Evidence map›Paper›PMID 35132056›Full record

SynthesisNature communications2022

Genome-wide association meta-analysis identifies 29 new acne susceptibility loci.

Brittany L Mitchell, Jake R Saklatvala, Nick Dand, Fiona A Hagenbeek, Xin Li, Josine L Min, Laurent Thomas, Meike Bartels, Jouke Jan Hottenga, Michelle K Lupton and 10 more

Open access · goldAbstract readMeta-Analysis
In one paragraph

Synthesis in Nature communications, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed, 1 pooled it
10.6field-weighted citation impact, top 1% 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

29 citing papers in PubMed, 1 synthesis or guideline pooled it, 55 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. From pixels to pimples.JID innovations : skin science from molecules to population health · 2026
    Article
  5. Article
  6. Hidden immune memory niches in inflammatory skin diseases.bioRxiv : the preprint server for biology · 2026
    Article
  7. Review
  8. Review
  9. Acne tarda: Recommendations for classification, treatment and care as a result of an expert discussion.Journal der Deutschen Dermatologischen Gesellschaft = Journal of the German Society of Dermatology : JDDG · 2026
    Review
  10. Article
  11. Article
  12. The Genetics of Acne.Annals of human genetics · 2025
    Review
  13. Article
  14. Article
  15. Review
  16. Article
  17. Review
  18. Article
  19. Article
  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

20 authors at 8 institutions in 5 countries.

Brittany L Mitchell *Department of Genetics and Computational Biology, QIMR Berghofer Medical Research Institute, Brisbane, Australia.ORCID http://orcid.org/0000-0002-9050-1516
Jake R Saklatvala *Department of Medical and Molecular Genetics, King's College London, London, UK.ORCID http://orcid.org/0000-0003-0836-4928
Nick DandDepartment of Medical and Molecular Genetics, King's College London, London, UK.ORCID http://orcid.org/0000-0002-1805-6278
Fiona A HagenbeekDepartment of Biological Psychology, Vrije Universiteit Amsterdam, Amsterdam, The Netherlands.ORCID http://orcid.org/0000-0002-8773-0430
Xin LiDepartment of Epidemiology, Indiana University Richard M. Fairbanks School of Public Health, Indianapolis, US.ORCID http://orcid.org/0000-0002-0135-8800
Josine L MinMRC Integrative Epidemiology Unit, University of Bristol, Bristol, UK.ORCID http://orcid.org/0000-0003-4456-9824
Laurent ThomasDepartment of Clinical and Molecular Medicine, Norwegian University of Science and Technology, Trondheim, Norway.ORCID http://orcid.org/0000-0003-0548-2486
Meike BartelsDepartment of Biological Psychology, Vrije Universiteit Amsterdam, Amsterdam, The Netherlands.ORCID http://orcid.org/0000-0002-9667-7555
Jouke Jan HottengaDepartment of Biological Psychology, Vrije Universiteit Amsterdam, Amsterdam, The Netherlands.ORCID http://orcid.org/0000-0002-5668-2368
Michelle K LuptonDepartment of Genetics and Computational Biology, QIMR Berghofer Medical Research Institute, Brisbane, Australia.
Dorret I BoomsmaDepartment of Biological Psychology, Vrije Universiteit Amsterdam, Amsterdam, The Netherlands.
Xianjun DongGenomics and Bioinformatics Hub, Brigham and Women's Hospital, Boston, MA, USA.ORCID http://orcid.org/0000-0002-8052-9320
Kristian HveemK.G. Jebsen Center for Genetic Epidemiology, Department of Public Health and Nursing, NTNU, Norwegian University of Science and Technology, Trondheim, Norway.
Mari LøsetK.G. Jebsen Center for Genetic Epidemiology, Department of Public Health and Nursing, NTNU, Norwegian University of Science and Technology, Trondheim, Norway.ORCID http://orcid.org/0000-0003-3736-6551
Nicholas G MartinDepartment of Genetics and Computational Biology, QIMR Berghofer Medical Research Institute, Brisbane, Australia.ORCID http://orcid.org/0000-0003-4069-8020
Jonathan N BarkerSt John's Institute of Dermatology, Faculty of Life Sciences & Medicine, King's College London, London, UK.
Jiali HanDepartment of Epidemiology, Indiana University Richard M. Fairbanks School of Public Health, Indianapolis, US.
Catherine H SmithSt John's Institute of Dermatology, Faculty of Life Sciences & Medicine, King's College London, London, UK.
Miguel E RenteríaDepartment of Genetics and Computational Biology, QIMR Berghofer Medical Research Institute, Brisbane, Australia. miguel.renteria@qimrberghofer.edu.au.ORCID http://orcid.org/0000-0003-4626-7248
Michael A SimpsonDepartment of Medical and Molecular Genetics, King's College London, London, UK. michael.simpson@kcl.ac.uk.ORCID http://orcid.org/0000-0002-8539-8753
King's College London · GBVrije Universiteit Amsterdam · NLNorwegian University of Science and Technology · NOIndiana University Health · USQIMR Berghofer Medical Research Institute · AUQueensland University of Technology · AUBrigham and Women's Hospital · USUniversity of Bristol · GB

Funding

Medical Research Council MC_UU_00011/5Medical Research Council MR/S003126/1
6 · The paper itself

Abstract

Acne vulgaris is a highly heritable skin disorder that primarily impacts facial skin. Severely inflamed lesions may leave permanent scars that have been associated with long-term psychosocial consequences. Here, we perform a GWAS meta-analysis comprising 20,165 individuals with acne from nine independent European ancestry cohorts. We identify 29 novel genome-wide significant loci and replicate 14 of the 17 previously identified risk loci, bringing the total number of reported acne risk loci to 46. Using fine-mapping and eQTL colocalisation approaches, we identify putative causal genes at several acne susceptibility loci that have previously been implicated in Mendelian hair and skin disorders, including pustular psoriasis. We identify shared genetic aetiology between acne, hormone levels, hormone-sensitive cancers and psychiatric traits. Finally, we show that a polygenic risk score calculated from our results explains up to 5.6% of the variance in acne liability in an independent cohort.

Indexed as

Acne VulgarisGenetic Predisposition to DiseaseGenome-Wide Association StudyHumansMultifactorial InheritancePhenotypePolymorphism, Single NucleotideQuantitative Trait LociRisk

Identifiers

PMID35132056
PMCPMC8821634
OpenAlexW4210762175

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.