Evidence map›Paper›PMID 19175525›Full record

SynthesisPigment cell & melanoma research2009

CTLA4 and generalized vitiligo: two genetic association studies and a meta-analysis of published data.

Stanca A Birlea, Greggory S Laberge, Lucia M Procopciuc, Pamela R Fain, Richard A Spritz

Open access · greenAbstract readMeta-Analysis
In one paragraph

Synthesis in Pigment cell & melanoma research, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed, 2 pooled it
2.0field-weighted citation impact, top 15% 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

20 citing papers in PubMed, 2 syntheses or guidelines pooled it, 39 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Vitiligo.Nature reviews. Disease primers · 2025
    Review
  4. Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Review
  10. Article
  11. Article
  12. Review
  13. Article
  14. Genetics of Vitiligo.Dermatologic clinics · 2017
    Review
  15. Review
  16. Article
  17. Recent progress in the genetics of generalized vitiligo.Journal of genetics and genomics = Yi chuan xue bao · 2011
    Review
  18. Shared genetic relationships underlying generalized vitiligo and autoimmune thyroid disease.Thyroid : official journal of the American Thyroid Association · 2010
    Review
  19. Article
  20. Vitiligo--part 1.Anais brasileiros de dermatologia
    Review
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

5 authors at 3 institutions in 3 countries.

Stanca A BirleaHuman Medical Genetics Program, University of Colorado, Denver, Colorado, USA.
Greggory S Laberge
Lucia M Procopciuc
Pamela R Fain
Richard A Spritz
University of Colorado Denver · USMedical Genetics Center · DEUniversity of Colorado Anschutz Medical Campus · US

Funding

MHC peptide tetramers in type 1 diabetesU19AI046374 · NIAID · UNIVERSITY OF COLORADO DENVER · PI HOLERS, VERNON MICHAEL · 1999 to 2007
$9.6M
VitiligoR01AR045584 · NIAMS · UNIVERSITY OF COLORADO DENVER · PI SPRITZ, RICHARD ANDREW · 1999 to 2014
$6.2M
IMMUNOGENETICS OF TYPE 1 DIABETES IN A BEDOUIN FAMILYR01DK057538 · NIDDK · UNIVERSITY OF COLORADO DENVER · PI FAIN, PAMELA R · 2000 to 2003
$1.4M
NIAID NIH HHS U19 AI046374NIAMS NIH HHS AR45584NIAMS NIH HHS R01 AR045584NIDDK NIH HHS DK57538NIDDK NIH HHS R01 DK057538
6 · The paper itself

Abstract

Several lines of evidence have implicated the gene encoding cytotoxic T lymphocyte antigen 4 (CTLA4) in susceptibility to various autoimmune diseases. However, published studies of genetic association between CTLA4 polymorphisms and vitiligo have yielded conflicting results. Here, we describe two new genetic association studies of CTLA4 single-nucleotide polymorphisms (SNPs) and generalized vitiligo in two independent Romanian Caucasian (CEU) case-control cohorts. The first study, of SNPs rs1863800, rs231806, rs231775, rs3087243, rs11571302, rs11571297, and rs10932037, showed no allelic, genotypic, or haplotypic association with generalized vitiligo. The second study, of SNP rs231775, likewise showed no significant association. To enhance statistical power over that of any individual study, we carried out a meta-analysis that incorporated these two new studies and all other published genetic association studies of CTLA4 SNPs and vitiligo in CEU populations. While there was no association with vitiligo overall, the meta-analysis showed significant association of SNP rs231775 in that subgroup of vitiligo patients who also had other concomitant autoimmune diseases. Similarly, there was near-significant association in this same patient subgroup with several other CTLA4 SNPs that are in linkage disequilibrium with rs231775. Our results indicate that the association of CTLA4 with vitiligo is weak, and indeed may be secondary, driven by primary genetic association of CTLA4 with other autoimmune diseases that are epidemiologically associated with vitiligo.

Indexed as

Genetic Predisposition to DiseaseAllelesAntigens, CDCase-Control StudiesCTLA-4 AntigenHumansModels, StatisticalOdds RatioPolymorphism, Single NucleotideRomaniaVitiligoWhite PeopleAntigens, CDCTLA-4 AntigenCTLA4 protein, human

Identifiers

PMID19175525
PMCPMC2745263
OpenAlexW1998985848

What OpenQuestion holds

Textmetadata
LicenceTDM
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.