Evidence map›Paper›PMID 34997172›Full record

ArticleScientific reports2022

Accurate diagnosis of atopic dermatitis by combining transcriptome and microbiota data with supervised machine learning.

Ziyuan Jiang, Jiajin Li, Nahyun Kong, Jeong-Hyun Kim, Bong-Soo Kim, Min-Jung Lee, Yoon Mee Park, So-Yeon Lee, Soo-Jong Hong, Jae Hoon Sul

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed, 1 pooled it
7.8field-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

20 citing papers in PubMed, 1 synthesis or guideline pooled it, 42 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Review
  4. Review
  5. Review
  6. Article
  7. Review
  8. Article
  9. Review
  10. Article
  11. Review
  12. Artificial intelligence in pediatric allergy research.European journal of pediatrics · 2024
    Review
  13. Review
  14. Review
  15. Review
  16. Review
  17. Review
  18. Review
  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

10 authors at 7 institutions in 3 countries.

Ziyuan Jiang *Department of Automation, Tsinghua University, Beijing, 100084, China.
Jiajin Li *Department of Human Genetics, David Geffen School of Medicine, University of California, Los Angeles, Los Angeles, CA, 90095, USA.
Nahyun KongDepartment of Biological Sciences, Korea Advanced Institute of Science and Technology, Daejeon, Daejeon, 34141, Republic of Korea.
Jeong-Hyun KimDepartment of Medicine, University of Ulsan College of Medicine, Seoul, 05505, Republic of Korea.
Bong-Soo KimDepartment of Life Science, Multidisciplinary Genome Institute, Hallym University, Chuncheon, 24252, Republic of Korea.
Min-Jung LeeDepartment of Life Science, Multidisciplinary Genome Institute, Hallym University, Chuncheon, 24252, Republic of Korea.
Yoon Mee ParkDepartment of Medicine, University of Ulsan College of Medicine, Seoul, 05505, Republic of Korea.
So-Yeon LeeDepartment of Pediatrics, Asan Medical Center, Childhood Asthma Atopy Center, Humidifier Disinfectant Health Center, University of Ulsan College of Medicine, Seoul, 05505, Republic of Korea.
Soo-Jong HongDepartment of Pediatrics, Asan Medical Center, Childhood Asthma Atopy Center, Humidifier Disinfectant Health Center, University of Ulsan College of Medicine, Seoul, 05505, Republic of Korea. sjhong@amc.seoul.kr.
Jae Hoon SulDepartment of Psychiatry and Biobehavioral Sciences, University of California, Los Angeles, Los Angeles, CA, 90095, USA. jaehoonsul@mednet.ucla.edu.
Hallym University · KRUniversity of California, Los Angeles · USUniversity of Ulsan · KRAsan Medical Center · KRKorea Advanced Institute of Science and Technology · KRTsinghua University · CNUlsan College · KR

Funding

Integrating Common and Rare Variation to Discover Genes Associated with Tourette SyndromeR01NS102371 · NINDS · MASSACHUSETTS GENERAL HOSPITAL · PI MATHEWS, CAROL A, OPHOFF, ROEL A · 2018 to 2022
$7.4M
A computational genomics approach to identify roles of rare genetic variants in psychiatric disorders and gene expressionK01ES028064 · NIEHS · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI SUL, JAE HOON · 2017 to 2020
$819k
Dissecting the spectrum of genetic architectures underlying congenital heart defects.R03HL150604 · NHLBI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI ARBOLEDA, VALERIE A · 2020 to 2021
$312k
National Research Foundation of Korea 2017M3A9F3043834National Science Foundation #1705197NHLBI NIH HHS R03 HL150604NIEHS NIH HHS K01 ES028064NINDS NIH HHS R01 NS102371
6 · The paper itself

Abstract

Atopic dermatitis (AD) is a common skin disease in childhood whose diagnosis requires expertise in dermatology. Recent studies have indicated that host genes-microbial interactions in the gut contribute to human diseases including AD. We sought to develop an accurate and automated pipeline for AD diagnosis based on transcriptome and microbiota data. Using these data of 161 subjects including AD patients and healthy controls, we trained a machine learning classifier to predict the risk of AD. We found that the classifier could accurately differentiate subjects with AD and healthy individuals based on the omics data with an average F1-score of 0.84. With this classifier, we also identified a set of 35 genes and 50 microbiota features that are predictive for AD. Among the selected features, we discovered at least three genes and three microorganisms directly or indirectly associated with AD. Although further replications in other cohorts are needed, our findings suggest that these genes and microbiota features may provide novel biological insights and may be developed into useful biomarkers of AD prediction.

Indexed as

Diagnosis, Computer-AssistedGastrointestinal MicrobiomeGene Expression ProfilingSupervised Machine LearningTranscriptomeCase-Control StudiesColonDermatitis, AtopicDysbiosisFemaleHost-Pathogen InteractionsHumansInfantMalePredictive Value of Tests

Identifiers

PMID34997172
PMCPMC8741793
OpenAlexW4205621089

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.