Evidence map›Paper›PMID 37783685›Full record

ArticleNature communications2023

Multifaceted analysis of cross-tissue transcriptomes reveals phenotype-endotype associations in atopic dermatitis.

Aiko Sekita, Hiroshi Kawasaki, Ayano Fukushima-Nomura, Kiyoshi Yashiro, Keiji Tanese, Susumu Toshima, Koichi Ashizaki, Tomohiro Miyai, Junshi Yazaki, Atsuo Kobayashi and 10 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
7.4field-weighted citation impact, top 2% 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

14 citing papers in PubMed, 26 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Alzheimer's Disease Risk Factor APOE4 Exerts Dimorphic Effects on Female Bone.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Article
  5. Review
  6. Review
  7. Multiomic approaches for endotype discovery in allergy/immunology.The Journal of allergy and clinical immunology · 2025
    Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Review
  14. 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 7 institutions in 1 country.

Aiko SekitaRIKEN Center for Integrative Medical Sciences, Yokohama, Japan.ORCID http://orcid.org/0009-0005-4622-395X
Hiroshi KawasakiRIKEN Center for Integrative Medical Sciences, Yokohama, Japan.
Ayano Fukushima-NomuraDepartment of Dermatology, Keio University School of Medicine, Tokyo, Japan.ORCID http://orcid.org/0000-0002-9482-5008
Kiyoshi YashiroDepartment of Dermatology, Keio University School of Medicine, Tokyo, Japan.
Keiji TaneseDepartment of Dermatology, Keio University School of Medicine, Tokyo, Japan.
Susumu ToshimaRIKEN Center for Integrative Medical Sciences, Yokohama, Japan.
Koichi AshizakiRIKEN Center for Integrative Medical Sciences, Yokohama, Japan.
Tomohiro MiyaiRIKEN Center for Integrative Medical Sciences, Yokohama, Japan.ORCID http://orcid.org/0000-0003-1952-0228
Junshi YazakiRIKEN Center for Integrative Medical Sciences, Yokohama, Japan.ORCID http://orcid.org/0000-0002-0697-8320
Atsuo KobayashiRIKEN Center for Integrative Medical Sciences, Yokohama, Japan.
Shinichi NambaDepartment of Statistical Genetics, Osaka University Graduate School of Medicine, Osaka, Japan.ORCID http://orcid.org/0000-0002-7486-3146
Tatsuhiko NaitoDepartment of Statistical Genetics, Osaka University Graduate School of Medicine, Osaka, Japan.ORCID http://orcid.org/0000-0002-2779-4600
Qingbo S WangRIKEN Center for Integrative Medical Sciences, Yokohama, Japan.
Eiryo KawakamiAdvanced Data Science Project, RIKEN Information R&D and Strategy Headquarters, Tokyo, Japan.ORCID http://orcid.org/0000-0001-9955-4342
Jun SeitaRIKEN Center for Integrative Medical Sciences, Yokohama, Japan.ORCID http://orcid.org/0000-0002-3008-3615
Osamu OharaKazusa DNA Research Institute, Chiba, Japan.ORCID http://orcid.org/0000-0002-3328-9571
Kazuhiro SakuradaAdvanced Data Science Project, RIKEN Information R&D and Strategy Headquarters, Tokyo, Japan.
Yukinori OkadaRIKEN Center for Integrative Medical Sciences, Yokohama, Japan. yuki-okada@m.u-tokyo.ac.jp.ORCID http://orcid.org/0000-0002-0311-8472
Masayuki AmagaiRIKEN Center for Integrative Medical Sciences, Yokohama, Japan. amagai@keio.jp.ORCID http://orcid.org/0000-0003-3314-7052
Haruhiko KosekiRIKEN Center for Integrative Medical Sciences, Yokohama, Japan. haruhiko.koseki@riken.jp.ORCID http://orcid.org/0000-0001-8424-5854
Keio University · JPRIKEN Center for Integrative Medical Sciences · JPChiba University · JPKazusa DNA Research Institute · JPRIKEN Center for Advanced Intelligence Project · JPThe University of Osaka · JPThe University of Tokyo · JP

Funding

Japan Agency for Medical Research and Development (AMED) JP22ek0410079
6 · The paper itself

Abstract

Atopic dermatitis (AD) is a skin disease that is heterogeneous both in terms of clinical manifestations and molecular profiles. It is increasingly recognized that AD is a systemic rather than a local disease and should be assessed in the context of whole-body pathophysiology. Here we show, via integrated RNA-sequencing of skin tissue and peripheral blood mononuclear cell (PBMC) samples along with clinical data from 115 AD patients and 14 matched healthy controls, that specific clinical presentations associate with matching differential molecular signatures. We establish a regression model based on transcriptome modules identified in weighted gene co-expression network analysis to extract molecular features associated with detailed clinical phenotypes of AD. The two main, qualitatively differential skin manifestations of AD, erythema and papulation are distinguished by differential immunological signatures. We further apply the regression model to a longitudinal dataset of 30 AD patients for personalized monitoring, highlighting patient heterogeneity in disease trajectories. The longitudinal features of blood tests and PBMC transcriptome modules identify three patient clusters which are aligned with clinical severity and reflect treatment history. Our approach thus serves as a framework for effective clinical investigation to gain a holistic view on the pathophysiology of complex human diseases.

Indexed as

Dermatitis, AtopicHumansLeukocytes, MononuclearPhenotypeSkinTranscriptome

Identifiers

PMID37783685
PMCPMC10545679
OpenAlexW4387264896

What OpenQuestion holds

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LicenceCC BY
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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.