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Integration of GWAS, QTLs and keratinocyte functional assays reveals molecular mechanisms of atopic dermatitis

Author

Listed:
  • Meritxell Oliva

    (AbbVie Inc.)

  • Mrinal K. Sarkar

    (University of Michigan)

  • Michael E. March

    (Children’s Hospital of Philadelphia)

  • Amir Hossein Saeidian

    (Children’s Hospital of Philadelphia)

  • Frank D. Mentch

    (Children’s Hospital of Philadelphia)

  • Chen-Lin Hsieh

    (AbbVie Inc.)

  • Fanying Tang

    (AbbVie Inc.)

  • Ranjitha Uppala

    (University of Michigan)

  • Matthew T. Patrick

    (University of Michigan)

  • Qinmengge Li

    (University of Michigan)

  • Rachael Bogle

    (University of Michigan)

  • J. Michelle Kahlenberg

    (University of Michigan)

  • Deborah Watson

    (Children’s Hospital of Philadelphia)

  • Joseph T. Glessner

    (Children’s Hospital of Philadelphia)

  • Leila Youssefian

    (Children’s Hospital of Philadelphia
    City of Hope National Medical Center)

  • Hassan Vahidnezhad

    (Children’s Hospital of Philadelphia
    Perelman School of Medicine)

  • Lam C. Tsoi

    (University of Michigan)

  • Hakon Hakonarson

    (Children’s Hospital of Philadelphia)

  • Johann E. Gudjonsson

    (University of Michigan)

  • Kathleen M. Smith

    (AbbVie Inc.)

  • Bridget Riley-Gillis

    (AbbVie Inc.)

Abstract

Atopic dermatitis is a highly heritable and common inflammatory skin condition affecting children and adults worldwide. Multi-ancestry approaches to atopic dermatitis genetic association studies are poised to boost power to detect genetic signal and identify loci contributing to atopic dermatitis risk. Here, we present a multi-ancestry GWAS meta-analysis of twelve atopic dermatitis cohorts from five ancestral populations totaling 56,146 cases and 602,280 controls. We report 101 genomic loci associated with atopic dermatitis, including 16 loci that have not been previously associated with atopic dermatitis or eczema. Fine-mapping, QTL colocalization, and cell-type enrichment analyses identified genes and cell types implicated in atopic dermatitis pathophysiology. Functional analyses in keratinocytes provide evidence for genes that could play a role in atopic dermatitis through epidermal barrier function. Our study provides insights into the etiology of atopic dermatitis by harnessing multiple genetic and functional approaches to unveil the mechanisms by which atopic dermatitis-associated variants impact genes and cell types.

Suggested Citation

  • Meritxell Oliva & Mrinal K. Sarkar & Michael E. March & Amir Hossein Saeidian & Frank D. Mentch & Chen-Lin Hsieh & Fanying Tang & Ranjitha Uppala & Matthew T. Patrick & Qinmengge Li & Rachael Bogle & , 2025. "Integration of GWAS, QTLs and keratinocyte functional assays reveals molecular mechanisms of atopic dermatitis," Nature Communications, Nature, vol. 16(1), pages 1-17, December.
  • Handle: RePEc:nat:natcom:v:16:y:2025:i:1:d:10.1038_s41467-025-58310-7
    DOI: 10.1038/s41467-025-58310-7
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    1. Aigar Ottas & Dmytro Fishman & Tiia-Linda Okas & Tõnu Püssa & Peeter Toomik & Aare Märtson & Külli Kingo & Ursel Soomets, 2017. "Blood serum metabolome of atopic dermatitis: Altered energy cycle and the markers of systemic inflammation," PLOS ONE, Public Library of Science, vol. 12(11), pages 1-14, November.
    2. Clare Bycroft & Colin Freeman & Desislava Petkova & Gavin Band & Lloyd T. Elliott & Kevin Sharp & Allan Motyer & Damjan Vukcevic & Olivier Delaneau & Jared O’Connell & Adrian Cortes & Samantha Welsh &, 2018. "The UK Biobank resource with deep phenotyping and genomic data," Nature, Nature, vol. 562(7726), pages 203-209, October.
    3. Benjamin B. Sun & Joseph C. Maranville & James E. Peters & David Stacey & James R. Staley & James Blackshaw & Stephen Burgess & Tao Jiang & Ellie Paige & Praveen Surendran & Clare Oliver-Williams & Mi, 2018. "Genomic atlas of the human plasma proteome," Nature, Nature, vol. 558(7708), pages 73-79, June.
    4. Yi Han & Qiong Jia & Pedram Shafiei Jahani & Benjamin P. Hurrell & Calvin Pan & Pin Huang & Janet Gukasyan & Nicholas C. Woodward & Eleazar Eskin & Frank D. Gilliland & Omid Akbari & Jaana A. Hartiala, 2020. "Genome-wide analysis highlights contribution of immune system pathways to the genetic architecture of asthma," Nature Communications, Nature, vol. 11(1), pages 1-13, December.
    5. Ashley Budu-Aggrey & Anna Kilanowski & Maria K. Sobczyk & Suyash S. Shringarpure & Ruth Mitchell & Kadri Reis & Anu Reigo & Reedik Mägi & Mari Nelis & Nao Tanaka & Ben M. Brumpton & Laurent F. Thomas , 2023. "European and multi-ancestry genome-wide association meta-analysis of atopic dermatitis highlights importance of systemic immune regulation," Nature Communications, Nature, vol. 14(1), pages 1-18, December.
    6. Tune H. Pers & Juha M. Karjalainen & Yingleong Chan & Harm-Jan Westra & Andrew R. Wood & Jian Yang & Julian C. Lui & Sailaja Vedantam & Stefan Gustafsson & Tonu Esko & Tim Frayling & Elizabeth K. Spel, 2015. "Biological interpretation of genome-wide association studies using predicted gene functions," Nature Communications, Nature, vol. 6(1), pages 1-9, May.
    7. Daniel Taliun & Daniel N. Harris & Michael D. Kessler & Jedidiah Carlson & Zachary A. Szpiech & Raul Torres & Sarah A. Gagliano Taliun & André Corvelo & Stephanie M. Gogarten & Hyun Min Kang & Achille, 2021. "Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program," Nature, Nature, vol. 590(7845), pages 290-299, February.
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