Whole exome sequencing in Alopecia Areata identifies rare variants in KRT82

Stephanie O. Erjavec, Sahar Gelfman, Alexa R. Abdelaziz, Eunice Y. Lee, Isha Monga, Anna Alkelai, Iuliana Ionita-Laza, Lynn Petukhova and Angela M. Christiano ()
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Stephanie O. Erjavec: Columbia University
Sahar Gelfman: Columbia University Irving Medical Center
Alexa R. Abdelaziz: Columbia University
Eunice Y. Lee: Columbia University
Isha Monga: Columbia University
Anna Alkelai: Columbia University Irving Medical Center
Iuliana Ionita-Laza: Columbia University
Lynn Petukhova: Columbia University
Angela M. Christiano: Columbia University

Nature Communications, 2022, vol. 13, issue 1, 1-13

Abstract: Abstract Alopecia areata is a complex genetic disease that results in hair loss due to the autoimmune-mediated attack of the hair follicle. We previously defined a role for both rare and common variants in our earlier GWAS and linkage studies. Here, we identify rare variants contributing to Alopecia Areata using a whole exome sequencing and gene-level burden analyses approach on 849 Alopecia Areata patients compared to 15,640 controls. KRT82 is identified as an Alopecia Areata risk gene with rare damaging variants in 51 heterozygous Alopecia Areata individuals (6.01%), achieving genome-wide significance (p = 2.18E−07). KRT82 encodes a hair-specific type II keratin that is exclusively expressed in the hair shaft cuticle during anagen phase, and its expression is decreased in Alopecia Areata patient skin and hair follicles. Finally, we find that cases with an identified damaging KRT82 variant and reduced KRT82 expression have elevated perifollicular CD8 infiltrates. In this work, we utilize whole exome sequencing to successfully identify a significant Alopecia Areata disease-relevant gene, KRT82, and reveal a proposed mechanism for rare variant predisposition leading to disrupted hair shaft integrity.

Date: 2022
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DOI: 10.1038/s41467-022-28343-3

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