# Shorter Anogenital Distance in Women with Adenomyosis Diagnosed by MUSA 2022 Criteria: A Prospective Case–Control Study

**Authors:** Berivan Guzelbag, Aysegul Bestel, Sevim Ezgi Katran, Betul Averbek, Hale Goksever Celik

PMC · DOI: 10.3390/jcm15041319 · Journal of Clinical Medicine · 2026-02-07

## TL;DR

This study found that women with adenomyosis have a shorter anogenital distance, suggesting a possible link to prenatal hormonal exposure.

## Contribution

The study introduces AGD-af as a potential non-invasive biomarker for adenomyosis.

## Key findings

- Women with adenomyosis had significantly shorter AGD-af compared to controls.
- AGD-af remained independently associated with adenomyosis after adjusting for age and BMI.
- AGD-af showed fair diagnostic accuracy with an AUC of 0.658.

## Abstract

Objective: The objective was to investigate the association between anogenital distance (AGD) and adenomyosis in reproductive-age women and to evaluate the potential of AGD as a non-invasive biomarker reflecting prenatal hormonal environment. Methods: This prospective case–control study included 40 women with adenomyosis diagnosed according to the Morphological Uterus Sonographic Assessment (MUSA) 2022 criteria and 40 age-matched healthy controls. Two AGD measurements were obtained: AGD-af (anus to posterior fourchette) and AGD-act (anus to clitoral tip). Measurements were performed by two independent observers using vernier calipers. Hormonal parameters, reliability analyses, receiver operating characteristic (ROC) curve analysis, and logistic regression were conducted. Results: Women with adenomyosis had significantly shorter AGD-af compared to controls (23.78 ± 7.20 vs. 27.88 ± 7.50 mm, p = 0.015), whereas AGD-act did not differ significantly (p = 0.574). Inter- and intra-observer reliability was excellent (intraclass correlation coefficient [ICC] = 0.87–0.93). ROC analysis revealed an area under the curve (AUC) of 0.658 (95% confidence interval [CI]: 0.55–0.76) for AGD-af (optimal cut-off = 24 mm; sensitivity: 57.5%, specificity: 67.5%). In multivariate logistic regression, AGD-af remained independently associated with adenomyosis after adjusting for age and body mass index (BMI) (adjusted odds ratio [OR] = 0.925, 95% CI = 0.866–0.989, p = 0.022). No significant difference was observed in hormonal parameters between groups. Conclusions: Women with adenomyosis exhibit a modest but significant reduction in AGD-af, suggesting a possible influence of prenatal hormonal environment in disease pathogenesis. Although its diagnostic accuracy is fair, AGD-af may serve as a complementary, non-invasive biomarker in clinical assessment of adenomyosis.

## Linked entities

- **Diseases:** adenomyosis (MONDO:0010888)

## Full-text entities

- **Genes:** SHBG (sex hormone binding globulin) [NCBI Gene 6462] {aka ABP, SBP, TEBG}, CYP19A1 (cytochrome P450 family 19 subfamily A member 1) [NCBI Gene 1588] {aka ARO, ARO1, CPV1, CYAR, CYP19, CYPXIX}, PRL (prolactin) [NCBI Gene 5617] {aka GHA1, pPRL}, AMH (anti-Mullerian hormone) [NCBI Gene 268] {aka MIF, MIS}
- **Diseases:** congenital adrenal hyperplasia (MESH:D000312), hypospadias (MESH:D007021), progesterone (MESH:C564871), diabetes mellitus (MESH:D003920), oncological (MESH:D000072716), impaired fertility (MESH:D007246), reproductive disorders (MESH:D060737), cryptorchidism (MESH:D003456), myometrial cysts (MESH:D003560), pelvic organ prolapse (MESH:D056887), uterine leiomyomas (OMIM:150699), androgen excess (MESH:D014770), miscarriage (MESH:D000022), gynecological disorders (MESH:D005831), bleeding (MESH:D006470), AGD (MESH:C567475), injury to (MESH:D014947), Adenomyosis (MESH:D062788), thyroid disorders (MESH:D013959), Endometriosis (MESH:D004715), dysmenorrhea (MESH:D004412), hyperprolactinemia (MESH:D006966), pelvic pain (MESH:D017699), PCOS (MESH:D011085)
- **Chemicals:** androstenedione (MESH:D000735), alcohol (MESH:D000438), progesterone (MESH:D011374), DHEAS (MESH:D019314), hormonal contraceptives (-), bisphenol A (MESH:C006780), diethylstilbestrol (MESH:D004054), testosterone (MESH:D013739), 17-OHP (MESH:D019326)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

47 references — full list in the complete paper: https://tomesphere.com/paper/PMC12941305/full.md

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Source: https://tomesphere.com/paper/PMC12941305