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GWAS Study

Meta-analysis of genome-wide association studies in celiac disease and rheumatoid arthritis identifies fourteen non-HLA shared loci.

Zhernakova A, Stahl EA, Trynka G et al.

21383967 PubMed ID
GWAS Study Type
50266 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

ZA
Zhernakova A
SE
Stahl EA
TG
Trynka G
RS
Raychaudhuri S
FE
Festen EA
FL
Franke L
WH
Westra HJ
FR
Fehrmann RS
KF
Kurreeman FA
TB
Thomson B
GN
Gupta N
RJ
Romanos J
MR
McManus R
RA
Ryan AW
TG
Turner G
BE
Brouwer E
PM
Posthumus MD
RE
Remmers EF
TF
Tucci F
TR
Toes R
GE
Grandone E
MM
Mazzilli MC
RA
Rybak A
CB
Cukrowska B
CM
Coenen MJ
RT
Radstake TR
VR
van Riel PL
LY
Li Y
DB
de Bakker PI
GP
Gregersen PK
WJ
Worthington J
SK
Siminovitch KA
KL
Klareskog L
HT
Huizinga TW
WC
Wijmenga C
PR
Plenge RM
Chapter II

Abstract

Summary of the research findings

Epidemiology and candidate gene studies indicate a shared genetic basis for celiac disease (CD) and rheumatoid arthritis (RA), but the extent of this sharing has not been systematically explored. Previous studies demonstrate that 6 of the established non-HLA CD and RA risk loci (out of 26 loci for each disease) are shared between both diseases. We hypothesized that there are additional shared risk alleles and that combining genome-wide association study (GWAS) data from each disease would increase power to identify these shared risk alleles. We performed a meta-analysis of two published GWAS on CD (4,533 cases and 10,750 controls) and RA (5,539 cases and 17,231 controls). After genotyping the top associated SNPs in 2,169 CD cases and 2,255 controls, and 2,845 RA cases and 4,944 controls, 8 additional SNPs demonstrated P<5 × 10(-8) in a combined analysis of all 50,266 samples, including four SNPs that have not been previously confirmed in either disease: rs10892279 near the DDX6 gene (P(combined) = 1.2 × 10(-12)), rs864537 near CD247 (P(combined) = 2.2 × 10(-11)), rs2298428 near UBE2L3 (P(combined) = 2.5 × 10(-10)), and rs11203203 near UBASH3A (P(combined) = 1.1 × 10(-8)). We also confirmed that 4 gene loci previously established in either CD or RA are associated with the other autoimmune disease at combined P<5 × 10(-8) (SH2B3, 8q24, STAT4, and TRAF1-C5). From the 14 shared gene loci, 7 SNPs showed a genome-wide significant effect on expression of one or more transcripts in the linkage disequilibrium (LD) block around the SNP. These associations implicate antigen presentation and T-cell activation as a shared mechanism of disease pathogenesis and underscore the utility of cross-disease meta-analysis for identification of genetic risk factors with pleiotropic effects between two clinically distinct diseases.

4,533 European ancestry celiac disease cases, 5,539 European ancestry rheumatoid arthritis cases, 27,981 European ancestry controls

Chapter III

Study Statistics

Key metrics and study information

50266
Total Participants
GWAS
Study Type
Yes
Replicated
2,169 European ancestry celiac disease cases, 2,845 European ancestry rheumatoid arthritis cases, 7,199 European ancestry controls
Replication Participants
European
Ancestry
U.K., U.S., Poland, Italy, Netherlands
Recruitment Country
Chapter IV

Analysis

Comprehensive review of health and genetic findings

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Analysis In Progress

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