A partitioned 88-loci psoriasis genetic risk score reveals HLA and non-HLA contributions to clinical phenotypes in a Newfoundland psoriasis cohort

Psoriasis is an immune-mediated inflammatory skin disease typically characterized by erythematous and scaly plaques. It affects 3% of the Newfoundland population while only affecting 1.7% of the general Canadian population. Recent genome-wide association studies (GWAS) in psoriasis have identified m...

Full description

Bibliographic Details
Published in:Frontiers in Genetics
Main Authors: Bui, Audrey, Kumar, Sugandh, Liu, Jared, Orcales, Faye, Gulliver, Susanne, Tsoi, Lam C., Gulliver, Wayne, Liao, Wilson
Format: Article in Journal/Newspaper
Language:unknown
Published: Frontiers Media SA 2023
Subjects:
Online Access:http://dx.doi.org/10.3389/fgene.2023.1141010
https://www.frontiersin.org/articles/10.3389/fgene.2023.1141010/full
id crfrontiers:10.3389/fgene.2023.1141010
record_format openpolar
spelling crfrontiers:10.3389/fgene.2023.1141010 2024-05-19T07:44:14+00:00 A partitioned 88-loci psoriasis genetic risk score reveals HLA and non-HLA contributions to clinical phenotypes in a Newfoundland psoriasis cohort Bui, Audrey Kumar, Sugandh Liu, Jared Orcales, Faye Gulliver, Susanne Tsoi, Lam C. Gulliver, Wayne Liao, Wilson 2023 http://dx.doi.org/10.3389/fgene.2023.1141010 https://www.frontiersin.org/articles/10.3389/fgene.2023.1141010/full unknown Frontiers Media SA https://creativecommons.org/licenses/by/4.0/ Frontiers in Genetics volume 14 ISSN 1664-8021 journal-article 2023 crfrontiers https://doi.org/10.3389/fgene.2023.1141010 2024-04-24T07:11:45Z Psoriasis is an immune-mediated inflammatory skin disease typically characterized by erythematous and scaly plaques. It affects 3% of the Newfoundland population while only affecting 1.7% of the general Canadian population. Recent genome-wide association studies (GWAS) in psoriasis have identified more than 63 genetic susceptibility loci that individually have modest effects. Prior studies have shown that a genetic risk score (GRS) combining multiple loci can improve psoriasis disease prediction. However, these prior GRS studies have not fully explored the association of GRS with patient clinical characteristics. In this study, we calculated three types of GRS: one using all known GWAS SNPs (GRS-ALL), one using a subset of SNPs from the HLA region (GRS-HLA), and the last using non-HLA SNPs (GRS-noHLA). We examined the relationship between these GRS and a number of psoriasis features within a well characterized Newfoundland psoriasis cohort. We found that both GRS-ALL and GRS-HLA were significantly associated with early age of psoriasis onset, psoriasis severity, first presentation of psoriasis at the elbow or knee, and the total number of body locations affected, while only GRS-ALL was associated with a positive family history of psoriasis. GRS-noHLA was uniquely associated with genital psoriasis. These findings clarify the relationship of the HLA and non-HLA components of GRS with important clinical features of psoriasis. Article in Journal/Newspaper Newfoundland Frontiers (Publisher) Frontiers in Genetics 14
institution Open Polar
collection Frontiers (Publisher)
op_collection_id crfrontiers
language unknown
description Psoriasis is an immune-mediated inflammatory skin disease typically characterized by erythematous and scaly plaques. It affects 3% of the Newfoundland population while only affecting 1.7% of the general Canadian population. Recent genome-wide association studies (GWAS) in psoriasis have identified more than 63 genetic susceptibility loci that individually have modest effects. Prior studies have shown that a genetic risk score (GRS) combining multiple loci can improve psoriasis disease prediction. However, these prior GRS studies have not fully explored the association of GRS with patient clinical characteristics. In this study, we calculated three types of GRS: one using all known GWAS SNPs (GRS-ALL), one using a subset of SNPs from the HLA region (GRS-HLA), and the last using non-HLA SNPs (GRS-noHLA). We examined the relationship between these GRS and a number of psoriasis features within a well characterized Newfoundland psoriasis cohort. We found that both GRS-ALL and GRS-HLA were significantly associated with early age of psoriasis onset, psoriasis severity, first presentation of psoriasis at the elbow or knee, and the total number of body locations affected, while only GRS-ALL was associated with a positive family history of psoriasis. GRS-noHLA was uniquely associated with genital psoriasis. These findings clarify the relationship of the HLA and non-HLA components of GRS with important clinical features of psoriasis.
format Article in Journal/Newspaper
author Bui, Audrey
Kumar, Sugandh
Liu, Jared
Orcales, Faye
Gulliver, Susanne
Tsoi, Lam C.
Gulliver, Wayne
Liao, Wilson
spellingShingle Bui, Audrey
Kumar, Sugandh
Liu, Jared
Orcales, Faye
Gulliver, Susanne
Tsoi, Lam C.
Gulliver, Wayne
Liao, Wilson
A partitioned 88-loci psoriasis genetic risk score reveals HLA and non-HLA contributions to clinical phenotypes in a Newfoundland psoriasis cohort
author_facet Bui, Audrey
Kumar, Sugandh
Liu, Jared
Orcales, Faye
Gulliver, Susanne
Tsoi, Lam C.
Gulliver, Wayne
Liao, Wilson
author_sort Bui, Audrey
title A partitioned 88-loci psoriasis genetic risk score reveals HLA and non-HLA contributions to clinical phenotypes in a Newfoundland psoriasis cohort
title_short A partitioned 88-loci psoriasis genetic risk score reveals HLA and non-HLA contributions to clinical phenotypes in a Newfoundland psoriasis cohort
title_full A partitioned 88-loci psoriasis genetic risk score reveals HLA and non-HLA contributions to clinical phenotypes in a Newfoundland psoriasis cohort
title_fullStr A partitioned 88-loci psoriasis genetic risk score reveals HLA and non-HLA contributions to clinical phenotypes in a Newfoundland psoriasis cohort
title_full_unstemmed A partitioned 88-loci psoriasis genetic risk score reveals HLA and non-HLA contributions to clinical phenotypes in a Newfoundland psoriasis cohort
title_sort partitioned 88-loci psoriasis genetic risk score reveals hla and non-hla contributions to clinical phenotypes in a newfoundland psoriasis cohort
publisher Frontiers Media SA
publishDate 2023
url http://dx.doi.org/10.3389/fgene.2023.1141010
https://www.frontiersin.org/articles/10.3389/fgene.2023.1141010/full
genre Newfoundland
genre_facet Newfoundland
op_source Frontiers in Genetics
volume 14
ISSN 1664-8021
op_rights https://creativecommons.org/licenses/by/4.0/
op_doi https://doi.org/10.3389/fgene.2023.1141010
container_title Frontiers in Genetics
container_volume 14
_version_ 1799483991722557440