Evidence map›Paper›PMID 35633118›Full record

ArticleThe British journal of dermatology2022

Distinct skin microbiome community structures in congenital ichthyosis.

Khek-Chian Tham, Rachel Lefferdink, Kaibo Duan, Seong Soo Lim, X F Colin C Wong, Erin Ibler, Benedict Wu, Hajar Abu-Zayed, Stephanie M Rangel, Ester Del Duca and 7 more

Open access · greenAbstract read
In one paragraph

Article in The British journal of dermatology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed, 1 pooled it
14.2field-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

15 citing papers in PubMed, 1 synthesis or guideline pooled it, 56 citations in OpenAlex.

  1. Pooled it
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  3. Article
  4. Article
  5. Article
  6. Review
  7. Review
  8. Review
  9. The skin microbiome in dermatologic disease.Journal of the American Academy of Dermatology · 2025
    Review
  10. Article
  11. The Carcinogenesis of the Human Scalp: An Immunometabolic-Centered View.International journal of molecular sciences · 2024
    Review
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  14. Article
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

17 authors at 3 institutions in 2 countries.

Khek-Chian ThamA*STAR Skin Research Labs, Agency for Science, Technology and Research, 8A Biomedical Grove, #06-10 Immunos, Singapore, 138648, Singapore.ORCID 0000-0002-5702-2986
Rachel LefferdinkNorthwestern University Feinberg School of Medicine, Chicago, IL, USA.
Kaibo DuanSingapore Immunology Network, Agency for Science, Technology and Research, 8A Biomedical Grove, #03 Immunos, Singapore, 138648, Singapore.
Seong Soo LimA*STAR Skin Research Labs, Agency for Science, Technology and Research, 8A Biomedical Grove, #06-10 Immunos, Singapore, 138648, Singapore.
X F Colin C WongA*STAR Skin Research Labs, Agency for Science, Technology and Research, 8A Biomedical Grove, #06-10 Immunos, Singapore, 138648, Singapore.
Erin IblerNorthwestern University Feinberg School of Medicine, Chicago, IL, USA.
Benedict WuNorthwestern University Feinberg School of Medicine, Chicago, IL, USA.
Hajar Abu-ZayedNorthwestern University Feinberg School of Medicine, Chicago, IL, USA.
Stephanie M RangelNorthwestern University Feinberg School of Medicine, Chicago, IL, USA.
Ester Del DucaIcahn School of Medicine at Mount Sinai Medical Center, New York, NY, USA.ORCID 0000-0001-7948-8536
Mashkura ChowdhuryIcahn School of Medicine at Mount Sinai Medical Center, New York, NY, USA.
Margot ChimaIcahn School of Medicine at Mount Sinai Medical Center, New York, NY, USA.
Hee Jee KimIcahn School of Medicine at Mount Sinai Medical Center, New York, NY, USA.
Bernett LeeSingapore Immunology Network, Agency for Science, Technology and Research, 8A Biomedical Grove, #03 Immunos, Singapore, 138648, Singapore.
Emma Guttman-YasskyIcahn School of Medicine at Mount Sinai Medical Center, New York, NY, USA.ORCID 0000-0002-9363-324X
Amy S PallerNorthwestern University Feinberg School of Medicine, Chicago, IL, USA.ORCID 0000-0001-6187-6549
John E A CommonA*STAR Skin Research Labs, Agency for Science, Technology and Research, 8A Biomedical Grove, #06-10 Immunos, Singapore, 138648, Singapore.ORCID 0000-0002-3280-7365
Agency for Science, Technology and Research · SGNorthwestern University · USMount Sinai Medical Center · US

Funding

Northwestern University Skin Disease Research Center Resource-based CenterP30AR075049 · NIAMS · NORTHWESTERN UNIVERSITY AT CHICAGO · PI Amy S Paller · 2019 to 2026
$6.6M
NIAMS NIH HHS P30 AR075049
6 · The paper itself

Abstract

backgroundThe ichthyoses are rare genetic keratinizing disorders that share the characteristics of an impaired epidermal barrier and increased risk of microbial infections. Although ichthyotic diseases share a T helper (Th) 17 cell immune signature, including increased expression of antimicrobial peptides, the skin microbiota of ichthyoses is virtually unexplored.

objectivesTo analyse the metagenome profile of skin microbiome for major congenital ichthyosis subtypes.

methodsBody site-matched skin surface samples were collected from the scalp, upper arm and upper buttocks of 16 healthy control participants and 22 adult patients with congenital forms of ichthyosis for whole metagenomics sequencing analysis.

resultsTaxonomic profiling showed significant shifts in bacteria and fungi abundance and sporadic viral increases across ichthyosis subtypes. Cutibacterium acnes and Malassezia were significantly reduced across body sites, consistent with skin barrier disruption and depletion of lipids. Microbial richness was reduced, with specific increases in Staphylococcus and Corynebacterium genera, as well as shifts in fungal species, including Malassezia. Malassezia globosa was reduced at all body sites, whereas M. sympodialis was reduced in the ichthyotic upper arm and upper buttocks. Malassezia slooffiae, by contrast, was strikingly increased at all body sites in participants with congenital ichthyosiform erythroderma (CIE) and lamellar ichthyosis (LI). A previously undescribed Trichophyton species was also detected as sporadically colonizing the skin of patients with CIE, LI and epidermolytic ichthyosis subtypes.

conclusionsThe ichthyosis skin microbiome is significantly altered from healthy skin with specific changes predominating among ichthyosis subtypes. Skewing towards the Th17 pathway may represent a response to the altered microbial colonization in ichthyosis. What is already known about this topic? The skin microbiome of congenital ichthyoses is largely unexplored. Microbes play an important role in pathogenesis, as infections are common. The relative abundances of staphylococci and corynebacteria is increased in the cutaneous microbiome of patients with Netherton syndrome, but extension of these abundances to all congenital ichthyoses is unexplored. What does this study add? A common skin microbiome signature was observed across congenital ichthyoses. Distinct microbiome features were associated with ichthyosis subtypes. Changes in microbiome may contribute to T helper 17 cell immune polarization. What is the translational message? These data provide the basis for comparison of the microbiome with lipidomic and transcriptomic alterations in these forms of ichthyosis and consideration of correcting the dysbiosis as a therapeutic intervention.

Indexed as

Ichthyosiform Erythroderma, CongenitalIchthyosisIchthyosis, LamellarMicrobiotaAdultHumansLipidsSkinLipids

Identifiers

PMID35633118
PMCPMC10234690
OpenAlexW4281772150

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.