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Introduction <p>Alopecia areata (AA) is an immune-mediated inflammatory skin disease that targets hair follicles. Current research yields varied lists of differentially expressed genes (DEGs). A meta-analytic approach is essential to consolidate these findings into a consistent tissue signature. This study aimed to perform a meta-analysis of gene expression datasets to establish a comprehensive molecular signature of AA lesional scalp.</p> Methods <p>We conducted a meta-analysis of transcriptomic data from human studies on lesional skin gene expression in AA. Reanalyzing 132 samples (82 patients with AA and 50 controls) from five Gene Expression Omnibus (GEO) datasets (GSE68801, GSE45512, GSE80342, GSE58573, GSE74761), we employed an effect size approach within a random-effects model to identify unique and shared DEGs and enriched biological pathways. The protocol is registered in PROSPERO (CRD42024559847).</p> Results <p>The meta-analysis identified 5109 DEGs, with 2710 upregulated and 2399 downregulated genes, significantly more than the 120 DEGs shared across the five studies. Consistently expressed genes included <i>CXCL9</i>, <i>CCL18</i>, <i>CXCL10</i>, <i>CD8A</i>, and <i>GZMB</i> (FDR &lt; 0.05). The analysis highlighted chemokines/receptors (<i>CCL13</i>, <i>CCR1</i>, <i>XCL1</i>) and markers of cytotoxic T&#xa0;lymphocytes (<i>GZMA</i>, <i>GZMH</i>, <i>GZMK</i>) and NK cells (<i>NKG2A</i>, <i>NKG2D</i>). Downregulated genes involved type&#xa0;I (<i>KRT31–35</i>, <i>KRT38</i>) and type&#xa0;II (<i>KRT81-86</i>) keratins and proteins crucial for hair follicle structure and function (<i>PADI3</i>, <i>GPRC5D</i>, <i>DSG4</i>, <i>FGF18</i>). Functional analysis showed enrichment in Th1, Th2, and Th17 pathways, particularly through JAK-STAT signaling (<i>p</i> &lt; 0.01).</p> Conclusion <p>This core transcriptome of AA lesions provides new insights into the disease’s pathogenesis and identifies potential targets for treatment.</p>

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Meta-Analysis of Gene Expression Reveals the Core Transcriptomic Profile of Lesional Scalp in Alopecia Areata

  • 期刊论文

  • 出版模式：

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  • 发表日期：

    2025年8月1日

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  • Irene Rivera-Ruiz,
  • Jesús Gay-Mimbrera,
  • Pedro J. Gómez-Arias,
  • Macarena Aguilar-Luque,
  • Miguel Juan-Cencerrado,
  • Carmen Mochón-Jiménez,
  • Esmeralda Parra-Peralbo,
  • Beatriz Isla-Tejera,
  • Francisco Gómez-García,
  • Juan Ruano

摘要

Introduction

Alopecia areata (AA) is an immune-mediated inflammatory skin disease that targets hair follicles. Current research yields varied lists of differentially expressed genes (DEGs). A meta-analytic approach is essential to consolidate these findings into a consistent tissue signature. This study aimed to perform a meta-analysis of gene expression datasets to establish a comprehensive molecular signature of AA lesional scalp.

Methods

We conducted a meta-analysis of transcriptomic data from human studies on lesional skin gene expression in AA. Reanalyzing 132 samples (82 patients with AA and 50 controls) from five Gene Expression Omnibus (GEO) datasets (GSE68801, GSE45512, GSE80342, GSE58573, GSE74761), we employed an effect size approach within a random-effects model to identify unique and shared DEGs and enriched biological pathways. The protocol is registered in PROSPERO (CRD42024559847).

Results

The meta-analysis identified 5109 DEGs, with 2710 upregulated and 2399 downregulated genes, significantly more than the 120 DEGs shared across the five studies. Consistently expressed genes included CXCL9, CCL18, CXCL10, CD8A, and GZMB (FDR < 0.05). The analysis highlighted chemokines/receptors (CCL13, CCR1, XCL1) and markers of cytotoxic T lymphocytes (GZMA, GZMH, GZMK) and NK cells (NKG2A, NKG2D). Downregulated genes involved type I (KRT31–35, KRT38) and type II (KRT81-86) keratins and proteins crucial for hair follicle structure and function (PADI3, GPRC5D, DSG4, FGF18). Functional analysis showed enrichment in Th1, Th2, and Th17 pathways, particularly through JAK-STAT signaling (p < 0.01).

Conclusion

This core transcriptome of AA lesions provides new insights into the disease’s pathogenesis and identifies potential targets for treatment.