# Role of insulin-regulated aminopeptidase as potential biomarker in insulin resistant polycystic ovary syndrome patients

**Authors:** Osman Köse, Koray Gök, Elif Köse, Sezen Irmak Gözükara, Abdullah Tüten, Mehmet Sühha Bostancı

PMC · DOI: 10.20945/2359-4292-2026-0011 · Archives of Endocrinology and Metabolism · 2026-02-16

## TL;DR

This study found that lower levels of insulin-regulated aminopeptidase in women with polycystic ovary syndrome may indicate insulin resistance, suggesting it could be a useful biomarker.

## Contribution

The study identifies insulin-regulated aminopeptidase as a potential biomarker for insulin resistance in polycystic ovary syndrome.

## Key findings

- Serum insulin-regulated aminopeptidase levels were significantly lower in polycystic ovary syndrome patients compared to healthy controls.
- Insulin-regulated aminopeptidase levels were even lower in insulin-resistant polycystic ovary syndrome patients.
- The levels showed a negative correlation with markers of insulin resistance like fasting blood glucose and HOMA-IR.

## Abstract

To measure serum insulin-regulated aminopeptidase levels in women diagnosed
with polycystic ovary syndrome and to investigate their potential
contribution of these levels to the development of insulin resistance, which
plays a central role in the pathophysiology of polycystic ovary
syndrome.

The study group, recruited between May and December 2021, consisted of 40
patients diagnosed with polycystic ovary syndrome and 40 age-matched healthy
controls. Serum insulin-regulated aminopeptidase levels were compared
between the groups using the ELISA method.

Serum insulin-regulated aminopeptidase levels were significantly lower in the
polycystic ovary syndrome group compared with the control group (p <
0.001). Subparameter assessments revealed that insulin-regulated
aminopeptidase levels were even lower in insulin-resistant polycystic ovary
syndrome patients (p = 0.001). Moreover, insulin-regulated aminopeptidase
levels demonstrated a statistically significant negative correlation with
fasting blood glucose, insulin, glycated hemoglobin, and HOMA-IR values.

Serum insulin-regulated aminopeptidase levels were found to be lower in women
with polycystic ovary syndrome than those in healthy controls. Furthermore,
these levels appear to reflect insulin resistance, a key factor in the
pathogenesis of polycystic ovary syndrome. Overall, these findings suggest
that insulin-regulated aminopeptidase may serve as a potential biomarker for
the identifification of insulin resistance in women with polycystic ovary
syndrome.

## Linked entities

- **Diseases:** polycystic ovary syndrome (MONDO:0008487)

## Full-text entities

- **Genes:** NLRC4 (NLR family CARD domain containing 4) [NCBI Gene 58484] {aka AIFEC, CARD12, CLAN, CLAN1, CLANA, CLANB}, PRL (prolactin) [NCBI Gene 5617] {aka GHA1, pPRL}, SLC2A4 (solute carrier family 2 member 4) [NCBI Gene 6517] {aka GLUT4}, AMH (anti-Mullerian hormone) [NCBI Gene 268] {aka MIF, MIS}, LNPEP (leucyl and cystinyl aminopeptidase) [NCBI Gene 4012] {aka CAP, IRAP, P-LAP, PLAP}, INS (insulin) [NCBI Gene 3630] {aka IDDM, IDDM1, IDDM2, ILPR, IRDN, MODY10}, HK1 (hexokinase 1) [NCBI Gene 3098] {aka CNSHA5, HK, HK1-ta, HK1-tb, HK1-tc, HKD}
- **Diseases:** heart disease (MESH:D006331), thyroid disorders (MESH:D013959), T2DM (MESH:D003924), IR (MESH:D007333), hormonal disorders (MESH:C565870), endocrine disorder (MESH:D004700), dysmenorrhea (MESH:D004412), hyperinsulinemic (MESH:D044903), PCOS (MESH:D011085), hyperandrogenism (MESH:D017588), epilepsy (MESH:D004827), anovulation (MESH:D000858), premenstrual syndrome (MESH:D011293), metabolic abnormalities (MESH:D008659), reproductive dysfunction (MESH:D060737), metabolic dysregulation (MESH:D021081), obesity (MESH:D009765), gestational diabetes (MESH:D016640), cancer (MESH:D009369), diabetic (MESH:D003920), congenital adrenal hyperplasia (MESH:D000312), renal failure (MESH:D051437), endometrioma (MESH:D004715), metabolic disturbances (MESH:D024821), inflammation (MESH:D007249), hirsutism (MESH:D006628)
- **Chemicals:** glucose (MESH:D005947), DHEA-S. (MESH:D003687), carbohydrate (MESH:D002241), PCOSInsulin (-), testosterone (MESH:D013739), DHEAS (MESH:D019314), cortisol (MESH:D006854), 17-OH progesterone (MESH:D019326)
- **Species:** Homo sapiens (human, species) [taxon 9606], Rattus norvegicus (brown rat, species) [taxon 10116]

## Full text

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## Figures

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## References

23 references — full list in the complete paper: https://tomesphere.com/paper/PMC12927181/full.md

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Source: https://tomesphere.com/paper/PMC12927181