# Differences in the Expression of Insulin‐Like Growth Factor Signaling Pathway Members in Patients With Psoriasis Vulgaris and Controls

**Authors:** Holmannova Drahomira, Borska Lenka, Fiala Zdenek, Krejsek Jan, Hamakova Kvetoslava, Cermakova Eva, Rehacek Vit, Fiala Ondrej, Maresova Tereza, Borsky Pavel

PMC · DOI: 10.1155/mi/2136373 · Mediators of Inflammation · 2026-02-02

## TL;DR

This study compares insulin-like growth factor signaling in psoriasis patients and healthy controls, finding differences that may explain metabolic comorbidities.

## Contribution

The study provides a comprehensive assessment of IGF-1 signaling pathway involvement in psoriasis and its metabolic comorbidities.

## Key findings

- Higher fasting glucose, insulin, IGFBP3, and IGFBP6 levels were found in psoriasis patients.
- Controls had higher levels of IGF-1, IGF-1R, and IGFBP4.
- The IGF-1 signaling pathway may contribute to psoriasis and related metabolic disorders.

## Abstract

Insulin‐like growth factors (IGFs) and IGF–binding proteins (IGFBPs) regulate cell proliferation, differentiation, metabolic processes, and immune activities. Psoriasis is a systemic inflammatory disease with metabolic disorders as an important comorbidity in the pathogenesis of which members of the IGF family could also play a role. Therefore, we decided to evaluate the levels of members of the IGF signaling pathway in patients with psoriasis. Sixty‐nine people were enrolled in our study: 34 patients with psoriasis and 35 controls. The following parameters were evaluated in serum obtained from peripheral blood: total cholesterol, triglycerides, high‐density lipoprotein, fasting glucose, IGF‐1, IGF‐1R, IGF‐2, IGF‐2R, IGFBP1, IGFBP2, IGFBP3, IGFBP4, IGFBP6, and insulin. The levels of several parameters differed between groups. The levels of fasting glucose, insulin, IGFBP3, and IGFBP6 were higher in patients with psoriasis, while the levels of IGF‐1, IGF‐1R, and IGBP4 were higher in controls. The results suggested that the IGF‐1 signaling pathway can be involved in the pathogenesis of psoriasis and its comorbidities, especially metabolic disorders such as insulin resistance, diabetes, and metabolic syndrome. The novelty of our study is in its comprehensive assessment of the involvement of the IGF‐1 signaling pathway in the pathogenesis of psoriasis and advances the understanding of the pathogenesis of psoriasis and its comorbidities.

## Linked entities

- **Genes:** IGF1 (insulin like growth factor 1) [NCBI Gene 3479], IGF1R (insulin like growth factor 1 receptor) [NCBI Gene 3480], IGF2 (insulin like growth factor 2) [NCBI Gene 3481], IGF2R (insulin like growth factor 2 receptor) [NCBI Gene 3482], IGFBP1 (insulin like growth factor binding protein 1) [NCBI Gene 3484], IGFBP2 (insulin like growth factor binding protein 2) [NCBI Gene 3485], IGFBP3 (insulin like growth factor binding protein 3) [NCBI Gene 3486], IGFBP4 (insulin like growth factor binding protein 4) [NCBI Gene 3487], IGFBP6 (insulin like growth factor binding protein 6) [NCBI Gene 3489]
- **Diseases:** psoriasis (MONDO:0005083), diabetes (MONDO:0005015), metabolic syndrome (MONDO:0000816)

## Full-text entities

- **Genes:** INS (insulin) [NCBI Gene 3630] {aka IDDM, IDDM1, IDDM2, ILPR, IRDN, MODY10}, IGF1 (insulin like growth factor 1) [NCBI Gene 3479] {aka IGF, IGF-I, IGFI, MGF}, IGF1R (insulin like growth factor 1 receptor) [NCBI Gene 3480] {aka CD221, IGFIR, IGFR, JTK13}, IGFBP1 (insulin like growth factor binding protein 1) [NCBI Gene 3484] {aka AFBP, IBP1, IGF-BP25, PP12, hIGFBP-1}, IGFBP6 (insulin like growth factor binding protein 6) [NCBI Gene 3489] {aka IBP6}, IGFBP4 (insulin like growth factor binding protein 4) [NCBI Gene 3487] {aka BP-4, HT29-IGFBP, IBP4, IGFBP-4}, IGFBP2 (insulin like growth factor binding protein 2) [NCBI Gene 3485] {aka IBP2, IGF-BP53}, IGF2 (insulin like growth factor 2) [NCBI Gene 3481] {aka C11orf43, GRDF, IGF-II, PP9974, SRS3}, IGFBP3 (insulin like growth factor binding protein 3) [NCBI Gene 3486] {aka BP-53, IBP-3, IBP3, IGFBP-3}, IGF2R (insulin like growth factor 2 receptor) [NCBI Gene 3482] {aka CD222, CI-M6PR, CIMPR, M6P-R, M6P/IGF2R, MPR 300}
- **Diseases:** Psoriasis (MESH:D011565), diabetes (MESH:D003920), metabolic syndrome (MESH:D024821), insulin resistance (MESH:D007333), metabolic disorders (MESH:D008659), inflammatory disease (MESH:D007249)
- **Chemicals:** triglycerides (MESH:D014280), cholesterol (MESH:D002784), glucose (MESH:D005947)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12862997/full.md

## References

96 references — full list in the complete paper: https://tomesphere.com/paper/PMC12862997/full.md

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Source: https://tomesphere.com/paper/PMC12862997