Evidence map›Paper›PMID 42311022›Full record

ArticleExperimental dermatology2026

Do Alopecia Areata and Hair Colour Have a Shared Genetic Component?

Leonie Rieger-Molitor, Carlo Maj, Silke Redler, Yasmina Gossmann, Stephan Ripke, Lynn Pethukova, Angela M Christiano, Markus M Nöthen, F Buket Basmanav, Regina C Betz

Abstract read
In one paragraph

Article in Experimental dermatology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

10 authors.

Leonie Rieger-MolitorInstitute of Human Genetics, University of Bonn, Medical Faculty & University Hospital Bonn, Bonn, Germany.
Carlo MajInstitute for Genomic Statistics and Bioinformatics, University of Bonn, Medical Faculty & University Hospital Bonn, Bonn, Germany.
Silke RedlerInstitute of Human Genetics, University of Bonn, Medical Faculty & University Hospital Bonn, Bonn, Germany.
Yasmina GossmannInstitute of Human Genetics, University of Bonn, Medical Faculty & University Hospital Bonn, Bonn, Germany.
Stephan RipkeDepartment of Psychiatry and Psychotherapy, Charité - Universitätsmedizin, Berlin, Germany.
Lynn PethukovaRonald O. Perlemen Department of Dermatology, NYU Langone Health, New York, New York, USA.ORCID https://orcid.org/0000-0002-1573-1653
Angela M ChristianoDepartment of Population Health, NYU Langone Health, New York, New York, USA.
Markus M NöthenInstitute of Human Genetics, University of Bonn, Medical Faculty & University Hospital Bonn, Bonn, Germany.
F Buket BasmanavInstitute of Human Genetics, University of Bonn, Medical Faculty & University Hospital Bonn, Bonn, Germany.ORCID https://orcid.org/0000-0001-6411-4275
Regina C BetzInstitute of Human Genetics, University of Bonn, Medical Faculty & University Hospital Bonn, Bonn, Germany.

Funding

Identification of biologically relevant subtypes of hidradenitis suppurativaK01AR075111 · NIAMS · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI PETUKHOVA, LYNN · 2020 to 2024
$534k
Deutsche Forschungsgemeinschaft EXC2151-390873048NIH HHS K01AR075111
6 · The paper itself

Abstract

Alopecia areata (AA) is a common T-cell mediated autoimmune disorder, which leads to sudden, non-scarring hair loss. An association between hair pigmentation and AA pathogenesis has long been postulated. Recent epidemiological evidence supports this link, indicating that individuals with darker hair colours have a higher risk of AA, while those with lighter hair colours exhibit a lower risk. This study aimed to investigate whether a shared genetic basis between hair colour determination and AA risk underlies this observation. To explore this, we analysed data from our AA genome-wide association study (GWAS) of 16 310 Caucasians from the US and Central Europe and a recently published GWAS of hair colour that involved 343 234 UK Biobank participants. Genetic correlations between the two traits were investigated using both polygenic risk score and linkage disequilibrium score regression (LDSC) analyses. No evidence was found for a strong, broadly shared genetic component for hair colour and AA. However, a suggestive weak inverse association with genetically predicted blond hair and AA risk was observed. Given the modest sample size of the AA-GWAS (~4100 cases), these findings are likely underpowered and should be interpreted as exploratory and hypothesis-generating, warranting replication in larger, independent cohorts.

Indexed as

Alopecia AreataHair ColorFemaleGenetic Predisposition to DiseaseGenetic Risk ScoreGenome-Wide Association StudyHumansLinkage DisequilibriumMalePolymorphism, Single NucleotideUnited StatesWhite Peoplealopeciageneticshair colourimmunology

Identifiers

PMID42311022
PMCPMC13276438

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