# Gut microbiota and brain aging: a comparative review of African and western populations

**Authors:** Beulah Favour Ortutu, Abidemi Oluwasanmi Okin, Kwame Osei Darkwah, Uju Maryanne Onuorah, Abdulkadir Yusif Maigoro, Gideon Onyedikachi Iheme

PMC · DOI: 10.3389/fnagi.2026.1740408 · Frontiers in Aging Neuroscience · 2026-02-12

## TL;DR

This review compares gut microbiota differences between African and Western populations and their potential impact on brain aging and neurodegenerative diseases.

## Contribution

It synthesizes evidence on how traditional African diets may influence gut microbiota and neuroprotection through the gut-brain axis.

## Key findings

- African populations show higher abundance of Prevotella, Faecalibacterium, and Ruminococcus linked to better gut health.
- These microbial profiles are associated with reduced inflammation and short-chain fatty acid production, potentially delaying brain aging.
- Lower dementia rates in African populations may be partly explained by gut microbiota differences.

## Abstract

As the population ages, cognitive decline and neurodegenerative diseases have become major public health concerns. The human gut microbiota plays a major role in regulating neurodevelopment, neuroinflammation, and cognitive decline through the gut-brain axis. Emerging evidence reveals a possible association between alterations in gut microbial diversity and age-related neurological disorders, including Alzheimer’s disease and neurodegeneration. Regional and dietary differences shape the gut microbiome. These variations may, in turn, be associated with differences in brain aging across populations. Several cross-sectional studies indicate that rural African communities consuming predominantly fiber-rich diets exhibit distinct gut microbiota profiles characterized by increased abundance of genera, including Prevotella, Faecalibacterium, and Ruminococcus. These microbial configurations have been associated with improved gut barrier integrity, reduced systemic inflammation, and enhanced production of short-chain fatty acids in some preclinical and human studies. All these factors have been studied as potential mechanisms linked to delayed brain aging. Furthermore, epidemiological reports suggest lower prevalence rates of dementia and other neurodegenerative disorders in these populations, although such comparisons may be influenced by differences in study design, diagnosis, and case ascertainment across regions. This narrative review synthesized current understanding of the gut microbiota’s role in brain aging, summarized available data on gut microbiota composition in African versus Western populations, and explored the pathways by which traditional African diets may contribute to neuroprotection. By critically examining this evidence and highlighting major research gaps, the review advocates for region-specific investigations and future longitudinal studies to validate causal links.

## Linked entities

- **Diseases:** Alzheimer’s disease (MONDO:0004975), dementia (MONDO:0001627)

## Full-text entities

- **Genes:** Trem2 (triggering receptor expressed on myeloid cells 2) [NCBI Gene 83433] {aka TREM-2, Trem2a, Trem2b, Trem2c}, IL17A (interleukin 17A) [NCBI Gene 3605] {aka CTLA-8, CTLA8, IL-17, IL-17A, IL17, ILA17}, FFAR2 (free fatty acid receptor 2) [NCBI Gene 2867] {aka FFA2R, GPR43}, HDAC9 (histone deacetylase 9) [NCBI Gene 9734] {aka HD7, HD7b, HD9, HDAC, HDAC7B, HDAC9B}, BDNF (brain derived neurotrophic factor) [NCBI Gene 627] {aka ANON2, BULN2}, SNCA (synuclein alpha) [NCBI Gene 6622] {aka NACP, PARK1, PARK4, PD1}, App (amyloid beta precursor protein) [NCBI Gene 11820] {aka Abeta, Abpp, Adap, Ag, Cvap, E030013M08Rik}, Ppargc1a (peroxisome proliferative activated receptor, gamma, coactivator 1 alpha) [NCBI Gene 19017] {aka A830037N07Rik, Gm11133, PGC-1, PPARGC-1-alpha, Pgc-1alpha, Pgc1}, mucin [NCBI Gene 100508689], Bdnf (brain derived neurotrophic factor) [NCBI Gene 12064], Tfam (transcription factor A, mitochondrial) [NCBI Gene 21780] {aka Hmgts, mtTFA, tsHMG}, HCAR2 (hydroxycarboxylic acid receptor 2) [NCBI Gene 338442] {aka GPR109A, HCA2, HM74a, HM74b, NIACR1, PUMAG}, APP (amyloid beta precursor protein) [NCBI Gene 351] {aka AAA, ABETA, ABPP, AD1, APPI, CTFgamma}, TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}, FFAR3 (free fatty acid receptor 3) [NCBI Gene 2865] {aka FFA3R, GPR41}, Nfe2l2 (nuclear factor, erythroid derived 2, like 2) [NCBI Gene 18024] {aka Nrf2}
- **Diseases:** dementia (MESH:D003704), neuronal loss (MESH:D009410), depressive (MESH:D003866), cognitive decline (MESH:D003072), chronic (MESH:D002908), synaptic dysfunction (MESH:C536122), colorectal cancer (MESH:D015179), astrogliosis (MESH:D005911), neurological disorders (MESH:D009461), metabolic disorders (MESH:D008659), Alzheimer's and Parkinson's diseases (MESH:D010300), mitochondrial damage (MESH:D028361), NDs (MESH:D019636), inflammation (MESH:D007249), BBB dysfunction (MESH:C536830), anxiety (MESH:D001007), Neuroinflammation (MESH:D000090862), ND (MESH:C537849), AD (MESH:D000544), dysbiosis (MESH:D064806)
- **Chemicals:** LPS (MESH:D008070), fructose (MESH:D005632), serotonin (MESH:D012701), SCFA (MESH:D005232), ROS (MESH:D017382), folate (MESH:D005492), Acetate (MESH:D000085), lysine (MESH:D008239), Aromatic AAs (-), propionate (MESH:D011422), starch (MESH:D013213), carbohydrates (MESH:D002241), catecholamines (MESH:D002395), Butyrate (MESH:D002087), homocysteine (MESH:D006710), amino acid (MESH:D000596), nicotinamide (MESH:D009536), BCAA (MESH:D000597), GABA (MESH:D005680), inulin (MESH:D007444), sugars (MESH:D000073893), aromatic amino acids (MESH:D024322), proline (MESH:D011392), mannose (MESH:D008358), lactate (MESH:D019344), polysaccharides (MESH:D011134), histidine (MESH:D006639), methane (MESH:D008697)
- **Species:** Akkermansia (genus) [taxon 239934], Sorghum bicolor (broomcorn, species) [taxon 4558], Enterobacteriaceae (enterobacteria, family) [taxon 543], gut metagenome (species) [taxon 749906], Subdoligranulum (genus) [taxon 292632], Manihot esculenta (cassava, species) [taxon 3983], Homo sapiens (human, species) [taxon 9606], Bacteroides fragilis (species) [taxon 817], Staphylococcus aureus (species) [taxon 1280], Collinsella (genus) [taxon 102106], Methanobrevibacter (genus) [taxon 2172], Veillonella (genus) [taxon 29465], Salmonella enterica (species) [taxon 28901], Bifidobacterium adolescentis (species) [taxon 1680], Ruminococcus (genus) [taxon 1263], Megasphaera (genus) [taxon 906], Escherichia coli (E. coli, species) [taxon 562], Dioscorea alata (greater yam, species) [taxon 55571], Faecalibacterium (genus) [taxon 216851], Clostridium perfringens (species) [taxon 1502], Lactobacillus (genus) [taxon 1578], Panicum miliaceum (broomcorn millet, species) [taxon 4540], Prevotella (genus) [taxon 838], Mus musculus (house mouse, species) [taxon 10090], Pseudomonas aeruginosa (species) [taxon 287]

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC12935954/full.md

## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12935954/full.md

## References

169 references — full list in the complete paper: https://tomesphere.com/paper/PMC12935954/full.md

---
Source: https://tomesphere.com/paper/PMC12935954