Evidence map›Paper›PMID 20338887›Full record

SynthesisRheumatology (Oxford, England)2010

Non-synonymous variant (Gly307Ser) in CD226 is associated with susceptibility to multiple autoimmune diseases.

Amit K Maiti, Xana Kim-Howard, Parvathi Viswanathan, Laura Guillén, Xiaoxia Qian, Adriana Rojas-Villarraga, Celi Sun, Carlos Cañas, Gabriel J Tobón, Koichi Matsuda and 4 more

Open access · bronzeAbstract readMeta-Analysis
In one paragraph

Synthesis in Rheumatology (Oxford, England), 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed, 1 pooled it
3.6field-weighted citation impact, top 7% of its field
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

34 citing papers in PubMed, 1 synthesis or guideline pooled it, 74 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Impact of the Multiple Sclerosis-Associated Genetic VariantNeurology(R) neuroimmunology & neuroinflammation · 2024
    Article
  4. Review
  5. Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Increased Proportion of CD226Frontiers in immunology · 2021
    Article
  11. Review
  12. Review
  13. Helios but not CD226, TIGIT and Foxp3 is a Potential Marker for CD4Cellular physiology and biochemistry : international journal of experimental cellular physiology, biochemistry, and pharmacology · 2019
    Article
  14. Article
  15. Article
  16. Review
  17. Review
  18. Article
  19. Review
  20. Article
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

14 authors at 2 institutions in 2 countries.

Amit K MaitiGenetic Epidemiology Unit, Arthritis and Immunology Research Program, Oklahoma Medical Research Foundation, Oklahoma City, OK 73104, USA.
Xana Kim-Howard
Parvathi Viswanathan
Laura Guillén
Xiaoxia Qian
Adriana Rojas-Villarraga
Celi Sun
Carlos Cañas
Gabriel J Tobón
Koichi Matsuda
Nan Shen
Alejandra C Cherñavsky
Juan-Manuel Anaya
Swapan K Nath
Fundación Valle del Lili · COOklahoma Medical Research Foundation · US

Funding

SNP Confirmation and High Throughput Genotyping CoreP30AR053483 · NIAMS · OKLAHOMA MEDICAL RESEARCH FOUNDATION · PI GUTHRIDGE, JOEL MARVIN · 2007 to 2017
$6.7M
Identifying the novel SLE susceptibility gene on 5p15.3R01AI063622 · NIAID · OKLAHOMA MEDICAL RESEARCH FOUNDATION · PI NATH, SWAPAN K. · 2005 to 2009
$1.5M
NIAID NIH HHS R01 AI063622NIAID NIH HHS R01AI063622NIAMS NIH HHS P30 AR053483
6 · The paper itself

Abstract

objectivesRecently, a non-synonymous (Gly307Ser) variant, rs763361, in the CD226 gene was shown to be associated with multiple autoimmune diseases (ADs) in European Caucasian populations. However, shared autoimmunity with CD226 has not been evaluated in non-European populations. The aim of the present study is to assess the association of this single nucleotide polymorphism (SNP) with ADs in non-European populations.

methodsTo replicate this association in non-European populations, we evaluated case-control association between rs763361 and coeliac disease (CED) samples from Argentina; SLE, RA, type-1 diabetes (T1D) and primary SS (pSS) from Colombia; and SLE samples from China and Japan. We genotyped rs763361 and evaluated its genetic association with multiple ADs, using chi(2)-test. For each association, odds ratio (OR) and 95% CI were calculated.

resultsWe show that rs763361 is significantly associated with Argentinean CED (P = 0.0009, OR = 1.60). We also observed a trend of possible association with Chinese SLE (P = 0.01, OR = 1.19), RA (P = 0.047, OR = 1.25), SLE (P = 0.0899, OR = 1.24) and pSS (P = 0.09, OR = 1.33) in Colombians. Meta-analyses for SLE (using our three populations) and T1D (our population and three published populations) yielded significant association with rs763361, P = 0.009 (OR = 1.16) and P = 1.1.46 x 10(-9) (OR = 1.14), respectively.

conclusionsOur results demonstrate that the coding variant rs763361 in CD226 gene is associated with multiple ADs in non-European populations.

Indexed as

Antigens, Differentiation, T-LymphocyteArgentinaAsian PeopleAutoimmune DiseasesCase-Control StudiesColombiaGene FrequencyGenetic Predisposition to DiseaseGenotypeHumansStatistics as TopicT Lineage-Specific Activation Antigen 1White PeopleAntigens, Differentiation, T-LymphocyteT Lineage-Specific Activation Antigen 1

Identifiers

PMID20338887
PMCPMC2909799
OpenAlexW2152655560

What OpenQuestion holds

Textmetadata
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 OpenQuestion graph.