# Serum Chemerin Levels in Polish Women with PCOS-Phenotype D

**Authors:** Justyna Kuliczkowska-Płaksej, Jowita Halupczok-Żyła, Łukasz Gojny, Agnieszka Zembska, Aneta Zimoch, Monika Skrzypiec-Spring, Marek Bolanowski, Aleksandra Jawiarczyk-Przybyłowska

PMC · DOI: 10.3390/jcm15020772 · Journal of Clinical Medicine · 2026-01-17

## TL;DR

This study found that chemerin levels in women with a specific type of PCOS are linked to metabolic and inflammatory factors, but not to hyperandrogenism.

## Contribution

The study is the first to investigate chemerin levels in normoandrogenic PCOS and their relationship with metabolic and inflammatory markers.

## Key findings

- Serum chemerin levels did not differ significantly between PCOS and control groups.
- Chemerin correlated with metabolic and inflammatory markers in both groups.
- Chemerin was weakly associated with androgen-related parameters in PCOS patients.

## Abstract

Objectives: Polycystic ovary syndrome (PCOS) is a heterogeneous disorder with diverse pathogenetic mechanisms and clinical manifestations. Phenotype D PCOS is characterized by oligomenorrhoea and polycystic ovaries without hyperandrogenism. Altered adipokine profiles may contribute to reproductive and metabolic disturbances. Chemerin is an adipokine involved in inflammatory and metabolic processes. It remains unclear whether altered chemerin levels in PCOS reflect metabolic dysfunction alone or are directly associated with hyperandrogenism. The aim of this study was to compare serum chemerin levels in women with normoandrogenic PCOS and a control group. Methods: This cross-sectional preliminary study included 49 women with phenotype D PCOS and 40 healthy, age- and body mass index (BMI)-matched controls. Anthropometric, biochemical, hormonal parameters, and serum chemerin concentrations were assessed. Results: Serum chemerin concentrations did not differ significantly between the groups. In the PCOS group, the 95% confidence interval ranged from 198.61 to 234.37, while in the controls, it ranged from 187.13 to 216.21. In women with PCOS, chemerin showed significant positive correlations with weight, BMI, waist and hip circumference, total adipose tissue, and both gynoid and android fat content. Positive correlations were also observed with highly sensitive C-reactive protein (hs-CRP), insulin, glucose, triglycerides, and Homeostasis Model Assessment of Insulin Resistance (HOMA-IR), and a negative correlation was found with high-density lipoprotein (HDL) cholesterol. Chemerin was weakly negatively correlated with sex hormone binding globulin (SHBG) and positively correlated with the free androgen index (FAI). In the control group, chemerin correlated positively with CRP, insulin, triglycerides, total and gynoid adipose tissue, and negatively correlated with HDL cholesterol and SHBG. Conclusions Although chemerin levels did not differ from controls, chemerin was associated with metabolic and inflammatory markers in both groups. These findings should be considered preliminary due to the limited sample size. Chemerin may reflect metabolic and inflammatory status rather than hyperandrogenism in normoandrogenic PCOS.

## Linked entities

- **Proteins:** RARRES2 (retinoic acid receptor responder (tazarotene induced) 2)
- **Diseases:** Polycystic ovary syndrome (MONDO:0008487), PCOS (MONDO:0008487)

## Full-text entities

- **Genes:** RARRES2 (retinoic acid receptor responder 2) [NCBI Gene 5919] {aka HP10433, TIG2}, SHBG (sex hormone binding globulin) [NCBI Gene 6462] {aka ABP, SBP, TEBG}, CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}, INS (insulin) [NCBI Gene 3630] {aka IDDM, IDDM1, IDDM2, ILPR, IRDN, MODY10}
- **Diseases:** PCOS (MESH:D011085), metabolic disturbances (MESH:D024821), Insulin Resistance (MESH:D007333), hyperandrogenism (MESH:D017588), metabolic dysfunction (MESH:D008659), inflammatory (MESH:D007249)
- **Chemicals:** glucose (MESH:D005947), free androgen (-), triglycerides (MESH:D014280)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12842525/full.md

## References

76 references — full list in the complete paper: https://tomesphere.com/paper/PMC12842525/full.md

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Source: https://tomesphere.com/paper/PMC12842525