Evidence map›Paper›PMID 21326295›Full record

ArticleThe Journal of investigative dermatology2011

Genome-wide analysis identifies a quantitative trait locus in the MHC class II region associated with generalized vitiligo age of onset.

Ying Jin, Stanca A Birlea, Pamela R Fain, Katherine Gowan, Sheri L Riccardi, Paulene J Holland, Dorothy C Bennett, Deborah M Herbstman, Margaret R Wallace, Wayne T McCormack and 12 more

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of investigative dermatology, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed, 1 pooled it
4.8field-weighted citation impact, top 5% 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

28 citing papers in PubMed, 1 synthesis or guideline pooled it, 85 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Article
  6. Aetiopathogenesis of Vitiligo.Dermatology practical & conceptual · 2023
    Review
  7. Article
  8. Article
  9. Vitamin D protects human melanocytes against oxidative damage by activation of Wnt/β-catenin signaling.Laboratory investigation; a journal of technical methods and pathology · 2018
    Article
  10. Clinical and Molecular Aspects of Vitiligo Treatments.International journal of molecular sciences · 2018
    Review
  11. Vitiligo: Focus on Clinical Aspects, Immunopathogenesis, and Therapy.Clinical reviews in allergy & immunology · 2018
    Review
  12. Genetics of Vitiligo.Dermatologic clinics · 2017
    Review
  13. Article
  14. The role of IL-17 in vitiligo: A review.Autoimmunity reviews · 2016
    Review
  15. Review
  16. Article
  17. Article
  18. Article
  19. Current aspects of vitiligo genetics.Postepy dermatologii i alergologii · 2014
    Review
  20. Genetic analysis in young-age-of-onset Graves' disease reveals new susceptibility loci.The Journal of clinical endocrinology and metabolism · 2014
    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

22 authors at 8 institutions in 5 countries.

Ying JinHuman Medical Genetics Program, University of Colorado Denver School of Medicine, Aurora, Colorado 80045, USA.
Stanca A Birlea
Pamela R Fain
Katherine Gowan
Sheri L Riccardi
Paulene J Holland
Dorothy C Bennett
Deborah M Herbstman
Margaret R Wallace
Wayne T McCormack
E Helen Kemp
David J Gawkrodger
Anthony P Weetman
Mauro Picardo
Giovanni Leone
Alain Taïeb
Thomas Jouary
Khaled Ezzedine
Nanny van Geel
Jo Lambert
Andreas Overbeck
Richard A Spritz
University of Colorado Denver · USHôpital Saint-André · FRUniversity of Florida · USGhent University Hospital · BESan Gallicano Hospital · ITUniversity of Sheffield · GBRoyal Hallamshire Hospital · GBSt George's, University of London · GB

Funding

VitGene International Consortium to Identify Susceptibility Genes for GeneralizedR01AR056292 · NIAMS · UNIVERSITY OF COLORADO DENVER · PI SPRITZ, RICHARD ANDREW · 2008 to 2016
$6.9M
VitiligoR01AR045584 · NIAMS · UNIVERSITY OF COLORADO DENVER · PI SPRITZ, RICHARD ANDREW · 1999 to 2014
$6.2M
NIAMS NIH HHS AR056292NIAMS NIH HHS AR45584NIAMS NIH HHS R01 AR045584NIAMS NIH HHS R01 AR056292
6 · The paper itself

Abstract

Generalized vitiligo is a common autoimmune disease in which acquired patchy depigmentation of skin, hair, and mucous membranes results from loss of melanocytes from involved areas. Previous genetic analyses have focused on vitiligo susceptibility, and have identified a number of genes involved in disease risk. Age of onset of generalized vitiligo also involves a substantial genetic component, but has not previously been studied systematically. In this study, we report a genome-wide association study of vitiligo age of onset in 1,339 generalized vitiligo patients, with replication in an independent cohort of 677 cases. We identified a quantitative trait locus for vitiligo age of onset in the major histocompatibility complex (MHC) class II region, located near c6orf10-BTNL2 (rs7758128; P=8.14 × 10(-11)), a region that is also associated with generalized vitiligo susceptibility. In contrast, there was no association of vitiligo age of onset with any other MHC or non-MHC loci that are associated with vitiligo susceptibility. These findings highlight the differing roles played by genes involved in vitiligo susceptibility versus vitiligo age of onset, and illustrate that genome-wide analyses can be used to identify genes involved in quantitative aspects of disease natural history, as well as disease susceptibility per se.

Indexed as

Genes, MHC Class IIGenome-Wide Association StudyQuantitative Trait LociAdultAge of OnsetFemaleGenetic Predisposition to DiseaseHumansMaleMiddle AgedPolymorphism, Single NucleotideProportional Hazards ModelsVitiligo

Identifiers

PMID21326295
PMCPMC3172680
OpenAlexW2076024357

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.