| Literature DB >> 26590448 |
Ali Ramezani1, Ziad A Massy2, Björn Meijers3, Pieter Evenepoel3, Raymond Vanholder4, Dominic S Raj5.
Abstract
Also known as the "second human genome," the gut microbiome plays important roles in both the maintenance of health and the pathogenesis of disease. The symbiotic relationship between host and microbiome is disturbed due to the proliferation of dysbiotic bacteria in patients with chronic kidney disease (CKD). Fermentation of protein and amino acids by gut bacteria generates excess amounts of potentially toxic compounds such as ammonia, amines, thiols, phenols, and indoles, but the generation of short-chain fatty acids is reduced. Impaired intestinal barrier function in patients with CKD permits translocation of gut-derived uremic toxins into the systemic circulation, contributing to the progression of CKD, cardiovascular disease, insulin resistance, and protein-energy wasting. The field of microbiome research is still nascent, but is evolving rapidly. Establishing symbiosis to treat uremic syndrome is a novel concept, but if proved effective, it will have a significant impact on the management of patients with CKD.Entities:
Keywords: Gut microbiome; amine; ammonia; chronic kidney disease (CKD); end-stage renal disease (ESRD); indole; metabolome; microbial metabolite; p-cresyl sulfate (PCS); phenol; review; thiol; urea; uremic syndrome; uremic toxin
Mesh:
Year: 2015 PMID: 26590448 PMCID: PMC5408507 DOI: 10.1053/j.ajkd.2015.09.027
Source DB: PubMed Journal: Am J Kidney Dis ISSN: 0272-6386 Impact factor: 8.860