# Gut microbiota alliance to shape sceneries of familial Mediterranean fever: a scoping review detailing difference between children and adults

**Authors:** Camilla Maria Pisa, Angelo Verrone, Martha Mazuy, Lorenzo Ientile, Donato Rigante, Susanna Esposito

PMC · DOI: 10.3389/fimmu.2026.1814103 · Frontiers in Immunology · 2026-03-18

## TL;DR

This review explores how gut microbiota influences Familial Mediterranean Fever, highlighting differences in children and adults.

## Contribution

The paper provides a scoping review focusing on gut microbiota's role in shaping FMF expression, particularly in children.

## Key findings

- Pediatric FMF patients show intestinal dysbiosis with reduced microbial diversity and pro-inflammatory taxa.
- Gut microbiota alterations may modulate pyrin-inflammasome activation and influence disease phenotype.
- Colchicine therapy partially remodels the gut microbiome, promoting an anti-inflammatory profile.

## Abstract

Familial Mediterranean fever (FMF) is the most common monogenic autoinflammatory disease worldwide and a key-model to illustrate dysregulation of innate immunity, etiologically determined by pathogenic variants in the MEFV gene, encoding pyrin, leading to uncontrolled interleukin-1β and interleukin-18 release. Despite its genetic basis, FMF shows marked clinical heterogeneity in all-aged patients, mostly in children, suggesting a role of potential environmental modifiers which are far to be exactly unraveled. Recent medical literature has increasingly illuminated the importance of gut microbiota in maintaining overall health and immune functions, and its contribution has been claimed also to explain both FMF inflammatory activity and heterogeneous disease expression. This narrative review summarizes current evidence on the interaction between gut microbiota and FMF, with a specific focus on differences between children and adults. Pediatric studies dedicated to FMF have reported intestinal dysbiosis in terms of reduced microbial diversity and depletion of short-chain fatty acid-producing bacteria, with subsequent enrichment of pro-inflammatory taxa: such alteration could modulate pyrin-inflammasome activation and contribute to systemic inflammation, disease phenotype, and response to colchicine or to other drugs specifically used in colchicine-resistant FMF. Geographic and lifestyle factors may shape intestinal microbiota composition early in life, reinforcing the relevance of gut flora and confirming its activity as a crucial tessera to determine FMF sceneries, mostly in children, and a potential target for future add-on therapeutic strategies. In addition, colchicine therapy appears to partially remodel the gut microbiome, empowering a local beneficial anti-inflammatory microbial profile.

## Linked entities

- **Genes:** MEFV (MEFV innate immunity regulator, pyrin) [NCBI Gene 4210]
- **Proteins:** Mefv (Mediterranean fever), IL18 (interleukin 18)
- **Diseases:** Familial Mediterranean fever (MONDO:0009572), FMF (MONDO:0009572)

## Full-text entities

- **Genes:** MEFV (MEFV innate immunity regulator, pyrin) [NCBI Gene 4210] {aka FMF, MEF, PAAND, TRIM20}, IL1B (interleukin 1 beta) [NCBI Gene 3553] {aka IL-1, IL1-BETA, IL1F2, IL1beta}, IL18 (interleukin 18) [NCBI Gene 3606] {aka IGIF, IL-18, IL-1g, IL1F4}
- **Diseases:** FMF (MESH:D010505), autoinflammatory disease (MESH:D056660), inflammation (MESH:D007249), intestinal dysbiosis (MESH:D064806)
- **Chemicals:** colchicine (MESH:D003078), short-chain fatty acid (MESH:D005232)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC13038611/full.md

## Figures

1 figure with captions in the complete paper: https://tomesphere.com/paper/PMC13038611/full.md

## References

18 references — full list in the complete paper: https://tomesphere.com/paper/PMC13038611/full.md

---
Source: https://tomesphere.com/paper/PMC13038611