Key result
Gut dysbiosis and altered microbial metabolites link to the development and progression of cardiovascular disease.
Answers are grounded in this paper and cite their sources.
The microbiota of the gastrointestinal tract (GIT) is an extremely diverse community of microorganisms, and their collective genomes (microbiome) provide a vast arsenal of biological activities, particularly enzymatic ones, which are far from being fully elucidated. The study of the microbiota (and the microbiome) is receiving great interest from the biomedical community because it carries the potential to improve risk prediction models, refine primary and secondary prevention efforts, and also design more appropriate and personalized therapies, including pharmacological ones. A growing body of evidence, although sometimes impaired by the limited number of subjects involved in the studies, suggests that GIT dysbiosis, that is, the altered microbial composition, has an important role in causing and/or worsening cardiovascular disease (CVD). Bacterial translocation and the alteration of levels of microbe-derived metabolites can thus be important to monitor and modulate because they may lead to initiation and progression of CVD and to its establishment as chronic state. We hereby aim to provide readers with details on available resources and experimental approaches that are used in this fascinating field of biomedical research and on some novelties on the impact of GIT microbiota on CVD.
No takes yet. Share an insight, caveat, or question.
Akyıldız et al. (2022) conducted a review in Cardiovascular disease. Gastrointestinal tract dysbiosis was evaluated. Gastrointestinal tract dysbiosis and altered microbe-derived metabolites appear to play an important role in initiating and worsening cardiovascular disease.
Synapse has enriched 10 related papers. Consider them for comparative context: