Evidence map›Paper›PMID 39468434›Full record

ArticleBMC microbiology2024

Insights into the gut microbiome of vitiligo patients from India.

Sudhir Kumar, Shruti Mahajan, Deeksha Kale, Nidhi Chourasia, Anam Khan, Dinesh Asati, Ashwin Kotnis, Vineet K Sharma

Abstract read
In one paragraph

Article in BMC microbiology, 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.

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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

8 authors.

Sudhir KumarDepartment of Biological Sciences, Indian Institute of Science Education and Research Bhopal, Bhopal, India.
Shruti MahajanDepartment of Biological Sciences, Indian Institute of Science Education and Research Bhopal, Bhopal, India.
Deeksha KaleDepartment of Biological Sciences, Indian Institute of Science Education and Research Bhopal, Bhopal, India.
Nidhi ChourasiaDepartment of Biochemistry, All India Institute of Medical Sciences (AIIMS), Bhopal, India.
Anam KhanDepartment of Biochemistry, All India Institute of Medical Sciences (AIIMS), Bhopal, India.
Dinesh AsatiDepartment of Biochemistry, All India Institute of Medical Sciences (AIIMS), Bhopal, India.
Ashwin KotnisDepartment of Biochemistry, All India Institute of Medical Sciences (AIIMS), Bhopal, India. Ashwin.BioChemistry@aiimsbhopal.edu.in.
Vineet K SharmaDepartment of Biological Sciences, Indian Institute of Science Education and Research Bhopal, Bhopal, India. vineetks@iiserb.ac.in.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundVitiligo is an autoimmune disease characterized by loss of pigmentation in the skin. It affects 0.4 to 2% of the global population, but the factors that trigger autoimmunity remain elusive. Previous work on several immune-mediated dermatological disorders has illuminated the substantial roles of the gut microbiome in disease pathogenesis. Here, we examined the gut microbiome composition in a cohort of vitiligo patients and healthy controls from India, including patients with a family history of the disease.

resultsOur results show significant alterations in the gut microbiome of vitiligo patients compared to healthy controls, affecting taxonomic and functional profiles as well as community structure. We observed a reduction in the abundance of several bacterial taxa commonly associated with a healthy gut microbiome and noted a decrease in the abundance of SCFA (Short Chain Fatty Acids) producing taxa in the vitiligo group. Observation of a higher abundance of genes linked to bacteria-mediated degradation of intestinal mucus suggested a potential compromise of the gut mucus barrier in vitiligo. Functional analysis also revealed a higher abundance of fatty acid and lipid metabolism-related genes in the vitiligo group. Combined analysis with data from a French cohort of vitiligo also led to the identification of common genera differentiating healthy and gut microbiome across populations.

conclusionOur observations, together with available data, strengthen the role of gut microbiome dysbiosis in symptom exacerbation and possibly pathogenesis in vitiligo. The reported microbiome changes also showed similarities with other autoimmune disorders, suggesting common gut microbiome-mediated mechanisms in autoimmune diseases. Further investigation can lead to the exploration of dietary interventions and probiotics for the management of these conditions.

Indexed as

BacteriaGastrointestinal MicrobiomeVitiligoAdultCase-Control StudiesCohort StudiesDysbiosisFatty Acids, VolatileFemaleHumansIndiaLipid MetabolismMaleMiddle AgedRNA, Ribosomal, 16SYoung AdultFatty Acids, VolatileRNA, Ribosomal, 16SAutoimmune diseaseDysbiosisGut MicrobiomeGut-skin axisVitiligo

Identifiers

PMID39468434
PMCPMC11514916

What Socratic holds

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LicenceCC BY-NC-ND
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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 Socratic graph.