Dietary Strategies for Management of Metabolic Syndrome: Role of Gut Microbiota Metabolites.
Sonia CrociLina Ilaras D'ApolitoValeria GasperiMaria Valeria CataniIsabella SaviniPublished in: Nutrients (2021)
Metabolic syndrome (MetS) is a complex pathophysiological state with incidence similar to that of a global epidemic and represents a risk factor for the onset of chronic non-communicable degenerative diseases (NCDDs), including cardiovascular disease (CVD), type 2 diabetes mellitus, chronic kidney disease, and some types of cancer. A plethora of literature data suggest the potential role of gut microbiota in interfering with the host metabolism, thus influencing several MetS risk factors. Perturbation of the gut microbiota's composition and activity, a condition known as dysbiosis, is involved in the etiopathogenesis of multiple chronic diseases. Recent studies have shown that some micro-organism-derived metabolites (including trimethylamine N-oxide (TMAO), lipopolysaccharide (LPS) of Gram-negative bacteria, indoxyl sulfate and p-cresol sulfate) induce subclinical inflammatory processes involved in MetS. Gut microbiota's taxonomic species or abundance are modified by many factors, including diet, lifestyle and medications. The main purpose of this review is to highlight the correlation between different dietary strategies and changes in gut microbiota metabolites. We mainly focus on the validity/inadequacy of specific dietary patterns to reduce inflammatory processes, including leaky gut and subsequent endotoxemia. We also describe the chance of probiotic supplementation to interact with the immune system and limit negative consequences associated with MetS.
Keyphrases
- metabolic syndrome
- risk factors
- cardiovascular disease
- chronic kidney disease
- ms ms
- inflammatory response
- physical activity
- cardiovascular risk factors
- type diabetes
- end stage renal disease
- oxidative stress
- weight loss
- uric acid
- lps induced
- squamous cell carcinoma
- immune response
- toll like receptor
- machine learning
- young adults
- electronic health record
- antibiotic resistance genes
- peritoneal dialysis
- microbial community
- glycemic control
- anaerobic digestion