Evidence map›Paper›PMID 42516970›Full record

ArticleFrontiers in microbiology2026

Gut microbiota profiles in pediatric atopic dermatitis and their relationship with skin microbiota: an Indonesian case-control study.

Raden Mohamad Rendy Ariezal Effendi, Hok Bing Thio, Robert Kraaij, Chrysanti Murad, Reiva Farah Dwiyana, Oki Suwarsa, Tamar E C Nijsten, Luba M Pardo

Abstract read
In one paragraph

Article in Frontiers in microbiology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

8 authors.

Raden Mohamad Rendy Ariezal EffendiDepartment of Dermatology, Erasmus MC, University Medical Center Rotterdam, Rotterdam, Netherlands.
Hok Bing ThioDepartment of Dermatology, Erasmus MC, University Medical Center Rotterdam, Rotterdam, Netherlands.
Robert KraaijDepartment of Internal Medicine, Erasmus MC, University Medical Center Rotterdam, Rotterdam, Netherlands.
Chrysanti MuradDivision of Microbiology, Department of Biomedical Sciences, Faculty of Medicine Universitas Padjadjaran, Bandung, West Java, Indonesia.
Reiva Farah DwiyanaDepartment of Dermatology, Venereology, and Aesthetics, Faculty of Medicine Universitas Padjadjaran, Dr. Hasan Sadikin Hospital, Bandung, West Java, Indonesia.
Oki SuwarsaDepartment of Dermatology, Venereology, and Aesthetics, Faculty of Medicine Universitas Padjadjaran, Dr. Hasan Sadikin Hospital, Bandung, West Java, Indonesia.
Tamar E C NijstenDepartment of Dermatology, Erasmus MC, University Medical Center Rotterdam, Rotterdam, Netherlands.
Luba M PardoDepartment of Dermatology, Erasmus MC, University Medical Center Rotterdam, Rotterdam, Netherlands.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: The bacterial gut microbiota has been implicated in the pathophysiology of atopic dermatitis (AD), yet most studies have focused on Western populations and have typically examined the gut or skin microbiota in isolation. Evidence for interactions between skin and gut microbiota in inflammatory skin diseases remains limited, particularly in pediatric cohorts from non-Western settings. Here, we profiled the bacterial gut microbiota in children with AD from Indonesia, and evaluated the relationship with bacterial skin microbiota using paired gut and skin samples from the same individuals. Methods: Skin and fecal swabs were collected from children and adolescents aged 4-18 years (111 AD cases and 107 controls) recruited from the Pediatric Dermatology Clinic of Dr. Hasan Sadikin General Hospital, an urban tertiary-care referral center in Bandung, West Java, Indonesia. Both skin and gut bacterial microbiota was profiled using 16S rRNA sequencing and bacteria were identified using DADA2 pipeline, previously published skin microbiota data from the same participants were paired with the gut microbiota data for skin-gut analyses. Alpha diversity was compared between AD cases and controls, beta diversity assessed using permutational multivariate analysis of variance (PERMANOVA) and univariable differential analysis was tested using ANCOM-BC2. Results: Gut alpha diversity did not differ between AD cases and controls, although hand feeding was associated with a higher Shannon diversity (β = 0.20; adjusted Conclusion: Gut microbiota differences by AD were modest. ASV-level, predicted stool functional pathways, and skin-gut correlation analyses suggested selective cross-site associations.

Indexed as

16S rRNA sequencingdermatitis and atopicgut microbiotaIndonesiapediatricpredicted functional pathwaysskin-gut correlationsskin microbiota

Identifiers

PMID42516970
PMCPMC13402473

What Socratic 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 Socratic graph.