Evidence map›Paper›PMID 42070004›Full record

ReviewCurrent microbiology2026

Medicinal Plants and the Gastrointestinal Microbiota in Chronic Diseases Modulation: A Structured Mechanistic and Translational Review.

Esther Ugo Alum, Daniel Ejim Uti, Okechukwu Paul-Chima Ugwu, Michael Ben Okon, Waheeb Sami Aggad, Hailah M Almohaimeed, Neeraj Bainsal, Sandeep Kumar Shukla, Kranti Kiran Reddy Ealla

Erratum issuedAbstract readReview
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In one paragraph

Review in Current microbiology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. 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

5 · Who and what money

Authors and funding

9 authors.

Esther Ugo AlumDepartment of Research and Publications, Kampala International University, P. O. Box 20000, Kampala, Uganda. esther.alum@kiu.ac.ug.ORCID http://orcid.org/0000-0003-4105-8615
Daniel Ejim UtiDepartment of Research and Publications, Kampala International University, P. O. Box 20000, Kampala, Uganda.
Okechukwu Paul-Chima UgwuDepartment of Research and Publications, Kampala International University, P. O. Box 20000, Kampala, Uganda.
Michael Ben OkonDepartment of Research and Publications, Kampala International University, P. O. Box 20000, Kampala, Uganda.
Waheeb Sami AggadDivision of Anatomy, Department of Basic Medical Sciences, College of Medicine, University of Jeddah, Jeddah, 23890, Saudi Arabia.
Hailah M AlmohaimeedDepartment of Basic Science, College of Medicine, Princess Nourah bint Abdulrahman University, P. O. Box 84428, Riyadh, 11671, Saudi Arabia.
Neeraj BainsalUniversity Institute of Pharma Sciences, Chandigarh University, Mohali, Punjab, India.
Sandeep Kumar ShuklaSharda School of Pharmacy, Sharda University, Greater, Noida, India.
Kranti Kiran Reddy EallaDepartment of Oral and Maxillofacial Pathology, Malla Reddy Institute of Dental Sciences, Malla Reddy Vishwavidyapeeth, Suraram, Hyderabad, 500055, Telangana, India.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The gut microbiome supports digestion, immunity, and metabolism; its imbalance (dysbiosis) drives inflammation and metabolic dysfunction, contributing to chronic diseases such as diabetes, cardiovascular disease, inflammatory bowel disease, and autoimmune disorders. Medicinal plants provide a wide range of phytochemicals (such as polyphenols, flavonoids, alkaloids, saponins), which reach the colon and undergo two-sided interactions with microbes in the gut, acting as potential microbiome modulators and substrates of biotransformation into bioactive metabolites. This structured narrative review synthesises evidence from peer-reviewed studies indexed in PubMed, Scopus, and Web of Science over the last 10 years on the role of medicinal plants in microbiome-mediated chronic disease modulation. This literature is organised into three mechanistic axes: (i) perturbations, defined here as measurable shifts in microbial diversity or taxonomic composition relative to a baseline or healthy reference state, together with beneficial taxa enrichment; (ii) alterations in microbial metabolite output, especially short-chain fatty acids (SCFAs) and other immunometabolic mediators; and (iii) downstream host metabolic and immune signalling. Rather than broad descriptive summaries, the literature is organised using an axis-based mechanistic framework, highlighting key translational constraints such as botanical heterogeneity, dose/formulation variability, and inconsistent microbiome endpoint standardisation, that must be addressed to strengthen human evidence and clinical relevance. Illustrative microbiome-mediated processes involve botanicals such as turmeric (curcumin), ginseng (ginsenosides), and green tea (catechins), though evidence strength varies by study design. Future progress requires standardised phytochemical characterisation, microbiome-stratified trials, and integration of multi-omics with artificial intelligence analytics to enhance mechanistic insight, identify responders, and enable personalised plant-based microbiome therapies.

Indexed as

Gastrointestinal MicrobiomePlants, MedicinalAnimalsBacteriaChronic DiseaseHumansPhytochemicalsPhytochemicals

Identifiers

What Socratic holds

Textmetadata
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.