Evidence map›Paper›PMID 20169177›Full record

ArticlePLoS genetics2010

Genome-wide association study in Asian populations identifies variants in ETS1 and WDFY4 associated with systemic lupus erythematosus.

Wanling Yang, Nan Shen, Dong-Qing Ye, Qiji Liu, Yan Zhang, Xiao-Xia Qian, Nattiya Hirankarn, Dingge Ying, Hai-Feng Pan, Chi Chiu Mok and 22 more

Abstract read
In one paragraph

Article in PLoS genetics, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 213 papers, 23 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
213citing papers in PubMed, 23 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

213 citing papers in PubMed, 23 syntheses or guidelines pooled it.

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153 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

32 authors.

Wanling YangDepartment of Paediatrics and Adolescent Medicine, LKS Faculty of Medicine, The University of Hong Kong, Pokfulam, Hong Kong.
Nan Shen
Dong-Qing Ye
Qiji Liu
Yan Zhang
Xiao-Xia Qian
Nattiya Hirankarn
Dingge Ying
Hai-Feng Pan
Chi Chiu Mok
Tak Mao Chan
Raymond Woon Sing Wong
Ka Wing Lee
Mo Yin Mok
Sik Nin Wong
Alexander Moon Ho Leung
Xiang-Pei Li
Yingyos Avihingsanon
Chun-Ming Wong
Tsz Leung Lee
Marco Hok Kung Ho
Pamela Pui Wah Lee
Yuk Kwan Chang
Philip H Li
Ruo-Jie Li
Lu Zhang
Wilfred Hing Sang Wong
Irene Oi Lin Ng
Chak Sing Lau
Pak Chung Sham
Yu Lung Lau
Asian Lupus Genetics Consortium

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Systemic lupus erythematosus is a complex and potentially fatal autoimmune disease, characterized by autoantibody production and multi-organ damage. By a genome-wide association study (320 patients and 1,500 controls) and subsequent replication altogether involving a total of 3,300 Asian SLE patients from Hong Kong, Mainland China, and Thailand, as well as 4,200 ethnically and geographically matched controls, genetic variants in ETS1 and WDFY4 were found to be associated with SLE (ETS1: rs1128334, P = 2.33x10(-11), OR = 1.29; WDFY4: rs7097397, P = 8.15x10(-12), OR = 1.30). ETS1 encodes for a transcription factor known to be involved in a wide range of immune functions, including Th17 cell development and terminal differentiation of B lymphocytes. SNP rs1128334 is located in the 3'-UTR of ETS1, and allelic expression analysis from peripheral blood mononuclear cells showed significantly lower expression level from the risk allele. WDFY4 is a conserved protein with unknown function, but is predominantly expressed in primary and secondary immune tissues, and rs7097397 in WDFY4 changes an arginine residue to glutamine (R1816Q) in this protein. Our study also confirmed association of the HLA locus, STAT4, TNFSF4, BLK, BANK1, IRF5, and TNFAIP3 with SLE in Asians. These new genetic findings may help us to gain a better understanding of the disease and the functions of the genes involved.

Indexed as

Genetic Predisposition to DiseaseGenome-Wide Association StudyAdaptor Proteins, Signal TransducingAdultAllelesAsian PeopleCohort StudiesDNA-Binding ProteinsFemaleHaplotypesHumansInterferon Regulatory FactorsIntracellular Signaling Peptides and ProteinsLeukocytes, MononuclearLinkage DisequilibriumLupus Erythematosus, SystemicAdaptor Proteins, Signal TransducingBANK1 protein, humanDNA-Binding ProteinsETS1 protein, humanInterferon Regulatory FactorsIntracellular Signaling Peptides and ProteinsIRF5 protein, humanMembrane ProteinsNuclear Proteinsprotein-tyrosine kinase p55(blk)Proto-Oncogene Protein c-ets-1src-Family KinasesSTAT4 Transcription FactorTNFAIP3 protein, humanTumor Necrosis Factor alpha-Induced Protein 3WDFY4 protein, human

Identifiers

PMID20169177
PMCPMC2820522

What Socratic holds

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Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.