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HLA-DQ and HLA-DRB1 alleles associated with Henoch-Schönlein purpura nephritis in Finnish pediatric population: a genome-wide association study

Authors :
Koskela, Mikael
Nihtilä, Julia
Ylinen, Elisa
Kolho, Kaija-Leena
Nuutinen, Matti
Ritari, Jarmo
Jahnukainen, Timo
Source :
Pediatric Nephrology. August, 2021, Vol. 36 Issue 8, p2311, 8 p.
Publication Year :
2021

Abstract

Background The pathophysiology of Henoch-Schönlein purpura (HSP) is still unclear, but several findings suggest that genetic factors may influence disease susceptibility. We aimed to perform a genome-wide association study (GWAS) in pediatric HSP patients with an emphasis on severe HSP nephritis. Methods The study included 46 HSP patients, 42 of whom had undergone kidney biopsy. Forty-nine pediatric patients with an inflammatory bowel disease (IBD) served as an autoimmune disease control group while Finnish bone marrow and blood donors represented the general reference population (n = 18,757). GWAS was performed for HSP and IBD samples in a case-control manner against the reference population. The analysis also included imputation of human leukocyte antigen (HLA) alleles. Results GWAS analysis in HSP revealed several polymorphisms from the HLA region that surpassed the genome-wide significance level. Three HLA class II alleles were also significantly more frequent in HSP than in the reference population: DQA1*01:01, DQB1*05:01, and DRB1*01:01. Haplotype DQA1*01:01/DQB1*05:01/DRB1*01:01 occurred in 43.5% of HSP patients, whereas its frequency was 8.2% in IBD patients and 15.0% in the reference population. HSP patients with this haplotype showed similar baseline clinical findings and outcome as HSP patients negative for the haplotype. In IBD patients, no polymorphism or HLA allele appeared significant at the genome-wide level. Conclusions Our results suggest that haplotype DQA1*01:01/DQB1*05:01/DRB1*01:01 is associated with susceptibility to HSP, but not with the severity of the kidney involvement. These HLA associations did not occur in IBD patients, suggesting that they are specific to HSP and not related to susceptibility to autoimmune diseases in general. Graphical abstract<br />Author(s): Mikael Koskela [sup.1] [sup.2] , Julia Nihtilä [sup.3] [sup.4] , Elisa Ylinen [sup.2] , Kaija-Leena Kolho [sup.1] [sup.5] , Matti Nuutinen [sup.6] [sup.7] , Jarmo Ritari [sup.4] , Timo [...]

Details

Language :
English
ISSN :
0931041X
Volume :
36
Issue :
8
Database :
Gale General OneFile
Journal :
Pediatric Nephrology
Publication Type :
Academic Journal
Accession number :
edsgcl.667704976
Full Text :
https://doi.org/10.1007/s00467-021-04955-7