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Microbiome-targeted interventions for the control of oral-gut dysbiosis and chronic systemic inflammation

March 18, 2025

Last Updated: 2024

Microbiome Signatures identifies and validates condition-specific microbiome shifts and interventions to accelerate clinical translation. Our multidisciplinary team supports clinicians, researchers, and innovators in turning microbiome science into actionable medicine.

Karen Pendergrass

Karen Pendergrass is a microbiome researcher specializing in microbiome-targeted interventions (MBTIs). She systematically analyzes scientific literature to identify microbial patterns, develop hypotheses, and validate interventions. As the founder of the Microbiome Signatures Database, she bridges microbiome research with clinical practice. In 2012, based on her own investigative research, she became the first documented case of FMT for Celiac Disease—four years before the first published case study.

What was studied?

The study focused on the relationship between oral-gut dysbiosis and chronic systemic inflammation, particularly in the context of periodontitis and its associated diseases. It reviewed the mechanisms underlying the crosstalk between the microbiome and the host, and explored novel precision medicine approaches aimed at controlling systemic inflammation by modulating the microbiome. The study emphasized the need to understand the causal relationships between the microbiome and its metabolites that contribute to periodontitis and chronic inflammation.

 

Who was studied?

The review incorporated findings from various research studies involving human and animal models to understand the interactions between the oral and gut microbiomes and their impact on systemic inflammatory conditions. The focus was on individuals with conditions such as periodontitis, diabetes, Alzheimer’s disease, and cardiovascular diseases, as these conditions have been linked to imbalances in the oral and gut microbiome.

What were the most important findings of this study?

Oral-Gut Dysbiosis and Systemic Inflammation: The study confirmed a strong connection between imbalances in the oral and gut microbiomes (oral-gut dysbiosis) and chronic systemic inflammation, which is implicated in various inflammatory diseases such as periodontitis, diabetes, Alzheimer’s disease, and cardiovascular diseases.

Microbiome-Host Crosstalk: The review detailed the mechanisms of microbiome-host interactions, highlighting how these interactions contribute to systemic inflammation and disease. It emphasized the role of microbial metabolites, particularly short-chain fatty acids (SCFAs), in mediating these effects.

Precision Medicine Approaches: The study discussed emerging precision medicine strategies for modulating the microbiome to control systemic inflammation. These approaches include targeted therapies that aim to restore a healthy microbiome balance and reduce the risk of periodontitis-associated diseases.

Knowledge Gaps: Despite advances, significant knowledge gaps remain, particularly in understanding the causal relationships between specific microbiome alterations and the metabolites they produce, and how these contribute to periodontitis and systemic inflammation.

What are the greatest implications of this study?

Potential for New Therapies: Understanding the microbiome-host interactions and the role of microbial metabolites in systemic inflammation could lead to the development of novel therapeutic strategies. These therapies could potentially reduce the risk of periodontitis-associated diseases and other inflammatory conditions by restoring a healthy microbiome balance.

Precision Medicine: The move towards precision medicine approaches in microbiome modulation represents a significant shift in treating inflammatory diseases. These strategies could offer more personalized and effective treatments by targeting specific microbiome imbalances and their metabolic byproducts.

Interconnected Health: The study underscores the interconnected nature of oral and gut health with overall systemic health. By addressing oral-gut dysbiosis, it may be possible to mitigate chronic systemic inflammation and its related diseases, highlighting the importance of holistic approaches in healthcare.

Need for Further Research: The study highlights critical areas for future research, particularly the need for more clinical trials to validate the efficacy of microbiome-targeted therapies. Understanding the specific mechanisms of microbiome-host interactions and their impact on systemic inflammation remains essential for advancing these therapeutic approaches.

Preventive Health: The findings suggest that microbiome modulation could play a crucial role in the prevention of chronic inflammatory diseases. This preventative approach could improve health outcomes and reduce the burden of these diseases on healthcare systems.

 

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