Evidence map›Paper›PMID 36699026›Full record

ReviewFrontiers in endocrinology2022

Gut bacteriome, mycobiome and virome alterations in rheumatoid arthritis.

Sonali Dagar, Jagdeep Singh, Aastha Saini, Yashwant Kumar, Seema Chhabra, Ranjana Walker Minz, Lekha Rani

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in endocrinology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed, 1 pooled it
4.3field-weighted citation impact, top 5% 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

21 citing papers in PubMed, 1 synthesis or guideline pooled it, 28 citations in OpenAlex.

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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

7 authors at 1 institution in 1 country.

Sonali DagarDepartment of Immunopathology, Postgraduate Institute of Medical Education and Research, Chandigarh, India.
Jagdeep SinghDepartment of Immunopathology, Postgraduate Institute of Medical Education and Research, Chandigarh, India.
Aastha SainiDepartment of Immunopathology, Postgraduate Institute of Medical Education and Research, Chandigarh, India.
Yashwant KumarDepartment of Immunopathology, Postgraduate Institute of Medical Education and Research, Chandigarh, India.
Seema ChhabraDepartment of Immunopathology, Postgraduate Institute of Medical Education and Research, Chandigarh, India.
Ranjana Walker MinzDepartment of Immunopathology, Postgraduate Institute of Medical Education and Research, Chandigarh, India.
Lekha RaniDepartment of Immunopathology, Postgraduate Institute of Medical Education and Research, Chandigarh, India.
Post Graduate Institute of Medical Education and Research · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Rheumatoid arthritis (RA) is a chronic destructive autoimmune disease of the joints which causes significant pain, functional disability, and mortality. Although aberrant immune cell activation induced by the imbalance between T helper Th1/Th17 and Treg cells is implicated in the RA development, its etiopathogenesis remains unclear. The presence of mucosal inflammation and systemic IgA-isotype-autoantibodies (anti-citrullinated peptide antibodies and rheumatoid factor) in pre-clinical RA supports the mucosal origin hypothesis involving altered microbiota in disease development. The gut microbiota comprises diverse bacteria, fungal and viral components, which are critical in developing host immunity. Alterations in microbial abundance are known to exacerbate or attenuate immune responses in the gut microenvironment subsequently affecting the joints. Further, these changes can provide biomarkers for disease activity and outcome in RA. Most of the research till date has been focused on describing gut bacterial components in RA. Studies on gut mycobiome and virome components in RA are relatively new and burgeoning field. Given the paucity of mycobiome or virome specific studies in RA, this review, discusses the recent findings on alterations in gut bacterial, fungal, and viral components as well as their role in regulating the spectrum of immune-pathogenic events occurring in RA which might be explored in future as a potential therapeutic target. Further, we provide an overview on inter-kingdom interactions between bacteria, fungi, and viruses in RA. The current understanding on gut microbiota modulation for managing RA is also summarised.

Indexed as

Arthritis, RheumatoidAutoimmune DiseasesGastrointestinal MicrobiomeMycobiomeAutoantibodiesBacteriaHumansViromeAutoantibodiesadjuvant therapydysbiosisgut microbiotaimmune responsesrheumatoid arthritis

Identifiers

PMID36699026
PMCPMC9868751
OpenAlexW4313889061

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.