Evidence map›Paper›PMID 38997299›Full record

Observational studyScientific reports2024

Familial clustering of dysbiotic oral and fecal microbiomes in juvenile dermatomyositis.

Sean T Koester, Albert Chow, Evan Pepper-Tunick, Peggy Lee, Mary Eckert, Laurie Brenchley, Pamela Gardner, Hyun Jung Song, Naisi Li, Adam Schiffenbauer and 7 more

Abstract readObservational StudyMulticenter Study
In one paragraph

Observational study in Scientific reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Review
  2. Review
  3. Review
  4. Review
  5. 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

17 authors.

Sean T Koester *Translational Science and Therapeutics Division, Fred Hutchinson Cancer Center, Seattle, WA, USA.
Albert Chow *Department of Pediatrics, Division of Rheumatology, University of Washington, Seattle, WA, USA.
Evan Pepper-TunickMolecular Engineering and Sciences Institute, University of Washington, Seattle, WA, USA.
Peggy LeeSchool of Dentistry, University of Washington, Seattle, WA, USA.
Mary EckertCenter for Clinical and Translational Research, Seattle Children's Research Institute, Seattle, WA, USA.
Laurie BrenchleyOffice of the Clinical Director, NIDCR, National Institutes of Health, Bethesda, MD, USA.
Pamela GardnerOffice of the Clinical Director, NIDCR, National Institutes of Health, Bethesda, MD, USA.
Hyun Jung SongSchool of Dentistry, University of Washington, Seattle, WA, USA.
Naisi LiTranslational Science and Therapeutics Division, Fred Hutchinson Cancer Center, Seattle, WA, USA.
Adam SchiffenbauerEnvironmental Autoimmunity Group, Clinical Research Branch, National Institute of Environmental Health Sciences, National Institutes of Health, Bethesda, MD, USA.
Rita VolochayevEnvironmental Autoimmunity Group, Clinical Research Branch, National Institute of Environmental Health Sciences, National Institutes of Health, Bethesda, MD, USA.
Nastaran BayatEnvironmental Autoimmunity Group, Clinical Research Branch, National Institute of Environmental Health Sciences, National Institutes of Health, Bethesda, MD, USA.
Jeffrey S McLeanDepartment of Periodontics, University of Washington, Seattle, WA, USA.
Lisa G RiderEnvironmental Autoimmunity Group, Clinical Research Branch, National Institute of Environmental Health Sciences, National Institutes of Health, Bethesda, MD, USA.
Susan ShenoiDepartment of Pediatrics, Division of Rheumatology, University of Washington, Seattle, WA, USA.
Anne M StevensDepartment of Pediatrics, Division of Rheumatology, University of Washington, Seattle, WA, USA.
Neelendu DeyTranslational Science and Therapeutics Division, Fred Hutchinson Cancer Center, Seattle, WA, USA. ndey@fredhutch.org.

Funding

Environmental/genetic Risk Factors and Pathogenesis of Autoimmune DiseaseZIAES101074 · NIEHS · NATIONAL INSTITUTE OF ENVIRONMENTAL HEALTH SCIENCES · PI RIDER, LISA · 2009 to 2025
$34.6M
Understanding adenoma progression: Interplay among tissue microenvironment, clonal architecture, and gut microbiomeU54CA274374 · NCI · FRED HUTCHINSON CANCER CENTER · PI Kristina A. Matkowskyj · 2022 to 2026
$10.7M
The gut microbiota, bile acid-mediated enteric nervous system signaling, and modulation of gastrointestinal motilityK08DK111941 · NIDDK · WASHINGTON UNIVERSITY · PI DEY, NEELENDU · 2016 to 2020
$809k
Intramural NIH HHS ZIA ES101074NCI NIH HHS U54 CA274374NIDDK NIH HHS DK111941NIDDK NIH HHS K08 DK111941NIEHS NIH HHS HHSN2732016000021NIH HHS ZIAES101074
6 · The paper itself

Abstract

Juvenile dermatomyositis (JDM) is a rare immune-mediated disease of childhood with putative links to microbial exposures. In this multi-center, prospective, observational cohort study, we evaluated whether JDM is associated with discrete oral and gut microbiome signatures. We generated 16S rRNA sequencing data from fecal, saliva, supragingival, and subgingival plaque samples from JDM probands (n = 28). To control for genetic and environmental determinants of microbiome community structure, we also profiled microbiomes of unaffected family members (n = 27 siblings, n = 26 mothers, and n = 17 fathers). Sample type (oral-vs-fecal) and nuclear family unit were the predominant variables explaining variance in microbiome diversity, more so than having a diagnosis of JDM. The oral and gut microbiomes of JDM probands were more similar to their own unaffected siblings than they were to the microbiomes of other JDM probands. In a sibling-paired within-family analysis, several potentially immunomodulatory bacterial taxa were differentially abundant in the microbiomes of JDM probands compared to their unaffected siblings, including Faecalibacterium (gut) and Streptococcus (oral cavity). While microbiome features of JDM are often shared by unaffected family members, the loss or gain of specific fecal and oral bacteria may play a role in disease pathogenesis or be secondary to immune dysfunction in susceptible individuals.

Indexed as

DermatomyositisFecesGastrointestinal MicrobiomeMouthRNA, Ribosomal, 16SAdolescentAdultChildChild, PreschoolDysbiosisFemaleHumansMaleMicrobiotaProspective StudiesSalivaRNA, Ribosomal, 16S

Identifiers

PMID38997299
PMCPMC11245510

What OpenQuestion holds

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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.