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GWAS Study

Immunochip identifies novel, and replicates known, genetic risk loci for rheumatoid arthritis in black South Africans.

Govind N, Choudhury A, Hodkinson B et al.

25014791 PubMed ID
GWAS Study Type
637 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

GN
Govind N
CA
Choudhury A
HB
Hodkinson B
IC
Ickinger C
FJ
Frost J
LA
Lee A
GP
Gregersen PK
RR
Reynolds RJ
BS
Bridges SL
HS
Hazelhurst S
RM
Ramsay M
TM
Tikly M
Chapter II

Abstract

Summary of the research findings

The aim of this study was to identify genetic variants associated with rheumatoid arthritis (RA) risk in black South Africans. Black South African RA patients (n = 263) were compared with healthy controls (n = 374). Genotyping was performed using the Immunochip, and four-digit high-resolution human leukocyte antigen (HLA) typing was performed by DNA sequencing of exon 2. Standard quality control measures were implemented on the data. The strongest associations were in the intergenic region between the HLA-DRB1 and HLA-DQA1 loci. After conditioning on HLA-DRB1 alleles, the effect in the rest of the extended major histocompatibility (MHC) diminished. Non-HLA single nucleotide polymorphisms (SNPs) in the intergenic regions LOC389203|RBPJ, LOC100131131|IL1R1, KIAA1919|REV3L, LOC643749|TRAF3IP2, and SNPs in the intron and untranslated regions (UTR) of IRF1 and the intronic region of ICOS and KIAA1542 showed association with RA (p < 5 × 10(-5)). Of the SNPs previously associated with RA in Caucasians, one SNP, rs874040, locating to the intergenic region LOC389203|RBPJ was replicated in this study. None of the variants in the PTPN22 gene was significantly associated. The seropositive subgroups showed similar results to the overall cohort. The effects observed across the HLA region are most likely due to HLA-DRB1, and secondary effects in the extended MHC cannot be detected. Seven non-HLA loci are associated with RA in black South Africans. Similar to Caucasians, the intergenic region between LOC38920 and RBPJ is associated with RA in this population. The strong association of the R620W variant of the PTPN22 gene with RA in Caucasians was not replicated since this variant was monomorphic in our study, but other SNP variants of the PTPN22 gene were also not associated with RA in black South Africans, suggesting that this locus does not play a major role in RA in this population.

263 South African Black cases and 374 South African Black controls

Chapter III

Study Statistics

Key metrics and study information

637
Total Participants
GWAS
Study Type
No
Replicated
Sub-Saharan African
Ancestry
South Africa
Recruitment Country
Chapter IV

Analysis

Comprehensive review of health and genetic findings

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