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Microbiome & Gut Health
GMJ News knowledge hub · last reviewed August 2026 · Georgian Medical Journal
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The human gut microbiome — approximately 100 trillion microorganisms (bacteria, archaea, viruses, fungi) encoding approximately 3 million unique genes vs the ~22,000 of the human genome — communicates bidirectionally with the immune system (70% of immune tissue is gut-associated), the brain (gut-brain axis via vagus nerve, metabolites and immune signalling), and virtually every major organ system, with dysbiosis (disruption of normal microbial ecology) associated — though not always causally proven — with IBD, obesity, type 2 diabetes, depression and colorectal cancer (WHO). The most important clinical advance: faecal microbiota transplantation (FMT) received FDA approval in 2022-2023 (Rebyota — Ferring; Vowst — Seres Therapeutics) specifically for recurrent Clostridioides difficile infection — achieving approximately 90% cure rates vs approximately 30% for repeat antibiotics — while the multi-billion-dollar probiotic supplement market operates largely on marketing rather than clinical evidence for most claimed benefits beyond C. diff and antibiotic-associated diarrhoea.
Key messages
FDA-approved FMT — 90% cure for recurrent C. diff
Faecal microbiota transplantation (FMT) received FDA approval in 2022-2023: Rebyota (Ferring, RBX2660 — enema) November 2022; Vowst (Seres Therapeutics, SER-109 — oral capsules) May 2023 — both for recurrent Clostridioides difficile infection. FMT achieves approximately 90% cure vs approximately 30% for repeated antibiotics. This is the strongest clinical evidence in all of microbiome medicine — and the only FDA-approved microbiome-based therapy.
The gut microbiome — 100 trillion organisms, 3 million genes
The human gut contains approximately 100 trillion microorganisms encoding approximately 3 million unique microbial genes — dwarfing the approximately 22,000 genes in the human genome. These microorganisms co-evolved with humans over millions of years. The dominant phyla: Firmicutes and Bacteroidetes (accounting for approximately 90%); also Actinobacteria, Proteobacteria, Verrucomicrobia.
Gut-brain axis — the second brain
The enteric nervous system (500 million neurons in the gut wall — comparable to the spinal cord) communicates bidirectionally with the brain via the vagus nerve, microbial metabolites (SCFAs, tryptophan metabolites), immune signalling and the HPA stress axis. The microbiome produces approximately 90% of the body's serotonin (in enterochromaffin cells). Germ-free mouse experiments show profound alterations in behaviour, stress response and brain development — establishing a causal microbiome-brain link in animal models.
Probiotics — evidence is condition-specific, not generic
Strong evidence: C. diff prevention during antibiotic therapy (Cochrane 2017: approximately 60% risk reduction; Lactobacillus rhamnosus GG and Saccharomyces boulardii have best evidence); rotavirus and infectious diarrhoea in children; necrotising enterocolitis prevention in premature infants. Modest/inconsistent evidence: IBS (some strains reduce bloating/pain); antibiotic-associated diarrhoea; ulcerative colitis maintenance. Insufficient/no evidence: depression; autism; weight loss; immune function in healthy adults; most other marketed uses. The multi-billion-dollar probiotic market vastly outpaces the evidence.
Fibre — the most evidence-based microbiome intervention
Dietary fibre is metabolised by gut bacteria to produce short-chain fatty acids (SCFAs): butyrate (principal fuel for colonocytes; anti-inflammatory; anti-cancer properties via histone deacetylase inhibition); propionate (liver gluconeogenesis regulation; appetite suppression); acetate (peripheral energy metabolism). Higher fibre intake consistently associated with: lower colorectal cancer risk; lower cardiovascular disease; better insulin sensitivity; greater microbiome diversity. The WHO recommends ≥25g fibre/day for adults; most people in HICs consume approximately 15g.
The hype-evidence gap — microbiome is not a panacea
The microbiome field suffers from a massive hype-evidence gap: preclinical and observational data are exciting; causality from association is frequently over-claimed; "dysbiosis" is loosely defined and varies by condition and study. Interventions with strong evidence: FMT for C. diff; specific probiotic strains for specific conditions. Interventions with insufficient evidence: personalised microbiome testing (direct-to-consumer gut microbiome tests have no validated clinical utility); probiotic supplements for most health claims; prebiotic supplements beyond standard high-fibre diet.
Key statistics
500M neurons
in the enteric nervous system (the "second brain") — communicates with CNS
NeurogastroenterologyMicrobiome intervention evidence — by clinical application (Cochrane/FDA)
Glossary of key terms
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Frequently asked questions 12 Q&A — structured for Google featured snippets and AI discovery
Knowledge hub: guidelines, conventions and reports
Organizations working in migration and health
Related health topics
Clostridioides difficile (FMT primary indication)Nutrition and dietIBD (FMT trials)Mental health (gut-brain axis)Antibiotics and microbiomeObesity (microbiome associations)
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