fold in cumulus oocyte complexes from High A4 cows, whereas NLRP5 abundance tended to be 19.8-fold greater (P = 0.07). There was a tendency for reduction in stage 4 follicles in ovarian cortex samples from High A4 cows suggesting that progression to antral stages were impaired. High A4 cows tended (P<0.07) to have a 17% reduction in calving rate compared with Low A4 cows suggesting reduced fertility in the High A4 population. These data suggest that the dominant follicle environment of High A4 cows including reduced estrogen conversion and androgen excess contributes to infertility in part through altered follicular and oocyte development.

Abstract reproduced from the open-access article under the recorded cc0 licence; © the authors. PMID 25330369 · DOI · PMC4199720

Development and validation of a predictive model for cervical insufficiency incorporating AMH and androstenedione [4]

Research article Zhao X, Ma M, Liu Y, Ma Y, Li R, Wang Y · · 2025 · cited 1 times (Europe PMC)

Abstract reading summary — source excerpts
Opening excerpt
This study aims to develop a predictive model for cervical insufficiency (CI) in women who undergo in vitro fertilization and embryo transfer (IVF-ET) based on relevant indicators measured prior to pregnancy.
Closing excerpt
Despite the lack of external validation from independent cohorts, this study successfully developed a comprehensive predictive model for CI in women undergoing IVF-ET, providing a preliminary exploration for early prediction and intervention strategies.
Interpretation limits
Verbatim excerpts from the authors’ abstract; the closing excerpt may describe a finding, limitation or recommendation. Design, population, effect size and uncertainty have not been independently extracted or appraised. Read the complete abstract and linked paper before interpreting the findings.
Read complete abstract (252 words)

This study aims to develop a predictive model for cervical insufficiency (CI) in women who undergo in vitro fertilization and embryo transfer (IVF-ET) based on relevant indicators measured prior to pregnancy. A total of 2,494 women who received IVF-ET at the Reproductive Medical Center of the Third Hospital of Peking University between 2016 and 2022 were included. All participants ultimately delivered at the same institution. 1,745 patients were assigned to the training cohort and 749 to the validation cohort. Both univariate logistic regression analysis and multiple logistic regression analysis were conducted to establish the CI prediction model. Among the 2,494 cases, the incidence rate of CI was 3.2%. Risk factors identified to be associated with CI included body mass index (BMI) > 22.83 kg/m2, testosterone (T) level > 0.74 nmol/L, androstenedione (A) level > 11.45 nmol/L, anti-Müllerian hormone (AMH) level > 3.50 ng/ml, frequency of hysteroscopic surgery, number of previous pregnancies (gravidity), and pre-pregnancy diabetes. Cervical length > 3.15 cm is a protective factor for cervical insufficiency. Conversely, factors such as the endometrial preparation regimen, occurrence of an intrauterine operation within six months before pregnancy, and the uterine length were not found to be significant risk factors for CI. The area under the curve (AUC) for this model achieved 0.819, with a 95% confidence interval of 0.758 to 0.881. Despite the lack of external validation from independent cohorts, this study successfully developed a comprehensive predictive model for CI in women undergoing IVF-ET, providing a preliminary exploration for early prediction and intervention strategies.

Abstract reproduced from the open-access article under the recorded cc by licence; © the authors. PMID 41387944 · DOI · PMC12808648

Key reviews and meta-analyses

The most cited review-type papers among PubMed’s best-match results for this heading, listed with bibliographic details only. Follow the links for the full text and access terms.

  • Research article Harnessing the catabolic diversity of rhodococci for environmental and biotechnological applications [5]
    van der Geize R, Dijkhuizen L · Curr Opin Microbiol · 2004 · cited 168 times (Europe PMC)
  • Research article Androstenedione production by biotransformation of phytosterols [6]
    Malaviya A, Gomes J · Bioresour Technol · 2008 · cited 123 times (Europe PMC)
  • Research article Androgen excess: Investigations and management [7]
    Lizneva D, Lizneva D, Gavrilova-Jordan L, Walker W, Azziz R · Best Pract Res Clin Obstet Gynaecol · 2016 · cited 72 times (Europe PMC)
  • Research article 11β-Hydroxyandrostenedione: Downstream metabolism by 11βHSD, 17βHSD and SRD5A produces novel substrates in familiar pathways [8]
    Swart AC, Storbeck KH · Mol Cell Endocrinol · 2015 · cited 57 times (Europe PMC)
  • Research article Aromatization inhibition alone or in combination with GnRH agonists for the treatment of premenopausal breast cancer patients [9]
    Dowsett M, Stein RC, Coombes RC · J Steroid Biochem Mol Biol · 1992 · cited 51 times (Europe PMC)
  • Research article Exemestane, a new steroidal aromatase inhibitor of clinical relevance [10]
    Lombardi P · Biochim Biophys Acta · 2002 · cited 50 times (Europe PMC)

References

  1. Lerchbaum E, Schwetz V, Rabe T, Giuliani A, Obermayer-Pietsch B. Hyperandrogenemia in polycystic ovary syndrome: exploration of the role of free testosterone and androstenedione in metabolic phenotype. . 2014. PMID 25310562 · DOI · PMC4195601
  2. Stein RC, Dowsett M, Hedley A, Gazet JC, Ford HT, Coombes RC. The clinical and endocrine effects of 4-hydroxyandrostenedione alone and in combination with goserelin in premenopausal women with advanced breast cancer. . 1990. PMID 2145964 · DOI · PMC1971476
  3. Summers AF, Pohlmeier WE, Sargent KM, Cole BD, Vinton RJ, Kurz SG, et al.. Altered theca and cumulus oocyte complex gene expression, follicular arrest and reduced fertility in cows with dominant follicle follicular fluid androgen excess. . 2014. PMID 25330369 · DOI · PMC4199720
  4. Zhao X, Ma M, Liu Y, Ma Y, Li R, Wang Y. Development and validation of a predictive model for cervical insufficiency incorporating AMH and androstenedione. . 2025. PMID 41387944 · DOI · PMC12808648
  5. van der Geize R, Dijkhuizen L. Harnessing the catabolic diversity of rhodococci for environmental and biotechnological applications. Curr Opin Microbiol. 2004. PMID 15196492 · DOI
  6. Malaviya A, Gomes J. Androstenedione production by biotransformation of phytosterols. Bioresour Technol. 2008. PMID 18329874 · DOI
  7. Lizneva D, Lizneva D, Gavrilova-Jordan L, Walker W, Azziz R. Androgen excess: Investigations and management. Best Pract Res Clin Obstet Gynaecol. 2016. PMID 27387253 · DOI
  8. Swart AC, Storbeck KH. 11β-Hydroxyandrostenedione: Downstream metabolism by 11βHSD, 17βHSD and SRD5A produces novel substrates in familiar pathways. Mol Cell Endocrinol. 2015. PMID 25542845 · DOI
  9. Dowsett M, Stein RC, Coombes RC. Aromatization inhibition alone or in combination with GnRH agonists for the treatment of premenopausal breast cancer patients. J Steroid Biochem Mol Biol. 1992. PMID 1388047 · DOI
  10. Lombardi P. Exemestane, a new steroidal aromatase inhibitor of clinical relevance. Biochim Biophys Acta. 2002. PMID 12084475 · DOI

About this article

Sources
NLM Medical Subject Headings (definition, synonyms); NCBI PubMed (counts, identifiers); Europe PMC (open-access abstracts and citation counts).
Verification
Every reference was resolved against PubMed on 2026-10-31; title, year and DOI matched.
Review state
automated source verified; no human expert review has been recorded yet.
Version
1, last updated 2026-10-31.

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At a glance

7,318
PubMed records on this heading
6%
published since 2020
254
review articles
212
randomized trials
10
verified references below

Counts come from PubMed on 2026-10-31; they show how much has been written, not how strong the evidence is.

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