Evidence map›Paper›PMID 36224329›Full record

Observational studyLeukemia2022

Disturbances in microbial skin recolonization and cutaneous immune response following allogeneic stem cell transfer.

Nadine Bayer, Bela Hausmann, Ram Vinay Pandey, Florian Deckert, Laura-Marie Gail, Johanna Strobl, Petra Pjevac, Christoph Krall, Luisa Unterluggauer, Anna Redl and 15 more

Erratum issuedAbstract readObservational Study
PubMed Publisher
In one paragraph

Observational study in Leukemia, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.5field-weighted citation impact, top 17% 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

4 citing papers in PubMed, 7 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

25 authors at 6 institutions in 2 countries.

Nadine BayerDepartment of Dermatology, Medical University of Vienna, 1090, Vienna, Austria.ORCID http://orcid.org/0000-0002-9759-8728
Bela HausmannJoint Microbiome Facility of the Medical University of Vienna and the University of Vienna, 1030, Vienna, Austria.ORCID http://orcid.org/0000-0002-0846-1202
Ram Vinay PandeyDepartment of Dermatology, Medical University of Vienna, 1090, Vienna, Austria.
Florian DeckertCeMM Research Center for Molecular Medicine of the Austrian Academy of Sciences, 1090, Vienna, Austria.ORCID http://orcid.org/0000-0002-3075-6808
Laura-Marie GailDepartment of Dermatology, Medical University of Vienna, 1090, Vienna, Austria.ORCID http://orcid.org/0000-0002-2525-9399
Johanna StroblDepartment of Dermatology, Medical University of Vienna, 1090, Vienna, Austria.ORCID http://orcid.org/0000-0003-3606-2185
Petra PjevacJoint Microbiome Facility of the Medical University of Vienna and the University of Vienna, 1030, Vienna, Austria.
Christoph KrallCentre for Medical Statistics, Informatics, and Intelligent Systems, Medical University of Vienna, 1090, Vienna, Austria.
Luisa UnterluggauerDepartment of Dermatology, Medical University of Vienna, 1090, Vienna, Austria.
Anna RedlDepartment of Dermatology, Medical University of Vienna, 1090, Vienna, Austria.
Victoria BachmayrDepartment of Dermatology, Medical University of Vienna, 1090, Vienna, Austria.ORCID http://orcid.org/0000-0002-4585-1736
Lisa KleisslDepartment of Dermatology, Medical University of Vienna, 1090, Vienna, Austria.ORCID http://orcid.org/0000-0001-8011-796X
Marion NehrDivision of Clinical Microbiology, Department of Laboratory Medicine, Medical University of Vienna, 1090, Vienna, Austria.
Rasmus KirkegaardJoint Microbiome Facility of the Medical University of Vienna and the University of Vienna, 1030, Vienna, Austria.ORCID http://orcid.org/0000-0003-3349-3617
Athanasios MakristathisDivision of Clinical Microbiology, Department of Laboratory Medicine, Medical University of Vienna, 1090, Vienna, Austria.ORCID http://orcid.org/0000-0002-1593-571X
Martin L WatzenboeckDepartment of Biomedical Imaging and Image-guided Therapy, Medical University of Vienna, Vienna, Austria.
Robert NicaTissueGnostics GmbH, 1020, Vienna, Austria.
Clement StaudDivision of Plastic and Reconstructive Surgery, Department of Surgery, Medical University of Vienna, 1090, Vienna, Austria.
Lukas HammerlDepartment of Dermatology, Medical University of Vienna, 1090, Vienna, Austria.
Philipp WohlfarthDepartment of Internal Medicine I, Hematopoietic Stem Cell Transplantation Unit, Medical University of Vienna, 1090, Vienna, Austria.
Rupert C EckerTissueGnostics GmbH, 1020, Vienna, Austria.
Sylvia KnappDepartment of Medicine I, Laboratory of Infection Biology, Medical University of Vienna, 1090, Vienna, Austria.ORCID http://orcid.org/0000-0001-9016-5244
Werner RabitschDepartment of Internal Medicine I, Hematopoietic Stem Cell Transplantation Unit, Medical University of Vienna, 1090, Vienna, Austria.
David BerryJoint Microbiome Facility of the Medical University of Vienna and the University of Vienna, 1030, Vienna, Austria.ORCID http://orcid.org/0000-0002-8997-608X
Georg StaryDepartment of Dermatology, Medical University of Vienna, 1090, Vienna, Austria. georg.stary@meduniwien.ac.at.ORCID http://orcid.org/0000-0003-1746-4250
Medical University of Vienna · ATAustrian Academy of Sciences · ATUniversity of Vienna · ATCeMM Research Center for Molecular Medicine · ATLudwig Boltzmann Institute for Rare and Undiagnosed Diseases · ATQueensland University of Technology · AU

Funding

Austrian Science Fund FWF P 31494
6 · The paper itself

Abstract

The composition of the gut microbiome influences the clinical course after allogeneic hematopoietic stem cell transplantation (HSCT), but little is known about the relevance of skin microorganisms. In a single-center, observational study, we recruited a cohort of 50 patients before undergoing conditioning treatment and took both stool and skin samples up to one year after HSCT. We could confirm intestinal dysbiosis following HSCT and report that the skin microbiome is likewise perturbed in HSCT-recipients. Overall bacterial colonization of the skin was decreased after conditioning. Particularly patients that developed acute skin graft-versus-host disease (aGVHD) presented with an overabundance of Staphylococcus spp. In addition, a loss in alpha diversity was indicative of aGVHD development already before disease onset and correlated with disease severity. Further, co-localization of CD45

Indexed as

Gastrointestinal MicrobiomeGraft vs Host DiseaseHematopoietic Stem Cell TransplantationHumansImmunity

Identifiers

PMID36224329
OpenAlexW4304695196

What OpenQuestion holds

Textmetadata
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.