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September 18, 2025International Journal of Molecular Sciences2 citationsOpen Access

Shared Genetic Architecture Between Atopic Dermatitis and Autoimmune Diseases

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PLPanagiotis LazanasCACharalabos AntonatosKTKonstantina T. Tsoumani

Key Points

  • Independent pleiotropic loci shared among atopic dermatitis and autoimmune diseases numbered 113, indicating significant genetic overlap.
  • Among the loci, 11 showed concordant effects across all three autoimmune diseases analyzed, highlighting shared genetic pathways.
  • Gene-set enrichment analyses supported inflammatory links between pleiotropic associations, underscoring the inflammatory nature of these conditions.
  • Mendelian randomization indicated that genetic liability to inflammatory bowel disease increased atopic dermatitis risk, while vitiligo offered a protective effect.

Abstract

Atopic dermatitis (AD) and autoimmune diseases exhibit epidemiological comorbidity, yet the shared genetic architecture remains incompletely understood. We investigated the genetic overlap between AD and three autoimmune disorders including inflammatory bowel disease (IBD), rheumatoid arthritis (RA), and vitiligo, leveraging genome-wide association data. Despite modest evidence for global genetic correlations, we found 113 independent pleiotropic loci shared among AD and autoimmune diseases, with 11 displaying a concordant effect across all 3 pairwise comparisons. Gene-set and tissue enrichment analyses evidenced the inflammatory background of pleiotropic associations. Multi-trait colocalization analysis prioritized 22 loci, linking the tissue-specific expression of DOK2, GPR132, RERE, RERE-AS1, SUOX, TNFRSF11A, and TRAF1 pleiotropic genes with AD risk. Mendelian randomization revealed no causal effect of genetic liability to AD on autoimmune diseases. Nevertheless, genetic liability to IBD increased AD risk, while vitiligo exhibited a protective effect post outlier correction. Our findings provide mechanistic insights into the multimorbidity of atopic dermatitis (AD) and autoimmune diseases, offering additional evidence for the pleiotropic genetic architecture of AD that contributes to systemic immune dysregulation across multiple organ systems.

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Cite This Study

Lazanas et al. (2025) studied this question.

synapsesocial.com/papers/68d463e231b076d99fa631b6https://doi.org/10.3390/ijms26189124
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