Evidence map›Paper›PMID 29717136›Full record

ArticleNature communications2018

Ancient DNA study reveals HLA susceptibility locus for leprosy in medieval Europeans.

Ben Krause-Kyora, Marcel Nutsua, Lisa Boehme, Federica Pierini, Dorthe Dangvard Pedersen, Sabin-Christin Kornell, Dmitriy Drichel, Marion Bonazzi, Lena Möbus, Peter Tarp and 13 more

Abstract read
In one paragraph

Article in Nature communications, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 50 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
50citing papers in PubMed, 2 pooled it
–field-weighted citation impact
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

50 citing papers in PubMed, 2 syntheses or guidelines pooled it.

  1. Pooled it
  2. Major histocompatibility complex-associated odour preferences and human mate choice: near and far horizons.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2020
    Pooled it
  3. Trial
  4. Ancient DNA and Human Physiology.Physiology (Bethesda, Md.) · 2026
    Review
  5. Article
  6. Article
  7. Article
  8. Detection ofVirulence · 2025
    Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Review
  16. Article
  17. Article
  18. Article
  19. HLA Genes: A Hallmark of Functional Genetic Variation and Complex Evolution.Methods in molecular biology (Clifton, N.J.) · 2024
    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

23 authors.

Ben Krause-KyoraInstitute of Clinical Molecular Biology, Kiel University, Kiel, 24105, Germany. b.krause-kyora@ikmb.uni-kiel.de.ORCID http://orcid.org/0000-0001-9435-2872
Marcel NutsuaInstitute of Clinical Molecular Biology, Kiel University, Kiel, 24105, Germany.
Lisa BoehmeInstitute of Clinical Molecular Biology, Kiel University, Kiel, 24105, Germany.
Federica PieriniDepartment of Evolutionary Ecology, Research Group for Evolutionary Immunogenomics, Max Planck Institute for Evolutionary Biology, Plön, 24306, Germany.
Dorthe Dangvard PedersenDepartment of Forensic Medicine, Unit of Anthropology (ADBOU), University of Southern Denmark, Odense S, 5260, Denmark.ORCID http://orcid.org/0000-0002-4709-9170
Sabin-Christin KornellInstitute of Clinical Molecular Biology, Kiel University, Kiel, 24105, Germany.
Dmitriy DrichelDepartment of Statistical Genetics and Bioinformatics, Cologne Center for Genomics (CCG), University of Cologne, Cologne, 50931, Germany.
Marion BonazziInstitute of Clinical Molecular Biology, Kiel University, Kiel, 24105, Germany.
Lena MöbusInstitute of Clinical Molecular Biology, Kiel University, Kiel, 24105, Germany.
Peter TarpDepartment of Forensic Medicine, Unit of Anthropology (ADBOU), University of Southern Denmark, Odense S, 5260, Denmark.
Julian SusatInstitute of Clinical Molecular Biology, Kiel University, Kiel, 24105, Germany.
Esther BosseInstitute of Clinical Molecular Biology, Kiel University, Kiel, 24105, Germany.
Beatrix WillburgerDKMS, Tübingen, 72072, Germany.
Alexander H SchmidtDKMS, Tübingen, 72072, Germany.
Jürgen SauterDKMS, Tübingen, 72072, Germany.
Andre FrankeInstitute of Clinical Molecular Biology, Kiel University, Kiel, 24105, Germany.ORCID http://orcid.org/0000-0003-1530-5811
Michael WittigInstitute of Clinical Molecular Biology, Kiel University, Kiel, 24105, Germany.
Amke CaliebeInstitute of Medical Informatics and Statistics, Kiel University, Kiel, 24105, Germany.
Michael NothnagelDepartment of Statistical Genetics and Bioinformatics, Cologne Center for Genomics (CCG), University of Cologne, Cologne, 50931, Germany.ORCID http://orcid.org/0000-0001-8305-7114
Stefan SchreiberInstitute of Clinical Molecular Biology, Kiel University, Kiel, 24105, Germany.
Jesper L BoldsenDepartment of Forensic Medicine, Unit of Anthropology (ADBOU), University of Southern Denmark, Odense S, 5260, Denmark.
Tobias L LenzDepartment of Evolutionary Ecology, Research Group for Evolutionary Immunogenomics, Max Planck Institute for Evolutionary Biology, Plön, 24306, Germany.
Almut NebelInstitute of Clinical Molecular Biology, Kiel University, Kiel, 24105, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Leprosy, a chronic infectious disease caused by Mycobacterium leprae (M. leprae), was very common in Europe till the 16th century. Here, we perform an ancient DNA study on medieval skeletons from Denmark that show lesions specific for lepromatous leprosy (LL). First, we test the remains for M. leprae DNA to confirm the infection status of the individuals and to assess the bacterial diversity. We assemble 10 complete M. leprae genomes that all differ from each other. Second, we evaluate whether the human leukocyte antigen allele DRB1*15:01, a strong LL susceptibility factor in modern populations, also predisposed medieval Europeans to the disease. The comparison of genotype data from 69 M. leprae DNA-positive LL cases with those from contemporary and medieval controls reveals a statistically significant association in both instances. In addition, we observe that DRB1*15:01 co-occurs with DQB1*06:02 on a haplotype that is a strong risk factor for inflammatory diseases today.

Indexed as

DNA, AncientGenetic Predisposition to DiseaseDenmarkDNA, BacterialFossilsGenome, BacterialHigh-Throughput Screening AssaysHLA-DQ beta-ChainsHLA-DRB1 ChainsHumansLeprosyMycobacterium lepraeWhite PeopleDNA, AncientDNA, BacterialHLA-DQB1 antigenHLA-DQ beta-ChainsHLA-DRB1 Chains

Identifiers

PMID29717136
PMCPMC5931558

What OpenQuestion holds

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Registered trials

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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.