# Association of Serum IL-17A and IL-23 Levels With Alopecia Areata: A Cross-Sectional Comparative Study

**Authors:** Md. Shihab Talukder, A.T.M. Asaduzzaman, Mohammad Abul Kalam Azad, Mohammad Jamal Uddin, Pranam Swapan Dash, Wasi Deen Ahmed

PMC · DOI: 10.7759/cureus.100011 · Cureus · 2025-12-24

## TL;DR

This study found that higher levels of IL-17A and IL-23 in blood are linked to alopecia areata severity, suggesting these cytokines may be important in disease progression and diagnosis.

## Contribution

The study identifies elevated IL-17A and IL-23 as potential biomarkers for alopecia areata severity and subtype differentiation.

## Key findings

- Serum IL-17A and IL-23 levels were significantly higher in alopecia areata patients compared to healthy controls.
- IL-17A levels correlated with disease severity and varied across clinical subtypes.
- A strong positive correlation exists between IL-17A and IL-23 in patients with alopecia areata.

## Abstract

Background and objective: Alopecia areata (AA) is an autoimmune, non-scarring hair loss disorder in which T helper 17 (Th17) cells play a key role. Interleukin-23 (IL-23) promotes the differentiation and expansion of Th17 cells from naïve CD4+ T cells. This study aimed to evaluate the association between serum IL-17A and IL-23 levels and disease severity in patients with AA.

Methods: A cross-sectional comparative study was conducted at the Department of Dermatology and Venereology, Bangladesh Medical University, Dhaka, from October 2022 to September 2024. Forty-three AA patients and 43 age- and sex-matched healthy controls were enrolled. Serum IL-17A and IL-23 levels were measured using enzyme-linked immunosorbent assay (ELISA) (Elabscience, USA). Disease severity was assessed using the Severity of Alopecia Tool (SALT) score. Data were analyzed with IBM SPSS Statistics for Windows, Version 26 (released 2018; IBM Corp., Armonk, New York, United States) using chi-square, t-test, Mann-Whitney U, and Spearman’s correlation tests, with p<0.05 considered statistically significant.

Results: Serum IL-17A and IL-23 levels were significantly higher in AA patients than controls (IL-17A: 39.4 ± 38.3 vs. 13.7 ± 10.7 pg/mL; IL-23: 48.2 ± 57.0 vs. 15.5 ± 15.5 pg/mL; both p<0.001). IL-17A correlated positively with disease severity (p=0.016), increasing from 21.17 ± 33.26 pg/mL in mild cases (S1, <25% hair loss) to 63.47 ± 50.33 pg/mL in severe cases (S4, 75-99% hair loss). IL-17A levels varied across clinical subtypes (single patch: 20.70 ± 24.46 pg/mL; sisaipho: 53.37 ± 1.33 pg/mL; p=0.044). IL-23 levels remained elevated regardless of disease severity (p=0.118) or clinical subtype (p=0.378). A significant positive correlation existed between IL-17A and IL-23 (p<0.001).

Conclusions: Elevated IL-17A levels are associated with AA severity and differ across clinical subtypes, suggesting a role in disease progression and phenotype variation. IL-23 is consistently elevated in AA, highlighting its potential as a biomarker for disease activity. These findings provide insight into cytokine dysregulation in AA and may inform future therapeutic strategies.

## Linked entities

- **Proteins:** IL17A (interleukin 17A), IL37 (interleukin 37)
- **Diseases:** Alopecia Areata (MONDO:0004907)

## Full-text entities

- **Genes:** CD4 (CD4 molecule) [NCBI Gene 920] {aka CD4mut, IMD79, Leu-3, OKT4D, T4}, IL37 (interleukin 37) [NCBI Gene 27178] {aka FIL1, FIL1(ZETA), FIL1Z, IL-1F7, IL-1H, IL-1H4}, IL17A (interleukin 17A) [NCBI Gene 3605] {aka CTLA-8, CTLA8, IL-17, IL-17A, IL17, ILA17}
- **Diseases:** Alopecia (MESH:D000505), autoimmune (MESH:D001327), AA (MESH:D000506)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

25 references — full list in the complete paper: https://tomesphere.com/paper/PMC12830056/full.md

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Source: https://tomesphere.com/paper/PMC12830056