Evidence map›Paper›PMID 42700342›Full record

ReviewJournal of physiology and biochemistry2026

Decoding dysbiosis: the role of gut microbiota in MASLD progression and emerging therapeutic interventions.

Dinesh Mohan Swamikkannu, Santhosha Dasarapu, Kanishk Dinesh Mohan, Allimalarkodi Shanmugam

Abstract readReview
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In one paragraph

Review in Journal of physiology and biochemistry, 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

4 authors.

Dinesh Mohan SwamikkannuDepartment of Pharmaceutics, Vishnu Institute of Pharmaceutical Education & Research Sangareddy-Narsapur Rd, Narsapur, Tuljaraopet, Hyderabad Telangana, 502313, India. dineshmohan.s@viper.ac.in.
Santhosha DasarapuDepartment of Pharmacognosy, Vishnu Institute of Pharmaceutical Education & Research Sangareddy-Narsapur Rd, Narsapur, Tuljaraopet, Hyderabad Telangana, 502313, India.
Kanishk Dinesh MohanDepartment of Computational Biology, Mahindra University, No: 62/1A, Bahadurpally, Jeedimetla, Hyderabad, Telangana, 500043, India.
Allimalarkodi ShanmugamDepartment of Pharmaceutical microbiology, The Erode College of Pharmacy, 7MX5+9H3, Veppampalayam, Pavalathampalayam, Erode, Tamil Nadu, 638112, India.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Metabolic dysfunction-associated steatotic liver disease (MASLD), affects a substantial proportion of the global population and is closely associated with metabolic disorders. The gut microbiota, comprising a diverse community of microorganisms within the gastrointestinal tract, plays a crucial role in maintaining host health. Dysbiosis, defined as an imbalance in this microbial ecosystem, has been increasingly implicated in the development and progression of liver diseases, including MASLD. This review examines the role of the gut microbiota in MASLD pathogenesis and highlights its potential as a therapeutic target. The gut-liver axis facilitates bidirectional communication between the intestine and the liver, thereby influencing metabolic regulation. In MASLD, dysbiosis characterized by reduced microbial diversity and an increased abundance of Gram-negative bacteria leads to altered bile acid metabolism, increased intestinal permeability, enhanced endotoxin translocation, and hepatic inflammation. Additionally, it disrupts short-chain fatty acid production and interferes with the endocannabinoid system and choline metabolism, collectively driving disease progression. Emerging non-invasive diagnostic approaches, including gut microbiome profiling, show promise for early detection. Although specific pharmacological treatments remain limited, microbiota-targeted strategies such as probiotics, prebiotics, and synbiotics aim to restore microbial balance. Furthermore, emerging modalities within microbiome-based therapies, including mesenchymal stromal cell therapy and bacteriophage therapy, offer potential for targeted modulation of the gut microbiota and liver repair. The gut microbiota-liver axis plays a central role in the pathogenesis of MASLD. Growing insights into this relationship have driven the development of microbiome-based diagnostic and therapeutic approaches. Non-invasive diagnostic tools, particularly gut microbiome profiling, show promise for early detection. Therapeutically, microbiota-targeted strategies including probiotics, prebiotics, synbiotics, and emerging modalities such as cellular and bacteriophage-based therapies offer potential to restore microbial balance and improve liver function. Nevertheless, robust clinical studies are essential to validate their efficacy, safety, and applicability in personalized MASLD management.

Indexed as

DysbiosisFatty LiverGastrointestinal MicrobiomeAnimalsBile Acids and SaltsDisease ProgressionHumansLiverMesenchymal Stem Cell TransplantationPrebioticsProbioticsSynbioticsBile Acids and SaltsPrebioticsDysbiosisGut–liver axisGut microbiotaMASLDMicrobiome profilingMicrobiota-based therapy

Identifiers

What Socratic holds

Textmetadata
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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.