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GWAS Study

GWAS identifies novel SLE susceptibility genes and explains the association of the HLA region.

Armstrong DL, Zidovetzki R, Alarcón-Riquelme ME et al.

24871463 PubMed ID
GWAS Study Type
3163 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

AD
Armstrong DL
ZR
Zidovetzki R
AM
Alarcón-Riquelme ME
TB
Tsao BP
CL
Criswell LA
KR
Kimberly RP
HJ
Harley JB
SK
Sivils KL
VT
Vyse TJ
GP
Gaffney PM
LC
Langefeld CD
JC
Jacob CO
Chapter II

Abstract

Summary of the research findings

In a genome-wide association study (GWAS) of individuals of European ancestry afflicted with systemic lupus erythematosus (SLE) the extensive utilization of imputation, step-wise multiple regression, lasso regularization and increasing study power by utilizing false discovery rate instead of a Bonferroni multiple test correction enabled us to identify 13 novel non-human leukocyte antigen (HLA) genes and confirmed the association of four genes previously reported to be associated. Novel genes associated with SLE susceptibility included two transcription factors (EHF and MED1), two components of the NF-κB pathway (RASSF2 and RNF114), one gene involved in adhesion and endothelial migration (CNTN6) and two genes involved in antigen presentation (BIN1 and SEC61G). In addition, the strongly significant association of multiple single-nucleotide polymorphisms (SNPs) in the HLA region was assigned to HLA alleles and serotypes and deconvoluted into four primary signals. The novel SLE-associated genes point to new directions for both the diagnosis and treatment of this debilitating autoimmune disease.

725 European ancestry cases, 2,438 European ancestry controls

Chapter III

Study Statistics

Key metrics and study information

3163
Total Participants
GWAS
Study Type
No
Replicated
European
Ancestry
Chapter IV

AI-Generated Summary

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