# Differential Oral Microbiota and Serum Cytokine Signatures in Age-Grouped Patients with Marfan Syndrome

**Authors:** Erick Ricardo Ordaz-Robles, María Elena Soto, Paulina Hernández-Ruiz, Alma Reyna Escalona-Montaño, Luis Alejandro Constantino-Jonapa, Amedeo Amedei, María Magdalena Aguirre-García

PMC · DOI: 10.3390/biomedicines13020330 · Biomedicines · 2025-01-31

## TL;DR

This study explores differences in oral bacteria and immune markers in Marfan syndrome patients with and without aortic issues.

## Contribution

The study is the first to investigate oral microbiota differences in Marfan syndrome patients with aortic dilatation.

## Key findings

- Actinomyces and Rothia were more abundant in patients with aortic dilatation.
- Fusobacterium was more abundant in patients without aortic dilatation.
- IL-1β levels were higher in non-dilatation patients but not significantly different.

## Abstract

Introduction: Marfan syndrome (MFS) is an autosomal dominant genetic disorder, caused by a mutation in the FBN-1 gene, affecting the cardiovascular, musculoskeletal, ocular, and central nervous systems. Cardiovascular abnormalities associated with MFS lead to different pathological conditions, such as cardiac arrhythmias, coronary artery disease, and aortic dilatation. The latter are the primary causes of mortality in MFS patients. To date, the role of altered oral microbiota (OM) in MFS is unknown, and so the aim of our study was to determine whether there are differences in the oral microbiota of MFS patients with aortic dilatation and non-dilatation. Methods: We enrolled 36 MFS patients, who were divided into groups with aortic non-dilatation (n = 12) and with aortic dilatation (n = 24). Dental plaque samples were used for OM analysis, and serum was used for cytokine evaluation. Results: The main genera were compared between patients with aortic dilatation and non-dilatation, revealing three genera with significant differences: Actinomyces (p = 0.007) and Rothia (p = 0.002) were more abundant in those with aortic dilatation, while Fusobacterium (p = 0.044) was more abundant in non-dilatation patients. However, no significant differences in cytokine levels were observed between the presence and absence of aortic dilatation, except that the IL-1β levels were higher in non-dilatation patients (165.09 pg/mL) than in those with dilatation (117.15 pg/mL), with a significance of p = 0.057. Conclusions: This study represents the initial, tentative pilot study to understand the relationship between oral health and systemic conditions in patients with Marfan syndrome.

## Linked entities

- **Genes:** FBN1 (fibrillin 1) [NCBI Gene 2200]
- **Diseases:** Marfan syndrome (MONDO:0007947), coronary artery disease (MONDO:0005010)

## Full-text entities

- **Genes:** FBN1 (fibrillin 1) [NCBI Gene 2200] {aka ACMICD, ECTOL1, FBN, GPHYSD2, MASS, MFLS}, IL1B (interleukin 1 beta) [NCBI Gene 3553] {aka IL-1, IL1-BETA, IL1F2, IL1beta}
- **Diseases:** cardiac arrhythmias (MESH:D001145), MFS (MESH:D008382), autosomal dominant genetic disorder (MESH:D030342), aortic dilatation (MESH:D002311), coronary artery disease (MESH:D003324), Cardiovascular abnormalities (MESH:D018376)
- **Species:** Fusobacterium (genus) [taxon 848], Homo sapiens (human, species) [taxon 9606], Actinomyces (genus) [taxon 1654]

## Full text

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## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC11853651/full.md

## References

42 references — full list in the complete paper: https://tomesphere.com/paper/PMC11853651/full.md

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Source: https://tomesphere.com/paper/PMC11853651