The Human Gut Microbiome in the Development of Chronic Disease: A Comprehensive Review
Sr No:
Page No:
9-14
Language:
English
Authors:
Mika`ilu Mainasara, Balkisu*, Bunza Jafaru Muhammad, Umar Asiya Imam, Bunza, Nura Muhammad, Mudathir, Abdul Mustapha, Malimi, Hafsat, Dogondaji, Muhammad, Yazid, Bukkuyum, Sani, Hassan, Tambari, Muhammad, Bello, and Jidda, Muhammad Lawal
Received:
2026-02-24
Accepted:
2026-03-27
Published Date:
2026-04-11
Abstract:
The human gut microbiome, comprising trillions of microorganisms, functions as an
"essential organ" with metabolic, immunological, and protective roles critical to host health.
This review synthesizes current evidence on the relationship between gut microbiota and
chronic disease pathogenesis, drawing from 50 high-impact studies identified through a
comprehensive literature search. Dysbiosis microbial imbalance is strongly associated with
metabolic disorders (obesity, type 2 diabetes, NAFLD), cardiovascular disease, inflammatory
bowel disease, autoimmune conditions, neurodegenerative diseases, and certain cancers. Key
mechanisms include immune modulation, regulation of intestinal barrier integrity, and
production of bioactive metabolites (short-chain fatty acids, trimethylamine N-oxide) that
influence host physiology. Environmental factors, particularly diet and lifestyle, shape
microbial composition, while therapeutic interventions including dietary modification,
probiotics, and faecal microbiota transplantation show promise but variable efficacy. Despite
significant advances in understanding microbiome-disease associations through highthroughput sequencing, challenges remain in establishing causality due to confounding
variables and inter-individual variability. This review highlights the gut microbiome's pivotal
role in chronic disease pathogenesis while identifying critical research gaps requiring
longitudinal studies, standardised dysbiosis definitions, and rigorous validation of personalised
therapeutic approaches.
Keywords:
Gut microbiome, dysbiosis, chronic disease, metabolic disorders, inflammation, therapeutic interventions.